Links from Gene
Items: 1 to 20 of 1000
1.
rs1491547169 [Homo sapiens]- Variant type:
- DEL
- Alleles:
- AT>-
[Show Flanks]
- Chromosome:
- 3:194025296
(GRCh38)
3:193743085
(GRCh37)
- Canonical SPDI:
- NC_000003.12:194025295:AT:
- Gene:
- LINC02028 (Varview)
- Functional Consequence:
- intron_variant,genic_downstream_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
-=0.00008/1
(
ALFA)
-=0.00005/4
(GnomAD)
- HGVS:
3.
rs1491468358 has merged into rs147816788 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- AAAAAAAAAAAAAA>-,A,AA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
[Show Flanks]
- Chromosome:
- 3:194028375
(GRCh38)
3:193746164
(GRCh37)
- Canonical SPDI:
- NC_000003.12:194028364:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000003.12:194028364:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000003.12:194028364:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000003.12:194028364:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000003.12:194028364:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000003.12:194028364:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000003.12:194028364:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000003.12:194028364:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000003.12:194028364:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000003.12:194028364:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:194028364:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:194028364:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:194028364:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:194028364:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:194028364:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:194028364:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:194028364:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:194028364:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:194028364:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:194028364:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:194028364:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:194028364:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:194028364:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:194028364:AAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
- Gene:
- LINC02028 (Varview)
- Functional Consequence:
- intron_variant,genic_downstream_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
AAAAAAAAAAA=0./0
(
ALFA)
-=0.3538/1772
(1000Genomes)
- HGVS:
NC_000003.12:g.194028375_194028388del, NC_000003.12:g.194028376_194028388del, NC_000003.12:g.194028377_194028388del, NC_000003.12:g.194028380_194028388del, NC_000003.12:g.194028381_194028388del, NC_000003.12:g.194028382_194028388del, NC_000003.12:g.194028383_194028388del, NC_000003.12:g.194028385_194028388del, NC_000003.12:g.194028386_194028388del, NC_000003.12:g.194028387_194028388del, NC_000003.12:g.194028388del, NC_000003.12:g.194028388dup, NC_000003.12:g.194028387_194028388dup, NC_000003.12:g.194028386_194028388dup, NC_000003.12:g.194028385_194028388dup, NC_000003.12:g.194028384_194028388dup, NC_000003.12:g.194028383_194028388dup, NC_000003.12:g.194028382_194028388dup, NC_000003.12:g.194028381_194028388dup, NC_000003.12:g.194028380_194028388dup, NC_000003.12:g.194028379_194028388dup, NC_000003.12:g.194028388_194028389insAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000003.12:g.194028388_194028389insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000003.12:g.194028388_194028389insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000003.11:g.193746164_193746177del, NC_000003.11:g.193746165_193746177del, NC_000003.11:g.193746166_193746177del, NC_000003.11:g.193746169_193746177del, NC_000003.11:g.193746170_193746177del, NC_000003.11:g.193746171_193746177del, NC_000003.11:g.193746172_193746177del, NC_000003.11:g.193746174_193746177del, NC_000003.11:g.193746175_193746177del, NC_000003.11:g.193746176_193746177del, NC_000003.11:g.193746177del, NC_000003.11:g.193746177dup, NC_000003.11:g.193746176_193746177dup, NC_000003.11:g.193746175_193746177dup, NC_000003.11:g.193746174_193746177dup, NC_000003.11:g.193746173_193746177dup, NC_000003.11:g.193746172_193746177dup, NC_000003.11:g.193746171_193746177dup, NC_000003.11:g.193746170_193746177dup, NC_000003.11:g.193746169_193746177dup, NC_000003.11:g.193746168_193746177dup, NC_000003.11:g.193746177_193746178insAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000003.11:g.193746177_193746178insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000003.11:g.193746177_193746178insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
4.
rs1491463415 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- ->T
[Show Flanks]
- Chromosome:
- 3:194068665
(GRCh38)
3:193786455
(GRCh37)
- Canonical SPDI:
- NC_000003.12:194068665:TT:TTT
- Gene:
- LINC02028 (Varview), LOC102724877 (Varview)
- Functional Consequence:
- intron_variant,upstream_transcript_variant,2KB_upstream_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
TTT=0.00017/2
(
ALFA)
T=0.0005/8
(TOMMO)
- HGVS:
5.
rs1491385248 [Homo sapiens]- Variant type:
- DEL
- Alleles:
- AT>-
[Show Flanks]
- Chromosome:
- 3:194025434
(GRCh38)
3:193743223
(GRCh37)
- Canonical SPDI:
- NC_000003.12:194025433:AT:
- Gene:
- LINC02028 (Varview)
- Functional Consequence:
- intron_variant,genic_downstream_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
-=0./0
(
ALFA)
-=0.000043/6
(GnomAD)
-=0.000177/3
(TOMMO)
-=0.001638/3
(Korea1K)
- HGVS:
6.
rs1491375839 [Homo sapiens]- Variant type:
- DEL
- Alleles:
- TC>-
[Show Flanks]
- Chromosome:
- 3:194014128
(GRCh38)
3:193731917
(GRCh37)
- Canonical SPDI:
- NC_000003.12:194014127:TC:
- Gene:
- LINC02028 (Varview)
- Functional Consequence:
- intron_variant,genic_downstream_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
-=0./0
(
ALFA)
-=0.00004/1
(TOMMO)
-=0.00018/16
(GnomAD)
- HGVS:
7.
rs1491365982 [Homo sapiens]- Variant type:
- DEL
- Alleles:
- CA>-
[Show Flanks]
- Chromosome:
- 3:194028364
(GRCh38)
3:193746153
(GRCh37)
- Canonical SPDI:
- NC_000003.12:194028363:CA:
- Gene:
- LINC02028 (Varview)
- Functional Consequence:
- intron_variant,genic_downstream_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
-=0.01619/192
(
ALFA)
-=0.00036/16
(GnomAD)
-=0.002/56
(TOMMO)
- HGVS:
8.
rs1491289493 [Homo sapiens]- Variant type:
- INS
- Alleles:
- ->GC,GCATGC,GCATGCGTGTGC,GCATGCGTGTGCATGC,GTGCATGCGTGTGCATGC
[Show Flanks]
- Chromosome:
- 3:194025271
(GRCh38)
3:193743061
(GRCh37)
- Canonical SPDI:
- NC_000003.12:194025271::GC,NC_000003.12:194025271::GCATGC,NC_000003.12:194025271::GCATGCGTGTGC,NC_000003.12:194025271::GCATGCGTGTGCATGC,NC_000003.12:194025271::GTGCATGCGTGTGCATGC
- Gene:
- LINC02028 (Varview)
- Functional Consequence:
- intron_variant,genic_downstream_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
- HGVS:
9.
rs1491267027 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- AT>-
[Show Flanks]
- Chromosome:
- 3:194025169
(GRCh38)
3:193742958
(GRCh37)
- Canonical SPDI:
- NC_000003.12:194025167:TAT:T
- Gene:
- LINC02028 (Varview)
- Functional Consequence:
- intron_variant,genic_downstream_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
T=0./0
(
ALFA)
-=0.000004/1
(TOPMED)
-=0.000779/13
(TOMMO)
-=0.000898/115
(GnomAD)
-=0.001638/3
(Korea1K)
-=0.005449/21
(ALSPAC)
-=0.007012/26
(TWINSUK)
- HGVS:
10.
rs1491261549 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- ->CATG,CCTG,CTTG
[Show Flanks]
- Chromosome:
- 3:194025228
(GRCh38)
3:193743018
(GRCh37)
- Canonical SPDI:
- NC_000003.12:194025228:TG:TGCATG,NC_000003.12:194025228:TG:TGCCTG,NC_000003.12:194025228:TG:TGCTTG
- Gene:
- LINC02028 (Varview)
- Functional Consequence:
- intron_variant,genic_downstream_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
TGCCTG=0./0
(
ALFA)
TGCC=0.000035/1
(TOMMO)
TGCA=0.000084/11
(GnomAD)
- HGVS:
11.
rs1491252976 has merged into rs11333787 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- AAAAAAAAAAAA>-,A,AAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
[Show Flanks]
- Chromosome:
- 3:194024848
(GRCh38)
3:193742637
(GRCh37)
- Canonical SPDI:
- NC_000003.12:194024839:AAAAAAAAAAAAAAAAAAAA:AAAAAAAA,NC_000003.12:194024839:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAA,NC_000003.12:194024839:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000003.12:194024839:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000003.12:194024839:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000003.12:194024839:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000003.12:194024839:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000003.12:194024839:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000003.12:194024839:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:194024839:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:194024839:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:194024839:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:194024839:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:194024839:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:194024839:AAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
- Gene:
- LINC02028 (Varview)
- Functional Consequence:
- intron_variant,genic_downstream_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
AAAAAAAAA=0./0
(
ALFA)
-=0.2674/1339
(1000Genomes)
- HGVS:
NC_000003.12:g.194024848_194024859del, NC_000003.12:g.194024849_194024859del, NC_000003.12:g.194024854_194024859del, NC_000003.12:g.194024856_194024859del, NC_000003.12:g.194024857_194024859del, NC_000003.12:g.194024858_194024859del, NC_000003.12:g.194024859del, NC_000003.12:g.194024859dup, NC_000003.12:g.194024858_194024859dup, NC_000003.12:g.194024857_194024859dup, NC_000003.12:g.194024856_194024859dup, NC_000003.12:g.194024855_194024859dup, NC_000003.12:g.194024852_194024859dup, NC_000003.12:g.194024841_194024859dup, NC_000003.12:g.194024859_194024860insAAAAAAAAAAAAAAAAAAAAAAAA, NC_000003.11:g.193742637_193742648del, NC_000003.11:g.193742638_193742648del, NC_000003.11:g.193742643_193742648del, NC_000003.11:g.193742645_193742648del, NC_000003.11:g.193742646_193742648del, NC_000003.11:g.193742647_193742648del, NC_000003.11:g.193742648del, NC_000003.11:g.193742648dup, NC_000003.11:g.193742647_193742648dup, NC_000003.11:g.193742646_193742648dup, NC_000003.11:g.193742645_193742648dup, NC_000003.11:g.193742644_193742648dup, NC_000003.11:g.193742641_193742648dup, NC_000003.11:g.193742630_193742648dup, NC_000003.11:g.193742648_193742649insAAAAAAAAAAAAAAAAAAAAAAAA
14.
rs1491201939 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- AT>-
[Show Flanks]
- Chromosome:
- 3:194025272
(GRCh38)
3:193743061
(GRCh37)
- Canonical SPDI:
- NC_000003.12:194025270:TAT:T
- Gene:
- LINC02028 (Varview)
- Functional Consequence:
- intron_variant,genic_downstream_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
T=0./0
(
ALFA)
-=0.000018/2
(GnomAD)
- HGVS:
15.
rs1491173363 has merged into rs529089271 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- AAAAAAAAAAA>-,A,AA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA
[Show Flanks]
- Chromosome:
- 3:194041452
(GRCh38)
3:193759241
(GRCh37)
- Canonical SPDI:
- NC_000003.12:194041441:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000003.12:194041441:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000003.12:194041441:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000003.12:194041441:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000003.12:194041441:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000003.12:194041441:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000003.12:194041441:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000003.12:194041441:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000003.12:194041441:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000003.12:194041441:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:194041441:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:194041441:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:194041441:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA
- Gene:
- LINC02028 (Varview)
- Functional Consequence:
- intron_variant,genic_downstream_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
AAAAAAAAAA=0./0
(
ALFA)
-=0.3169/1587
(1000Genomes)
- HGVS:
NC_000003.12:g.194041452_194041462del, NC_000003.12:g.194041453_194041462del, NC_000003.12:g.194041454_194041462del, NC_000003.12:g.194041457_194041462del, NC_000003.12:g.194041458_194041462del, NC_000003.12:g.194041459_194041462del, NC_000003.12:g.194041460_194041462del, NC_000003.12:g.194041461_194041462del, NC_000003.12:g.194041462del, NC_000003.12:g.194041462dup, NC_000003.12:g.194041461_194041462dup, NC_000003.12:g.194041459_194041462dup, NC_000003.12:g.194041458_194041462dup, NC_000003.11:g.193759241_193759251del, NC_000003.11:g.193759242_193759251del, NC_000003.11:g.193759243_193759251del, NC_000003.11:g.193759246_193759251del, NC_000003.11:g.193759247_193759251del, NC_000003.11:g.193759248_193759251del, NC_000003.11:g.193759249_193759251del, NC_000003.11:g.193759250_193759251del, NC_000003.11:g.193759251del, NC_000003.11:g.193759251dup, NC_000003.11:g.193759250_193759251dup, NC_000003.11:g.193759248_193759251dup, NC_000003.11:g.193759247_193759251dup
16.
rs1491167620 has merged into rs375091103 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- GTGT>-,GT,GTGTGT
[Show Flanks]
- Chromosome:
- 3:194025442
(GRCh38)
3:193743231
(GRCh37)
- Canonical SPDI:
- NC_000003.12:194025434:TGTGTGTGTGT:TGTGTGT,NC_000003.12:194025434:TGTGTGTGTGT:TGTGTGTGT,NC_000003.12:194025434:TGTGTGTGTGT:TGTGTGTGTGTGT
- Gene:
- LINC02028 (Varview)
- Functional Consequence:
- intron_variant,genic_downstream_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
TGTGTGTGTGTGT=0./0
(
ALFA)
-=0.00152/26
(TOMMO)
-=0.0018/9
(1000Genomes)
-=0.00273/5
(Korea1K)
- HGVS:
19.
rs1491130188 has merged into rs3054789 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- TGTG>-,TG,TGTGTG,TGTGTGTGTGTGTG
[Show Flanks]
- Chromosome:
- 3:194025303
(GRCh38)
3:193743092
(GRCh37)
- Canonical SPDI:
- NC_000003.12:194025296:TGTGTGTGTG:TGTGTG,NC_000003.12:194025296:TGTGTGTGTG:TGTGTGTG,NC_000003.12:194025296:TGTGTGTGTG:TGTGTGTGTGTG,NC_000003.12:194025296:TGTGTGTGTG:TGTGTGTGTGTGTGTGTGTG
- Gene:
- LINC02028 (Varview)
- Functional Consequence:
- genic_downstream_transcript_variant,intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
TGTGTGTG=0./0
(
ALFA)
-=0.00026/1
(ALSPAC)
TG=0.35333/212
(NorthernSweden)
-=0.36593/6123
(TOMMO)
- HGVS:
20.
rs1491116160 has merged into rs59184462 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- CACACACACACACACA>-,CA,CACA,CACACA,CACACACA,CACACACACA,CACACACACACA,CACACACACACACA,CACACACACACACACACA,CACACACACACACACACACA,CACACACACACACACACACACA,CACACACACACACACACACACACA,CACACACACACACACACACACACACA,CACACACACACACACACACACACACACA,CACACACACACACACACACACACACACACA,CACACACACACACACACACACACACACACACA,CACACACACACACACACACACACACACACACACA,CACACACACACACACACACACACACACACACACACA,CACACACACACACACACACACACACACACACACACACA
[Show Flanks]
- Chromosome:
- 3:194014143
(GRCh38)
3:193731932
(GRCh37)
- Canonical SPDI:
- NC_000003.12:194014128:CACACACACACACACACACACACACACACA:CACACACACACACA,NC_000003.12:194014128:CACACACACACACACACACACACACACACA:CACACACACACACACA,NC_000003.12:194014128:CACACACACACACACACACACACACACACA:CACACACACACACACACA,NC_000003.12:194014128:CACACACACACACACACACACACACACACA:CACACACACACACACACACA,NC_000003.12:194014128:CACACACACACACACACACACACACACACA:CACACACACACACACACACACA,NC_000003.12:194014128:CACACACACACACACACACACACACACACA:CACACACACACACACACACACACA,NC_000003.12:194014128:CACACACACACACACACACACACACACACA:CACACACACACACACACACACACACA,NC_000003.12:194014128:CACACACACACACACACACACACACACACA:CACACACACACACACACACACACACACA,NC_000003.12:194014128:CACACACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACA,NC_000003.12:194014128:CACACACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACACA,NC_000003.12:194014128:CACACACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACACACA,NC_000003.12:194014128:CACACACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACACACACA,NC_000003.12:194014128:CACACACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACACACACACA,NC_000003.12:194014128:CACACACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACACACACACACA,NC_000003.12:194014128:CACACACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACACACACACACACA,NC_000003.12:194014128:CACACACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACACACACACACACACA,NC_000003.12:194014128:CACACACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACACACACACACACACACA,NC_000003.12:194014128:CACACACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACACACACACACACACACACA,NC_000003.12:194014128:CACACACACACACACACACACACACACACA:CACACACACACACACACACACACACACACACACACACACACACACACACACA
- Gene:
- LINC02028 (Varview)
- Functional Consequence:
- intron_variant,genic_downstream_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
CACACACACACACA=0./0
(
ALFA)
- HGVS:
NC_000003.12:g.194014129CA[7], NC_000003.12:g.194014129CA[8], NC_000003.12:g.194014129CA[9], NC_000003.12:g.194014129CA[10], NC_000003.12:g.194014129CA[11], NC_000003.12:g.194014129CA[12], NC_000003.12:g.194014129CA[13], NC_000003.12:g.194014129CA[14], NC_000003.12:g.194014129CA[16], NC_000003.12:g.194014129CA[17], NC_000003.12:g.194014129CA[18], NC_000003.12:g.194014129CA[19], NC_000003.12:g.194014129CA[20], NC_000003.12:g.194014129CA[21], NC_000003.12:g.194014129CA[22], NC_000003.12:g.194014129CA[23], NC_000003.12:g.194014129CA[24], NC_000003.12:g.194014129CA[25], NC_000003.12:g.194014129CA[26], NC_000003.11:g.193731918CA[7], NC_000003.11:g.193731918CA[8], NC_000003.11:g.193731918CA[9], NC_000003.11:g.193731918CA[10], NC_000003.11:g.193731918CA[11], NC_000003.11:g.193731918CA[12], NC_000003.11:g.193731918CA[13], NC_000003.11:g.193731918CA[14], NC_000003.11:g.193731918CA[16], NC_000003.11:g.193731918CA[17], NC_000003.11:g.193731918CA[18], NC_000003.11:g.193731918CA[19], NC_000003.11:g.193731918CA[20], NC_000003.11:g.193731918CA[21], NC_000003.11:g.193731918CA[22], NC_000003.11:g.193731918CA[23], NC_000003.11:g.193731918CA[24], NC_000003.11:g.193731918CA[25], NC_000003.11:g.193731918CA[26]