Links from Gene
Items: 1 to 20 of 14915
2.
rs1491518058 has merged into rs748042243 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- TTTTTTTTTTTTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
[Show Flanks]
- Chromosome:
- 21:36351066
(GRCh38)
21:37723364
(GRCh37)
- Canonical SPDI:
- NC_000021.9:36351057:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTT,NC_000021.9:36351057:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT,NC_000021.9:36351057:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000021.9:36351057:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000021.9:36351057:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000021.9:36351057:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000021.9:36351057:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000021.9:36351057:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000021.9:36351057:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000021.9:36351057:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000021.9:36351057:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000021.9:36351057:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000021.9:36351057:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000021.9:36351057:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000021.9:36351057:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000021.9:36351057:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000021.9:36351057:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000021.9:36351057:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000021.9:36351057:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000021.9:36351057:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000021.9:36351057:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000021.9:36351057:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000021.9:36351057:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000021.9:36351057:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000021.9:36351057:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000021.9:36351057:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000021.9:36351057:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000021.9:36351057:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000021.9:36351057:TTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- Gene:
- MORC3 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
TTTTTTTT=0./0
(
ALFA)
-=0.175/7
(GENOME_DK)
- HGVS:
NC_000021.9:g.36351066_36351083del, NC_000021.9:g.36351067_36351083del, NC_000021.9:g.36351068_36351083del, NC_000021.9:g.36351069_36351083del, NC_000021.9:g.36351070_36351083del, NC_000021.9:g.36351071_36351083del, NC_000021.9:g.36351072_36351083del, NC_000021.9:g.36351073_36351083del, NC_000021.9:g.36351074_36351083del, NC_000021.9:g.36351075_36351083del, NC_000021.9:g.36351076_36351083del, NC_000021.9:g.36351077_36351083del, NC_000021.9:g.36351078_36351083del, NC_000021.9:g.36351079_36351083del, NC_000021.9:g.36351080_36351083del, NC_000021.9:g.36351081_36351083del, NC_000021.9:g.36351082_36351083del, NC_000021.9:g.36351083del, NC_000021.9:g.36351083dup, NC_000021.9:g.36351082_36351083dup, NC_000021.9:g.36351081_36351083dup, NC_000021.9:g.36351080_36351083dup, NC_000021.9:g.36351079_36351083dup, NC_000021.9:g.36351078_36351083dup, NC_000021.9:g.36351077_36351083dup, NC_000021.9:g.36351076_36351083dup, NC_000021.9:g.36351075_36351083dup, NC_000021.9:g.36351073_36351083dup, NC_000021.9:g.36351072_36351083dup, NC_000021.8:g.37723364_37723381del, NC_000021.8:g.37723365_37723381del, NC_000021.8:g.37723366_37723381del, NC_000021.8:g.37723367_37723381del, NC_000021.8:g.37723368_37723381del, NC_000021.8:g.37723369_37723381del, NC_000021.8:g.37723370_37723381del, NC_000021.8:g.37723371_37723381del, NC_000021.8:g.37723372_37723381del, NC_000021.8:g.37723373_37723381del, NC_000021.8:g.37723374_37723381del, NC_000021.8:g.37723375_37723381del, NC_000021.8:g.37723376_37723381del, NC_000021.8:g.37723377_37723381del, NC_000021.8:g.37723378_37723381del, NC_000021.8:g.37723379_37723381del, NC_000021.8:g.37723380_37723381del, NC_000021.8:g.37723381del, NC_000021.8:g.37723381dup, NC_000021.8:g.37723380_37723381dup, NC_000021.8:g.37723379_37723381dup, NC_000021.8:g.37723378_37723381dup, NC_000021.8:g.37723377_37723381dup, NC_000021.8:g.37723376_37723381dup, NC_000021.8:g.37723375_37723381dup, NC_000021.8:g.37723374_37723381dup, NC_000021.8:g.37723373_37723381dup, NC_000021.8:g.37723371_37723381dup, NC_000021.8:g.37723370_37723381dup
3.
rs1491516264 [Homo sapiens]- Variant type:
- INS
- Alleles:
- ->C
[Show Flanks]
- Chromosome:
- 21:36351058
(GRCh38)
21:37723357
(GRCh37)
- Canonical SPDI:
- NC_000021.9:36351058::C
- Gene:
- MORC3 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
C=0./0
(
ALFA)
C=0.0001/3
(GnomAD)
C=0.00165/3
(Korea1K)
C=0.00458/68
(TOMMO)
- HGVS:
4.
rs1491512258 [Homo sapiens]- Variant type:
- INS
- Alleles:
- ->A,AA,ATA,ATATA,ATATATA,ATATATATA,ATATATATATA
[Show Flanks]
- Chromosome:
- 21:36370640
(GRCh38)
21:37742939
(GRCh37)
- Canonical SPDI:
- NC_000021.9:36370640::A,NC_000021.9:36370640::AA,NC_000021.9:36370640::ATA,NC_000021.9:36370640::ATATA,NC_000021.9:36370640::ATATATA,NC_000021.9:36370640::ATATATATA,NC_000021.9:36370640::ATATATATATA
- Gene:
- MORC3 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
- HGVS:
NC_000021.9:g.36370640_36370641insA, NC_000021.9:g.36370640_36370641insAA, NC_000021.9:g.36370640_36370641insATA, NC_000021.9:g.36370640_36370641insATATA, NC_000021.9:g.36370640_36370641insATATATA, NC_000021.9:g.36370640_36370641insATATATATA, NC_000021.9:g.36370640_36370641insATATATATATA, NC_000021.8:g.37742938_37742939insA, NC_000021.8:g.37742938_37742939insAA, NC_000021.8:g.37742938_37742939insATA, NC_000021.8:g.37742938_37742939insATATA, NC_000021.8:g.37742938_37742939insATATATA, NC_000021.8:g.37742938_37742939insATATATATA, NC_000021.8:g.37742938_37742939insATATATATATA
5.
rs1491496224 has merged into rs869169013 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- TTTTTTTTTTTTTTTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
[Show Flanks]
- Chromosome:
- 21:36370651
(GRCh38)
21:37742949
(GRCh37)
- Canonical SPDI:
- NC_000021.9:36370639:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000021.9:36370639:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000021.9:36370639:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000021.9:36370639:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000021.9:36370639:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000021.9:36370639:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000021.9:36370639:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000021.9:36370639:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000021.9:36370639:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000021.9:36370639:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000021.9:36370639:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000021.9:36370639:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000021.9:36370639:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000021.9:36370639:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000021.9:36370639:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000021.9:36370639:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000021.9:36370639:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000021.9:36370639:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000021.9:36370639:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000021.9:36370639:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000021.9:36370639:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000021.9:36370639:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000021.9:36370639:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000021.9:36370639:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000021.9:36370639:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000021.9:36370639:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000021.9:36370639:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000021.9:36370639:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000021.9:36370639:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- Gene:
- MORC3 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
TTTTTTTTTTT=0./0
(
ALFA)
-=0.000004/1
(TOPMED)
- HGVS:
NC_000021.9:g.36370651_36370671del, NC_000021.9:g.36370652_36370671del, NC_000021.9:g.36370653_36370671del, NC_000021.9:g.36370654_36370671del, NC_000021.9:g.36370655_36370671del, NC_000021.9:g.36370656_36370671del, NC_000021.9:g.36370657_36370671del, NC_000021.9:g.36370658_36370671del, NC_000021.9:g.36370659_36370671del, NC_000021.9:g.36370660_36370671del, NC_000021.9:g.36370661_36370671del, NC_000021.9:g.36370662_36370671del, NC_000021.9:g.36370663_36370671del, NC_000021.9:g.36370664_36370671del, NC_000021.9:g.36370665_36370671del, NC_000021.9:g.36370666_36370671del, NC_000021.9:g.36370667_36370671del, NC_000021.9:g.36370668_36370671del, NC_000021.9:g.36370669_36370671del, NC_000021.9:g.36370670_36370671del, NC_000021.9:g.36370671del, NC_000021.9:g.36370671dup, NC_000021.9:g.36370670_36370671dup, NC_000021.9:g.36370669_36370671dup, NC_000021.9:g.36370667_36370671dup, NC_000021.9:g.36370666_36370671dup, NC_000021.9:g.36370664_36370671dup, NC_000021.9:g.36370653_36370671dup, NC_000021.9:g.36370645_36370671dup, NC_000021.8:g.37742949_37742969del, NC_000021.8:g.37742950_37742969del, NC_000021.8:g.37742951_37742969del, NC_000021.8:g.37742952_37742969del, NC_000021.8:g.37742953_37742969del, NC_000021.8:g.37742954_37742969del, NC_000021.8:g.37742955_37742969del, NC_000021.8:g.37742956_37742969del, NC_000021.8:g.37742957_37742969del, NC_000021.8:g.37742958_37742969del, NC_000021.8:g.37742959_37742969del, NC_000021.8:g.37742960_37742969del, NC_000021.8:g.37742961_37742969del, NC_000021.8:g.37742962_37742969del, NC_000021.8:g.37742963_37742969del, NC_000021.8:g.37742964_37742969del, NC_000021.8:g.37742965_37742969del, NC_000021.8:g.37742966_37742969del, NC_000021.8:g.37742967_37742969del, NC_000021.8:g.37742968_37742969del, NC_000021.8:g.37742969del, NC_000021.8:g.37742969dup, NC_000021.8:g.37742968_37742969dup, NC_000021.8:g.37742967_37742969dup, NC_000021.8:g.37742965_37742969dup, NC_000021.8:g.37742964_37742969dup, NC_000021.8:g.37742962_37742969dup, NC_000021.8:g.37742951_37742969dup, NC_000021.8:g.37742943_37742969dup
7.
rs1491377045 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- ->G
[Show Flanks]
- Chromosome:
- 21:36359581
(GRCh38)
21:37731880
(GRCh37)
- Canonical SPDI:
- NC_000021.9:36359581:G:GG
- Gene:
- MORC3 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa
- MAF:
GG=0./0
(
ALFA)
G=0.00007/5
(GnomAD)
- HGVS:
8.
rs1491339397 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- GA>-
[Show Flanks]
- Chromosome:
- 21:36328921
(GRCh38)
21:37701219
(GRCh37)
- Canonical SPDI:
- NC_000021.9:36328919:AGA:A
- Gene:
- MORC3 (Varview)
- Functional Consequence:
- genic_upstream_transcript_variant,intron_variant
- Validated:
- by frequency,by alfa
- MAF:
A=0.000184/3
(
ALFA)
-=0.000029/4
(GnomAD)
- HGVS:
9.
rs1491320831 has merged into rs545030354 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- TTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTTTTTT
[Show Flanks]
- Chromosome:
- 21:36371824
(GRCh38)
21:37744122
(GRCh37)
- Canonical SPDI:
- NC_000021.9:36371815:TTTTTTTTTTTTTTT:TTTTTTTT,NC_000021.9:36371815:TTTTTTTTTTTTTTT:TTTTTTTTT,NC_000021.9:36371815:TTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000021.9:36371815:TTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000021.9:36371815:TTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000021.9:36371815:TTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000021.9:36371815:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000021.9:36371815:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000021.9:36371815:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000021.9:36371815:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000021.9:36371815:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000021.9:36371815:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000021.9:36371815:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT
- Gene:
- MORC3 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
TTTTTTTTT=0./0
(
ALFA)
TTTTT=0.0003/5
(TOMMO)
T=0.01638/30
(Korea1K)
T=0.05/2
(GENOME_DK)
- HGVS:
NC_000021.9:g.36371824_36371830del, NC_000021.9:g.36371825_36371830del, NC_000021.9:g.36371826_36371830del, NC_000021.9:g.36371827_36371830del, NC_000021.9:g.36371828_36371830del, NC_000021.9:g.36371829_36371830del, NC_000021.9:g.36371830del, NC_000021.9:g.36371830dup, NC_000021.9:g.36371829_36371830dup, NC_000021.9:g.36371828_36371830dup, NC_000021.9:g.36371827_36371830dup, NC_000021.9:g.36371826_36371830dup, NC_000021.9:g.36371821_36371830dup, NC_000021.8:g.37744122_37744128del, NC_000021.8:g.37744123_37744128del, NC_000021.8:g.37744124_37744128del, NC_000021.8:g.37744125_37744128del, NC_000021.8:g.37744126_37744128del, NC_000021.8:g.37744127_37744128del, NC_000021.8:g.37744128del, NC_000021.8:g.37744128dup, NC_000021.8:g.37744127_37744128dup, NC_000021.8:g.37744126_37744128dup, NC_000021.8:g.37744125_37744128dup, NC_000021.8:g.37744124_37744128dup, NC_000021.8:g.37744119_37744128dup
10.
rs1491314567 has merged into rs35837458 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- AAAAAAAAAAAAAAAAAAAAA>-,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAA
[Show Flanks]
- Chromosome:
- 21:36353360
(GRCh38)
21:37725658
(GRCh37)
- Canonical SPDI:
- NC_000021.9:36353355:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAA,NC_000021.9:36353355:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000021.9:36353355:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000021.9:36353355:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000021.9:36353355:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000021.9:36353355:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000021.9:36353355:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000021.9:36353355:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000021.9:36353355:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000021.9:36353355:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000021.9:36353355:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000021.9:36353355:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000021.9:36353355:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000021.9:36353355:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000021.9:36353355:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000021.9:36353355:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000021.9:36353355:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000021.9:36353355:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000021.9:36353355:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000021.9:36353355:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000021.9:36353355:AAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
- Gene:
- MORC3 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
AAAAAAAAAAAAA=0./0
(
ALFA)
AAAAAAAAAAAAAAAAAAAAA=0./0
(GENOME_DK)
- HGVS:
NC_000021.9:g.36353360_36353380del, NC_000021.9:g.36353369_36353380del, NC_000021.9:g.36353370_36353380del, NC_000021.9:g.36353371_36353380del, NC_000021.9:g.36353372_36353380del, NC_000021.9:g.36353373_36353380del, NC_000021.9:g.36353374_36353380del, NC_000021.9:g.36353375_36353380del, NC_000021.9:g.36353376_36353380del, NC_000021.9:g.36353377_36353380del, NC_000021.9:g.36353378_36353380del, NC_000021.9:g.36353379_36353380del, NC_000021.9:g.36353380del, NC_000021.9:g.36353380dup, NC_000021.9:g.36353379_36353380dup, NC_000021.9:g.36353378_36353380dup, NC_000021.9:g.36353377_36353380dup, NC_000021.9:g.36353376_36353380dup, NC_000021.9:g.36353375_36353380dup, NC_000021.9:g.36353374_36353380dup, NC_000021.9:g.36353373_36353380dup, NC_000021.8:g.37725658_37725678del, NC_000021.8:g.37725667_37725678del, NC_000021.8:g.37725668_37725678del, NC_000021.8:g.37725669_37725678del, NC_000021.8:g.37725670_37725678del, NC_000021.8:g.37725671_37725678del, NC_000021.8:g.37725672_37725678del, NC_000021.8:g.37725673_37725678del, NC_000021.8:g.37725674_37725678del, NC_000021.8:g.37725675_37725678del, NC_000021.8:g.37725676_37725678del, NC_000021.8:g.37725677_37725678del, NC_000021.8:g.37725678del, NC_000021.8:g.37725678dup, NC_000021.8:g.37725677_37725678dup, NC_000021.8:g.37725676_37725678dup, NC_000021.8:g.37725675_37725678dup, NC_000021.8:g.37725674_37725678dup, NC_000021.8:g.37725673_37725678dup, NC_000021.8:g.37725672_37725678dup, NC_000021.8:g.37725671_37725678dup
11.
rs1491243339 has merged into rs5843757 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- TTTTTTTTTTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
[Show Flanks]
- Chromosome:
- 21:36359566
(GRCh38)
21:37731864
(GRCh37)
- Canonical SPDI:
- NC_000021.9:36359556:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT,NC_000021.9:36359556:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000021.9:36359556:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000021.9:36359556:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000021.9:36359556:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000021.9:36359556:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000021.9:36359556:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000021.9:36359556:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000021.9:36359556:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000021.9:36359556:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000021.9:36359556:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000021.9:36359556:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000021.9:36359556:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000021.9:36359556:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000021.9:36359556:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000021.9:36359556:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000021.9:36359556:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000021.9:36359556:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000021.9:36359556:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000021.9:36359556:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000021.9:36359556:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000021.9:36359556:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000021.9:36359556:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000021.9:36359556:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000021.9:36359556:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000021.9:36359556:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000021.9:36359556:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000021.9:36359556:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000021.9:36359556:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000021.9:36359556:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000021.9:36359556:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000021.9:36359556:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000021.9:36359556:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000021.9:36359556:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000021.9:36359556:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000021.9:36359556:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000021.9:36359556:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000021.9:36359556:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000021.9:36359556:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000021.9:36359556:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000021.9:36359556:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000021.9:36359556:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000021.9:36359556:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000021.9:36359556:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000021.9:36359556:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- Gene:
- MORC3 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
TTTTTTTTT=0./0
(
ALFA)
TTT=0.2442/1223
(1000Genomes)
- HGVS:
NC_000021.9:g.36359566_36359581del, NC_000021.9:g.36359567_36359581del, NC_000021.9:g.36359568_36359581del, NC_000021.9:g.36359569_36359581del, NC_000021.9:g.36359570_36359581del, NC_000021.9:g.36359571_36359581del, NC_000021.9:g.36359572_36359581del, NC_000021.9:g.36359573_36359581del, NC_000021.9:g.36359574_36359581del, NC_000021.9:g.36359575_36359581del, NC_000021.9:g.36359576_36359581del, NC_000021.9:g.36359577_36359581del, NC_000021.9:g.36359578_36359581del, NC_000021.9:g.36359579_36359581del, NC_000021.9:g.36359580_36359581del, NC_000021.9:g.36359581del, NC_000021.9:g.36359581dup, NC_000021.9:g.36359580_36359581dup, NC_000021.9:g.36359579_36359581dup, NC_000021.9:g.36359578_36359581dup, NC_000021.9:g.36359577_36359581dup, NC_000021.9:g.36359576_36359581dup, NC_000021.9:g.36359575_36359581dup, NC_000021.9:g.36359574_36359581dup, NC_000021.9:g.36359573_36359581dup, NC_000021.9:g.36359572_36359581dup, NC_000021.9:g.36359571_36359581dup, NC_000021.9:g.36359570_36359581dup, NC_000021.9:g.36359569_36359581dup, NC_000021.9:g.36359568_36359581dup, NC_000021.9:g.36359567_36359581dup, NC_000021.9:g.36359566_36359581dup, NC_000021.9:g.36359565_36359581dup, NC_000021.9:g.36359564_36359581dup, NC_000021.9:g.36359563_36359581dup, NC_000021.9:g.36359561_36359581dup, NC_000021.9:g.36359560_36359581dup, NC_000021.9:g.36359559_36359581dup, NC_000021.9:g.36359558_36359581dup, NC_000021.9:g.36359581_36359582insTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000021.9:g.36359581_36359582insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000021.9:g.36359581_36359582insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000021.9:g.36359581_36359582insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000021.9:g.36359581_36359582insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000021.9:g.36359581_36359582insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000021.8:g.37731864_37731879del, NC_000021.8:g.37731865_37731879del, NC_000021.8:g.37731866_37731879del, NC_000021.8:g.37731867_37731879del, NC_000021.8:g.37731868_37731879del, NC_000021.8:g.37731869_37731879del, NC_000021.8:g.37731870_37731879del, NC_000021.8:g.37731871_37731879del, NC_000021.8:g.37731872_37731879del, NC_000021.8:g.37731873_37731879del, NC_000021.8:g.37731874_37731879del, NC_000021.8:g.37731875_37731879del, NC_000021.8:g.37731876_37731879del, NC_000021.8:g.37731877_37731879del, NC_000021.8:g.37731878_37731879del, NC_000021.8:g.37731879del, NC_000021.8:g.37731879dup, NC_000021.8:g.37731878_37731879dup, NC_000021.8:g.37731877_37731879dup, NC_000021.8:g.37731876_37731879dup, NC_000021.8:g.37731875_37731879dup, NC_000021.8:g.37731874_37731879dup, NC_000021.8:g.37731873_37731879dup, NC_000021.8:g.37731872_37731879dup, NC_000021.8:g.37731871_37731879dup, NC_000021.8:g.37731870_37731879dup, NC_000021.8:g.37731869_37731879dup, NC_000021.8:g.37731868_37731879dup, NC_000021.8:g.37731867_37731879dup, NC_000021.8:g.37731866_37731879dup, NC_000021.8:g.37731865_37731879dup, NC_000021.8:g.37731864_37731879dup, NC_000021.8:g.37731863_37731879dup, NC_000021.8:g.37731862_37731879dup, NC_000021.8:g.37731861_37731879dup, NC_000021.8:g.37731859_37731879dup, NC_000021.8:g.37731858_37731879dup, NC_000021.8:g.37731857_37731879dup, NC_000021.8:g.37731856_37731879dup, NC_000021.8:g.37731879_37731880insTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000021.8:g.37731879_37731880insTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000021.8:g.37731879_37731880insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000021.8:g.37731879_37731880insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000021.8:g.37731879_37731880insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000021.8:g.37731879_37731880insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
12.
rs1491220924 has merged into rs35441762 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- AAAAAAAAAAAAAAAAAAA>-,A,AA,AAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA
[Show Flanks]
- Chromosome:
- 21:36361550
(GRCh38)
21:37733848
(GRCh37)
- Canonical SPDI:
- NC_000021.9:36361540:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA,NC_000021.9:36361540:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000021.9:36361540:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000021.9:36361540:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000021.9:36361540:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000021.9:36361540:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000021.9:36361540:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000021.9:36361540:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000021.9:36361540:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000021.9:36361540:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000021.9:36361540:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000021.9:36361540:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000021.9:36361540:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000021.9:36361540:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000021.9:36361540:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000021.9:36361540:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000021.9:36361540:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000021.9:36361540:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000021.9:36361540:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000021.9:36361540:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000021.9:36361540:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000021.9:36361540:AAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
- Gene:
- MORC3 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
AAAAAAAAA=0./0
(
ALFA)
-=0.002/1
(NorthernSweden)
- HGVS:
NC_000021.9:g.36361550_36361568del, NC_000021.9:g.36361551_36361568del, NC_000021.9:g.36361552_36361568del, NC_000021.9:g.36361553_36361568del, NC_000021.9:g.36361556_36361568del, NC_000021.9:g.36361557_36361568del, NC_000021.9:g.36361558_36361568del, NC_000021.9:g.36361559_36361568del, NC_000021.9:g.36361560_36361568del, NC_000021.9:g.36361561_36361568del, NC_000021.9:g.36361562_36361568del, NC_000021.9:g.36361563_36361568del, NC_000021.9:g.36361564_36361568del, NC_000021.9:g.36361565_36361568del, NC_000021.9:g.36361566_36361568del, NC_000021.9:g.36361567_36361568del, NC_000021.9:g.36361568del, NC_000021.9:g.36361568dup, NC_000021.9:g.36361567_36361568dup, NC_000021.9:g.36361566_36361568dup, NC_000021.9:g.36361565_36361568dup, NC_000021.9:g.36361563_36361568dup, NC_000021.8:g.37733848_37733866del, NC_000021.8:g.37733849_37733866del, NC_000021.8:g.37733850_37733866del, NC_000021.8:g.37733851_37733866del, NC_000021.8:g.37733854_37733866del, NC_000021.8:g.37733855_37733866del, NC_000021.8:g.37733856_37733866del, NC_000021.8:g.37733857_37733866del, NC_000021.8:g.37733858_37733866del, NC_000021.8:g.37733859_37733866del, NC_000021.8:g.37733860_37733866del, NC_000021.8:g.37733861_37733866del, NC_000021.8:g.37733862_37733866del, NC_000021.8:g.37733863_37733866del, NC_000021.8:g.37733864_37733866del, NC_000021.8:g.37733865_37733866del, NC_000021.8:g.37733866del, NC_000021.8:g.37733866dup, NC_000021.8:g.37733865_37733866dup, NC_000021.8:g.37733864_37733866dup, NC_000021.8:g.37733863_37733866dup, NC_000021.8:g.37733861_37733866dup
15.
rs1491118383 [Homo sapiens]- Variant type:
- INS
- Alleles:
- ->CTCC
[Show Flanks]
- Chromosome:
- 21:36359557
(GRCh38)
21:37731856
(GRCh37)
- Canonical SPDI:
- NC_000021.9:36359557::CTCC
- Gene:
- MORC3 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa
- MAF:
CTCC=0./0
(
ALFA)
CTCC=0.000004/1
(TOPMED)
- HGVS:
18.
rs1491018994 has merged into rs71326676 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- TTTTTTTT>-,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT
[Show Flanks]
- Chromosome:
- 21:36336103
(GRCh38)
21:37708401
(GRCh37)
- Canonical SPDI:
- NC_000021.9:36336092:TTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000021.9:36336092:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000021.9:36336092:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000021.9:36336092:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000021.9:36336092:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000021.9:36336092:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000021.9:36336092:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000021.9:36336092:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT
- Gene:
- MORC3 (Varview)
- Functional Consequence:
- genic_upstream_transcript_variant,intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
TTTTTTTTTTTTTTTT=0./0
(
ALFA)
T=0.06856/41
(NorthernSweden)
-=0.1845/924
(1000Genomes)
T=0.25/2
(KOREAN)
T=0.5/20
(GENOME_DK)
- HGVS:
NC_000021.9:g.36336103_36336110del, NC_000021.9:g.36336107_36336110del, NC_000021.9:g.36336108_36336110del, NC_000021.9:g.36336109_36336110del, NC_000021.9:g.36336110del, NC_000021.9:g.36336110dup, NC_000021.9:g.36336109_36336110dup, NC_000021.9:g.36336108_36336110dup, NC_000021.8:g.37708401_37708408del, NC_000021.8:g.37708405_37708408del, NC_000021.8:g.37708406_37708408del, NC_000021.8:g.37708407_37708408del, NC_000021.8:g.37708408del, NC_000021.8:g.37708408dup, NC_000021.8:g.37708407_37708408dup, NC_000021.8:g.37708406_37708408dup
19.
rs1490945827 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- A>G
[Show Flanks]
- Chromosome:
- 21:36370067
(GRCh38)
21:37742365
(GRCh37)
- Canonical SPDI:
- NC_000021.9:36370066:A:G
- Gene:
- MORC3 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
G=0./0
(
ALFA)
G=0.000008/2
(TOPMED)
G=0.000021/3
(GnomAD)
- HGVS:
20.
rs1490866221 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- C>T
[Show Flanks]
- Chromosome:
- 21:36355055
(GRCh38)
21:37727353
(GRCh37)
- Canonical SPDI:
- NC_000021.9:36355054:C:T
- Gene:
- MORC3 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
T=0./0
(
ALFA)
T=0.000004/1
(TOPMED)
T=0.000007/1
(GnomAD)
- HGVS: