11-10597949-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10597949
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10597949
    reference: chr 11
allele count: 2
allele frequency: 1.657577616071872e-5
allele num: 120658
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*2194C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1724C>T
  hgvsp: ENSP00000453013.1:p.Thr575Ile
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.2396C>T
  hgvsp: ENSP00000432067.2:p.Thr799Ile
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1724C>T
  hgvsp: ENSP00000441971.1:p.Thr575Ile
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.2051C>T
  hgvsp: ENSP00000437784.1:p.Thr684Ile
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2669C>T
  hgvsp: ENSP00000412130.2:p.Thr890Ile
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.2396C>T
  hgvsp: ENSP00000446764.1:p.Thr799Ile
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2588C>T
  hgvsp: ENSP00000412229.1:p.Thr863Ile
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2645C>T
  hgvsp: ENSP00000432436.1:p.Thr882Ile
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-17715G>A
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.2396C>T
  hgvsp: ENSP00000448278.1:p.Thr799Ile
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1724C>T
  hgvsp: ENSP00000401205.1:p.Thr575Ile
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2642C>T
  hgvsp: ENSP00000414598.1:p.Thr881Ile
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.124-12172C>T
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.247-9625G>A
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1724C>T
  hgvsp: ENSP00000433296.2:p.Thr575Ile
  variant of: http://identifiers.org/hgnc/7237
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1041
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19888
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19040
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr890Ile
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum

11-10597949-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10597949
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10597949
    reference: chr 11
allele count: 3
allele frequency: 2.486366424107809e-5
allele num: 120658
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1724C>G
  hgvsp: ENSP00000441971.1:p.Thr575Ser
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.2396C>G
  hgvsp: ENSP00000432067.2:p.Thr799Ser
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*2194C>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.2396C>G
  hgvsp: ENSP00000446764.1:p.Thr799Ser
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.247-9625G>C
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1724C>G
  hgvsp: ENSP00000401205.1:p.Thr575Ser
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1724C>G
  hgvsp: ENSP00000453013.1:p.Thr575Ser
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.2396C>G
  hgvsp: ENSP00000448278.1:p.Thr799Ser
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2588C>G
  hgvsp: ENSP00000412229.1:p.Thr863Ser
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1724C>G
  hgvsp: ENSP00000433296.2:p.Thr575Ser
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2642C>G
  hgvsp: ENSP00000414598.1:p.Thr881Ser
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2669C>G
  hgvsp: ENSP00000412130.2:p.Thr890Ser
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.2051C>G
  hgvsp: ENSP00000437784.1:p.Thr684Ser
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2645C>G
  hgvsp: ENSP00000432436.1:p.Thr882Ser
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.124-12172C>G
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-17715G>C
  variant of: http://identifiers.org/hgnc/43434
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19040
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4436
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr890Ser
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: African
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

11-10597954-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10597954
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10597954
    reference: chr 11
allele count: 3
allele frequency: 2.486201581224206e-5
allele num: 120666
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*2189A>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.2391A>T
  hgvsp: ENSP00000446764.1:p.Arg797Ser
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2664A>T
  hgvsp: ENSP00000412130.2:p.Arg888Ser
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.2046A>T
  hgvsp: ENSP00000437784.1:p.Arg682Ser
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1719A>T
  hgvsp: ENSP00000433296.2:p.Arg573Ser
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.2391A>T
  hgvsp: ENSP00000448278.1:p.Arg797Ser
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1719A>T
  hgvsp: ENSP00000441971.1:p.Arg573Ser
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.124-12177A>T
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2637A>T
  hgvsp: ENSP00000414598.1:p.Arg879Ser
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.2391A>T
  hgvsp: ENSP00000432067.2:p.Arg797Ser
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-17710T>A
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2583A>T
  hgvsp: ENSP00000412229.1:p.Arg861Ser
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1719A>T
  hgvsp: ENSP00000401205.1:p.Arg573Ser
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.247-9620T>A
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1719A>T
  hgvsp: ENSP00000453013.1:p.Arg573Ser
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2640A>T
  hgvsp: ENSP00000432436.1:p.Arg880Ser
  variant of: http://identifiers.org/hgnc/7237
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19048
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4438
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Arg888Ser
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

11-10597964-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10597964
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10597964
    reference: chr 11
allele count: 1
allele frequency: 8.285553309249991e-6
allele num: 120692
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.2036C>A
  hgvsp: ENSP00000437784.1:p.Pro679His
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1709C>A
  hgvsp: ENSP00000433296.2:p.Pro570His
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.2381C>A
  hgvsp: ENSP00000448278.1:p.Pro794His
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1709C>A
  hgvsp: ENSP00000441971.1:p.Pro570His
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.2381C>A
  hgvsp: ENSP00000432067.2:p.Pro794His
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2627C>A
  hgvsp: ENSP00000414598.1:p.Pro876His
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.2381C>A
  hgvsp: ENSP00000446764.1:p.Pro794His
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1709C>A
  hgvsp: ENSP00000453013.1:p.Pro570His
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2630C>A
  hgvsp: ENSP00000432436.1:p.Pro877His
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-17700G>T
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2573C>A
  hgvsp: ENSP00000412229.1:p.Pro858His
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1709C>A
  hgvsp: ENSP00000401205.1:p.Pro570His
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.124-12187C>A
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2654C>A
  hgvsp: ENSP00000412130.2:p.Pro885His
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.247-9610G>T
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*2179C>A
  variant of: http://identifiers.org/hgnc/7237
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19057
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19811
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11600
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro885His
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
population: Latino
population: African
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff

11-10597965-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10597965
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10597965
    reference: chr 11
allele count: 1
allele frequency: 8.285004142502071e-6
allele num: 120700
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.124-12188C>G
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2629C>G
  hgvsp: ENSP00000432436.1:p.Pro877Ala
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.2035C>G
  hgvsp: ENSP00000437784.1:p.Pro679Ala
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.2380C>G
  hgvsp: ENSP00000446764.1:p.Pro794Ala
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*2178C>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2653C>G
  hgvsp: ENSP00000412130.2:p.Pro885Ala
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.247-9609G>C
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1708C>G
  hgvsp: ENSP00000401205.1:p.Pro570Ala
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1708C>G
  hgvsp: ENSP00000453013.1:p.Pro570Ala
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1708C>G
  hgvsp: ENSP00000433296.2:p.Pro570Ala
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.2380C>G
  hgvsp: ENSP00000432067.2:p.Pro794Ala
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.2380C>G
  hgvsp: ENSP00000448278.1:p.Pro794Ala
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2626C>G
  hgvsp: ENSP00000414598.1:p.Pro876Ala
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2572C>G
  hgvsp: ENSP00000412229.1:p.Pro858Ala
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1708C>G
  hgvsp: ENSP00000441971.1:p.Pro570Ala
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-17699G>C
  variant of: http://identifiers.org/hgnc/43434
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Pro885Ala
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/11-10597974-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10597974
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10597974
    reference: chr 11
allele count: 1
allele frequency: 8.283906027370025e-6
allele num: 120716
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1699G>T
  hgvsp: ENSP00000441971.1:p.Ala567Ser
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.2026G>T
  hgvsp: ENSP00000437784.1:p.Ala676Ser
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2644G>T
  hgvsp: ENSP00000412130.2:p.Ala882Ser
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.2371G>T
  hgvsp: ENSP00000446764.1:p.Ala791Ser
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2563G>T
  hgvsp: ENSP00000412229.1:p.Ala855Ser
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2617G>T
  hgvsp: ENSP00000414598.1:p.Ala873Ser
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1699G>T
  hgvsp: ENSP00000433296.2:p.Ala567Ser
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-17690C>A
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1699G>T
  hgvsp: ENSP00000453013.1:p.Ala567Ser
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.2371G>T
  hgvsp: ENSP00000432067.2:p.Ala791Ser
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2620G>T
  hgvsp: ENSP00000432436.1:p.Ala874Ser
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.124-12197G>T
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.247-9600C>A
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1699G>T
  hgvsp: ENSP00000401205.1:p.Ala567Ser
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.2371G>T
  hgvsp: ENSP00000448278.1:p.Ala791Ser
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*2169G>T
  variant of: http://identifiers.org/hgnc/7237
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19060
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11612
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala882Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: African
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

11-10597977-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10597977
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10597977
    reference: chr 11
allele count: 1
allele frequency: 8.28349430923941e-6
allele num: 120722
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2560C>G
  hgvsp: ENSP00000412229.1:p.Gln854Glu
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1696C>G
  hgvsp: ENSP00000453013.1:p.Gln566Glu
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.124-12200C>G
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-17687G>C
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.2023C>G
  hgvsp: ENSP00000437784.1:p.Gln675Glu
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.247-9597G>C
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2617C>G
  hgvsp: ENSP00000432436.1:p.Gln873Glu
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.2368C>G
  hgvsp: ENSP00000446764.1:p.Gln790Glu
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2614C>G
  hgvsp: ENSP00000414598.1:p.Gln872Glu
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1696C>G
  hgvsp: ENSP00000401205.1:p.Gln566Glu
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.2368C>G
  hgvsp: ENSP00000432067.2:p.Gln790Glu
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*2166C>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2641C>G
  hgvsp: ENSP00000412130.2:p.Gln881Glu
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.2368C>G
  hgvsp: ENSP00000448278.1:p.Gln790Glu
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1696C>G
  hgvsp: ENSP00000441971.1:p.Gln566Glu
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1696C>G
  hgvsp: ENSP00000433296.2:p.Gln566Glu
  variant of: http://identifiers.org/hgnc/7237
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19797
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln881Glu
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

11-10597984-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10597984
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10597984
    reference: chr 11
allele count: 4
allele frequency: 3.312958637711408e-5
allele num: 120738
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.2361T>C
  hgvsp: ENST00000527509.2:c.2361T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.2361T>C
  hgvsp: ENST00000552103.1:c.2361T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.2361T>C
  hgvsp: ENST00000547195.1:c.2361T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2553T>C
  hgvsp: ENST00000436272.1:c.2553T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-17680A>G
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1689T>C
  hgvsp: ENST00000424001.1:c.1689T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2634T>C
  hgvsp: ENST00000423302.2:c.2634T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2607T>C
  hgvsp: ENST00000421747.1:c.2607T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*2159T>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1689T>C
  hgvsp: ENST00000534266.2:c.1689T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.247-9590A>G
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.2016T>C
  hgvsp: ENST00000541483.1:c.2016T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2610T>C
  hgvsp: ENST00000531107.1:c.2610T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1689T>C
  hgvsp: ENST00000545852.1:c.1689T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1689T>C
  hgvsp: ENST00000558540.1:c.1689T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.124-12207T>C
  variant of: http://identifiers.org/hgnc/14687
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11607
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19794
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2024
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys878Cys
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
reference allele: A
site quality: FS
site quality: DP
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

11-10597986-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10597986
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10597986
    reference: chr 11
allele count: 1
allele frequency: 8.28239659427852e-6
allele num: 120738
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2608T>C
  hgvsp: ENSP00000432436.1:p.Cys870Arg
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.2359T>C
  hgvsp: ENSP00000432067.2:p.Cys787Arg
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.2014T>C
  hgvsp: ENSP00000437784.1:p.Cys672Arg
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2551T>C
  hgvsp: ENSP00000412229.1:p.Cys851Arg
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-17678A>G
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.247-9588A>G
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*2157T>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.2359T>C
  hgvsp: ENSP00000446764.1:p.Cys787Arg
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2632T>C
  hgvsp: ENSP00000412130.2:p.Cys878Arg
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2605T>C
  hgvsp: ENSP00000414598.1:p.Cys869Arg
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1687T>C
  hgvsp: ENSP00000441971.1:p.Cys563Arg
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.2359T>C
  hgvsp: ENSP00000448278.1:p.Cys787Arg
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1687T>C
  hgvsp: ENSP00000401205.1:p.Cys563Arg
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1687T>C
  hgvsp: ENSP00000433296.2:p.Cys563Arg
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.124-12209T>C
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1687T>C
  hgvsp: ENSP00000453013.1:p.Cys563Arg
  variant of: http://identifiers.org/hgnc/7237
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 595
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys878Arg
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: Other
reference allele: A
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: MQ

11-10597988-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10597988
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10597988
    reference: chr 11
allele count: 1
allele frequency: 8.282533792737874e-6
allele num: 120736
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2603C>A
  hgvsp: ENSP00000414598.1:p.Ser868Tyr
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.2357C>A
  hgvsp: ENSP00000448278.1:p.Ser786Tyr
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.124-12211C>A
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.2357C>A
  hgvsp: ENSP00000446764.1:p.Ser786Tyr
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.2357C>A
  hgvsp: ENSP00000432067.2:p.Ser786Tyr
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1685C>A
  hgvsp: ENSP00000441971.1:p.Ser562Tyr
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1685C>A
  hgvsp: ENSP00000401205.1:p.Ser562Tyr
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2630C>A
  hgvsp: ENSP00000412130.2:p.Ser877Tyr
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1685C>A
  hgvsp: ENSP00000433296.2:p.Ser562Tyr
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.2012C>A
  hgvsp: ENSP00000437784.1:p.Ser671Tyr
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1685C>A
  hgvsp: ENSP00000453013.1:p.Ser562Tyr
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2549C>A
  hgvsp: ENSP00000412229.1:p.Ser850Tyr
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-17676G>T
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*2155C>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.247-9586G>T
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2606C>A
  hgvsp: ENSP00000432436.1:p.Ser869Tyr
  variant of: http://identifiers.org/hgnc/7237
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19056
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11610
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2023
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4474
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser877Tyr
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

11-10597994-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10597994
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10597994
    reference: chr 11
allele count: 2
allele frequency: 1.656479318855704e-5
allele num: 120738
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.2351A>G
  hgvsp: ENSP00000448278.1:p.Tyr784Cys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.124-12217A>G
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-17670T>C
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1679A>G
  hgvsp: ENSP00000441971.1:p.Tyr560Cys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2597A>G
  hgvsp: ENSP00000414598.1:p.Tyr866Cys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2600A>G
  hgvsp: ENSP00000432436.1:p.Tyr867Cys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.247-9580T>C
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*2149A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.2006A>G
  hgvsp: ENSP00000437784.1:p.Tyr669Cys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.2351A>G
  hgvsp: ENSP00000432067.2:p.Tyr784Cys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2624A>G
  hgvsp: ENSP00000412130.2:p.Tyr875Cys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2543A>G
  hgvsp: ENSP00000412229.1:p.Tyr848Cys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1679A>G
  hgvsp: ENSP00000401205.1:p.Tyr560Cys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1679A>G
  hgvsp: ENSP00000433296.2:p.Tyr560Cys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.2351A>G
  hgvsp: ENSP00000446764.1:p.Tyr784Cys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1679A>G
  hgvsp: ENSP00000453013.1:p.Tyr560Cys
  variant of: http://identifiers.org/hgnc/7237
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4476
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr875Cys
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: T
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP

11-10598000-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10598000
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10598000
    reference: chr 11
allele count: 1
allele frequency: 8.282122210995345e-6
allele num: 120742
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.2000A>G
  hgvsp: ENSP00000437784.1:p.Asn667Ser
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1673A>G
  hgvsp: ENSP00000401205.1:p.Asn558Ser
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*2143A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.2345A>G
  hgvsp: ENSP00000446764.1:p.Asn782Ser
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2594A>G
  hgvsp: ENSP00000432436.1:p.Asn865Ser
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.2345A>G
  hgvsp: ENSP00000448278.1:p.Asn782Ser
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2537A>G
  hgvsp: ENSP00000412229.1:p.Asn846Ser
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1673A>G
  hgvsp: ENSP00000433296.2:p.Asn558Ser
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.2345A>G
  hgvsp: ENSP00000432067.2:p.Asn782Ser
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1673A>G
  hgvsp: ENSP00000441971.1:p.Asn558Ser
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1673A>G
  hgvsp: ENSP00000453013.1:p.Asn558Ser
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2591A>G
  hgvsp: ENSP00000414598.1:p.Asn864Ser
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2618A>G
  hgvsp: ENSP00000412130.2:p.Asn873Ser
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.124-12223A>G
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-17664T>C
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.247-9574T>C
  variant of: http://identifiers.org/hgnc/43434
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4478
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19045
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn873Ser
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: QD

11-10598005-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10598005
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10598005
    reference: chr 11
allele count: 1
allele frequency: 8.282122210995345e-6
allele num: 120742
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1995C>G
  hgvsp: ENST00000541483.1:c.1995C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2532C>G
  hgvsp: ENST00000436272.1:c.2532C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1668C>G
  hgvsp: ENST00000534266.2:c.1668C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1668C>G
  hgvsp: ENST00000424001.1:c.1668C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.247-9569G>C
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*2138C>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2586C>G
  hgvsp: ENST00000421747.1:c.2586C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-17659G>C
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.2340C>G
  hgvsp: ENST00000552103.1:c.2340C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1668C>G
  hgvsp: ENST00000545852.1:c.1668C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.2340C>G
  hgvsp: ENST00000547195.1:c.2340C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.124-12228C>G
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.2340C>G
  hgvsp: ENST00000527509.2:c.2340C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1668C>G
  hgvsp: ENST00000558540.1:c.1668C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2589C>G
  hgvsp: ENST00000531107.1:c.2589C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2613C>G
  hgvsp: ENST00000423302.2:c.2613C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2032
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 594
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19040
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu871Leu
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: African
reference allele: G
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

11-10598018-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10598018
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10598018
    reference: chr 11
allele count: 4
allele frequency: 3.312574532926991e-5
allele num: 120752
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1982T>C
  hgvsp: ENSP00000437784.1:p.Val661Ala
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2600T>C
  hgvsp: ENSP00000412130.2:p.Val867Ala
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2576T>C
  hgvsp: ENSP00000432436.1:p.Val859Ala
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1655T>C
  hgvsp: ENSP00000401205.1:p.Val552Ala
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1655T>C
  hgvsp: ENSP00000453013.1:p.Val552Ala
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1655T>C
  hgvsp: ENSP00000441971.1:p.Val552Ala
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.124-12241T>C
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.247-9556A>G
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.2327T>C
  hgvsp: ENSP00000432067.2:p.Val776Ala
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.2327T>C
  hgvsp: ENSP00000448278.1:p.Val776Ala
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1655T>C
  hgvsp: ENSP00000433296.2:p.Val552Ala
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2519T>C
  hgvsp: ENSP00000412229.1:p.Val840Ala
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.2327T>C
  hgvsp: ENSP00000446764.1:p.Val776Ala
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2573T>C
  hgvsp: ENSP00000414598.1:p.Val858Ala
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*2125T>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-17646A>G
  variant of: http://identifiers.org/hgnc/43434
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4477
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1062
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Val867Ala
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum

11-10598023-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10598023
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10598023
    reference: chr 11
allele count: 1
allele frequency: 8.281299170213822e-6
allele num: 120754
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1650G>A
  hgvsp: ENST00000558540.1:c.1650G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.247-9551C>T
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2568G>A
  hgvsp: ENST00000421747.1:c.2568G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1650G>A
  hgvsp: ENST00000545852.1:c.1650G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.2322G>A
  hgvsp: ENST00000527509.2:c.2322G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-17641C>T
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2595G>A
  hgvsp: ENST00000423302.2:c.2595G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1650G>A
  hgvsp: ENST00000424001.1:c.1650G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2571G>A
  hgvsp: ENST00000531107.1:c.2571G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1977G>A
  hgvsp: ENST00000541483.1:c.1977G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.2322G>A
  hgvsp: ENST00000552103.1:c.2322G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*2120G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1650G>A
  hgvsp: ENST00000534266.2:c.1650G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.124-12246G>A
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2514G>A
  hgvsp: ENST00000436272.1:c.2514G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.2322G>A
  hgvsp: ENST00000547195.1:c.2322G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4477
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11605
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19804
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu865Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Latino
population: Other
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ

http://identifiers.org/exac.variant/11-10598025-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10598025
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10598025
    reference: chr 11
allele count: 1
allele frequency: 8.281024859636628e-6
allele num: 120758
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.2320T>G
  hgvsp: ENSP00000448278.1:p.Leu774Val
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.247-9549A>C
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1975T>G
  hgvsp: ENSP00000437784.1:p.Leu659Val
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2512T>G
  hgvsp: ENSP00000412229.1:p.Leu838Val
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1648T>G
  hgvsp: ENSP00000453013.1:p.Leu550Val
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.2320T>G
  hgvsp: ENSP00000432067.2:p.Leu774Val
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.2320T>G
  hgvsp: ENSP00000446764.1:p.Leu774Val
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1648T>G
  hgvsp: ENSP00000441971.1:p.Leu550Val
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1648T>G
  hgvsp: ENSP00000433296.2:p.Leu550Val
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1648T>G
  hgvsp: ENSP00000401205.1:p.Leu550Val
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.124-12248T>G
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-17639A>C
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2566T>G
  hgvsp: ENSP00000414598.1:p.Leu856Val
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*2118T>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2593T>G
  hgvsp: ENSP00000412130.2:p.Leu865Val
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2569T>G
  hgvsp: ENSP00000432436.1:p.Leu857Val
  variant of: http://identifiers.org/hgnc/7237
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19804
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4478
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu865Val
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: African
reference allele: A
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQ

11-10598044-CATCATCCAG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10598044
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10598035
    reference: chr 11
allele count: 1
allele frequency: 8.281299170213822e-6
allele num: 120754
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsp: ENSP00000414598.1:p.Ile846_Met848del
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsp: ENSP00000453013.1:p.Ile540_Met542del
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsp: ENSP00000412130.2:p.Ile855_Met857del
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsp: ENSP00000432436.1:p.Ile847_Met849del
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsp: ENSP00000437784.1:p.Ile649_Met651del
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsp: ENSP00000441971.1:p.Ile540_Met542del
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsp: ENSP00000448278.1:p.Ile764_Met766del
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsp: ENSP00000432067.2:p.Ile764_Met766del
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsp: ENSP00000412229.1:p.Ile828_Met830del
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsp: ENSP00000401205.1:p.Ile540_Met542del
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsp: ENSP00000446764.1:p.Ile764_Met766del
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsp: ENSP00000433296.2:p.Ile540_Met542del
  variant of: http://identifiers.org/hgnc/7237
canonical: true
consequence: inframe deletion
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1062
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11603
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19036
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile855_Met857del
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: CATCATCCAG
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: DP

11-10598084-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10598084
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10598084
    reference: chr 11
allele count: 1
allele frequency: 8.281162012653616e-6
allele num: 120756
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.2261A>G
  hgvsp: ENSP00000432067.2:p.Tyr754Cys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2510A>G
  hgvsp: ENSP00000432436.1:p.Tyr837Cys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1916A>G
  hgvsp: ENSP00000437784.1:p.Tyr639Cys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1589A>G
  hgvsp: ENSP00000441971.1:p.Tyr530Cys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2453A>G
  hgvsp: ENSP00000412229.1:p.Tyr818Cys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1589A>G
  hgvsp: ENSP00000453013.1:p.Tyr530Cys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1589A>G
  hgvsp: ENSP00000401205.1:p.Tyr530Cys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.2261A>G
  hgvsp: ENSP00000446764.1:p.Tyr754Cys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.124-12307A>G
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2534A>G
  hgvsp: ENSP00000412130.2:p.Tyr845Cys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2507A>G
  hgvsp: ENSP00000414598.1:p.Tyr836Cys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-17580T>C
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.2261A>G
  hgvsp: ENSP00000448278.1:p.Tyr754Cys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1589A>G
  hgvsp: ENSP00000433296.2:p.Tyr530Cys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.247-9490T>C
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*2059A>G
  variant of: http://identifiers.org/hgnc/7237
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2033
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr845Cys
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: T
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: DP
site quality: VQSLOD

11-10598098-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10598098
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10598098
    reference: chr 11
allele count: 3
allele frequency: 2.484430899695243e-5
allele num: 120752
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.2247C>A
  hgvsp: ENSP00000446764.1:p.Phe749Leu
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.2247C>A
  hgvsp: ENSP00000432067.2:p.Phe749Leu
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.247-9476G>T
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.124-12321C>A
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2520C>A
  hgvsp: ENSP00000412130.2:p.Phe840Leu
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-17566G>T
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1902C>A
  hgvsp: ENSP00000437784.1:p.Phe634Leu
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1575C>A
  hgvsp: ENSP00000401205.1:p.Phe525Leu
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2439C>A
  hgvsp: ENSP00000412229.1:p.Phe813Leu
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1575C>A
  hgvsp: ENSP00000453013.1:p.Phe525Leu
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1575C>A
  hgvsp: ENSP00000441971.1:p.Phe525Leu
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.2247C>A
  hgvsp: ENSP00000448278.1:p.Phe749Leu
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*2045C>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1575C>A
  hgvsp: ENSP00000433296.2:p.Phe525Leu
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2493C>A
  hgvsp: ENSP00000414598.1:p.Phe831Leu
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2496C>A
  hgvsp: ENSP00000432436.1:p.Phe832Leu
  variant of: http://identifiers.org/hgnc/7237
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19795
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2033
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4475
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe840Leu
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff

11-10598101-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10598101
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10598101
    reference: chr 11
allele count: 1
allele frequency: 8.281710670156027e-6
allele num: 120748
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2493T>C
  hgvsp: ENST00000531107.1:c.2493T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.2244T>C
  hgvsp: ENST00000527509.2:c.2244T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2436T>C
  hgvsp: ENST00000436272.1:c.2436T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1899T>C
  hgvsp: ENST00000541483.1:c.1899T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.2244T>C
  hgvsp: ENST00000547195.1:c.2244T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1572T>C
  hgvsp: ENST00000534266.2:c.1572T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2517T>C
  hgvsp: ENST00000423302.2:c.2517T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.2244T>C
  hgvsp: ENST00000552103.1:c.2244T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1572T>C
  hgvsp: ENST00000545852.1:c.1572T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2490T>C
  hgvsp: ENST00000421747.1:c.2490T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*2042T>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1572T>C
  hgvsp: ENST00000558540.1:c.1572T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-17563A>G
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1572T>C
  hgvsp: ENST00000424001.1:c.1572T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.247-9473A>G
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.124-12324T>C
  variant of: http://identifiers.org/hgnc/14687
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19032
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11591
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19792
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His839His
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

11-10598131-GA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10598131
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10598130
    reference: chr 11
allele count: 9
allele frequency: 7.486897928624906e-5
allele num: 120210
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.2223-10delT
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1878-10delT
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2415-10delT
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.124-12355delT
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.2223-10delT
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.247-9435delA
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2472-10delT
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1551-10delT
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*2021-10delT
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1551-10delT
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1551-10delT
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2496-10delT
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2469-10delT
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-17525delA
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1551-10delT
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.2223-10delT
  variant of: http://identifiers.org/hgnc/7237
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 11435
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2081
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19513
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18806
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
reference allele: GA
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum

11-10598131-G-GA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10598131
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10598132
    reference: chr 11
allele count: 2
allele frequency: 1.663755095249979e-5
allele num: 120210
alternate allele: GA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2415-10dupT
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*2021-10dupT
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.2223-10dupT
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.2223-10dupT
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.2223-10dupT
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1551-10dupT
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2472-10dupT
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.124-12355dupT
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.247-9435dupA
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2496-10dupT
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2469-10dupT
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1878-10dupT
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1551-10dupT
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1551-10dupT
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-17525dupA
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1551-10dupT
  variant of: http://identifiers.org/hgnc/7237
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18806
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19513
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2081
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1107
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum

11-10598140-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10598140
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10598140
    reference: chr 11
allele count: 1
allele frequency: 8.302200083022e-6
allele num: 120450
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1551-18A>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.2223-18A>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1551-18A>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.2223-18A>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1551-18A>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1878-18A>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.124-12363A>T
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.247-9434T>A
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2496-18A>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.2223-18A>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1551-18A>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2472-18A>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2469-18A>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2415-18A>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*2021-18A>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-17524T>A
  variant of: http://identifiers.org/hgnc/43434
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18829
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19412
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1999
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: T
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS

11-10598141-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10598141
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10598141
    reference: chr 11
allele count: 1
allele frequency: 8.302475798283047e-6
allele num: 120446
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.2223-19T>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.124-12364T>A
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1551-19T>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*2021-19T>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.2223-19T>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2496-19T>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1878-19T>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2415-19T>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.247-9433A>T
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1551-19T>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2469-19T>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-17523A>T
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1551-19T>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2472-19T>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.2223-19T>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1551-19T>A
  variant of: http://identifiers.org/hgnc/7237
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19377
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18809
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum

11-10598142-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10598142
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10598142
    reference: chr 11
allele count: 1
allele frequency: 8.303165166561494e-6
allele num: 120436
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2469-20A>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1551-20A>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2472-20A>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*2021-20A>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1551-20A>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.124-12365A>T
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.2223-20A>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1551-20A>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2496-20A>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1878-20A>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.247-9432T>A
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2415-20A>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.2223-20A>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-17522T>A
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.2223-20A>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1551-20A>T
  variant of: http://identifiers.org/hgnc/7237
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18725
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19334
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: East Asian
population: African
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ

11-10598143-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10598143
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10598143
    reference: chr 11
allele count: 1
allele frequency: 8.304544246611745e-6
allele num: 120416
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.124-12366C>A
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2469-21C>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2496-21C>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2415-21C>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.2223-21C>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2472-21C>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1551-21C>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*2021-21C>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.2223-21C>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1551-21C>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1551-21C>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1878-21C>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-17521G>T
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1551-21C>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.247-9431G>T
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.2223-21C>A
  variant of: http://identifiers.org/hgnc/7237
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1993
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4394
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11321
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: South Asian
population: African
population: European (Finnish)
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: DP

11-10598148-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10598148
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10598148
    reference: chr 11
allele count: 1
allele frequency: 8.307579835842223e-6
allele num: 120372
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1551-26C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.2223-26C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1551-26C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2496-26C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*2021-26C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.247-9426G>A
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2469-26C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.2223-26C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1551-26C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.124-12371C>T
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1878-26C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2472-26C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1551-26C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2415-26C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-17516G>A
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.2223-26C>T
  variant of: http://identifiers.org/hgnc/7237
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19191
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD

11-10598150-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10598150
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10598150
    reference: chr 11
allele count: 1
allele frequency: 8.312137383006666e-6
allele num: 120306
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1551-28G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1878-28G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.2223-28G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.2223-28G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2472-28G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2415-28G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.2223-28G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.124-12373G>A
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1551-28G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1551-28G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1551-28G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.247-9424C>T
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*2021-28G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2496-28G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2469-28G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-17514C>T
  variant of: http://identifiers.org/hgnc/43434
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1032
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19031
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4328
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1048
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18283
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1980
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum

11-10598151-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10598151
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10598151
    reference: chr 11
allele count: 1
allele frequency: 8.311861025683651e-6
allele num: 120310
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.2223-29A>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1551-29A>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.247-9423T>G
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.2223-29A>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2415-29A>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1878-29A>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.2223-29A>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1551-29A>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.124-12374A>C
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*2021-29A>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2496-29A>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-17513T>G
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2469-29A>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2472-29A>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1551-29A>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1551-29A>C
  variant of: http://identifiers.org/hgnc/7237
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11047
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19037
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18317
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ

11-10598158-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10598158
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10598158
    reference: chr 11
allele count: 1
allele frequency: 8.317114959162966e-6
allele num: 120234
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-17506T>C
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1551-36A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1551-36A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.2223-36A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.247-9416T>C
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2415-36A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.2223-36A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2469-36A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*2021-36A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.2223-36A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.124-12381A>G
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1878-36A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2472-36A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1551-36A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2496-36A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1551-36A>G
  variant of: http://identifiers.org/hgnc/7237
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1103
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4286
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10875
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1048
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1768
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: VQSLOD

11-10598162-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10598162
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10598162
    reference: chr 11
allele count: 5
allele frequency: 4.161672659475296e-5
allele num: 120144
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2496-40C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2415-40C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.124-12385C>T
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.2223-40C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.2223-40C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2469-40C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1551-40C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2472-40C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.247-9412G>A
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*2021-40C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1551-40C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1878-40C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1551-40C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-17502G>A
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.2223-40C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1551-40C>T
  variant of: http://identifiers.org/hgnc/7237
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1108
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10765
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/11-10598165-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10598165
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10598165
    reference: chr 11
allele count: 1
allele frequency: 8.332361224523806e-6
allele num: 120014
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1551-43G>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2496-43G>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1551-43G>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2472-43G>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1551-43G>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.2223-43G>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*2021-43G>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2469-43G>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.2223-43G>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1878-43G>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2415-43G>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-17499C>A
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.124-12388G>T
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1551-43G>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.2223-43G>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.247-9409C>A
  variant of: http://identifiers.org/hgnc/43434
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4273
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19146
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: South Asian
population: East Asian
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

11-10598166-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10598166
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10598166
    reference: chr 11
allele count: 1
allele frequency: 8.327088017320342e-6
allele num: 120090
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-17498A>G
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1551-44T>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.247-9408A>G
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2496-44T>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.2223-44T>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1551-44T>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1878-44T>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.2223-44T>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2472-44T>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*2021-44T>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2415-44T>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1551-44T>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.124-12389T>C
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.2223-44T>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2469-44T>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1551-44T>C
  variant of: http://identifiers.org/hgnc/7237
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1115
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19205
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1966
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum

11-10598167-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10598167
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10598167
    reference: chr 11
allele count: 3
allele frequency: 2.49887550602229e-5
allele num: 120054
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-17497C>T
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2415-45G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1551-45G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2472-45G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1551-45G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.2223-45G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.124-12390G>A
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1878-45G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2469-45G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*2021-45G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2496-45G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.247-9407C>T
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1551-45G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.2223-45G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.2223-45G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1551-45G>A
  variant of: http://identifiers.org/hgnc/7237
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17313
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2083
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4273
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19269
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum

11-10598169-CAT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10598169
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10598167
    reference: chr 11
allele count: 1
allele frequency: 8.337224037884346e-6
allele num: 119944
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2472-49_2472-48delAT
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.124-12394_124-12393delAT
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.2223-49_2223-48delAT
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.247-9402_247-9401delAT
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.2223-49_2223-48delAT
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1551-49_1551-48delAT
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2415-49_2415-48delAT
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.2223-49_2223-48delAT
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2496-49_2496-48delAT
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1551-49_1551-48delAT
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1878-49_1878-48delAT
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-17492_272-17491delAT
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*2021-49_*2021-48delAT
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1551-49_1551-48delAT
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1551-49_1551-48delAT
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2469-49_2469-48delAT
  variant of: http://identifiers.org/hgnc/7237
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10612
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1968
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19361
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: CAT
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD

11-10598170-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10598170
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10598170
    reference: chr 11
allele count: 3
allele frequency: 2.500166677778519e-5
allele num: 119992
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1551-48T>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1551-48T>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.2223-48T>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2496-48T>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.124-12393T>A
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2469-48T>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1878-48T>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-17494A>T
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.247-9404A>T
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*2021-48T>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2472-48T>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1551-48T>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1551-48T>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.2223-48T>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.2223-48T>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2415-48T>A
  variant of: http://identifiers.org/hgnc/7237
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17275
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1108
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10605
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: African
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

11-10598172-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10598172
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10598172
    reference: chr 11
allele count: 1
allele frequency: 8.337085021593051e-6
allele num: 119946
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.2223-50T>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2472-50T>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1878-50T>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1551-50T>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*2021-50T>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.124-12395T>C
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1551-50T>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.247-9402A>G
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1551-50T>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2469-50T>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-17492A>G
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.2223-50T>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.2223-50T>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2496-50T>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1551-50T>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2415-50T>C
  variant of: http://identifiers.org/hgnc/7237
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2058
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4266
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1967
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17294
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10586
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

11-10601972-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10601972
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10601972
    reference: chr 11
allele count: 8
allele frequency: 6.747183051076176e-5
allele num: 118568
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.2222+30G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1550+30G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.124-16195G>A
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2468+30G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1550+30G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2414+30G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2471+30G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.247-5602C>T
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1550+30G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.2222+30G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1877+30G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2495+30G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1550+30G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*2020+30G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-13692C>T
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.2222+30G>A
  variant of: http://identifiers.org/hgnc/7237
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1543
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6346
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5398
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6326
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1025
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1581
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Finnish)
reference allele: C
site quality: FS
site quality: DP
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum

11-10601973-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10601973
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10601973
    reference: chr 11
allele count: 9
allele frequency: 7.582906443785387e-5
allele num: 118688
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2471+29C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2495+29C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1550+29C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.247-5601G>A
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.2222+29C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-13691G>A
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1550+29C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.2222+29C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.124-16196C>T
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*2020+29C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1877+29C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1550+29C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2468+29C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.2222+29C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2414+29C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1550+29C>T
  variant of: http://identifiers.org/hgnc/7237
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2535
  bin: 9.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 1025
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7249
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3418
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4769
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7240
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4384
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQ

11-10601975-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10601975
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10601975
    reference: chr 11
allele count: 1
allele frequency: 8.424032078714155e-6
allele num: 118708
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2495+27G>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1550+27G>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1550+27G>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2471+27G>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*2020+27G>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1550+27G>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2414+27G>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2468+27G>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1550+27G>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.247-5599C>G
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.124-16198G>C
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.2222+27G>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-13689C>G
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.2222+27G>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.2222+27G>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1877+27G>C
  variant of: http://identifiers.org/hgnc/7237
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4441
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2526
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1321
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6329
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3064
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum

11-10601984-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10601984
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10601984
    reference: chr 11
allele count: 1
allele frequency: 8.381808123648433e-6
allele num: 119306
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1550+18G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2495+18G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.2222+18G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-13680C>T
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.2222+18G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2468+18G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*2020+18G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.247-5590C>T
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1550+18G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.124-16207G>A
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1550+18G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1550+18G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2471+18G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.2222+18G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1877+18G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2414+18G>A
  variant of: http://identifiers.org/hgnc/7237
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1545
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7241
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4771
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7251
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3690
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4677
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: DP

11-10601988-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10601988
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10601988
    reference: chr 11
allele count: 1
allele frequency: 8.367780697203488e-6
allele num: 119506
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2468+14G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1550+14G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1550+14G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1550+14G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2495+14G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2471+14G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-13676C>T
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1550+14G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.124-16211G>A
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1877+14G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.247-5586C>T
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*2020+14G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2414+14G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.2222+14G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.2222+14G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.2222+14G>A
  variant of: http://identifiers.org/hgnc/7237
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5491
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4771
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2334
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7253
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6360
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum

11-10601992-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10601992
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10601992
    reference: chr 11
allele count: 1
allele frequency: 8.352962795903706e-6
allele num: 119718
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.2222+10C>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1550+10C>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.2222+10C>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2495+10C>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2414+10C>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1550+10C>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2468+10C>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.2222+10C>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.247-5582G>T
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-13672G>T
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1550+10C>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.124-16215C>A
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1877+10C>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2471+10C>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1550+10C>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*2020+10C>A
  variant of: http://identifiers.org/hgnc/7237
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2524
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3901
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7239
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4770
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7253
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5494
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3419
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: Latino
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

11-10601995-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10601995
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10601995
    reference: chr 11
allele count: 1
allele frequency: 8.337502084375522e-6
allele num: 119940
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-13669T>G
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1877+7A>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*2020+7A>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2468+7A>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1550+7A>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2414+7A>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1550+7A>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2495+7A>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1550+7A>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.247-5579T>G
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2471+7A>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.2222+7A>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1550+7A>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.2222+7A>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.124-16218A>C
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.2222+7A>C
  variant of: http://identifiers.org/hgnc/7237
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1546
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7254
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7239
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5035
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.2495+7A>C
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
reference allele: T
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: VQSLOD

11-10601999-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10601999
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10601999
    reference: chr 11
allele count: 1
allele frequency: 8.328058896032513e-6
allele num: 120076
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2468+3G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2414+3G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.2222+3G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2471+3G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.2222+3G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2495+3G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1877+3G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.124-16222G>A
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1550+3G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*2020+3G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1550+3G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.2222+3G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1550+3G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1550+3G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.247-5575C>T
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-13665C>T
  variant of: http://identifiers.org/hgnc/43434
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6364
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1546
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6331
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3419
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2334
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4770
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.2495+3G>A
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: DP

11-10602003-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10602003
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10602003
    reference: chr 11
allele count: 1
allele frequency: 8.314210648840998e-6
allele num: 120276
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1549A>G
  hgvsp: ENSP00000433296.2:p.Ser517Gly
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.124-16226A>G
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.2221A>G
  hgvsp: ENSP00000448278.1:p.Ser741Gly
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2467A>G
  hgvsp: ENSP00000414598.1:p.Ser823Gly
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2413A>G
  hgvsp: ENSP00000412229.1:p.Ser805Gly
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2470A>G
  hgvsp: ENSP00000432436.1:p.Ser824Gly
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2494A>G
  hgvsp: ENSP00000412130.2:p.Ser832Gly
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1876A>G
  hgvsp: ENSP00000437784.1:p.Ser626Gly
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1549A>G
  hgvsp: ENSP00000401205.1:p.Ser517Gly
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.2221A>G
  hgvsp: ENSP00000432067.2:p.Ser741Gly
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.247-5571T>C
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-13661T>C
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.2221A>G
  hgvsp: ENSP00000446764.1:p.Ser741Gly
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*2019A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1549A>G
  hgvsp: ENSP00000441971.1:p.Ser517Gly
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1549A>G
  hgvsp: ENSP00000453013.1:p.Ser517Gly
  variant of: http://identifiers.org/hgnc/7237
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6331
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4127
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3419
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser832Gly
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/11-10602005-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10602005
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10602005
    reference: chr 11
allele count: 1
allele frequency: 8.311308366163002e-6
allele num: 120318
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2411G>T
  hgvsp: ENSP00000412229.1:p.Ser804Ile
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1547G>T
  hgvsp: ENSP00000401205.1:p.Ser516Ile
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2492G>T
  hgvsp: ENSP00000412130.2:p.Ser831Ile
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.2219G>T
  hgvsp: ENSP00000432067.2:p.Ser740Ile
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1547G>T
  hgvsp: ENSP00000433296.2:p.Ser516Ile
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2465G>T
  hgvsp: ENSP00000414598.1:p.Ser822Ile
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1874G>T
  hgvsp: ENSP00000437784.1:p.Ser625Ile
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1547G>T
  hgvsp: ENSP00000453013.1:p.Ser516Ile
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.2219G>T
  hgvsp: ENSP00000446764.1:p.Ser740Ile
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2468G>T
  hgvsp: ENSP00000432436.1:p.Ser823Ile
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*2017G>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.2219G>T
  hgvsp: ENSP00000448278.1:p.Ser740Ile
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-13659C>A
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.124-16228G>T
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1547G>T
  hgvsp: ENSP00000441971.1:p.Ser516Ile
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.247-5569C>A
  variant of: http://identifiers.org/hgnc/43434
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4130
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2335
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7256
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5586
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser831Ile
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum

11-10602008-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10602008
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10602008
    reference: chr 11
allele count: 2
allele frequency: 1.660908849322349e-5
allele num: 120416
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2489G>C
  hgvsp: ENSP00000412130.2:p.Arg830Thr
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1544G>C
  hgvsp: ENSP00000433296.2:p.Arg515Thr
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1544G>C
  hgvsp: ENSP00000401205.1:p.Arg515Thr
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2408G>C
  hgvsp: ENSP00000412229.1:p.Arg803Thr
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1871G>C
  hgvsp: ENSP00000437784.1:p.Arg624Thr
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.124-16231G>C
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1544G>C
  hgvsp: ENSP00000453013.1:p.Arg515Thr
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.2216G>C
  hgvsp: ENSP00000446764.1:p.Arg739Thr
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.247-5566C>G
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2462G>C
  hgvsp: ENSP00000414598.1:p.Arg821Thr
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1544G>C
  hgvsp: ENSP00000441971.1:p.Arg515Thr
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.2216G>C
  hgvsp: ENSP00000448278.1:p.Arg739Thr
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.2216G>C
  hgvsp: ENSP00000432067.2:p.Arg739Thr
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2465G>C
  hgvsp: ENSP00000432436.1:p.Arg822Thr
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-13656C>G
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*2014G>C
  variant of: http://identifiers.org/hgnc/7237
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5592
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1546
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg830Thr
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum

11-10602014-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10602014
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10602014
    reference: chr 11
allele count: 7
allele frequency: 5.808550185873606e-5
allele num: 120512
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2459G>A
  hgvsp: ENSP00000432436.1:p.Gly820Asp
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1538G>A
  hgvsp: ENSP00000441971.1:p.Gly513Asp
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-13650C>T
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.2210G>A
  hgvsp: ENSP00000446764.1:p.Gly737Asp
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2483G>A
  hgvsp: ENSP00000412130.2:p.Gly828Asp
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.124-16237G>A
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2402G>A
  hgvsp: ENSP00000412229.1:p.Gly801Asp
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2456G>A
  hgvsp: ENSP00000414598.1:p.Gly819Asp
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*2008G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1538G>A
  hgvsp: ENSP00000433296.2:p.Gly513Asp
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1538G>A
  hgvsp: ENSP00000453013.1:p.Gly513Asp
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.2210G>A
  hgvsp: ENSP00000432067.2:p.Gly737Asp
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1538G>A
  hgvsp: ENSP00000401205.1:p.Gly513Asp
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1865G>A
  hgvsp: ENSP00000437784.1:p.Gly622Asp
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.2210G>A
  hgvsp: ENSP00000448278.1:p.Gly737Asp
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.247-5560C>T
  variant of: http://identifiers.org/hgnc/43434
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4189
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7259
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5497
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly828Asp
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: African
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ

11-10602017-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10602017
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10602017
    reference: chr 11
allele count: 1
allele frequency: 8.293386853323161e-6
allele num: 120578
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2480A>G
  hgvsp: ENSP00000412130.2:p.Lys827Arg
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.2207A>G
  hgvsp: ENSP00000446764.1:p.Lys736Arg
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.2207A>G
  hgvsp: ENSP00000448278.1:p.Lys736Arg
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*2005A>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1535A>G
  hgvsp: ENSP00000441971.1:p.Lys512Arg
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2453A>G
  hgvsp: ENSP00000414598.1:p.Lys818Arg
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1535A>G
  hgvsp: ENSP00000453013.1:p.Lys512Arg
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1535A>G
  hgvsp: ENSP00000401205.1:p.Lys512Arg
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.124-16240A>G
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1862A>G
  hgvsp: ENSP00000437784.1:p.Lys621Arg
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.2207A>G
  hgvsp: ENSP00000432067.2:p.Lys736Arg
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-13647T>C
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1535A>G
  hgvsp: ENSP00000433296.2:p.Lys512Arg
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.247-5557T>C
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2456A>G
  hgvsp: ENSP00000432436.1:p.Lys819Arg
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2399A>G
  hgvsp: ENSP00000412229.1:p.Lys800Arg
  variant of: http://identifiers.org/hgnc/7237
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 4168
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7241
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6362
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6330
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1546
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys827Arg
num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ

11-10602021-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10602021
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10602021
    reference: chr 11
allele count: 1
allele frequency: 8.290636555074699e-6
allele num: 120618
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2476G>A
  hgvsp: ENSP00000412130.2:p.Glu826Lys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-13643C>T
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1531G>A
  hgvsp: ENSP00000453013.1:p.Glu511Lys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.124-16244G>A
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1531G>A
  hgvsp: ENSP00000401205.1:p.Glu511Lys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*2001G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.2203G>A
  hgvsp: ENSP00000432067.2:p.Glu735Lys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1531G>A
  hgvsp: ENSP00000441971.1:p.Glu511Lys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2395G>A
  hgvsp: ENSP00000412229.1:p.Glu799Lys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2449G>A
  hgvsp: ENSP00000414598.1:p.Glu817Lys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1858G>A
  hgvsp: ENSP00000437784.1:p.Glu620Lys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.2203G>A
  hgvsp: ENSP00000446764.1:p.Glu735Lys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2452G>A
  hgvsp: ENSP00000432436.1:p.Glu818Lys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1531G>A
  hgvsp: ENSP00000433296.2:p.Glu511Lys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.247-5553C>T
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.2203G>A
  hgvsp: ENSP00000448278.1:p.Glu735Lys
  variant of: http://identifiers.org/hgnc/7237
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2513
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5625
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5609
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6359
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu826Lys
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff

11-10602024-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10602024
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10602024
    reference: chr 11
allele count: 2
allele frequency: 1.657769967839263e-5
allele num: 120644
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2473G>A
  hgvsp: ENSP00000412130.2:p.Glu825Lys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.124-16247G>A
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1855G>A
  hgvsp: ENSP00000437784.1:p.Glu619Lys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1528G>A
  hgvsp: ENSP00000401205.1:p.Glu510Lys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.2200G>A
  hgvsp: ENSP00000432067.2:p.Glu734Lys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.2200G>A
  hgvsp: ENSP00000446764.1:p.Glu734Lys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1528G>A
  hgvsp: ENSP00000453013.1:p.Glu510Lys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.247-5550C>T
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.2200G>A
  hgvsp: ENSP00000448278.1:p.Glu734Lys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2449G>A
  hgvsp: ENSP00000432436.1:p.Glu817Lys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2446G>A
  hgvsp: ENSP00000414598.1:p.Glu816Lys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2392G>A
  hgvsp: ENSP00000412229.1:p.Glu798Lys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1528G>A
  hgvsp: ENSP00000441971.1:p.Glu510Lys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1528G>A
  hgvsp: ENSP00000433296.2:p.Glu510Lys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*1998G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-13640C>T
  variant of: http://identifiers.org/hgnc/43434
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6360
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4214
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2512
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1547
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu825Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: African
population: East Asian
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum

11-10602057-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10602057
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10602057
    reference: chr 11
allele count: 1
allele frequency: 8.281985026171072e-6
allele num: 120744
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.2167G>C
  hgvsp: ENSP00000432067.2:p.Glu723Gln
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2413G>C
  hgvsp: ENSP00000414598.1:p.Glu805Gln
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1495G>C
  hgvsp: ENSP00000401205.1:p.Glu499Gln
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.2167G>C
  hgvsp: ENSP00000448278.1:p.Glu723Gln
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1495G>C
  hgvsp: ENSP00000441971.1:p.Glu499Gln
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1495G>C
  hgvsp: ENSP00000453013.1:p.Glu499Gln
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2359G>C
  hgvsp: ENSP00000412229.1:p.Glu787Gln
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2440G>C
  hgvsp: ENSP00000412130.2:p.Glu814Gln
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2416G>C
  hgvsp: ENSP00000432436.1:p.Glu806Gln
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1495G>C
  hgvsp: ENSP00000433296.2:p.Glu499Gln
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*1965G>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.247-5517C>G
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.2167G>C
  hgvsp: ENSP00000446764.1:p.Glu723Gln
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1822G>C
  hgvsp: ENSP00000437784.1:p.Glu608Gln
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-13607C>G
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.124-16280G>C
  variant of: http://identifiers.org/hgnc/14687
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7258
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5710
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4253
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4768
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu814Gln
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum

http://identifiers.org/exac.variant/11-10602061-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10602061
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10602061
    reference: chr 11
allele count: 1
allele frequency: 8.281985026171072e-6
allele num: 120744
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1491T>G
  hgvsp: ENSP00000441971.1:p.Ser497Arg
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2436T>G
  hgvsp: ENSP00000412130.2:p.Ser812Arg
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.2163T>G
  hgvsp: ENSP00000446764.1:p.Ser721Arg
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2412T>G
  hgvsp: ENSP00000432436.1:p.Ser804Arg
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.247-5513A>C
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*1961T>G
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1491T>G
  hgvsp: ENSP00000453013.1:p.Ser497Arg
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1491T>G
  hgvsp: ENSP00000401205.1:p.Ser497Arg
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.2163T>G
  hgvsp: ENSP00000432067.2:p.Ser721Arg
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2355T>G
  hgvsp: ENSP00000412229.1:p.Ser785Arg
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1491T>G
  hgvsp: ENSP00000433296.2:p.Ser497Arg
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-13603A>C
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.2163T>G
  hgvsp: ENSP00000448278.1:p.Ser721Arg
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2409T>G
  hgvsp: ENSP00000414598.1:p.Ser803Arg
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.124-16284T>G
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1818T>G
  hgvsp: ENSP00000437784.1:p.Ser606Arg
  variant of: http://identifiers.org/hgnc/7237
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1545
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7258
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4258
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6329
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7240
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser812Arg
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum

11-10602068-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10602068
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10602068
    reference: chr 11
allele count: 32
allele frequency: 2.650235208374743e-4
allele num: 120744
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.2156G>A
  hgvsp: ENSP00000432067.2:p.Ser719Asn
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1484G>A
  hgvsp: ENSP00000401205.1:p.Ser495Asn
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.124-16291G>A
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.2156G>A
  hgvsp: ENSP00000448278.1:p.Ser719Asn
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2402G>A
  hgvsp: ENSP00000414598.1:p.Ser801Asn
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2348G>A
  hgvsp: ENSP00000412229.1:p.Ser783Asn
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.2156G>A
  hgvsp: ENSP00000446764.1:p.Ser719Asn
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1484G>A
  hgvsp: ENSP00000453013.1:p.Ser495Asn
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-13596C>T
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1484G>A
  hgvsp: ENSP00000441971.1:p.Ser495Asn
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2405G>A
  hgvsp: ENSP00000432436.1:p.Ser802Asn
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.247-5506C>T
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*1954G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2429G>A
  hgvsp: ENSP00000412130.2:p.Ser810Asn
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1811G>A
  hgvsp: ENSP00000437784.1:p.Ser604Asn
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1484G>A
  hgvsp: ENSP00000433296.2:p.Ser495Asn
  variant of: http://identifiers.org/hgnc/7237
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6359
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7260
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1545
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4254
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser810Asn
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

11-10602073-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10602073
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10602073
    reference: chr 11
allele count: 2
allele frequency: 1.656561640658649e-5
allele num: 120732
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.247-5501C>G
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2397G>C
  hgvsp: ENSP00000414598.1:p.Gln799His
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1806G>C
  hgvsp: ENSP00000437784.1:p.Gln602His
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*1949G>C
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1479G>C
  hgvsp: ENSP00000453013.1:p.Gln493His
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2424G>C
  hgvsp: ENSP00000412130.2:p.Gln808His
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2343G>C
  hgvsp: ENSP00000412229.1:p.Gln781His
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2400G>C
  hgvsp: ENSP00000432436.1:p.Gln800His
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.2151G>C
  hgvsp: ENSP00000446764.1:p.Gln717His
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1479G>C
  hgvsp: ENSP00000441971.1:p.Gln493His
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.2151G>C
  hgvsp: ENSP00000432067.2:p.Gln717His
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.2151G>C
  hgvsp: ENSP00000448278.1:p.Gln717His
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-13591C>G
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1479G>C
  hgvsp: ENSP00000433296.2:p.Gln493His
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1479G>C
  hgvsp: ENSP00000401205.1:p.Gln493His
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.124-16296G>C
  variant of: http://identifiers.org/hgnc/14687
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2475
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2338
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4773
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6361
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7241
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln808His
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

11-10602075-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10602075
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10602075
    reference: chr 11
allele count: 1
allele frequency: 8.283357078956959e-6
allele num: 120724
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.124-16298C>T
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1804C>T
  hgvsp: ENSP00000437784.1:p.Gln602Ter
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*1947C>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.2149C>T
  hgvsp: ENSP00000448278.1:p.Gln717Ter
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1477C>T
  hgvsp: ENSP00000433296.2:p.Gln493Ter
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2398C>T
  hgvsp: ENSP00000432436.1:p.Gln800Ter
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.2149C>T
  hgvsp: ENSP00000432067.2:p.Gln717Ter
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1477C>T
  hgvsp: ENSP00000453013.1:p.Gln493Ter
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.247-5499G>A
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2395C>T
  hgvsp: ENSP00000414598.1:p.Gln799Ter
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1477C>T
  hgvsp: ENSP00000441971.1:p.Gln493Ter
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.2149C>T
  hgvsp: ENSP00000446764.1:p.Gln717Ter
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2422C>T
  hgvsp: ENSP00000412130.2:p.Gln808Ter
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1477C>T
  hgvsp: ENSP00000401205.1:p.Gln493Ter
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-13589G>A
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2341C>T
  hgvsp: ENSP00000412229.1:p.Gln781Ter
  variant of: http://identifiers.org/hgnc/7237
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6362
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7241
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5719
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 873
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln808Ter
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum

11-10602078-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10602078
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10602078
    reference: chr 11
allele count: 1
allele frequency: 8.282670995742708e-6
allele num: 120734
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2419G>A
  hgvsp: ENSP00000412130.2:p.Glu807Lys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.2146G>A
  hgvsp: ENSP00000446764.1:p.Glu716Lys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2392G>A
  hgvsp: ENSP00000414598.1:p.Glu798Lys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2338G>A
  hgvsp: ENSP00000412229.1:p.Glu780Lys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.124-16301G>A
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1474G>A
  hgvsp: ENSP00000401205.1:p.Glu492Lys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1474G>A
  hgvsp: ENSP00000441971.1:p.Glu492Lys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.2146G>A
  hgvsp: ENSP00000432067.2:p.Glu716Lys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.247-5496C>T
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-13586C>T
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*1944G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1801G>A
  hgvsp: ENSP00000437784.1:p.Glu601Lys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1474G>A
  hgvsp: ENSP00000453013.1:p.Glu492Lys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.2146G>A
  hgvsp: ENSP00000448278.1:p.Glu716Lys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1474G>A
  hgvsp: ENSP00000433296.2:p.Glu492Lys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2395G>A
  hgvsp: ENSP00000432436.1:p.Glu799Lys
  variant of: http://identifiers.org/hgnc/7237
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7263
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1026
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2470
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6335
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1546
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3420
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu807Lys
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum

11-10602079-TTCC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10602079
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10602076
    reference: chr 11
allele count: 236
allele frequency: 1.954677975086138e-3
allele num: 120736
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.124-16305_124-16303delGGA
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.2142_2144delGGA
  hgvsp: ENSP00000446764.1:p.Glu716del
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2415_2417delGGA
  hgvsp: ENSP00000412130.2:p.Glu807del
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.2142_2144delGGA
  hgvsp: ENSP00000432067.2:p.Glu716del
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1470_1472delGGA
  hgvsp: ENSP00000433296.2:p.Glu492del
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2388_2390delGGA
  hgvsp: ENSP00000414598.1:p.Glu798del
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.247-5484_247-5482delCCT
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2391_2393delGGA
  hgvsp: ENSP00000432436.1:p.Glu799del
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1797_1799delGGA
  hgvsp: ENSP00000437784.1:p.Glu601del
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1470_1472delGGA
  hgvsp: ENSP00000401205.1:p.Glu492del
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.2142_2144delGGA
  hgvsp: ENSP00000448278.1:p.Glu716del
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-13574_272-13572delCCT
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2334_2336delGGA
  hgvsp: ENSP00000412229.1:p.Glu780del
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1470_1472delGGA
  hgvsp: ENSP00000453013.1:p.Glu492del
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*1940_*1942delGGA
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1470_1472delGGA
  hgvsp: ENSP00000441971.1:p.Glu492del
  variant of: http://identifiers.org/hgnc/7237
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2336
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1547
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3424
  bin: 6.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7265
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5717
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu807del
num of homozygotes: 4
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: African
population: South Asian
population: Latino
reference allele: TTCC
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: QD

11-10602085-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10602085
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10602085
    reference: chr 11
allele count: 1
allele frequency: 8.282122210995345e-6
allele num: 120742
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.247-5489C>T
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2412G>A
  hgvsp: ENST00000423302.2:c.2412G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.2139G>A
  hgvsp: ENST00000552103.1:c.2139G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.124-16308G>A
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2388G>A
  hgvsp: ENST00000531107.1:c.2388G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1467G>A
  hgvsp: ENST00000534266.2:c.1467G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.2139G>A
  hgvsp: ENST00000547195.1:c.2139G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2385G>A
  hgvsp: ENST00000421747.1:c.2385G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1467G>A
  hgvsp: ENST00000545852.1:c.1467G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1794G>A
  hgvsp: ENST00000541483.1:c.1794G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.2139G>A
  hgvsp: ENST00000527509.2:c.2139G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2331G>A
  hgvsp: ENST00000436272.1:c.2331G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-13579C>T
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1467G>A
  hgvsp: ENST00000558540.1:c.1467G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*1937G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1467G>A
  hgvsp: ENST00000424001.1:c.1467G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7237
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2343
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4247
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7289
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6361
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5650
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu804Glu
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: African
population: European (Finnish)
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: QD

11-10602087-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10602087
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10602087
    reference: chr 11
allele count: 5
allele frequency: 4.14167853947848e-5
allele num: 120724
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1465G>A
  hgvsp: ENSP00000441971.1:p.Glu489Lys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.2137G>A
  hgvsp: ENSP00000432067.2:p.Glu713Lys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.2137G>A
  hgvsp: ENSP00000446764.1:p.Glu713Lys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2329G>A
  hgvsp: ENSP00000412229.1:p.Glu777Lys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2386G>A
  hgvsp: ENSP00000432436.1:p.Glu796Lys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1465G>A
  hgvsp: ENSP00000401205.1:p.Glu489Lys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1465G>A
  hgvsp: ENSP00000433296.2:p.Glu489Lys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2383G>A
  hgvsp: ENSP00000414598.1:p.Glu795Lys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*1935G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.247-5487C>T
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1792G>A
  hgvsp: ENSP00000437784.1:p.Glu598Lys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-13577C>T
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.2137G>A
  hgvsp: ENSP00000448278.1:p.Glu713Lys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1465G>A
  hgvsp: ENSP00000453013.1:p.Glu489Lys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.124-16310G>A
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2410G>A
  hgvsp: ENSP00000412130.2:p.Glu804Lys
  variant of: http://identifiers.org/hgnc/7237
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5737
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7260
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3432
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu804Lys
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: South Asian
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff

11-10602090-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10602090
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10602090
    reference: chr 11
allele count: 10
allele frequency: 8.283357078956959e-5
allele num: 120724
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*1932G>A
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2326G>A
  hgvsp: ENSP00000412229.1:p.Glu776Lys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.2134G>A
  hgvsp: ENSP00000432067.2:p.Glu712Lys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2380G>A
  hgvsp: ENSP00000414598.1:p.Glu794Lys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-13574C>T
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1462G>A
  hgvsp: ENSP00000433296.2:p.Glu488Lys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1462G>A
  hgvsp: ENSP00000453013.1:p.Glu488Lys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.2134G>A
  hgvsp: ENSP00000448278.1:p.Glu712Lys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1462G>A
  hgvsp: ENSP00000441971.1:p.Glu488Lys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1789G>A
  hgvsp: ENSP00000437784.1:p.Glu597Lys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.2134G>A
  hgvsp: ENSP00000446764.1:p.Glu712Lys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.124-16313G>A
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2383G>A
  hgvsp: ENSP00000432436.1:p.Glu795Lys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1462G>A
  hgvsp: ENSP00000401205.1:p.Glu488Lys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.247-5484C>T
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2407G>A
  hgvsp: ENSP00000412130.2:p.Glu803Lys
  variant of: http://identifiers.org/hgnc/7237
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6385
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5738
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3432
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2276
  bin: 9.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu803Lys
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ

11-10602092-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10602092
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10602092
    reference: chr 11
allele count: 1
allele frequency: 8.283768783445716e-6
allele num: 120718
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1787A>T
  hgvsp: ENSP00000437784.1:p.Lys596Met
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2324A>T
  hgvsp: ENSP00000412229.1:p.Lys775Met
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.2132A>T
  hgvsp: ENSP00000432067.2:p.Lys711Met
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2378A>T
  hgvsp: ENSP00000414598.1:p.Lys793Met
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1460A>T
  hgvsp: ENSP00000401205.1:p.Lys487Met
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*1930A>T
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2381A>T
  hgvsp: ENSP00000432436.1:p.Lys794Met
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1460A>T
  hgvsp: ENSP00000441971.1:p.Lys487Met
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-13572T>A
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1460A>T
  hgvsp: ENSP00000433296.2:p.Lys487Met
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.124-16315A>T
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2405A>T
  hgvsp: ENSP00000412130.2:p.Lys802Met
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.247-5482T>A
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1460A>T
  hgvsp: ENSP00000453013.1:p.Lys487Met
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.2132A>T
  hgvsp: ENSP00000446764.1:p.Lys711Met
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.2132A>T
  hgvsp: ENSP00000448278.1:p.Lys711Met
  variant of: http://identifiers.org/hgnc/7237
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3433
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6383
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6360
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5742
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys802Met
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum

11-10602102-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 10602102
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 10602102
    reference: chr 11
allele count: 2
allele frequency: 1.657028285472833e-5
allele num: 120698
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000453013
  ensembl transcript: ENST00000558540
  gene symbol: MRVI1
  hgvsc: ENST00000558540.1:c.1450C>A
  hgvsp: ENSP00000453013.1:p.Gln484Lys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432067
  ensembl transcript: ENST00000527509
  gene symbol: MRVI1
  hgvsc: ENST00000527509.2:c.2122C>A
  hgvsp: ENSP00000432067.2:p.Gln708Lys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412229
  ensembl transcript: ENST00000436272
  gene symbol: MRVI1
  hgvsc: ENST00000436272.1:c.2314C>A
  hgvsp: ENSP00000412229.1:p.Gln772Lys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000414598
  ensembl transcript: ENST00000421747
  gene symbol: MRVI1
  hgvsc: ENST00000421747.1:c.2368C>A
  hgvsp: ENSP00000414598.1:p.Gln790Lys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000448278
  ensembl transcript: ENST00000547195
  gene symbol: MRVI1
  hgvsc: ENST00000547195.1:c.2122C>A
  hgvsp: ENSP00000448278.1:p.Gln708Lys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: true
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529829
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529829.1:n.272-13562G>T
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000177112
  ensembl transcript: ENST00000529979
  gene symbol: MRVI1-AS1
  hgvsc: ENST00000529979.1:n.247-5472G>T
  variant of: http://identifiers.org/hgnc/43434
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000412130
  ensembl transcript: ENST00000423302
  gene symbol: MRVI1
  hgvsc: ENST00000423302.2:c.2395C>A
  hgvsp: ENSP00000412130.2:p.Gln799Lys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000432436
  ensembl transcript: ENST00000531107
  gene symbol: MRVI1
  hgvsc: ENST00000531107.1:c.2371C>A
  hgvsp: ENSP00000432436.1:p.Gln791Lys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000133800
  ensembl transcript: ENST00000531706
  gene symbol: LYVE1
  hgvsc: ENST00000531706.1:n.124-16325C>A
  variant of: http://identifiers.org/hgnc/14687
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000401205
  ensembl transcript: ENST00000424001
  gene symbol: MRVI1
  hgvsc: ENST00000424001.1:c.1450C>A
  hgvsp: ENSP00000401205.1:p.Gln484Lys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000446764
  ensembl transcript: ENST00000552103
  gene symbol: MRVI1
  hgvsc: ENST00000552103.1:c.2122C>A
  hgvsp: ENSP00000446764.1:p.Gln708Lys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000433296
  ensembl transcript: ENST00000534266
  gene symbol: MRVI1
  hgvsc: ENST00000534266.2:c.1450C>A
  hgvsp: ENSP00000433296.2:p.Gln484Lys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000441971
  ensembl transcript: ENST00000545852
  gene symbol: MRVI1
  hgvsc: ENST00000545852.1:c.1450C>A
  hgvsp: ENSP00000441971.1:p.Gln484Lys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000437784
  ensembl transcript: ENST00000541483
  gene symbol: MRVI1
  hgvsc: ENST00000541483.1:c.1777C>A
  hgvsp: ENSP00000437784.1:p.Gln593Lys
  variant of: http://identifiers.org/hgnc/7237
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000072952
  ensembl protein: ENSP00000434741
  ensembl transcript: ENST00000529448
  gene symbol: MRVI1
  hgvsc: ENST00000529448.1:c.*1920C>A
  variant of: http://identifiers.org/hgnc/7237
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4229
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Gln799Lys
num of homozygotes: 0
reference allele: G

GenotypeDepth
all individuals: 4436
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1997
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 103
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 57
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 11543
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 394
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 72
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 173
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 105
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 234
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 156
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 584
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 203
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25986
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9466
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5515
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4034
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1865
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 18
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4704
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 73
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6510
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2094
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.32396002788752e-4
allele num: 8606
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11526
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9798
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66706
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 6.33e-1

DP
type: SiteQuality
SIO_000300: 1.774776e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.3e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.554e0

QD
type: SiteQuality
SIO_000300: 1.274e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.21e-1

FS
type: SiteQuality
SIO_000300: 6.582e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.91e-1

GenotypeDepth
all individuals: 156
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 11543
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 584
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 77
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1997
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 394
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 57
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 19888
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 50
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 37
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 203
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 72
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1041
bin: 4.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1865
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4704
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2094
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 12
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4034
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25986
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 18
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6510
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 73
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5515
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9466
bin: 6.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 3
allele frequency: 1.817080557238038e-4
allele num: 16510
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66706
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8606
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11526
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9798
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.21e-1

FS
type: SiteQuality
SIO_000300: 6.582e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.554e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 6.33e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-3

QD
type: SiteQuality
SIO_000300: 1.274e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.3e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.91e-1

DP
type: SiteQuality
SIO_000300: 1.774776e6

GenotypeDepth
all individuals: 156
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 585
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 19858
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 106
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 72
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 45
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 11570
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 45
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 173
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 35
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 203
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2004
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 1043
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 14
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 25971
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5528
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4045
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4710
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6519
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 64
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2096
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1868
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9468
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 4.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11532
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9798
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.497211728728189e-5
allele num: 66708
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8604
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -4.65e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.73e0

VQSLOD
type: SiteQuality
SIO_000300: 2.89e0

MQRankSum
type: SiteQuality
SIO_000300: 8.0e-3

FS
type: SiteQuality
SIO_000300: 1.24e0

DP
type: SiteQuality
SIO_000300: 1.77565e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

MQ
type: SiteQuality
SIO_000300: 5.974e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.96e-1

QD
type: SiteQuality
SIO_000300: 1.355e1

GenotypeDepth
all individuals: 4460
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 35
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 173
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 273
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 82
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 588
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 105
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 234
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 156
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2015
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1051
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 203
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 103
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6539
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 9469
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2105
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1875
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 8
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4065
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4720
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5539
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25937
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.16144018583043e-4
allele num: 8610
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66724
num of homozygotes: 0

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9800
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.326e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.2e-1

DP
type: SiteQuality
SIO_000300: 1.777392e6

MQ
type: SiteQuality
SIO_000300: 5.847e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.124e0

QD
type: SiteQuality
SIO_000300: 4.07e0

FS
type: SiteQuality
SIO_000300: 2.951e0

VQSLOD
type: SiteQuality
SIO_000300: -3.424e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.265e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

GenotypeDepth
all individuals: 11603
bin: 3.25e1
variant carriers: 0

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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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African
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European (Non-Finnish)
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Latino
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East Asian
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QD
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BaseQRankSum
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MQRankSum
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MQ
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DP
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FS
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ClippingRankSum
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VQSLOD
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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VQSLOD
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BaseQRankSum
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MQRankSum
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FS
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ClippingRankSum
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QD
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MQ
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DP
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ReadPosRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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African
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European (Non-Finnish)
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European (Finnish)
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Latino
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Other
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FS
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VQSLOD
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DP
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MQ
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ClippingRankSum
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InbreedingCoeff
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QD
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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Other
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East Asian
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European (Finnish)
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European (Non-Finnish)
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African
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FS
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DP
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QD
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MQ
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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ReadPosRankSum
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European (Finnish)
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European (Non-Finnish)
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Latino
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South Asian
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East Asian
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BaseQRankSum
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MQRankSum
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QD
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ClippingRankSum
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FS
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InbreedingCoeff
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ReadPosRankSum
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DP
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MQ
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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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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East Asian
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ReadPosRankSum
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FS
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MQ
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InbreedingCoeff
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SIO_000300: 3.0e-4

VQSLOD
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DP
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MQRankSum
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BaseQRankSum
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ClippingRankSum
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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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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 frequency: 2.996793431028799e-5
allele num: 66738
num of homozygotes: 0

African
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East Asian
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South Asian
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Latino
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num of homozygotes: 0

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

Other
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VQSLOD
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ClippingRankSum
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MQ
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ReadPosRankSum
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QD
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InbreedingCoeff
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FS
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BaseQRankSum
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MQRankSum
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DP
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SIO_000300: 1.779432e6

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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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 frequency: 0.0e0
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Other
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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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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
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allele num: 66738
num of homozygotes: 0

European (Finnish)
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num of homozygotes: 0

South Asian
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FS
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SIO_000300: 6.058e0

ReadPosRankSum
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InbreedingCoeff
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ClippingRankSum
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MQ
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MQRankSum
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VQSLOD
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DP
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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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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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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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European (Finnish)
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Latino
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European (Non-Finnish)
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allele num: 66738
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Other
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African
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FS
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DP
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VQSLOD
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MQRankSum
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MQ
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ReadPosRankSum
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InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Latino
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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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South Asian
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InbreedingCoeff
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DP
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FS
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BaseQRankSum
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ClippingRankSum
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QD
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ReadPosRankSum
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MQ
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VQSLOD
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MQRankSum
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GenotypeQuality
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European (Finnish)
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East Asian
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South Asian
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African
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Latino
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Other
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VQSLOD
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FS
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BaseQRankSum
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ClippingRankSum
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QD
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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DP
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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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Latino
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Other
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South Asian
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East Asian
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European (Finnish)
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African
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DP
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QD
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BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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VQSLOD
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FS
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ClippingRankSum
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 0.0e0
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European (Finnish)
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Latino
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East Asian
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European (Non-Finnish)
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Other
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South Asian
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MQRankSum
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ReadPosRankSum
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QD
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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FS
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ClippingRankSum
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MQ
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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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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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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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South Asian
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Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.498486528606108e-5
allele num: 66734
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Latino
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ReadPosRankSum
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ClippingRankSum
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MQ
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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FS
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QD
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DP
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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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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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East Asian
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ClippingRankSum
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MQ
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BaseQRankSum
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DP
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FS
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QD
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MQRankSum
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VQSLOD
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ReadPosRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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East Asian
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Other
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European (Non-Finnish)
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South Asian
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MQRankSum
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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DP
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FS
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MQ
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ReadPosRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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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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Latino
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East Asian
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European (Finnish)
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African
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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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DP
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InbreedingCoeff
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QD
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ReadPosRankSum
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VQSLOD
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ClippingRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Finnish)
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allele frequency: 0.0e0
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Latino
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Other
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African
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allele num: 9722
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European (Non-Finnish)
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allele frequency: 1.504302304591131e-5
allele num: 66476
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East Asian
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InbreedingCoeff
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ClippingRankSum
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VQSLOD
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QD
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MQ
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FS
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BaseQRankSum
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DP
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ReadPosRankSum
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MQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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East Asian
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Other
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African
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European (Non-Finnish)
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European (Finnish)
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Latino
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MQ
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InbreedingCoeff
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ReadPosRankSum
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QD
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BaseQRankSum
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DP
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MQRankSum
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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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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Other
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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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South Asian
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European (Non-Finnish)
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Latino
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MQRankSum
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InbreedingCoeff
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FS
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QD
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ReadPosRankSum
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BaseQRankSum
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MQ
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DP
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VQSLOD
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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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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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num of homozygotes: 0

