Links from Gene
Items: 1 to 20 of 18585
2.
rs1491564446 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- CT>-
[Show Flanks]
- Chromosome:
- 3:177877593
(GRCh38)
3:177595381
(GRCh37)
- Canonical SPDI:
- NC_000003.12:177877591:TCT:T
- Gene:
- LINC02015 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
T=0.021518/351
(
ALFA)
-=0.000036/1
(TOMMO)
-=0.004372/8
(Korea1K)
-=0.005/3
(NorthernSweden)
-=0.023338/2995
(GnomAD)
- HGVS:
3.
rs1491485684 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- ->TGC
[Show Flanks]
- Chromosome:
- 3:177890240
(GRCh38)
3:177608029
(GRCh37)
- Canonical SPDI:
- NC_000003.12:177890240:TGCTGC:TGCTGCTGC
- Gene:
- LINC02015 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
TGCTGCTGC=0./0
(
ALFA)
TGC=0.000004/1
(TOPMED)
TGC=0.000007/1
(GnomAD)
- HGVS:
4.
rs1491478406 [Homo sapiens]- Variant type:
- DEL
- Alleles:
- AG>-
[Show Flanks]
- Chromosome:
- 3:177883751
(GRCh38)
3:177601539
(GRCh37)
- Canonical SPDI:
- NC_000003.12:177883750:AG:
- Gene:
- LINC02015 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa
- MAF:
-=0.00129/21
(
ALFA)
-=0.00032/9
(TOMMO)
- HGVS:
5.
rs1491477666 [Homo sapiens]- Variant type:
- INS
- Alleles:
- ->AAG,T
[Show Flanks]
- Chromosome:
- 3:177883751
(GRCh38)
3:177601540
(GRCh37)
- Canonical SPDI:
- NC_000003.12:177883751::AAG,NC_000003.12:177883751::T
- Gene:
- LINC02015 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
T=0./0
(
ALFA)
T=0.000004/1
(TOPMED)
AAG=0.001092/2
(Korea1K)
- HGVS:
6.
rs1491402247 has merged into rs57269502 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- AAAAAAAAAAAAAAAAAAAA>-,A,AA,AAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAACAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAACAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAACCAAACAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
[Show Flanks]
- Chromosome:
- 3:177886611
(GRCh38)
3:177604399
(GRCh37)
- Canonical SPDI:
- NC_000003.12:177886599:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000003.12:177886599:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000003.12:177886599:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000003.12:177886599:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000003.12:177886599:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000003.12:177886599:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000003.12:177886599:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000003.12:177886599:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000003.12:177886599:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000003.12:177886599:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000003.12:177886599:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:177886599:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:177886599:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:177886599:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:177886599:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:177886599:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:177886599:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:177886599:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:177886599:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:177886599:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:177886599:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:177886599:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:177886599:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:177886599:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:177886599:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:177886599:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:177886599:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:177886599:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:177886599:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:177886599:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:177886599:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:177886599:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:177886599:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:177886599:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:177886599:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:177886599:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:177886599:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:177886599:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:177886599:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:177886599:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:177886599:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:177886599:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:177886599:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:177886599:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:177886599:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:177886599:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:177886599:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:177886599:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:177886599:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:177886599:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:177886599:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:177886599:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:177886599:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:177886599:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:177886599:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAACAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:177886599:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAACAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:177886599:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAACCAAACAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
- Gene:
- LINC02015 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
- HGVS:
NC_000003.12:g.177886611_177886630del, NC_000003.12:g.177886612_177886630del, NC_000003.12:g.177886613_177886630del, NC_000003.12:g.177886614_177886630del, NC_000003.12:g.177886616_177886630del, NC_000003.12:g.177886617_177886630del, NC_000003.12:g.177886618_177886630del, NC_000003.12:g.177886619_177886630del, NC_000003.12:g.177886620_177886630del, NC_000003.12:g.177886621_177886630del, NC_000003.12:g.177886622_177886630del, NC_000003.12:g.177886623_177886630del, NC_000003.12:g.177886624_177886630del, NC_000003.12:g.177886625_177886630del, NC_000003.12:g.177886626_177886630del, NC_000003.12:g.177886628_177886630del, NC_000003.12:g.177886629_177886630del, NC_000003.12:g.177886630del, NC_000003.12:g.177886630dup, NC_000003.12:g.177886629_177886630dup, NC_000003.12:g.177886628_177886630dup, NC_000003.12:g.177886627_177886630dup, NC_000003.12:g.177886626_177886630dup, NC_000003.12:g.177886625_177886630dup, NC_000003.12:g.177886624_177886630dup, NC_000003.12:g.177886623_177886630dup, NC_000003.12:g.177886622_177886630dup, NC_000003.12:g.177886621_177886630dup, NC_000003.12:g.177886620_177886630dup, NC_000003.12:g.177886619_177886630dup, NC_000003.12:g.177886618_177886630dup, NC_000003.12:g.177886617_177886630dup, NC_000003.12:g.177886616_177886630dup, NC_000003.12:g.177886615_177886630dup, NC_000003.12:g.177886614_177886630dup, NC_000003.12:g.177886613_177886630dup, NC_000003.12:g.177886612_177886630dup, NC_000003.12:g.177886611_177886630dup, NC_000003.12:g.177886610_177886630dup, NC_000003.12:g.177886609_177886630dup, NC_000003.12:g.177886608_177886630dup, NC_000003.12:g.177886607_177886630dup, NC_000003.12:g.177886606_177886630dup, NC_000003.12:g.177886605_177886630dup, NC_000003.12:g.177886603_177886630dup, NC_000003.12:g.177886602_177886630dup, NC_000003.12:g.177886601_177886630dup, NC_000003.12:g.177886630_177886631insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000003.12:g.177886630_177886631insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000003.12:g.177886630_177886631insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000003.12:g.177886630_177886631insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000003.12:g.177886630_177886631insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000003.12:g.177886630_177886631insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000003.12:g.177886630_177886631insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000003.12:g.177886600_177886630A[45]CAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000003.12:g.177886600_177886630A[33]CAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000003.12:g.177886600_177886630A[32]CCAAACAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000003.11:g.177604399_177604418del, NC_000003.11:g.177604400_177604418del, NC_000003.11:g.177604401_177604418del, NC_000003.11:g.177604402_177604418del, NC_000003.11:g.177604404_177604418del, NC_000003.11:g.177604405_177604418del, NC_000003.11:g.177604406_177604418del, NC_000003.11:g.177604407_177604418del, NC_000003.11:g.177604408_177604418del, NC_000003.11:g.177604409_177604418del, NC_000003.11:g.177604410_177604418del, NC_000003.11:g.177604411_177604418del, NC_000003.11:g.177604412_177604418del, NC_000003.11:g.177604413_177604418del, NC_000003.11:g.177604414_177604418del, NC_000003.11:g.177604416_177604418del, NC_000003.11:g.177604417_177604418del, NC_000003.11:g.177604418del, NC_000003.11:g.177604418dup, NC_000003.11:g.177604417_177604418dup, NC_000003.11:g.177604416_177604418dup, NC_000003.11:g.177604415_177604418dup, NC_000003.11:g.177604414_177604418dup, NC_000003.11:g.177604413_177604418dup, NC_000003.11:g.177604412_177604418dup, NC_000003.11:g.177604411_177604418dup, NC_000003.11:g.177604410_177604418dup, NC_000003.11:g.177604409_177604418dup, NC_000003.11:g.177604408_177604418dup, NC_000003.11:g.177604407_177604418dup, NC_000003.11:g.177604406_177604418dup, NC_000003.11:g.177604405_177604418dup, NC_000003.11:g.177604404_177604418dup, NC_000003.11:g.177604403_177604418dup, NC_000003.11:g.177604402_177604418dup, NC_000003.11:g.177604401_177604418dup, NC_000003.11:g.177604400_177604418dup, NC_000003.11:g.177604399_177604418dup, NC_000003.11:g.177604398_177604418dup, NC_000003.11:g.177604397_177604418dup, NC_000003.11:g.177604396_177604418dup, NC_000003.11:g.177604395_177604418dup, NC_000003.11:g.177604394_177604418dup, NC_000003.11:g.177604393_177604418dup, NC_000003.11:g.177604391_177604418dup, NC_000003.11:g.177604390_177604418dup, NC_000003.11:g.177604389_177604418dup, NC_000003.11:g.177604418_177604419insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000003.11:g.177604418_177604419insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000003.11:g.177604418_177604419insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000003.11:g.177604418_177604419insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000003.11:g.177604418_177604419insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000003.11:g.177604418_177604419insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000003.11:g.177604418_177604419insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000003.11:g.177604388_177604418A[45]CAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000003.11:g.177604388_177604418A[33]CAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000003.11:g.177604388_177604418A[32]CCAAACAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1]
8.
rs1491316984 has merged into rs34071767 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- AAAAAAAAAAAAAA>-,A,AA,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
[Show Flanks]
- Chromosome:
- 3:177883738
(GRCh38)
3:177601526
(GRCh37)
- Canonical SPDI:
- NC_000003.12:177883728:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA,NC_000003.12:177883728:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000003.12:177883728:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000003.12:177883728:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000003.12:177883728:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000003.12:177883728:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000003.12:177883728:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000003.12:177883728:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000003.12:177883728:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000003.12:177883728:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000003.12:177883728:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000003.12:177883728:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000003.12:177883728:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000003.12:177883728:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:177883728:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:177883728:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:177883728:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:177883728:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:177883728:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:177883728:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:177883728:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:177883728:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:177883728:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:177883728:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:177883728:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:177883728:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:177883728:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000003.12:177883728:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
- Gene:
- LINC02015 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
AAAAAAAAA=0./0
(
ALFA)
-=0.4257/2132
(1000Genomes)
- HGVS:
NC_000003.12:g.177883738_177883751del, NC_000003.12:g.177883739_177883751del, NC_000003.12:g.177883740_177883751del, NC_000003.12:g.177883741_177883751del, NC_000003.12:g.177883742_177883751del, NC_000003.12:g.177883743_177883751del, NC_000003.12:g.177883744_177883751del, NC_000003.12:g.177883745_177883751del, NC_000003.12:g.177883746_177883751del, NC_000003.12:g.177883747_177883751del, NC_000003.12:g.177883748_177883751del, NC_000003.12:g.177883749_177883751del, NC_000003.12:g.177883750_177883751del, NC_000003.12:g.177883751del, NC_000003.12:g.177883751dup, NC_000003.12:g.177883750_177883751dup, NC_000003.12:g.177883749_177883751dup, NC_000003.12:g.177883748_177883751dup, NC_000003.12:g.177883747_177883751dup, NC_000003.12:g.177883746_177883751dup, NC_000003.12:g.177883744_177883751dup, NC_000003.12:g.177883743_177883751dup, NC_000003.12:g.177883742_177883751dup, NC_000003.12:g.177883741_177883751dup, NC_000003.12:g.177883740_177883751dup, NC_000003.12:g.177883731_177883751dup, NC_000003.12:g.177883751_177883752insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000003.12:g.177883751_177883752insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000003.11:g.177601526_177601539del, NC_000003.11:g.177601527_177601539del, NC_000003.11:g.177601528_177601539del, NC_000003.11:g.177601529_177601539del, NC_000003.11:g.177601530_177601539del, NC_000003.11:g.177601531_177601539del, NC_000003.11:g.177601532_177601539del, NC_000003.11:g.177601533_177601539del, NC_000003.11:g.177601534_177601539del, NC_000003.11:g.177601535_177601539del, NC_000003.11:g.177601536_177601539del, NC_000003.11:g.177601537_177601539del, NC_000003.11:g.177601538_177601539del, NC_000003.11:g.177601539del, NC_000003.11:g.177601539dup, NC_000003.11:g.177601538_177601539dup, NC_000003.11:g.177601537_177601539dup, NC_000003.11:g.177601536_177601539dup, NC_000003.11:g.177601535_177601539dup, NC_000003.11:g.177601534_177601539dup, NC_000003.11:g.177601532_177601539dup, NC_000003.11:g.177601531_177601539dup, NC_000003.11:g.177601530_177601539dup, NC_000003.11:g.177601529_177601539dup, NC_000003.11:g.177601528_177601539dup, NC_000003.11:g.177601519_177601539dup, NC_000003.11:g.177601539_177601540insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000003.11:g.177601539_177601540insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
9.
rs1491315010 [Homo sapiens]- Variant type:
- DEL
- Alleles:
- TC>-
[Show Flanks]
- Chromosome:
- 3:177865822
(GRCh38)
3:177583610
(GRCh37)
- Canonical SPDI:
- NC_000003.12:177865821:TC:
- Gene:
- LINC02015 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
-=0.000071/1
(
ALFA)
-=0.00003/8
(TOPMED)
-=0.000038/5
(GnomAD)
- HGVS:
10.
rs1491191191 [Homo sapiens]- Variant type:
- DEL
- Alleles:
- CA>-
[Show Flanks]
- Chromosome:
- 3:177875112
(GRCh38)
3:177592900
(GRCh37)
- Canonical SPDI:
- NC_000003.12:177875111:CA:
- Gene:
- LINC02015 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
-=0.00902/107
(
ALFA)
-=0.00012/2
(TOMMO)
-=0.00021/11
(GnomAD)
- HGVS:
11.
rs1491183031 has merged into rs11285520 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- AAAAAA>-,A,AA,AAA,AAAA,AAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA
[Show Flanks]
- Chromosome:
- 3:177822591
(GRCh38)
3:177540379
(GRCh37)
- Canonical SPDI:
- NC_000003.12:177822579:AAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000003.12:177822579:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAA,NC_000003.12:177822579:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000003.12:177822579:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000003.12:177822579:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000003.12:177822579:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000003.12:177822579:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000003.12:177822579:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000003.12:177822579:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000003.12:177822579:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA
- Gene:
- LINC02015 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
AAAAAAAAAAAAAAA=0./0
(
ALFA)
-=0.0695/268
(ALSPAC)
-=0.3913/198
(NorthernSweden)
A=0.4828/2418
(1000Genomes)
- HGVS:
NC_000003.12:g.177822591_177822596del, NC_000003.12:g.177822592_177822596del, NC_000003.12:g.177822593_177822596del, NC_000003.12:g.177822594_177822596del, NC_000003.12:g.177822595_177822596del, NC_000003.12:g.177822596del, NC_000003.12:g.177822596dup, NC_000003.12:g.177822595_177822596dup, NC_000003.12:g.177822594_177822596dup, NC_000003.12:g.177822593_177822596dup, NC_000003.11:g.177540379_177540384del, NC_000003.11:g.177540380_177540384del, NC_000003.11:g.177540381_177540384del, NC_000003.11:g.177540382_177540384del, NC_000003.11:g.177540383_177540384del, NC_000003.11:g.177540384del, NC_000003.11:g.177540384dup, NC_000003.11:g.177540383_177540384dup, NC_000003.11:g.177540382_177540384dup, NC_000003.11:g.177540381_177540384dup
13.
rs1491109338 has merged into rs1204049399 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- TTTTTTTTTT>-,TT,TTT,TTTT,TTTTTTT,TTTTTTTT,TTTTTTTTT,TTTTTTTTTTT,TTTTTTTTTTTT,TTTTTTTTTTTTT,TTTTTTTTTTTTTT,TTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTT,TTTTTTTTTTTTTTTTTTTTTTTT
[Show Flanks]
- Chromosome:
- 3:177877602
(GRCh38)
3:177595390
(GRCh37)
- Canonical SPDI:
- NC_000003.12:177877593:TTTTTTTTTTTTTTTTTT:TTTTTTTT,NC_000003.12:177877593:TTTTTTTTTTTTTTTTTT:TTTTTTTTTT,NC_000003.12:177877593:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000003.12:177877593:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000003.12:177877593:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTT,NC_000003.12:177877593:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000003.12:177877593:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000003.12:177877593:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000003.12:177877593:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTT,NC_000003.12:177877593:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTT,NC_000003.12:177877593:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:177877593:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:177877593:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:177877593:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:177877593:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:177877593:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:177877593:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:177877593:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTT,NC_000003.12:177877593:TTTTTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
