SNP Links for Gene (Select 283033) - SNP

Links from Gene

Items: 1 to 20 of 16741

<< First< Prev

Page of 838

Next >Last >>

Select item 14910437051.

rs1491043705 has merged into rs55640713 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAA>-,A,AA,AAA,AAAA,AAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 10:43933119 (GRCh38)
10:44428567 (GRCh37)
Canonical SPDI:: NC_000010.11:43933103:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000010.11:43933103:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000010.11:43933103:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000010.11:43933103:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000010.11:43933103:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000010.11:43933103:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000010.11:43933103:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:43933103:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:43933103:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:43933103:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:43933103:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:43933103:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:43933103:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:43933103:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:43933103:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000010.11:43933103:AAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: LINC00841 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAAAAAAAAA=0./0 (ALFA)
HGVS:: NC_000010.11:g.43933119_43933124del, NC_000010.11:g.43933120_43933124del, NC_000010.11:g.43933121_43933124del, NC_000010.11:g.43933122_43933124del, NC_000010.11:g.43933123_43933124del, NC_000010.11:g.43933124del, NC_000010.11:g.43933124dup, NC_000010.11:g.43933123_43933124dup, NC_000010.11:g.43933122_43933124dup, NC_000010.11:g.43933121_43933124dup, NC_000010.11:g.43933120_43933124dup, NC_000010.11:g.43933119_43933124dup, NC_000010.11:g.43933118_43933124dup, NC_000010.11:g.43933117_43933124dup, NC_000010.11:g.43933115_43933124dup, NC_000010.11:g.43933106_43933124dup, NC_000010.10:g.44428567_44428572del, NC_000010.10:g.44428568_44428572del, NC_000010.10:g.44428569_44428572del, NC_000010.10:g.44428570_44428572del, NC_000010.10:g.44428571_44428572del, NC_000010.10:g.44428572del, NC_000010.10:g.44428572dup, NC_000010.10:g.44428571_44428572dup, NC_000010.10:g.44428570_44428572dup, NC_000010.10:g.44428569_44428572dup, NC_000010.10:g.44428568_44428572dup, NC_000010.10:g.44428567_44428572dup, NC_000010.10:g.44428566_44428572dup, NC_000010.10:g.44428565_44428572dup, NC_000010.10:g.44428563_44428572dup, NC_000010.10:g.44428554_44428572dup

Select item 14910406892.

rs1491040689 has merged into rs373137014 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTTT>-,T,TT,TTT,TTTTT,TTTTTT,TTTTTTT,TTTTTTTT,TTTTTTTTTTTTTT [Show Flanks]
Chromosome:: 10:43908285 (GRCh38)
10:44403733 (GRCh37)
Canonical SPDI:: NC_000010.11:43908273:TTTTTTTTTTTTTTT:TTTTTTTTTTT,NC_000010.11:43908273:TTTTTTTTTTTTTTT:TTTTTTTTTTTT,NC_000010.11:43908273:TTTTTTTTTTTTTTT:TTTTTTTTTTTTT,NC_000010.11:43908273:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTT,NC_000010.11:43908273:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTT,NC_000010.11:43908273:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTT,NC_000010.11:43908273:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTT,NC_000010.11:43908273:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTT,NC_000010.11:43908273:TTTTTTTTTTTTTTT:TTTTTTTTTTTTTTTTTTTTTTTTT
Gene:: LINC00841 (Varview), LINC02659 (Varview)
Functional Consequence:: upstream_transcript_variant,intron_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTTTTTTTTT=0./0 (ALFA)
T=0.03167/19 (NorthernSweden)
HGVS:: NC_000010.11:g.43908285_43908288del, NC_000010.11:g.43908286_43908288del, NC_000010.11:g.43908287_43908288del, NC_000010.11:g.43908288del, NC_000010.11:g.43908288dup, NC_000010.11:g.43908287_43908288dup, NC_000010.11:g.43908286_43908288dup, NC_000010.11:g.43908285_43908288dup, NC_000010.11:g.43908279_43908288dup, NC_000010.10:g.44403733_44403736del, NC_000010.10:g.44403734_44403736del, NC_000010.10:g.44403735_44403736del, NC_000010.10:g.44403736del, NC_000010.10:g.44403736dup, NC_000010.10:g.44403735_44403736dup, NC_000010.10:g.44403734_44403736dup, NC_000010.10:g.44403733_44403736dup, NC_000010.10:g.44403727_44403736dup

Select item 14909813043.

rs1490981304 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 10:43978227 (GRCh38)
10:44473675 (GRCh37)
Canonical SPDI:: NC_000010.11:43978226:G:A
Gene:: LINC00841 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000084/1 (ALFA)
A=0./0 (Korea1K)
A=0.000014/2 (GnomAD)
A=0.000034/9 (TOPMED)
A=0.000684/2 (KOREAN)
HGVS:: NC_000010.11:g.43978227G>A, NC_000010.10:g.44473675G>A

Select item 14909046734.

rs1490904673 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 10:43963400 (GRCh38)
10:44458848 (GRCh37)
Canonical SPDI:: NC_000010.11:43963399:G:A
Gene:: LINC00841 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000010.11:g.43963400G>A, NC_000010.10:g.44458848G>A

Select item 14908975255.

rs1490897525 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 10:43948651 (GRCh38)
10:44444099 (GRCh37)
Canonical SPDI:: NC_000010.11:43948650:T:C
Gene:: LINC00841 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000010.11:g.43948651T>C, NC_000010.10:g.44444099T>C

Select item 14908491656.

rs1490849165 [Homo sapiens]

Variant type:: DELINS
Alleles:: T>- [Show Flanks]
Chromosome:: 10:43979453 (GRCh38)
10:44474901 (GRCh37)
Canonical SPDI:: NC_000010.11:43979452:TT:T
Gene:: LINC00841 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TT=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.000014/2 (GnomAD)
HGVS:: NC_000010.11:g.43979454del, NC_000010.10:g.44474902del

Select item 14908194847.

rs1490819484 [Homo sapiens]

Variant type:: INS
Alleles:: ->CTTAAC [Show Flanks]
Chromosome:: 10:43933137 (GRCh38)
10:44428586 (GRCh37)
Canonical SPDI:: NC_000010.11:43933137::CTTAAC
Gene:: LINC00841 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: CTTAAC=0./0 (ALFA)
CTTAAC=0.000004/1 (TOPMED)
HGVS:: NC_000010.11:g.43933137_43933138insCTTAAC, NC_000010.10:g.44428585_44428586insCTTAAC

Select item 14907449978.

rs1490744997 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 10:43919271 (GRCh38)
10:44414719 (GRCh37)
Canonical SPDI:: NC_000010.11:43919270:C:G,NC_000010.11:43919270:C:T
Gene:: LINC00841 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000010.11:g.43919271C>G, NC_000010.11:g.43919271C>T, NC_000010.10:g.44414719C>G, NC_000010.10:g.44414719C>T

Select item 14907214529.

rs1490721452 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 10:43920101 (GRCh38)
10:44415549 (GRCh37)
Canonical SPDI:: NC_000010.11:43920100:T:G
Gene:: LINC00841 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000010.11:g.43920101T>G, NC_000010.10:g.44415549T>G

Select item 149061902910.

rs1490619029 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 10:43970611 (GRCh38)
10:44466059 (GRCh37)
Canonical SPDI:: NC_000010.11:43970610:C:T
Gene:: LINC00841 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000010.11:g.43970611C>T, NC_000010.10:g.44466059C>T

Select item 149059675711.

rs1490596757 [Homo sapiens]

Variant type:: DEL
Alleles:: A>- [Show Flanks]
Chromosome:: 10:43956488 (GRCh38)
10:44451936 (GRCh37)
Canonical SPDI:: NC_000010.11:43956487:A:
Gene:: LINC00841 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.000004/1 (TOPMED)
HGVS:: NC_000010.11:g.43956488del, NC_000010.10:g.44451936del

Select item 149054622012.

rs1490546220 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 10:43955555 (GRCh38)
10:44451003 (GRCh37)
Canonical SPDI:: NC_000010.11:43955554:C:G
Gene:: LINC00841 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000021/3 (GnomAD)
G=0.000026/7 (TOPMED)
HGVS:: NC_000010.11:g.43955555C>G, NC_000010.10:g.44451003C>G

Select item 149048310113.

rs1490483101 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 10:43912939 (GRCh38)
10:44408387 (GRCh37)
Canonical SPDI:: NC_000010.11:43912938:C:T
Gene:: LINC00841 (Varview), LINC02659 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000010.11:g.43912939C>T, NC_000010.10:g.44408387C>T

Select item 149041583214.

rs1490415832 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 10:43962916 (GRCh38)
10:44458364 (GRCh37)
Canonical SPDI:: NC_000010.11:43962915:C:T
Gene:: LINC00841 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0./0 (KOREAN)
T=0.000007/1 (GnomAD)
T=0.000023/6 (TOPMED)
HGVS:: NC_000010.11:g.43962916C>T, NC_000010.10:g.44458364C>T

Select item 149036157015.

rs1490361570 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 10:43947966 (GRCh38)
10:44443414 (GRCh37)
Canonical SPDI:: NC_000010.11:43947965:T:C
Gene:: LINC00841 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000014/2 (GnomAD)
C=0.000038/10 (TOPMED)
HGVS:: NC_000010.11:g.43947966T>C, NC_000010.10:g.44443414T>C

Select item 149035856416.

rs1490358564 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 10:43980420 (GRCh38)
10:44475868 (GRCh37)
Canonical SPDI:: NC_000010.11:43980419:G:T
Gene:: LINC00841 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000010.11:g.43980420G>T, NC_000010.10:g.44475868G>T

Select item 149033087817.

rs1490330878 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 10:43942762 (GRCh38)
10:44438210 (GRCh37)
Canonical SPDI:: NC_000010.11:43942761:C:G
Gene:: LINC00841 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
G=0.000021/3 (GnomAD)
HGVS:: NC_000010.11:g.43942762C>G, NC_000010.10:g.44438210C>G

Select item 149027163018.

rs1490271630 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 10:43957381 (GRCh38)
10:44452829 (GRCh37)
Canonical SPDI:: NC_000010.11:43957380:G:A
Gene:: LINC00841 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000011/3 (TOPMED)
HGVS:: NC_000010.11:g.43957381G>A, NC_000010.10:g.44452829G>A

Select item 149024497119.

rs1490244971 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 10:43930785 (GRCh38)
10:44426233 (GRCh37)
Canonical SPDI:: NC_000010.11:43930784:G:A
Gene:: LINC00841 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
A=0.000021/3 (GnomAD)
HGVS:: NC_000010.11:g.43930785G>A, NC_000010.10:g.44426233G>A

Select item 149019834020.

rs1490198340 [Homo sapiens]

Variant type:: DELINS
Alleles:: CA>- [Show Flanks]
Chromosome:: 10:43941785 (GRCh38)
10:44437233 (GRCh37)
Canonical SPDI:: NC_000010.11:43941779:ACACACA:ACACA
Gene:: LINC00841 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: ACACA=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.000007/1 (GnomAD)
-=0.000035/1 (TOMMO)
HGVS:: NC_000010.11:g.43941781CA[2], NC_000010.10:g.44437229CA[2]

<< First< Prev

Page of 838

Next >Last >>

dbSNP

Result Filters

Validation Status

Publication

Function Class

Variation Class

Annotation

Global MAF

Custom range

Additional filters

Display Settings:

Send to:

Links from Gene

Items: 1 to 20 of 16741

Display Settings:

Send to:

Supplemental Content

Find related data

Recent activity