South Asian
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Other
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Latino
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East Asian
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African
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European (Finnish)
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InbreedingCoeff
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DP
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FS
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ReadPosRankSum
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BaseQRankSum
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MQRankSum
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QD
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VQSLOD
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ClippingRankSum
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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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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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European (Non-Finnish)
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Latino
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Other
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East Asian
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South Asian
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African
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European (Finnish)
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FS
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ReadPosRankSum
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VQSLOD
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MQRankSum
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BaseQRankSum
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ClippingRankSum
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InbreedingCoeff
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MQ
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QD
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Other
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East Asian
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European (Non-Finnish)
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European (Finnish)
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allele num: 6610
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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MQ
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VQSLOD
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FS
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BaseQRankSum
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ClippingRankSum
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DP
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66514
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.084945843981989e-5
allele num: 16434
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11540
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.198e0

DP
type: SiteQuality
SIO_000300: 1.750303e6

InbreedingCoeff
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SIO_000300: 7.0e-3

MQ
type: SiteQuality
SIO_000300: 5.963e1

MQRankSum
type: SiteQuality
SIO_000300: 1.18e0

FS
type: SiteQuality
SIO_000300: 5.093e0

ReadPosRankSum
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SIO_000300: 3.49e-1

QD
type: SiteQuality
SIO_000300: 1.411e1

VQSLOD
type: SiteQuality
SIO_000300: 3.35e-1

ClippingRankSum
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SIO_000300: -1.01e0

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11540
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503352476021528e-5
allele num: 66518
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
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.73e-1

FS
type: SiteQuality
SIO_000300: 1.696e0

QD
type: SiteQuality
SIO_000300: 1.633e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.46e-1

DP
type: SiteQuality
SIO_000300: 1.749836e6

BaseQRankSum
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SIO_000300: 1.1e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.59e-1

MQRankSum
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SIO_000300: 9.12e-1

MQ
type: SiteQuality
SIO_000300: 5.986e1

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9712
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66484
num of homozygotes: 0

East Asian
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allele count: 1
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allele num: 8574
num of homozygotes: 0

South Asian
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allele count: 0
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num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.0e0

MQRankSum
type: SiteQuality
SIO_000300: -3.39e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.5e-3

MQ
type: SiteQuality
SIO_000300: 5.985e1

FS
type: SiteQuality
SIO_000300: 6.31e-1

ReadPosRankSum
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SIO_000300: -3.53e-1

ClippingRankSum
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SIO_000300: 9.92e-1

QD
type: SiteQuality
SIO_000300: 1.496e1

DP
type: SiteQuality
SIO_000300: 1.741167e6

VQSLOD
type: SiteQuality
SIO_000300: 5.7e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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variant carriers: 2

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 5
allele frequency: 5.834305717619603e-4
allele num: 8570
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: 0
allele frequency: 0.0e0
allele num: 66436
num of homozygotes: 0

South Asian
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allele count: 0
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MQRankSum
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SIO_000300: 7.96e-1

DP
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.988e1

ClippingRankSum
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SIO_000300: -1.1e-2

QD
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InbreedingCoeff
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SIO_000300: 8.3e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.35e0

BaseQRankSum
type: SiteQuality
SIO_000300: 8.37e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.0e-2

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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: 11534
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66402
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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Other
type: Population
allele count: 0
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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 num: 16320
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
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DP
type: SiteQuality
SIO_000300: 1.73438e6

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

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6610
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9692
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66422
num of homozygotes: 0

East Asian
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allele num: 8566
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QD
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SIO_000300: 1.289e1

BaseQRankSum
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MQRankSum
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FS
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VQSLOD
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InbreedingCoeff
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DP
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MQ
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SIO_000300: 5.979e1

ReadPosRankSum
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ClippingRankSum
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SIO_000300: 4.16e-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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (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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Latino
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VQSLOD
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ClippingRankSum
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FS
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QD
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MQRankSum
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InbreedingCoeff
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DP
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MQ
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BaseQRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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Other
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Latino
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African
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European (Non-Finnish)
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East Asian
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South Asian
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ReadPosRankSum
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MQ
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VQSLOD
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DP
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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FS
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ClippingRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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East Asian
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Latino
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Other
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European (Finnish)
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South Asian
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African
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VQSLOD
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FS
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MQ
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DP
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MQRankSum
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InbreedingCoeff
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QD
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ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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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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European (Finnish)
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Latino
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African
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South Asian
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European (Non-Finnish)
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FS
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InbreedingCoeff
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MQRankSum
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DP
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VQSLOD
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MQ
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BaseQRankSum
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ReadPosRankSum
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QD
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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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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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Other
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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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European (Finnish)
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FS
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DP
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MQ
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QD
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BaseQRankSum
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ClippingRankSum
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InbreedingCoeff
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VQSLOD
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ReadPosRankSum
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MQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Other
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European (Finnish)
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East Asian
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European (Non-Finnish)
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Latino
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South Asian
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BaseQRankSum
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MQRankSum
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VQSLOD
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InbreedingCoeff
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QD
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ReadPosRankSum
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FS
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ClippingRankSum
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DP
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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African
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Latino
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East Asian
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South Asian
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European (Non-Finnish)
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VQSLOD
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FS
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InbreedingCoeff
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QD
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DP
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BaseQRankSum
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ClippingRankSum
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MQRankSum
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MQ
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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South Asian
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European (Non-Finnish)
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Latino
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East Asian
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European (Finnish)
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MQ
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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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InbreedingCoeff
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QD
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ClippingRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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African
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East Asian
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European (Finnish)
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Other
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Latino
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European (Non-Finnish)
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QD
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ReadPosRankSum
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FS
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InbreedingCoeff
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VQSLOD
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MQ
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BaseQRankSum
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DP
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MQRankSum
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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African
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South Asian
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Other
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Latino
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European (Finnish)
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VQSLOD
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MQRankSum
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FS
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QD
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DP
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MQ
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InbreedingCoeff
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BaseQRankSum
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ClippingRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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South Asian
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African
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European (Non-Finnish)
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East Asian
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European (Finnish)
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Latino
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MQ
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BaseQRankSum
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ClippingRankSum
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FS
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InbreedingCoeff
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ReadPosRankSum
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QD
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MQRankSum
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DP
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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Latino
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South Asian
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European (Finnish)
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East Asian
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European (Non-Finnish)
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FS
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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MQ
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BaseQRankSum
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ReadPosRankSum
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VQSLOD
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SIO_000300: 1.0e0

QD
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DP
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SIO_000300: 2.989899e6

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

European (Finnish)
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Other
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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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FS
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InbreedingCoeff
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QD
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MQ
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ReadPosRankSum
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MQRankSum
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VQSLOD
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ClippingRankSum
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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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African
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South Asian
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Latino
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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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InbreedingCoeff
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MQ
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FS
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VQSLOD
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MQRankSum
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ClippingRankSum
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BaseQRankSum
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DP
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QD
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Other
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European (Non-Finnish)
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European (Finnish)
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South Asian
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Latino
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African
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DP
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MQRankSum
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QD
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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FS
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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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Other
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African
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Latino
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European (Non-Finnish)
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European (Finnish)
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South Asian
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East Asian
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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DP
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VQSLOD
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QD
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ReadPosRankSum
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ClippingRankSum
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FS
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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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European (Finnish)
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Latino
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European (Non-Finnish)
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East Asian
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South Asian
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VQSLOD
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ClippingRankSum
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QD
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DP
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MQRankSum
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FS
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BaseQRankSum
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MQ
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ReadPosRankSum
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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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European (Non-Finnish)
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allele num: 66642
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Latino
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Other
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European (Finnish)
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African
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East Asian
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South Asian
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ClippingRankSum
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ReadPosRankSum
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MQ
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VQSLOD
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DP
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MQRankSum
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FS
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InbreedingCoeff
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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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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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African
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Latino
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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European (Finnish)
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Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
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allele num: 66724
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MQ
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MQRankSum
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QD
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ReadPosRankSum
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InbreedingCoeff
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SIO_000300: 1.3e-3

BaseQRankSum
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FS
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DP
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VQSLOD
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ClippingRankSum
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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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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 num: 16510
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East Asian
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European (Non-Finnish)
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African
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Latino
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European (Finnish)
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Other
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InbreedingCoeff
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MQ
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ReadPosRankSum
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FS
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MQRankSum
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VQSLOD
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BaseQRankSum
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QD
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DP
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ClippingRankSum
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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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East Asian
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African
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Other
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European (Non-Finnish)
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South Asian
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European (Finnish)
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InbreedingCoeff
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FS
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VQSLOD
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QD
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MQ
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MQRankSum
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DP
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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GenotypeQuality
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European (Finnish)
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East Asian
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Latino
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South Asian
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African
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European (Non-Finnish)
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InbreedingCoeff
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BaseQRankSum
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ClippingRankSum
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QD
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FS
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MQRankSum
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VQSLOD
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DP
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MQ
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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East Asian
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Other
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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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MQRankSum
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InbreedingCoeff
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FS
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QD
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VQSLOD
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DP
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BaseQRankSum
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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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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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num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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BaseQRankSum
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QD
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ClippingRankSum
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DP
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FS
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InbreedingCoeff
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MQRankSum
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VQSLOD
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MQ
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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European (Non-Finnish)
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allele frequency: 5.994664748373947e-5
allele num: 66726
num of homozygotes: 0

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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African
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allele frequency: 2.244897959183673e-2
allele num: 9800
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South Asian
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allele frequency: 6.05766900896535e-5
allele num: 16508
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Latino
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allele frequency: 7.781428324399101e-4
allele num: 11566
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.27e-1

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

European (Non-Finnish)
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East Asian
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African
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Other
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South Asian
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European (Finnish)
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ClippingRankSum
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QD
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BaseQRankSum
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FS
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ReadPosRankSum
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VQSLOD
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MQRankSum
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MQ
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DP
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InbreedingCoeff
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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South Asian
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European (Non-Finnish)
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allele num: 66720
num of homozygotes: 0

Latino
type: Population
allele count: 9
allele frequency: 7.782774126599793e-4
allele num: 11564
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: 2.33e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.8e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -6.125e0

QD
type: SiteQuality
SIO_000300: 1.406e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.56e-1

FS
type: SiteQuality
SIO_000300: 1.51e0

MQRankSum
type: SiteQuality
SIO_000300: -1.74e-1

DP
type: SiteQuality
SIO_000300: 2.960603e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.605e0

MQ
type: SiteQuality
SIO_000300: 6.001e1

GenotypeDepth
all individuals: 11
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 2345
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7261
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2268
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 5653
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4239
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 879
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 27
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 7295
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1548
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4787
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 673
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3153
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2607
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1502
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2920
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9282
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1653
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2848
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36355
bin: 9.75e1
variant carriers: 1

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9798
num of homozygotes: 0

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

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: -2.314e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.63e-1

QD
type: SiteQuality
SIO_000300: 1.424e1

FS
type: SiteQuality
SIO_000300: 1.907e0

DP
type: SiteQuality
SIO_000300: 2.959437e6

MQ
type: SiteQuality
SIO_000300: 5.654e1

MQRankSum
type: SiteQuality
SIO_000300: -9.94e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.34e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.829e0