- Gene:
- LINC02015 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
TTTTTTTT=0./0
(
ALFA)
-=0.000004/1
(TOPMED)
- HGVS:
NC_000003.12:g.177877602_177877611del, NC_000003.12:g.177877604_177877611del, NC_000003.12:g.177877605_177877611del, NC_000003.12:g.177877606_177877611del, NC_000003.12:g.177877609_177877611del, NC_000003.12:g.177877610_177877611del, NC_000003.12:g.177877611del, NC_000003.12:g.177877611dup, NC_000003.12:g.177877610_177877611dup, NC_000003.12:g.177877609_177877611dup, NC_000003.12:g.177877608_177877611dup, NC_000003.12:g.177877607_177877611dup, NC_000003.12:g.177877606_177877611dup, NC_000003.12:g.177877605_177877611dup, NC_000003.12:g.177877603_177877611dup, NC_000003.12:g.177877602_177877611dup, NC_000003.12:g.177877601_177877611dup, NC_000003.12:g.177877600_177877611dup, NC_000003.12:g.177877598_177877611dup, NC_000003.11:g.177595390_177595399del, NC_000003.11:g.177595392_177595399del, NC_000003.11:g.177595393_177595399del, NC_000003.11:g.177595394_177595399del, NC_000003.11:g.177595397_177595399del, NC_000003.11:g.177595398_177595399del, NC_000003.11:g.177595399del, NC_000003.11:g.177595399dup, NC_000003.11:g.177595398_177595399dup, NC_000003.11:g.177595397_177595399dup, NC_000003.11:g.177595396_177595399dup, NC_000003.11:g.177595395_177595399dup, NC_000003.11:g.177595394_177595399dup, NC_000003.11:g.177595393_177595399dup, NC_000003.11:g.177595391_177595399dup, NC_000003.11:g.177595390_177595399dup, NC_000003.11:g.177595389_177595399dup, NC_000003.11:g.177595388_177595399dup, NC_000003.11:g.177595386_177595399dup
14.
rs1491003079 [Homo sapiens]- Variant type:
- DEL
- Alleles:
- G>-
[Show Flanks]
- Chromosome:
- 3:177849552
(GRCh38)
3:177567340
(GRCh37)
- Canonical SPDI:
- NC_000003.12:177849551:G:
- Gene:
- LINC02015 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa
- MAF:
-=0./0
(
ALFA)
-=0.000021/3
(GnomAD)
-=0.000064/17
(TOPMED)
- HGVS:
15.
rs1490994182 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- G>A,C
[Show Flanks]
- Chromosome:
- 3:177870976
(GRCh38)
3:177588764
(GRCh37)
- Canonical SPDI:
- NC_000003.12:177870975:G:A,NC_000003.12:177870975:G:C
- Gene:
- LINC02015 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa
- MAF:
A=0./0
(
ALFA)
C=0.000007/1
(GnomAD)
- HGVS:
16.
rs1490873283 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- C>T
[Show Flanks]
- Chromosome:
- 3:177815279
(GRCh38)
3:177533067
(GRCh37)
- Canonical SPDI:
- NC_000003.12:177815278:C:T
- Gene:
- LINC02015 (Varview)
- Functional Consequence:
- upstream_transcript_variant,2KB_upstream_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
T=0./0
(
ALFA)
T=0.000004/1
(TOPMED)
T=0.000007/1
(GnomAD)
- HGVS:
17.
rs1490828956 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- G>A
[Show Flanks]
- Chromosome:
- 3:177873584
(GRCh38)
3:177591372
(GRCh37)
- Canonical SPDI:
- NC_000003.12:177873583:G:A
- Gene:
- LINC02015 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
A=0./0
(
ALFA)
A=0.000007/1
(GnomAD)
A=0.000008/2
(TOPMED)
- HGVS:
19.
rs1490814191 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- A>G
[Show Flanks]
- Chromosome:
- 3:177872860
(GRCh38)
3:177590648
(GRCh37)
- Canonical SPDI:
- NC_000003.12:177872859:A:G
- Gene:
- LINC02015 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
G=0.000071/1
(
ALFA)
G=0.000007/1
(GnomAD)
G=0.000008/2
(TOPMED)
- HGVS:
20.
rs1490768947 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- A>G,T
[Show Flanks]
- Chromosome:
- 3:177854190
(GRCh38)
3:177571978
(GRCh37)
- Canonical SPDI:
- NC_000003.12:177854189:A:G,NC_000003.12:177854189:A:T
- Gene:
- LINC02015 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
G=0.000054/1
(
ALFA)
G=0.000004/1
(TOPMED)
G=0.000007/1
(GnomAD)
G=0.000223/1
(Estonian)
T=0.001092/2
(Korea1K)
- HGVS: