SNP Links for Nucleotide (Select 206597531) - SNP

Links from Nucleotide

Items: 1 to 20 of 193

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Select item 14908256151.

rs1490825615 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 1:168792487 (GRCh38)
1:168761725 (GRCh37)
Canonical SPDI:: NC_000001.11:168792486:T:C
Gene:: LINC00626 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.168792487T>C, NC_000001.10:g.168761725T>C, NR_024160.1:n.554T>C, NM_080719.1:c.2T>C

Select item 14886130872.

rs1488613087 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:168792785 (GRCh38)
1:168762023 (GRCh37)
Canonical SPDI:: NC_000001.11:168792784:C:T
Gene:: LINC00626 (Varview)
Functional Consequence:: non_coding_transcript_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_000001.11:g.168792785C>T, NC_000001.10:g.168762023C>T, NR_024160.1:n.852C>T, NM_080719.1:c.*177C>T

Select item 14786856153.

rs1478685615 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 1:168787174 (GRCh38)
1:168756412 (GRCh37)
Canonical SPDI:: NC_000001.11:168787173:G:T
Gene:: LINC00626 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000014/2 (GnomAD)
HGVS:: NC_000001.11:g.168787174G>T, NC_000001.10:g.168756412G>T, NR_024160.1:n.234G>T, NM_080719.1:c.-319G>T

Select item 14778059634.

rs1477805963 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:168792768 (GRCh38)
1:168762006 (GRCh37)
Canonical SPDI:: NC_000001.11:168792767:A:G
Gene:: LINC00626 (Varview)
Functional Consequence:: non_coding_transcript_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_000001.11:g.168792768A>G, NC_000001.10:g.168762006A>G, NR_024160.1:n.835A>G, NM_080719.1:c.*160A>G

Select item 14765633105.

rs1476563310 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:168792407 (GRCh38)
1:168761645 (GRCh37)
Canonical SPDI:: NC_000001.11:168792406:G:A
Gene:: LINC00626 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.168792407G>A, NC_000001.10:g.168761645G>A, NR_024160.1:n.474G>A, NM_080719.1:c.-79G>A

Select item 14734450496.

rs1473445049 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C [Show Flanks]
Chromosome:: 1:168792503 (GRCh38)
1:168761741 (GRCh37)
Canonical SPDI:: NC_000001.11:168792502:T:A,NC_000001.11:168792502:T:C
Gene:: LINC00626 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.168792503T>A, NC_000001.11:g.168792503T>C, NC_000001.10:g.168761741T>A, NC_000001.10:g.168761741T>C, NR_024160.1:n.570T>A, NR_024160.1:n.570T>C, NM_080719.1:c.18T>A, NM_080719.1:c.18T>C

Select item 14647835587.

rs1464783558 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 1:168792852 (GRCh38)
1:168762090 (GRCh37)
Canonical SPDI:: NC_000001.11:168792851:G:T
Gene:: LINC00626 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.168792852G>T, NC_000001.10:g.168762090G>T, NR_024160.1:n.919G>T, NM_080719.1:c.*244G>T

Select item 14612752598.

rs1461275259 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:168787220 (GRCh38)
1:168756458 (GRCh37)
Canonical SPDI:: NC_000001.11:168787219:C:T
Gene:: LINC00626 (Varview)
Functional Consequence:: non_coding_transcript_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_000001.11:g.168787220C>T, NC_000001.10:g.168756458C>T, NR_024160.1:n.280C>T, NM_080719.1:c.-273C>T

Select item 14566223929.

rs1456622392 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 1:168792729 (GRCh38)
1:168761967 (GRCh37)
Canonical SPDI:: NC_000001.11:168792728:G:T
Gene:: LINC00626 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000071/1 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000011/3 (TOPMED)
HGVS:: NC_000001.11:g.168792729G>T, NC_000001.10:g.168761967G>T, NR_024160.1:n.796G>T, NM_080719.1:c.*121G>T

Select item 145113522710.

rs1451135227 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:168792665 (GRCh38)
1:168761903 (GRCh37)
Canonical SPDI:: NC_000001.11:168792664:G:A
Gene:: LINC00626 (Varview)
Functional Consequence:: non_coding_transcript_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_000001.11:g.168792665G>A, NC_000001.10:g.168761903G>A, NR_024160.1:n.732G>A, NM_080719.1:c.*57G>A

Select item 144989307411.

rs1449893074 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:168792878 (GRCh38)
1:168762116 (GRCh37)
Canonical SPDI:: NC_000001.11:168792877:G:A
Gene:: LINC00626 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.168792878G>A, NC_000001.10:g.168762116G>A, NR_024160.1:n.945G>A, NM_080719.1:c.*270G>A

Select item 144726082612.

rs1447260826 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 1:168786948 (GRCh38)
1:168756186 (GRCh37)
Canonical SPDI:: NC_000001.11:168786947:G:T
Gene:: LINC00626 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.168786948G>T, NC_000001.10:g.168756186G>T, NR_024160.1:n.8G>T, NM_080719.1:c.-545G>T

Select item 144658388313.

rs1446583883 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 1:168792782 (GRCh38)
1:168762020 (GRCh37)
Canonical SPDI:: NC_000001.11:168792781:G:T
Gene:: LINC00626 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000001.11:g.168792782G>T, NC_000001.10:g.168762020G>T, NR_024160.1:n.849G>T, NM_080719.1:c.*174G>T

Select item 144551277614.

rs1445512776 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G,T [Show Flanks]
Chromosome:: 1:168792635 (GRCh38)
1:168761873 (GRCh37)
Canonical SPDI:: NC_000001.11:168792634:A:C,NC_000001.11:168792634:A:G,NC_000001.11:168792634:A:T
Gene:: LINC00626 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.168792635A>C, NC_000001.11:g.168792635A>G, NC_000001.11:g.168792635A>T, NC_000001.10:g.168761873A>C, NC_000001.10:g.168761873A>G, NC_000001.10:g.168761873A>T, NR_024160.1:n.702A>C, NR_024160.1:n.702A>G, NR_024160.1:n.702A>T, NM_080719.1:c.*27A>C, NM_080719.1:c.*27A>G, NM_080719.1:c.*27A>T

Select item 144233811715.

rs1442338117 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:168787118 (GRCh38)
1:168756356 (GRCh37)
Canonical SPDI:: NC_000001.11:168787117:C:T
Gene:: LINC00626 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000014/2 (GnomAD)
HGVS:: NC_000001.11:g.168787118C>T, NC_000001.10:g.168756356C>T, NR_024160.1:n.178C>T, NM_080719.1:c.-375C>T

Select item 143992999416.

rs1439929994 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:168792521 (GRCh38)
1:168761759 (GRCh37)
Canonical SPDI:: NC_000001.11:168792520:G:A
Gene:: LINC00626 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000011/3 (TOPMED)
HGVS:: NC_000001.11:g.168792521G>A, NC_000001.10:g.168761759G>A, NR_024160.1:n.588G>A, NM_080719.1:c.36G>A

Select item 143562582617.

rs1435625826 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 1:168786984 (GRCh38)
1:168756222 (GRCh37)
Canonical SPDI:: NC_000001.11:168786983:T:C
Gene:: LINC00626 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.0002/1 (ALFA)
C=0.0002/1 (Estonian)
HGVS:: NC_000001.11:g.168786984T>C, NC_000001.10:g.168756222T>C, NR_024160.1:n.44T>C, NM_080719.1:c.-509T>C

Select item 143524674118.

rs1435246741 [Homo sapiens]

Variant type:: DEL
Alleles:: CCCCTCCC>- [Show Flanks]
Chromosome:: 1:168792709 (GRCh38)
1:168761947 (GRCh37)
Canonical SPDI:: NC_000001.11:168792708:CCCCTCCC:
Gene:: LINC00626 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.168792709_168792716del, NC_000001.10:g.168761947_168761954del, NR_024160.1:n.776_783del, NM_080719.1:c.*101_*108del

Select item 143484673719.

rs1434846737 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:168786944 (GRCh38)
1:168756182 (GRCh37)
Canonical SPDI:: NC_000001.11:168786943:G:A
Gene:: LINC00626 (Varview)
Functional Consequence:: non_coding_transcript_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_000001.11:g.168786944G>A, NC_000001.10:g.168756182G>A, NR_024160.1:n.4G>A, NM_080719.1:c.-549G>A

Select item 142549212620.

rs1425492126 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:168787105 (GRCh38)
1:168756343 (GRCh37)
Canonical SPDI:: NC_000001.11:168787104:G:A
Gene:: LINC00626 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.168787105G>A, NC_000001.10:g.168756343G>A, NR_024160.1:n.165G>A, NM_080719.1:c.-388G>A

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