Links from Gene
Items: 1 to 20 of 1000
1.
rs1491569830 has merged into rs3073324 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- TTTTTTTTTTTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
[Show Flanks]
- Chromosome:
- 10:24633894
(GRCh38)
10:24922823
(GRCh37)
- Canonical SPDI:
- NC_000010.11:24633883:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000010.11:24633883:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000010.11:24633883:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000010.11:24633883:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000010.11:24633883:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000010.11:24633883:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000010.11:24633883:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000010.11:24633883:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000010.11:24633883:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000010.11:24633883:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000010.11:24633883:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000010.11:24633883:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000010.11:24633883:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:24633883:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:24633883:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:24633883:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:24633883:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:24633883:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:24633883:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:24633883:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:24633883:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:24633883:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:24633883:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:24633883:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:24633883:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:24633883:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:24633883:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:24633883:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:24633883:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:24633883:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:24633883:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:24633883:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:24633883:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:24633883:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:24633883:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:24633883:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:24633883:TTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- Gene:
- ARHGAP21 (Varview)
- Functional Consequence:
- genic_upstream_transcript_variant,intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
TTTTTTTTTT=0./0
(
ALFA)
-=0.01025/38
(TWINSUK)
-=0.01323/51
(ALSPAC)
- HGVS:
NC_000010.11:g.24633894_24633910del, NC_000010.11:g.24633895_24633910del, NC_000010.11:g.24633896_24633910del, NC_000010.11:g.24633897_24633910del, NC_000010.11:g.24633898_24633910del, NC_000010.11:g.24633899_24633910del, NC_000010.11:g.24633900_24633910del, NC_000010.11:g.24633901_24633910del, NC_000010.11:g.24633902_24633910del, NC_000010.11:g.24633903_24633910del, NC_000010.11:g.24633904_24633910del, NC_000010.11:g.24633905_24633910del, NC_000010.11:g.24633906_24633910del, NC_000010.11:g.24633907_24633910del, NC_000010.11:g.24633908_24633910del, NC_000010.11:g.24633909_24633910del, NC_000010.11:g.24633910del, NC_000010.11:g.24633910dup, NC_000010.11:g.24633909_24633910dup, NC_000010.11:g.24633908_24633910dup, NC_000010.11:g.24633907_24633910dup, NC_000010.11:g.24633906_24633910dup, NC_000010.11:g.24633905_24633910dup, NC_000010.11:g.24633904_24633910dup, NC_000010.11:g.24633903_24633910dup, NC_000010.11:g.24633902_24633910dup, NC_000010.11:g.24633901_24633910dup, NC_000010.11:g.24633900_24633910dup, NC_000010.11:g.24633899_24633910dup, NC_000010.11:g.24633898_24633910dup, NC_000010.11:g.24633897_24633910dup, NC_000010.11:g.24633896_24633910dup, NC_000010.11:g.24633895_24633910dup, NC_000010.11:g.24633894_24633910dup, NC_000010.11:g.24633893_24633910dup, NC_000010.11:g.24633892_24633910dup, NC_000010.11:g.24633910_24633911insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000010.10:g.24922823_24922839del, NC_000010.10:g.24922824_24922839del, NC_000010.10:g.24922825_24922839del, NC_000010.10:g.24922826_24922839del, NC_000010.10:g.24922827_24922839del, NC_000010.10:g.24922828_24922839del, NC_000010.10:g.24922829_24922839del, NC_000010.10:g.24922830_24922839del, NC_000010.10:g.24922831_24922839del, NC_000010.10:g.24922832_24922839del, NC_000010.10:g.24922833_24922839del, NC_000010.10:g.24922834_24922839del, NC_000010.10:g.24922835_24922839del, NC_000010.10:g.24922836_24922839del, NC_000010.10:g.24922837_24922839del, NC_000010.10:g.24922838_24922839del, NC_000010.10:g.24922839del, NC_000010.10:g.24922839dup, NC_000010.10:g.24922838_24922839dup, NC_000010.10:g.24922837_24922839dup, NC_000010.10:g.24922836_24922839dup, NC_000010.10:g.24922835_24922839dup, NC_000010.10:g.24922834_24922839dup, NC_000010.10:g.24922833_24922839dup, NC_000010.10:g.24922832_24922839dup, NC_000010.10:g.24922831_24922839dup, NC_000010.10:g.24922830_24922839dup, NC_000010.10:g.24922829_24922839dup, NC_000010.10:g.24922828_24922839dup, NC_000010.10:g.24922827_24922839dup, NC_000010.10:g.24922826_24922839dup, NC_000010.10:g.24922825_24922839dup, NC_000010.10:g.24922824_24922839dup, NC_000010.10:g.24922823_24922839dup, NC_000010.10:g.24922822_24922839dup, NC_000010.10:g.24922821_24922839dup, NC_000010.10:g.24922839_24922840insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
2.
rs1491555555 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- ->G
[Show Flanks]
- Chromosome:
- 10:24676148
(GRCh38)
10:24965078
(GRCh37)
- Canonical SPDI:
- NC_000010.11:24676148:GGGGG:GGGGGG
- Gene:
- ARHGAP21 (Varview)
- Functional Consequence:
- genic_upstream_transcript_variant,intron_variant
- Validated:
- by frequency,by alfa
- MAF:
GGGGGG=0./0
(
ALFA)
G=0.000019/5
(TOPMED)
- HGVS:
3.
rs1491540239 [Homo sapiens]- Variant type:
- INS
- Alleles:
- ->C
[Show Flanks]
- Chromosome:
- 10:24633884
(GRCh38)
10:24922814
(GRCh37)
- Canonical SPDI:
- NC_000010.11:24633884::C
- Gene:
- ARHGAP21 (Varview)
- Functional Consequence:
- genic_upstream_transcript_variant,intron_variant
- Validated:
- by frequency,by alfa
- MAF:
C=0./0
(
ALFA)
C=0.00012/4
(GnomAD)
- HGVS:
5.
rs1491491351 [Homo sapiens]- Variant type:
- INS
- Alleles:
- ->T,TGT,TGTGT
[Show Flanks]
- Chromosome:
- 10:24625051
(GRCh38)
10:24913981
(GRCh37)
- Canonical SPDI:
- NC_000010.11:24625051::T,NC_000010.11:24625051::TGT,NC_000010.11:24625051::TGTGT
- Gene:
- ARHGAP21 (Varview)
- Functional Consequence:
- genic_upstream_transcript_variant,intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
TGT=0./0
(
ALFA)
T=0.00102/45
(GnomAD)
- HGVS:
6.
rs1491472636 has merged into rs57863565 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- ACACACACACACACAC>-,AC,ACAC,ACACAC,ACACACAC,ACACACACAC,ACACACACACAC,ACACACACACACAC,ACACACACACACACACAC,ACACACACACACACACACAC,ACACACACACACACACACACAC,ACACACACACACACACACACACAC,ACACACACACACACACACACACACAC,ACACACACACACACACACACACACACAC,ACACACACACACACACACACACACACACAC,ACACACACACACACACACACACACACACACAC,ACACACACACACACACACACACACACACACACAC,ACACACACACACACACACACACACACACACACACAC,ACACACACACACACACACACACACACACACACACACAC,ACACACACACACACACACACACACACACACACACACACAC
[Show Flanks]
- Chromosome:
- 10:24719115
(GRCh38)
10:25008044
(GRCh37)
- Canonical SPDI:
- NC_000010.11:24719098:ACACACACACACACACACACACACACACACAC:ACACACACACACACAC,NC_000010.11:24719098:ACACACACACACACACACACACACACACACAC:ACACACACACACACACAC,NC_000010.11:24719098:ACACACACACACACACACACACACACACACAC:ACACACACACACACACACAC,NC_000010.11:24719098:ACACACACACACACACACACACACACACACAC:ACACACACACACACACACACAC,NC_000010.11:24719098:ACACACACACACACACACACACACACACACAC:ACACACACACACACACACACACAC,NC_000010.11:24719098:ACACACACACACACACACACACACACACACAC:ACACACACACACACACACACACACAC,NC_000010.11:24719098:ACACACACACACACACACACACACACACACAC:ACACACACACACACACACACACACACAC,NC_000010.11:24719098:ACACACACACACACACACACACACACACACAC:ACACACACACACACACACACACACACACAC,NC_000010.11:24719098:ACACACACACACACACACACACACACACACAC:ACACACACACACACACACACACACACACACACAC,NC_000010.11:24719098:ACACACACACACACACACACACACACACACAC:ACACACACACACACACACACACACACACACACACAC,NC_000010.11:24719098:ACACACACACACACACACACACACACACACAC:ACACACACACACACACACACACACACACACACACACAC,NC_000010.11:24719098:ACACACACACACACACACACACACACACACAC:ACACACACACACACACACACACACACACACACACACACAC,NC_000010.11:24719098:ACACACACACACACACACACACACACACACAC:ACACACACACACACACACACACACACACACACACACACACAC,NC_000010.11:24719098:ACACACACACACACACACACACACACACACAC:ACACACACACACACACACACACACACACACACACACACACACAC,NC_000010.11:24719098:ACACACACACACACACACACACACACACACAC:ACACACACACACACACACACACACACACACACACACACACACACAC,NC_000010.11:24719098:ACACACACACACACACACACACACACACACAC:ACACACACACACACACACACACACACACACACACACACACACACACAC,NC_000010.11:24719098:ACACACACACACACACACACACACACACACAC:ACACACACACACACACACACACACACACACACACACACACACACACACAC,NC_000010.11:24719098:ACACACACACACACACACACACACACACACAC:ACACACACACACACACACACACACACACACACACACACACACACACACACAC,NC_000010.11:24719098:ACACACACACACACACACACACACACACACAC:ACACACACACACACACACACACACACACACACACACACACACACACACACACAC,NC_000010.11:24719098:ACACACACACACACACACACACACACACACAC:ACACACACACACACACACACACACACACACACACACACACACACACACACACACAC
- Gene:
- ARHGAP21 (Varview)
- Functional Consequence:
- intron_variant,genic_upstream_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
ACACACACACACACACAC=0./0
(
ALFA)
- HGVS:
NC_000010.11:g.24719099AC[8], NC_000010.11:g.24719099AC[9], NC_000010.11:g.24719099AC[10], NC_000010.11:g.24719099AC[11], NC_000010.11:g.24719099AC[12], NC_000010.11:g.24719099AC[13], NC_000010.11:g.24719099AC[14], NC_000010.11:g.24719099AC[15], NC_000010.11:g.24719099AC[17], NC_000010.11:g.24719099AC[18], NC_000010.11:g.24719099AC[19], NC_000010.11:g.24719099AC[20], NC_000010.11:g.24719099AC[21], NC_000010.11:g.24719099AC[22], NC_000010.11:g.24719099AC[23], NC_000010.11:g.24719099AC[24], NC_000010.11:g.24719099AC[25], NC_000010.11:g.24719099AC[26], NC_000010.11:g.24719099AC[27], NC_000010.11:g.24719099AC[28], NC_000010.10:g.25008028AC[8], NC_000010.10:g.25008028AC[9], NC_000010.10:g.25008028AC[10], NC_000010.10:g.25008028AC[11], NC_000010.10:g.25008028AC[12], NC_000010.10:g.25008028AC[13], NC_000010.10:g.25008028AC[14], NC_000010.10:g.25008028AC[15], NC_000010.10:g.25008028AC[17], NC_000010.10:g.25008028AC[18], NC_000010.10:g.25008028AC[19], NC_000010.10:g.25008028AC[20], NC_000010.10:g.25008028AC[21], NC_000010.10:g.25008028AC[22], NC_000010.10:g.25008028AC[23], NC_000010.10:g.25008028AC[24], NC_000010.10:g.25008028AC[25], NC_000010.10:g.25008028AC[26], NC_000010.10:g.25008028AC[27], NC_000010.10:g.25008028AC[28]
7.
rs1491450733 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- ->GT
[Show Flanks]
- Chromosome:
- 10:24628751
(GRCh38)
10:24917681
(GRCh37)
- Canonical SPDI:
- NC_000010.11:24628751:T:TGT
- Gene:
- ARHGAP21 (Varview)
- Functional Consequence:
- genic_upstream_transcript_variant,intron_variant
- Validated:
- by frequency,by alfa
- MAF:
TGT=0./0
(
ALFA)
TG=0.00001/1
(GnomAD)
- HGVS:
8.
rs1491407050 [Homo sapiens]- Variant type:
- INS
- Alleles:
- ->C
[Show Flanks]
- Chromosome:
- 10:24610373
(GRCh38)
10:24899303
(GRCh37)
- Canonical SPDI:
- NC_000010.11:24610373::C
- Gene:
- ARHGAP21 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa
- MAF:
C=0./0
(
ALFA)
C=0.000011/3
(TOPMED)
- HGVS:
9.
rs1491367328 [Homo sapiens]- Variant type:
- INS
- Alleles:
- ->TC
[Show Flanks]
- Chromosome:
- 10:24592181
(GRCh38)
10:24881111
(GRCh37)
- Canonical SPDI:
- NC_000010.11:24592181::TC
- Gene:
- ARHGAP21 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa
- MAF:
TC=0./0
(
ALFA)
TC=0.00001/1
(GnomAD)
- HGVS:
10.
rs1491341536 [Homo sapiens]- Variant type:
- INS
- Alleles:
- ->AGTTG
[Show Flanks]
- Chromosome:
- 10:24593988
(GRCh38)
10:24882918
(GRCh37)
- Canonical SPDI:
- NC_000010.11:24593988::AGTTG
- Gene:
- ARHGAP21 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency
- MAF:
AGTTG=0.000007/1
(GnomAD)
- HGVS:
11.
rs1491332687 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- GA>-
[Show Flanks]
- Chromosome:
- 10:24595048
(GRCh38)
10:24883977
(GRCh37)
- Canonical SPDI:
- NC_000010.11:24595046:AGA:A
- Gene:
- ARHGAP21 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
A=0./0
(
ALFA)
-=0.000004/1
(GnomAD_exomes)
-=0.000004/1
(TOPMED)
-=0.000008/1
(ExAC)
- HGVS:
12.
rs1491330410 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- TA>-
[Show Flanks]
- Chromosome:
- 10:24593989
(GRCh38)
10:24882918
(GRCh37)
- Canonical SPDI:
- NC_000010.11:24593987:ATA:A
- Gene:
- ARHGAP21 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa
- MAF:
A=0./0
(
ALFA)
-=0.000004/1
(TOPMED)
- HGVS:
13.
rs1491319915 has merged into rs1166249007 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- TTTTTTTTTTTTTTTTTTTT>-,TT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT
[Show Flanks]
- Chromosome:
- 10:24628994
(GRCh38)
10:24917923
(GRCh37)
- Canonical SPDI:
- NC_000010.11:24628982:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000010.11:24628982:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000010.11:24628982:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000010.11:24628982:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000010.11:24628982:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000010.11:24628982:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000010.11:24628982:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000010.11:24628982:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000010.11:24628982:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000010.11:24628982:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:24628982:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:24628982:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:24628982:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:24628982:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:24628982:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:24628982:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:24628982:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:24628982:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:24628982:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:24628982:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:24628982:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:24628982:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:24628982:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:24628982:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:24628982:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:24628982:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:24628982:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- Gene:
- ARHGAP21 (Varview)
- Functional Consequence:
- intron_variant,genic_upstream_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
TTTTTTTTTTT=0./0
(
ALFA)
TT=0.02024/407
(TOMMO)
- HGVS:
NC_000010.11:g.24628994_24629013del, NC_000010.11:g.24628996_24629013del, NC_000010.11:g.24628998_24629013del, NC_000010.11:g.24628999_24629013del, NC_000010.11:g.24629000_24629013del, NC_000010.11:g.24629001_24629013del, NC_000010.11:g.24629002_24629013del, NC_000010.11:g.24629003_24629013del, NC_000010.11:g.24629004_24629013del, NC_000010.11:g.24629005_24629013del, NC_000010.11:g.24629006_24629013del, NC_000010.11:g.24629007_24629013del, NC_000010.11:g.24629008_24629013del, NC_000010.11:g.24629009_24629013del, NC_000010.11:g.24629010_24629013del, NC_000010.11:g.24629011_24629013del, NC_000010.11:g.24629012_24629013del, NC_000010.11:g.24629013del, NC_000010.11:g.24629013dup, NC_000010.11:g.24629012_24629013dup, NC_000010.11:g.24629011_24629013dup, NC_000010.11:g.24629010_24629013dup, NC_000010.11:g.24629009_24629013dup, NC_000010.11:g.24629008_24629013dup, NC_000010.11:g.24629007_24629013dup, NC_000010.11:g.24629006_24629013dup, NC_000010.11:g.24629005_24629013dup, NC_000010.10:g.24917923_24917942del, NC_000010.10:g.24917925_24917942del, NC_000010.10:g.24917927_24917942del, NC_000010.10:g.24917928_24917942del, NC_000010.10:g.24917929_24917942del, NC_000010.10:g.24917930_24917942del, NC_000010.10:g.24917931_24917942del, NC_000010.10:g.24917932_24917942del, NC_000010.10:g.24917933_24917942del, NC_000010.10:g.24917934_24917942del, NC_000010.10:g.24917935_24917942del, NC_000010.10:g.24917936_24917942del, NC_000010.10:g.24917937_24917942del, NC_000010.10:g.24917938_24917942del, NC_000010.10:g.24917939_24917942del, NC_000010.10:g.24917940_24917942del, NC_000010.10:g.24917941_24917942del, NC_000010.10:g.24917942del, NC_000010.10:g.24917942dup, NC_000010.10:g.24917941_24917942dup, NC_000010.10:g.24917940_24917942dup, NC_000010.10:g.24917939_24917942dup, NC_000010.10:g.24917938_24917942dup, NC_000010.10:g.24917937_24917942dup, NC_000010.10:g.24917936_24917942dup, NC_000010.10:g.24917935_24917942dup, NC_000010.10:g.24917934_24917942dup
14.
rs1491311930 has merged into rs34672775 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- AAAA>-,A,AA,AAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAAAA
[Show Flanks]
- Chromosome:
- 10:24645598
(GRCh38)
10:24934527
(GRCh37)
- Canonical SPDI:
- NC_000010.11:24645585:AAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000010.11:24645585:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000010.11:24645585:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000010.11:24645585:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000010.11:24645585:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000010.11:24645585:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000010.11:24645585:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000010.11:24645585:AAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA
- Gene:
- ARHGAP21 (Varview)
- Functional Consequence:
- intron_variant,genic_upstream_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
AAAAAAAAAAAAAA=0./0
(
ALFA)
-=0.1788/93
(NorthernSweden)
- HGVS:
NC_000010.11:g.24645598_24645601del, NC_000010.11:g.24645599_24645601del, NC_000010.11:g.24645600_24645601del, NC_000010.11:g.24645601del, NC_000010.11:g.24645601dup, NC_000010.11:g.24645600_24645601dup, NC_000010.11:g.24645599_24645601dup, NC_000010.11:g.24645596_24645601dup, NC_000010.10:g.24934527_24934530del, NC_000010.10:g.24934528_24934530del, NC_000010.10:g.24934529_24934530del, NC_000010.10:g.24934530del, NC_000010.10:g.24934530dup, NC_000010.10:g.24934529_24934530dup, NC_000010.10:g.24934528_24934530dup, NC_000010.10:g.24934525_24934530dup
15.
rs1491274903 has merged into rs1214553998 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- CT>-,CTCT
[Show Flanks]
- Chromosome:
- 10:24592182
(GRCh38)
10:24881111
(GRCh37)
- Canonical SPDI:
- NC_000010.11:24592180:TCT:T,NC_000010.11:24592180:TCT:TCTCT
- Gene:
- ARHGAP21 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
T=0.000372/6
(
ALFA)
TC=0.000041/5
(GnomAD)
-=0.000179/3
(TOMMO)
- HGVS:
16.
rs1491272202 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- GT>-
[Show Flanks]
- Chromosome:
- 10:24584242
(GRCh38)
10:24873171
(GRCh37)
- Canonical SPDI:
- NC_000010.11:24584240:TGT:T
- Gene:
- ARHGAP21 (Varview)
- Functional Consequence:
- 3_prime_UTR_variant,genic_downstream_transcript_variant,non_coding_transcript_variant
- Validated:
- by frequency,by cluster
- MAF:
-=0.0197/76
(ALSPAC)
-=0.0332/123
(TWINSUK)
- HGVS:
NC_000010.11:g.24584242_24584243del, NC_000010.10:g.24873171_24873172del, XM_011519603.4:c.*170_*171del, XM_011519603.3:c.*170_*171del, XM_011519603.2:c.*170_*171del, XM_011519603.1:c.*170_*171del, NM_020824.4:c.*170_*171del, NM_020824.3:c.*170_*171del, XM_011519606.3:c.*170_*171del, XM_011519606.2:c.*170_*171del, XM_011519606.1:c.*170_*171del, XM_011519602.3:c.*170_*171del, XM_011519602.2:c.*170_*171del, XM_011519602.1:c.*170_*171del, XM_011519605.3:c.*170_*171del, XM_011519605.2:c.*170_*171del, XM_011519605.1:c.*170_*171del, XM_011519607.3:c.*1567_*1568del, XM_011519607.2:c.*1567_*1568del, XM_011519604.3:c.*170_*171del, XM_011519604.2:c.*170_*171del, XM_011519604.1:c.*170_*171del, NR_160023.1:n.6964_6965del, NR_160022.1:n.6883_6884del, NM_001367450.1:c.*170_*171del, NR_160021.1:n.6766_6767del, XM_047425556.1:c.*170_*171del, NM_001367447.1:c.*170_*171del, NM_001367453.1:c.*170_*171del, XM_047425560.1:c.*1567_*1568del, NM_001367454.1:c.*170_*171del, XM_047425561.1:c.*1567_*1568del, XM_047425557.1:c.*170_*171del, NM_001367449.1:c.*170_*171del, NM_001367448.1:c.*170_*171del, NM_001367451.1:c.*170_*171del, XM_047425562.1:c.*1567_*1568del, NM_001367452.1:c.*170_*171del, NR_160025.1:n.5985_5986del, NR_160024.1:n.5907_5908del, NM_001367455.1:c.*170_*171del
17.
rs1491218327 has merged into rs57313842 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- GGGGG>-,G,GG,GGG,GGGG,GGGGGG,GGGGGGG,GGGGGGGG,GGGGGGGGG,GGGGGGGGGG,GGGGGGGGGGG,GGGGGGGGGGGG,GGGGGGGGGGGGG,GGGGGGGGGGGGGG
[Show Flanks]
- Chromosome:
- 10:24625060
(GRCh38)
10:24913989
(GRCh37)
- Canonical SPDI:
- NC_000010.11:24625050:GGGGGGGGGGGGGG:GGGGGGGGG,NC_000010.11:24625050:GGGGGGGGGGGGGG:GGGGGGGGGG,NC_000010.11:24625050:GGGGGGGGGGGGGG:GGGGGGGGGGG,NC_000010.11:24625050:GGGGGGGGGGGGGG:GGGGGGGGGGGG,NC_000010.11:24625050:GGGGGGGGGGGGGG:GGGGGGGGGGGGG,NC_000010.11:24625050:GGGGGGGGGGGGGG:GGGGGGGGGGGGGGG,NC_000010.11:24625050:GGGGGGGGGGGGGG:GGGGGGGGGGGGGGGG,NC_000010.11:24625050:GGGGGGGGGGGGGG:GGGGGGGGGGGGGGGGG,NC_000010.11:24625050:GGGGGGGGGGGGGG:GGGGGGGGGGGGGGGGGG,NC_000010.11:24625050:GGGGGGGGGGGGGG:GGGGGGGGGGGGGGGGGGG,NC_000010.11:24625050:GGGGGGGGGGGGGG:GGGGGGGGGGGGGGGGGGGG,NC_000010.11:24625050:GGGGGGGGGGGGGG:GGGGGGGGGGGGGGGGGGGGG,NC_000010.11:24625050:GGGGGGGGGGGGGG:GGGGGGGGGGGGGGGGGGGGGG,NC_000010.11:24625050:GGGGGGGGGGGGGG:GGGGGGGGGGGGGGGGGGGGGGG
- Gene:
- ARHGAP21 (Varview)
- Functional Consequence:
- intron_variant,genic_upstream_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
GGGGGGGGGG=0./0
(
ALFA)
GGGGGGGGG=0.00154/2
(Korea1K)
- HGVS:
NC_000010.11:g.24625060_24625064del, NC_000010.11:g.24625061_24625064del, NC_000010.11:g.24625062_24625064del, NC_000010.11:g.24625063_24625064del, NC_000010.11:g.24625064del, NC_000010.11:g.24625064dup, NC_000010.11:g.24625063_24625064dup, NC_000010.11:g.24625062_24625064dup, NC_000010.11:g.24625061_24625064dup, NC_000010.11:g.24625060_24625064dup, NC_000010.11:g.24625059_24625064dup, NC_000010.11:g.24625058_24625064dup, NC_000010.11:g.24625057_24625064dup, NC_000010.11:g.24625056_24625064dup, NC_000010.10:g.24913989_24913993del, NC_000010.10:g.24913990_24913993del, NC_000010.10:g.24913991_24913993del, NC_000010.10:g.24913992_24913993del, NC_000010.10:g.24913993del, NC_000010.10:g.24913993dup, NC_000010.10:g.24913992_24913993dup, NC_000010.10:g.24913991_24913993dup, NC_000010.10:g.24913990_24913993dup, NC_000010.10:g.24913989_24913993dup, NC_000010.10:g.24913988_24913993dup, NC_000010.10:g.24913987_24913993dup, NC_000010.10:g.24913986_24913993dup, NC_000010.10:g.24913985_24913993dup
18.
rs1491096944 has merged into rs57846258 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- TTTTTTTTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
[Show Flanks]
- Chromosome:
- 10:24592168
(GRCh38)
10:24881097
(GRCh37)
- Canonical SPDI:
- NC_000010.11:24592156:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000010.11:24592156:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000010.11:24592156:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000010.11:24592156:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000010.11:24592156:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000010.11:24592156:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000010.11:24592156:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000010.11:24592156:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000010.11:24592156:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000010.11:24592156:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000010.11:24592156:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000010.11:24592156:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:24592156:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:24592156:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:24592156:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:24592156:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:24592156:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:24592156:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:24592156:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:24592156:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:24592156:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:24592156:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:24592156:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:24592156:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:24592156:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:24592156:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:24592156:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:24592156:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:24592156:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:24592156:TTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- Gene:
- ARHGAP21 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
TTTTTTTTTTT=0./0
(
ALFA)
-=0.000094/25
(TOPMED)
-=0.455471/2281
(1000Genomes)
- HGVS:
NC_000010.11:g.24592168_24592181del, NC_000010.11:g.24592169_24592181del, NC_000010.11:g.24592170_24592181del, NC_000010.11:g.24592171_24592181del, NC_000010.11:g.24592172_24592181del, NC_000010.11:g.24592173_24592181del, NC_000010.11:g.24592174_24592181del, NC_000010.11:g.24592175_24592181del, NC_000010.11:g.24592176_24592181del, NC_000010.11:g.24592177_24592181del, NC_000010.11:g.24592178_24592181del, NC_000010.11:g.24592179_24592181del, NC_000010.11:g.24592180_24592181del, NC_000010.11:g.24592181del, NC_000010.11:g.24592181dup, NC_000010.11:g.24592180_24592181dup, NC_000010.11:g.24592179_24592181dup, NC_000010.11:g.24592178_24592181dup, NC_000010.11:g.24592177_24592181dup, NC_000010.11:g.24592157_24592181T[30]ATTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000010.11:g.24592176_24592181dup, NC_000010.11:g.24592174_24592181dup, NC_000010.11:g.24592172_24592181dup, NC_000010.11:g.24592171_24592181dup, NC_000010.11:g.24592166_24592181dup, NC_000010.11:g.24592161_24592181dup, NC_000010.11:g.24592160_24592181dup, NC_000010.11:g.24592159_24592181dup, NC_000010.11:g.24592181_24592182insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000010.11:g.24592181_24592182insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000010.10:g.24881097_24881110del, NC_000010.10:g.24881098_24881110del, NC_000010.10:g.24881099_24881110del, NC_000010.10:g.24881100_24881110del, NC_000010.10:g.24881101_24881110del, NC_000010.10:g.24881102_24881110del, NC_000010.10:g.24881103_24881110del, NC_000010.10:g.24881104_24881110del, NC_000010.10:g.24881105_24881110del, NC_000010.10:g.24881106_24881110del, NC_000010.10:g.24881107_24881110del, NC_000010.10:g.24881108_24881110del, NC_000010.10:g.24881109_24881110del, NC_000010.10:g.24881110del, NC_000010.10:g.24881110dup, NC_000010.10:g.24881109_24881110dup, NC_000010.10:g.24881108_24881110dup, NC_000010.10:g.24881107_24881110dup, NC_000010.10:g.24881106_24881110dup, NC_000010.10:g.24881086_24881110T[30]ATTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NC_000010.10:g.24881105_24881110dup, NC_000010.10:g.24881103_24881110dup, NC_000010.10:g.24881101_24881110dup, NC_000010.10:g.24881100_24881110dup, NC_000010.10:g.24881095_24881110dup, NC_000010.10:g.24881090_24881110dup, NC_000010.10:g.24881089_24881110dup, NC_000010.10:g.24881088_24881110dup, NC_000010.10:g.24881110_24881111insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000010.10:g.24881110_24881111insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
19.
rs1491091181 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- ->T
[Show Flanks]
- Chromosome:
- 10:24628851
(GRCh38)
10:24917781
(GRCh37)
- Canonical SPDI:
- NC_000010.11:24628851:T:TT
- Gene:
- ARHGAP21 (Varview)
- Functional Consequence:
- genic_upstream_transcript_variant,intron_variant
- Validated:
- by frequency,by alfa
- MAF:
TT=0./0
(
ALFA)
T=0.000004/1
(TOPMED)
- HGVS:
20.
rs1491071611 has merged into rs71798625 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- TTTTTTTTTTTT>-,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
[Show Flanks]
- Chromosome:
- 10:24702137
(GRCh38)
10:24991066
(GRCh37)
- Canonical SPDI:
- NC_000010.11:24702127:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTT,NC_000010.11:24702127:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000010.11:24702127:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000010.11:24702127:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000010.11:24702127:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000010.11:24702127:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000010.11:24702127:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000010.11:24702127:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000010.11:24702127:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000010.11:24702127:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000010.11:24702127:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:24702127:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:24702127:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:24702127:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:24702127:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:24702127:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:24702127:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:24702127:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:24702127:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:24702127:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:24702127:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:24702127:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:24702127:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:24702127:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:24702127:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000010.11:24702127:TTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- Gene:
- ARHGAP21 (Varview)
- Functional Consequence:
- intron_variant,genic_upstream_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
- HGVS:
NC_000010.11:g.24702137_24702148del, NC_000010.11:g.24702140_24702148del, NC_000010.11:g.24702141_24702148del, NC_000010.11:g.24702142_24702148del, NC_000010.11:g.24702143_24702148del, NC_000010.11:g.24702144_24702148del, NC_000010.11:g.24702145_24702148del, NC_000010.11:g.24702146_24702148del, NC_000010.11:g.24702147_24702148del, NC_000010.11:g.24702148del, NC_000010.11:g.24702148dup, NC_000010.11:g.24702147_24702148dup, NC_000010.11:g.24702146_24702148dup, NC_000010.11:g.24702145_24702148dup, NC_000010.11:g.24702144_24702148dup, NC_000010.11:g.24702143_24702148dup, NC_000010.11:g.24702142_24702148dup, NC_000010.11:g.24702141_24702148dup, NC_000010.11:g.24702140_24702148dup, NC_000010.11:g.24702139_24702148dup, NC_000010.11:g.24702138_24702148dup, NC_000010.11:g.24702135_24702148dup, NC_000010.11:g.24702133_24702148dup, NC_000010.11:g.24702148_24702149insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000010.11:g.24702148_24702149insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000010.11:g.24702148_24702149insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000010.10:g.24991066_24991077del, NC_000010.10:g.24991069_24991077del, NC_000010.10:g.24991070_24991077del, NC_000010.10:g.24991071_24991077del, NC_000010.10:g.24991072_24991077del, NC_000010.10:g.24991073_24991077del, NC_000010.10:g.24991074_24991077del, NC_000010.10:g.24991075_24991077del, NC_000010.10:g.24991076_24991077del, NC_000010.10:g.24991077del, NC_000010.10:g.24991077dup, NC_000010.10:g.24991076_24991077dup, NC_000010.10:g.24991075_24991077dup, NC_000010.10:g.24991074_24991077dup, NC_000010.10:g.24991073_24991077dup, NC_000010.10:g.24991072_24991077dup, NC_000010.10:g.24991071_24991077dup, NC_000010.10:g.24991070_24991077dup, NC_000010.10:g.24991069_24991077dup, NC_000010.10:g.24991068_24991077dup, NC_000010.10:g.24991067_24991077dup, NC_000010.10:g.24991064_24991077dup, NC_000010.10:g.24991062_24991077dup, NC_000010.10:g.24991077_24991078insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000010.10:g.24991077_24991078insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000010.10:g.24991077_24991078insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT