Links from Gene
Items: 1 to 20 of 1000
1.
rs1491573908 [Homo sapiens]- Variant type:
- INS
- Alleles:
- ->C,CTC,CTCTC,CTCTCTC,CTCTCTCTC
[Show Flanks]
- Chromosome:
- 8:53889413
(GRCh38)
8:54801974
(GRCh37)
- Canonical SPDI:
- NC_000008.11:53889413::C,NC_000008.11:53889413::CTC,NC_000008.11:53889413::CTCTC,NC_000008.11:53889413::CTCTCTC,NC_000008.11:53889413::CTCTCTCTC
- Gene:
- RGS20 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
CTC=0./0
(
ALFA)
C=0.00016/2
(TOMMO)
C=0.00056/1
(Korea1K)
- HGVS:
2.
rs1491536262 has merged into rs34316630 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- TTTTTTTTTTTTTTTTTTTTTTTTTTTT>-,T,TT,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
[Show Flanks]
- Chromosome:
- 8:53889424
(GRCh38)
8:54801984
(GRCh37)
- Canonical SPDI:
- NC_000008.11:53889412:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000008.11:53889412:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000008.11:53889412:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000008.11:53889412:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000008.11:53889412:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000008.11:53889412:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000008.11:53889412:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000008.11:53889412:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000008.11:53889412:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000008.11:53889412:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000008.11:53889412:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000008.11:53889412:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:53889412:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:53889412:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:53889412:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:53889412:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:53889412:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:53889412:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:53889412:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:53889412:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:53889412:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:53889412:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:53889412:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:53889412:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:53889412:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:53889412:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:53889412:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:53889412:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:53889412:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:53889412:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:53889412:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:53889412:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:53889412:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:53889412:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:53889412:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:53889412:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:53889412:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:53889412:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:53889412:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:53889412:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:53889412:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:53889412:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:53889412:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:53889412:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:53889412:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:53889412:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:53889412:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:53889412:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:53889412:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:53889412:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:53889412:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- Gene:
- RGS20 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
- HGVS:
NC_000008.11:g.53889424_53889451del, NC_000008.11:g.53889425_53889451del, NC_000008.11:g.53889426_53889451del, NC_000008.11:g.53889427_53889451del, NC_000008.11:g.53889428_53889451del, NC_000008.11:g.53889429_53889451del, NC_000008.11:g.53889430_53889451del, NC_000008.11:g.53889431_53889451del, NC_000008.11:g.53889432_53889451del, NC_000008.11:g.53889433_53889451del, NC_000008.11:g.53889434_53889451del, NC_000008.11:g.53889435_53889451del, NC_000008.11:g.53889436_53889451del, NC_000008.11:g.53889437_53889451del, NC_000008.11:g.53889438_53889451del, NC_000008.11:g.53889439_53889451del, NC_000008.11:g.53889440_53889451del, NC_000008.11:g.53889441_53889451del, NC_000008.11:g.53889442_53889451del, NC_000008.11:g.53889443_53889451del, NC_000008.11:g.53889444_53889451del, NC_000008.11:g.53889445_53889451del, NC_000008.11:g.53889446_53889451del, NC_000008.11:g.53889447_53889451del, NC_000008.11:g.53889448_53889451del, NC_000008.11:g.53889449_53889451del, NC_000008.11:g.53889450_53889451del, NC_000008.11:g.53889451del, NC_000008.11:g.53889451dup, NC_000008.11:g.53889450_53889451dup, NC_000008.11:g.53889449_53889451dup, NC_000008.11:g.53889445_53889451dup, NC_000008.11:g.53889444_53889451dup, NC_000008.11:g.53889441_53889451dup, NC_000008.11:g.53889440_53889451dup, NC_000008.11:g.53889439_53889451dup, NC_000008.11:g.53889438_53889451dup, NC_000008.11:g.53889437_53889451dup, NC_000008.11:g.53889435_53889451dup, NC_000008.11:g.53889434_53889451dup, NC_000008.11:g.53889433_53889451dup, NC_000008.11:g.53889431_53889451dup, NC_000008.11:g.53889430_53889451dup, NC_000008.11:g.53889429_53889451dup, NC_000008.11:g.53889428_53889451dup, NC_000008.11:g.53889427_53889451dup, NC_000008.11:g.53889424_53889451dup, NC_000008.11:g.53889422_53889451dup, NC_000008.11:g.53889421_53889451dup, NC_000008.11:g.53889420_53889451dup, NC_000008.11:g.53889451_53889452insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000008.10:g.54801984_54802011del, NC_000008.10:g.54801985_54802011del, NC_000008.10:g.54801986_54802011del, NC_000008.10:g.54801987_54802011del, NC_000008.10:g.54801988_54802011del, NC_000008.10:g.54801989_54802011del, NC_000008.10:g.54801990_54802011del, NC_000008.10:g.54801991_54802011del, NC_000008.10:g.54801992_54802011del, NC_000008.10:g.54801993_54802011del, NC_000008.10:g.54801994_54802011del, NC_000008.10:g.54801995_54802011del, NC_000008.10:g.54801996_54802011del, NC_000008.10:g.54801997_54802011del, NC_000008.10:g.54801998_54802011del, NC_000008.10:g.54801999_54802011del, NC_000008.10:g.54802000_54802011del, NC_000008.10:g.54802001_54802011del, NC_000008.10:g.54802002_54802011del, NC_000008.10:g.54802003_54802011del, NC_000008.10:g.54802004_54802011del, NC_000008.10:g.54802005_54802011del, NC_000008.10:g.54802006_54802011del, NC_000008.10:g.54802007_54802011del, NC_000008.10:g.54802008_54802011del, NC_000008.10:g.54802009_54802011del, NC_000008.10:g.54802010_54802011del, NC_000008.10:g.54802011del, NC_000008.10:g.54802011dup, NC_000008.10:g.54802010_54802011dup, NC_000008.10:g.54802009_54802011dup, NC_000008.10:g.54802005_54802011dup, NC_000008.10:g.54802004_54802011dup, NC_000008.10:g.54802001_54802011dup, NC_000008.10:g.54802000_54802011dup, NC_000008.10:g.54801999_54802011dup, NC_000008.10:g.54801998_54802011dup, NC_000008.10:g.54801997_54802011dup, NC_000008.10:g.54801995_54802011dup, NC_000008.10:g.54801994_54802011dup, NC_000008.10:g.54801993_54802011dup, NC_000008.10:g.54801991_54802011dup, NC_000008.10:g.54801990_54802011dup, NC_000008.10:g.54801989_54802011dup, NC_000008.10:g.54801988_54802011dup, NC_000008.10:g.54801987_54802011dup, NC_000008.10:g.54801984_54802011dup, NC_000008.10:g.54801982_54802011dup, NC_000008.10:g.54801981_54802011dup, NC_000008.10:g.54801980_54802011dup, NC_000008.10:g.54802011_54802012insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
3.
rs1491529134 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- ->CA
[Show Flanks]
- Chromosome:
- 8:53948331
(GRCh38)
8:54860892
(GRCh37)
- Canonical SPDI:
- NC_000008.11:53948331:A:ACA
- Gene:
- RGS20 (Varview)
- Functional Consequence:
- genic_downstream_transcript_variant,intron_variant
- Validated:
- by frequency
- MAF:
AC=0.000008/1
(GnomAD)
- HGVS:
4.
rs1491509027 [Homo sapiens]- Variant type:
- INS
- Alleles:
- ->AA
[Show Flanks]
- Chromosome:
- 8:53948553
(GRCh38)
8:54861114
(GRCh37)
- Canonical SPDI:
- NC_000008.11:53948553::AA
- Gene:
- RGS20 (Varview)
- Functional Consequence:
- genic_downstream_transcript_variant,intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
AA=0.00632/75
(
ALFA)
AA=0.00035/19
(GnomAD)
- HGVS:
5.
rs1491506299 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- TA>-
[Show Flanks]
- Chromosome:
- 8:53948399
(GRCh38)
8:54860959
(GRCh37)
- Canonical SPDI:
- NC_000008.11:53948397:ATA:A
- Gene:
- RGS20 (Varview)
- Functional Consequence:
- genic_downstream_transcript_variant,intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
A=0.000796/13
(
ALFA)
-=0.000071/2
(TOMMO)
-=0.00069/89
(GnomAD)
- HGVS:
6.
rs1491452031 [Homo sapiens]- Variant type:
- DEL
- Alleles:
- GT>-
[Show Flanks]
- Chromosome:
- 8:53927201
(GRCh38)
8:54839761
(GRCh37)
- Canonical SPDI:
- NC_000008.11:53927200:GT:
- Gene:
- RGS20 (Varview)
- Functional Consequence:
- genic_downstream_transcript_variant,intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
-=0./0
(
ALFA)
-=0.00025/4
(TOMMO)
- HGVS:
7.
rs1491440781 has merged into rs1178436696 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- TATATATATATATATATATATATATATATATATATA>-,TA,TATA,TATATA,TATATATA,TATATATATA,TATATATATATA,TATATATATATATA,TATATATATATATATA,TATATATATATATATATA,TATATATATATATATATATA,TATATATATATATATATATATA,TATATATATATATATATATATATA,TATATATATATATATATATATATATA,TATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATATATATATATATATA,TATATATATATATATATATATATATATATATATATATATATATATATATATA
[Show Flanks]
- Chromosome:
- 8:53909220
(GRCh38)
8:54821780
(GRCh37)
- Canonical SPDI:
- NC_000008.11:53909209:TATATATATATATATATATATATATATATATATATATATATATATA:TATATATATA,NC_000008.11:53909209:TATATATATATATATATATATATATATATATATATATATATATATA:TATATATATATA,NC_000008.11:53909209:TATATATATATATATATATATATATATATATATATATATATATATA:TATATATATATATA,NC_000008.11:53909209:TATATATATATATATATATATATATATATATATATATATATATATA:TATATATATATATATA,NC_000008.11:53909209:TATATATATATATATATATATATATATATATATATATATATATATA:TATATATATATATATATA,NC_000008.11:53909209:TATATATATATATATATATATATATATATATATATATATATATATA:TATATATATATATATATATA,NC_000008.11:53909209:TATATATATATATATATATATATATATATATATATATATATATATA:TATATATATATATATATATATA,NC_000008.11:53909209:TATATATATATATATATATATATATATATATATATATATATATATA:TATATATATATATATATATATATA,NC_000008.11:53909209:TATATATATATATATATATATATATATATATATATATATATATATA:TATATATATATATATATATATATATA,NC_000008.11:53909209:TATATATATATATATATATATATATATATATATATATATATATATA:TATATATATATATATATATATATATATA,NC_000008.11:53909209:TATATATATATATATATATATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATA,NC_000008.11:53909209:TATATATATATATATATATATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATA,NC_000008.11:53909209:TATATATATATATATATATATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATATA,NC_000008.11:53909209:TATATATATATATATATATATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATATATA,NC_000008.11:53909209:TATATATATATATATATATATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATATATATA,NC_000008.11:53909209:TATATATATATATATATATATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATATATATATA,NC_000008.11:53909209:TATATATATATATATATATATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATATATATATATA,NC_000008.11:53909209:TATATATATATATATATATATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATATATATATATATA,NC_000008.11:53909209:TATATATATATATATATATATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATATATATATATATATATA,NC_000008.11:53909209:TATATATATATATATATATATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATATATATATATATATATATA,NC_000008.11:53909209:TATATATATATATATATATATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATATATATATATATATATATATA,NC_000008.11:53909209:TATATATATATATATATATATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATATATATATATATATATATATATA,NC_000008.11:53909209:TATATATATATATATATATATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATATATATATATATATATATATATATA,NC_000008.11:53909209:TATATATATATATATATATATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATATATATATATATATATATATATATATA,NC_000008.11:53909209:TATATATATATATATATATATATATATATATATATATATATATATA:TATATATATATATATATATATATATATATATATATATATATATATATATATATATATATATA
- Gene:
- RGS20 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
- HGVS:
NC_000008.11:g.53909210TA[5], NC_000008.11:g.53909210TA[6], NC_000008.11:g.53909210TA[7], NC_000008.11:g.53909210TA[8], NC_000008.11:g.53909210TA[9], NC_000008.11:g.53909210TA[10], NC_000008.11:g.53909210TA[11], NC_000008.11:g.53909210TA[12], NC_000008.11:g.53909210TA[13], NC_000008.11:g.53909210TA[14], NC_000008.11:g.53909210TA[15], NC_000008.11:g.53909210TA[16], NC_000008.11:g.53909210TA[17], NC_000008.11:g.53909210TA[18], NC_000008.11:g.53909210TA[19], NC_000008.11:g.53909210TA[20], NC_000008.11:g.53909210TA[21], NC_000008.11:g.53909210TA[22], NC_000008.11:g.53909210TA[24], NC_000008.11:g.53909210TA[25], NC_000008.11:g.53909210TA[26], NC_000008.11:g.53909210TA[27], NC_000008.11:g.53909210TA[28], NC_000008.11:g.53909210TA[29], NC_000008.11:g.53909210TA[31], NC_000008.10:g.54821770TA[5], NC_000008.10:g.54821770TA[6], NC_000008.10:g.54821770TA[7], NC_000008.10:g.54821770TA[8], NC_000008.10:g.54821770TA[9], NC_000008.10:g.54821770TA[10], NC_000008.10:g.54821770TA[11], NC_000008.10:g.54821770TA[12], NC_000008.10:g.54821770TA[13], NC_000008.10:g.54821770TA[14], NC_000008.10:g.54821770TA[15], NC_000008.10:g.54821770TA[16], NC_000008.10:g.54821770TA[17], NC_000008.10:g.54821770TA[18], NC_000008.10:g.54821770TA[19], NC_000008.10:g.54821770TA[20], NC_000008.10:g.54821770TA[21], NC_000008.10:g.54821770TA[22], NC_000008.10:g.54821770TA[24], NC_000008.10:g.54821770TA[25], NC_000008.10:g.54821770TA[26], NC_000008.10:g.54821770TA[27], NC_000008.10:g.54821770TA[28], NC_000008.10:g.54821770TA[29], NC_000008.10:g.54821770TA[31]
8.
rs1491422517 [Homo sapiens]- Variant type:
- DEL
- Alleles:
- TG>-
[Show Flanks]
- Chromosome:
- 8:53948584
(GRCh38)
8:54861144
(GRCh37)
- Canonical SPDI:
- NC_000008.11:53948583:TG:
- Gene:
- RGS20 (Varview)
- Functional Consequence:
- genic_downstream_transcript_variant,intron_variant
- Validated:
- by frequency,by cluster
- MAF:
-=0.01492/961
(GnomAD)
- HGVS:
9.
rs1491312735 has merged into rs553191513 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- TTTTT>-,T,TT,TTT,TTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
[Show Flanks]
- Chromosome:
- 8:53927214
(GRCh38)
8:54839774
(GRCh37)
- Canonical SPDI:
- NC_000008.11:53927201:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000008.11:53927201:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000008.11:53927201:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000008.11:53927201:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000008.11:53927201:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000008.11:53927201:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000008.11:53927201:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000008.11:53927201:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000008.11:53927201:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000008.11:53927201:TTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- Gene:
- RGS20 (Varview)
- Functional Consequence:
- intron_variant,genic_downstream_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
TTTTTTTTTTTTTT=0./0
(
ALFA)
-=0.26977/1351
(1000Genomes)
-=0.325/13
(GENOME_DK)
- HGVS:
NC_000008.11:g.53927214_53927218del, NC_000008.11:g.53927215_53927218del, NC_000008.11:g.53927216_53927218del, NC_000008.11:g.53927217_53927218del, NC_000008.11:g.53927218del, NC_000008.11:g.53927218dup, NC_000008.11:g.53927217_53927218dup, NC_000008.11:g.53927216_53927218dup, NC_000008.11:g.53927215_53927218dup, NC_000008.11:g.53927218_53927219insTTTTTTTTTTTTTTTTTTTTTTTTTTT, NC_000008.10:g.54839774_54839778del, NC_000008.10:g.54839775_54839778del, NC_000008.10:g.54839776_54839778del, NC_000008.10:g.54839777_54839778del, NC_000008.10:g.54839778del, NC_000008.10:g.54839778dup, NC_000008.10:g.54839777_54839778dup, NC_000008.10:g.54839776_54839778dup, NC_000008.10:g.54839775_54839778dup, NC_000008.10:g.54839778_54839779insTTTTTTTTTTTTTTTTTTTTTTTTTTT
10.
rs1491300679 [Homo sapiens]- Variant type:
- INS
- Alleles:
- ->CACAG
[Show Flanks]
- Chromosome:
- 8:53948398
(GRCh38)
8:54860959
(GRCh37)
- Canonical SPDI:
- NC_000008.11:53948398::CACAG
- Gene:
- RGS20 (Varview)
- Functional Consequence:
- genic_downstream_transcript_variant,intron_variant
- Validated:
- by frequency,by cluster
- MAF:
CACAG=0.000142/2
(TOMMO)
CACAG=0.000311/41
(GnomAD)
- HGVS:
11.
rs1491240899 [Homo sapiens]- Variant type:
- INS
- Alleles:
- ->TAT,TG,TGATAT
[Show Flanks]
- Chromosome:
- 8:53948211
(GRCh38)
8:54860772
(GRCh37)
- Canonical SPDI:
- NC_000008.11:53948211::TAT,NC_000008.11:53948211::TG,NC_000008.11:53948211::TGATAT
- Gene:
- RGS20 (Varview)
- Functional Consequence:
- genic_downstream_transcript_variant,intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
TG=0.00059/7
(
ALFA)
TG=0.00011/2
(TOMMO)
- HGVS:
12.
rs1491214117 [Homo sapiens]- Variant type:
- DEL
- Alleles:
- TG>-
[Show Flanks]
- Chromosome:
- 8:53948553
(GRCh38)
8:54861113
(GRCh37)
- Canonical SPDI:
- NC_000008.11:53948552:TG:
- Gene:
- RGS20 (Varview)
- Functional Consequence:
- genic_downstream_transcript_variant,intron_variant
- Validated:
- by frequency,by cluster
- MAF:
-=0.00108/18
(TOMMO)
- HGVS:
13.
rs1491077947 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- AT>-
[Show Flanks]
- Chromosome:
- 8:53948320
(GRCh38)
8:54860880
(GRCh37)
- Canonical SPDI:
- NC_000008.11:53948317:ATAT:AT
- Gene:
- RGS20 (Varview)
- Functional Consequence:
- genic_downstream_transcript_variant,intron_variant
- Validated:
- by frequency,by alfa
- MAF:
ATAT=0.000084/1
(
ALFA)
-=0.000016/2
(GnomAD)
- HGVS:
14.
rs1491032918 has merged into rs34526937 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- AAA>-,A,AA,AAAA,AAAAA,AAAAAA
[Show Flanks]
- Chromosome:
- 8:53915157
(GRCh38)
8:54827717
(GRCh37)
- Canonical SPDI:
- NC_000008.11:53915144:AAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000008.11:53915144:AAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000008.11:53915144:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000008.11:53915144:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000008.11:53915144:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000008.11:53915144:AAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA
- Gene:
- RGS20 (Varview)
- Functional Consequence:
- intron_variant,genic_downstream_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
AAAAAAAAAAAAA=0.0004/2
(
ALFA)
A=0.2845/1425
(1000Genomes)
- HGVS:
NC_000008.11:g.53915157_53915159del, NC_000008.11:g.53915158_53915159del, NC_000008.11:g.53915159del, NC_000008.11:g.53915159dup, NC_000008.11:g.53915158_53915159dup, NC_000008.11:g.53915157_53915159dup, NC_000008.10:g.54827717_54827719del, NC_000008.10:g.54827718_54827719del, NC_000008.10:g.54827719del, NC_000008.10:g.54827719dup, NC_000008.10:g.54827718_54827719dup, NC_000008.10:g.54827717_54827719dup
15.
rs1491011698 has merged into rs367844788 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- TTTTTTTTTT>-,TTT,TTTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT
[Show Flanks]
- Chromosome:
- 8:53901072
(GRCh38)
8:54813632
(GRCh37)
- Canonical SPDI:
- NC_000008.11:53901062:TTTTTTTTTTTTTTTTTTT:TTTTTTTTT,NC_000008.11:53901062:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000008.11:53901062:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000008.11:53901062:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000008.11:53901062:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000008.11:53901062:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000008.11:53901062:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000008.11:53901062:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000008.11:53901062:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000008.11:53901062:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000008.11:53901062:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000008.11:53901062:TTTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT
- Gene:
- RGS20 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
TTTTTTTTTTTT=0./0
(
ALFA)
TTTT=0.000004/1
(TOPMED)
- HGVS:
NC_000008.11:g.53901072_53901081del, NC_000008.11:g.53901075_53901081del, NC_000008.11:g.53901076_53901081del, NC_000008.11:g.53901077_53901081del, NC_000008.11:g.53901078_53901081del, NC_000008.11:g.53901079_53901081del, NC_000008.11:g.53901080_53901081del, NC_000008.11:g.53901081del, NC_000008.11:g.53901081dup, NC_000008.11:g.53901080_53901081dup, NC_000008.11:g.53901079_53901081dup, NC_000008.11:g.53901078_53901081dup, NC_000008.10:g.54813632_54813641del, NC_000008.10:g.54813635_54813641del, NC_000008.10:g.54813636_54813641del, NC_000008.10:g.54813637_54813641del, NC_000008.10:g.54813638_54813641del, NC_000008.10:g.54813639_54813641del, NC_000008.10:g.54813640_54813641del, NC_000008.10:g.54813641del, NC_000008.10:g.54813641dup, NC_000008.10:g.54813640_54813641dup, NC_000008.10:g.54813639_54813641dup, NC_000008.10:g.54813638_54813641dup
16.
rs1490988476 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- T>A,C
[Show Flanks]
- Chromosome:
- 8:53948069
(GRCh38)
8:54860629
(GRCh37)
- Canonical SPDI:
- NC_000008.11:53948068:T:A,NC_000008.11:53948068:T:C
- Gene:
- RGS20 (Varview)
- Functional Consequence:
- genic_downstream_transcript_variant,intron_variant
- Validated:
- by frequency,by alfa
- MAF:
A=0.000084/1
(
ALFA)
C=0.000004/1
(TOPMED)
- HGVS:
17.
rs1490969653 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- T>-,TT
[Show Flanks]
- Chromosome:
- 8:53856383
(GRCh38)
8:54768943
(GRCh37)
- Canonical SPDI:
- NC_000008.11:53856382:TTTTTTTT:TTTTTTT,NC_000008.11:53856382:TTTTTTTT:TTTTTTTTT
- Gene:
- RGS20 (Varview)
- Functional Consequence:
- intron_variant,genic_upstream_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
TTTTTTTTT=0./0
(
ALFA)
-=0.000008/2
(TOPMED)
- HGVS:
18.
rs1490961202 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- T>C,G
[Show Flanks]
- Chromosome:
- 8:53890011
(GRCh38)
8:54802571
(GRCh37)
- Canonical SPDI:
- NC_000008.11:53890010:T:C,NC_000008.11:53890010:T:G
- Gene:
- RGS20 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
G=0./0
(
ALFA)
C=0.000007/1
(GnomAD)
- HGVS:
20.
rs1490943114 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- C>A,G,T
[Show Flanks]
- Chromosome:
- 8:53947392
(GRCh38)
8:54859952
(GRCh37)
- Canonical SPDI:
- NC_000008.11:53947391:C:A,NC_000008.11:53947391:C:G,NC_000008.11:53947391:C:T
- Gene:
- RGS20 (Varview)
- Functional Consequence:
- genic_downstream_transcript_variant,intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
T=0./0
(
ALFA)
T=0.00021/4
(TOMMO)
- HGVS: