SNP Links for Nucleotide (Select 262206343) - SNP

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Links from Nucleotide

Items: 1 to 20 of 22

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Select item 14314729181.

rs1431472918 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 11:75335179 (GRCh38)
11:75046223 (GRCh37)
Canonical SPDI:: NC_000011.10:75335178:C:G
Gene:: ARRB1 (Varview), MIR326 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000008/2 (TOPMED)
HGVS:: NC_000011.10:g.75335179C>G, NC_000011.9:g.75046223C>G, NG_028118.1:g.21653G>C, NR_029891.1:n.8G>C

Select item 13796810752.

rs1379681075 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:75335102 (GRCh38)
11:75046146 (GRCh37)
Canonical SPDI:: NC_000011.10:75335101:T:C
Gene:: ARRB1 (Varview), MIR326 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant,genic_upstream_transcript_variant
Validated:: by frequency
MAF:: C=0.00003/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.75335102T>C, NC_000011.9:g.75046146T>C, NG_028118.1:g.21730A>G, NR_029891.1:n.85A>G

Select item 13110789293.

rs1311078929 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:75335125 (GRCh38)
11:75046169 (GRCh37)
Canonical SPDI:: NC_000011.10:75335124:A:G
Gene:: ARRB1 (Varview), MIR326 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000094/1 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.75335125A>G, NC_000011.9:g.75046169A>G, NG_028118.1:g.21707T>C, NR_029891.1:n.62T>C

Select item 11791557864.

rs1179155786 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 11:75335152 (GRCh38)
11:75046196 (GRCh37)
Canonical SPDI:: NC_000011.10:75335151:C:A
Gene:: ARRB1 (Varview), MIR326 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant,non_coding_transcript_variant
HGVS:: NC_000011.10:g.75335152C>A, NC_000011.9:g.75046196C>A, NG_028118.1:g.21680G>T, NR_029891.1:n.35G>T

Select item 10370810705.

rs1037081070 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 11:75335103 (GRCh38)
11:75046147 (GRCh37)
Canonical SPDI:: NC_000011.10:75335102:C:A,NC_000011.10:75335102:C:T
Gene:: ARRB1 (Varview), MIR326 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.75335103C>A, NC_000011.10:g.75335103C>T, NC_000011.9:g.75046147C>A, NC_000011.9:g.75046147C>T, NG_028118.1:g.21729G>T, NG_028118.1:g.21729G>A, NR_029891.1:n.84G>T, NR_029891.1:n.84G>A

Select item 10193448986.

rs1019344898 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:75335098 (GRCh38)
11:75046142 (GRCh37)
Canonical SPDI:: NC_000011.10:75335097:C:T
Gene:: ARRB1 (Varview), MIR326 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.75335098C>T, NC_000011.9:g.75046142C>T, NG_028118.1:g.21734G>A, NR_029891.1:n.89G>A

Select item 9986218837.

rs998621883 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:75335095 (GRCh38)
11:75046139 (GRCh37)
Canonical SPDI:: NC_000011.10:75335094:A:G
Gene:: ARRB1 (Varview), MIR326 (Varview)
Functional Consequence:: non_coding_transcript_variant,genic_upstream_transcript_variant,intron_variant
HGVS:: NC_000011.10:g.75335095A>G, NC_000011.9:g.75046139A>G, NG_028118.1:g.21737T>C, NR_029891.1:n.92T>C

Select item 9543011268.

rs954301126 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,G [Show Flanks]
Chromosome:: 11:75335132 (GRCh38)
11:75046176 (GRCh37)
Canonical SPDI:: NC_000011.10:75335131:C:A,NC_000011.10:75335131:C:G
Gene:: ARRB1 (Varview), MIR326 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
A=0.00005/7 (GnomAD)
HGVS:: NC_000011.10:g.75335132C>A, NC_000011.10:g.75335132C>G, NC_000011.9:g.75046176C>A, NC_000011.9:g.75046176C>G, NG_028118.1:g.21700G>T, NG_028118.1:g.21700G>C, NR_029891.1:n.55G>T, NR_029891.1:n.55G>C

Select item 9527470749.

rs952747074 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 11:75335144 (GRCh38)
11:75046188 (GRCh37)
Canonical SPDI:: NC_000011.10:75335143:C:A,NC_000011.10:75335143:C:T
Gene:: ARRB1 (Varview), MIR326 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000015/4 (TOPMED)
T=0.000029/4 (GnomAD)
T=0.000684/2 (KOREAN)
HGVS:: NC_000011.10:g.75335144C>A, NC_000011.10:g.75335144C>T, NC_000011.9:g.75046188C>A, NC_000011.9:g.75046188C>T, NG_028118.1:g.21688G>T, NG_028118.1:g.21688G>A, NR_029891.1:n.43G>T, NR_029891.1:n.43G>A

Select item 92500367010.

rs925003670 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:75335186 (GRCh38)
11:75046230 (GRCh37)
Canonical SPDI:: NC_000011.10:75335185:G:A
Gene:: ARRB1 (Varview), MIR326 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,non_coding_transcript_variant,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:: NC_000011.10:g.75335186G>A, NC_000011.9:g.75046230G>A, NG_028118.1:g.21646C>T, NR_029891.1:n.1C>T

Select item 89867432011.

rs898674320 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 11:75335128 (GRCh38)
11:75046172 (GRCh37)
Canonical SPDI:: NC_000011.10:75335127:C:A,NC_000011.10:75335127:C:T
Gene:: ARRB1 (Varview), MIR326 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.75335128C>A, NC_000011.10:g.75335128C>T, NC_000011.9:g.75046172C>A, NC_000011.9:g.75046172C>T, NG_028118.1:g.21704G>T, NG_028118.1:g.21704G>A, NR_029891.1:n.59G>T, NR_029891.1:n.59G>A

Select item 77455151712.

rs774551517 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:75335101 (GRCh38)
11:75046145 (GRCh37)
Canonical SPDI:: NC_000011.10:75335100:C:T
Gene:: ARRB1 (Varview), MIR326 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0./0 (ExAC)
T=0./0 (GnomAD)
HGVS:: NC_000011.10:g.75335101C>T, NC_000011.9:g.75046145C>T, NG_028118.1:g.21731G>A, NR_029891.1:n.86G>A

Select item 77299247713.

rs772992477 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 11:75335139 (GRCh38)
11:75046183 (GRCh37)
Canonical SPDI:: NC_000011.10:75335138:C:A
Gene:: ARRB1 (Varview), MIR326 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000014/2 (GnomAD)
A=0.000015/4 (TOPMED)
A=0.000092/1 (ExAC)
HGVS:: NC_000011.10:g.75335139C>A, NC_000011.9:g.75046183C>A, NG_028118.1:g.21693G>T, NR_029891.1:n.48G>T

Select item 77086087814.

rs770860878 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:75335168 (GRCh38)
11:75046212 (GRCh37)
Canonical SPDI:: NC_000011.10:75335167:A:G
Gene:: ARRB1 (Varview), MIR326 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0./0 (TWINSUK)
G=0.000007/1 (GnomAD)
G=0.000008/2 (TOPMED)
G=0.000259/1 (ALSPAC)
HGVS:: NC_000011.10:g.75335168A>G, NC_000011.9:g.75046212A>G, NG_028118.1:g.21664T>C, NR_029891.1:n.19T>C

Select item 76635883615.

rs766358836 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:75335143 (GRCh38)
11:75046187 (GRCh37)
Canonical SPDI:: NC_000011.10:75335142:C:T
Gene:: ARRB1 (Varview), MIR326 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant,genic_upstream_transcript_variant
Validated:: by frequency,by cluster
MAF:: T=0.00009/1 (ExAC)
HGVS:: NC_000011.10:g.75335143C>T, NC_000011.9:g.75046187C>T, NG_028118.1:g.21689G>A, NR_029891.1:n.44G>A

Select item 75450964416.

rs754509644 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:75335174 (GRCh38)
11:75046218 (GRCh37)
Canonical SPDI:: NC_000011.10:75335173:A:G
Gene:: ARRB1 (Varview), MIR326 (Varview)
Functional Consequence:: non_coding_transcript_variant,genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0./0 (ExAC)
G=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.75335174A>G, NC_000011.9:g.75046218A>G, NG_028118.1:g.21658T>C, NR_029891.1:n.13T>C

Select item 75376453617.

rs753764536 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 11:75335145 (GRCh38)
11:75046189 (GRCh37)
Canonical SPDI:: NC_000011.10:75335144:G:A,NC_000011.10:75335144:G:T
Gene:: ARRB1 (Varview), MIR326 (Varview)
Functional Consequence:: non_coding_transcript_variant,genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
A=0.000041/3 (GnomAD_exomes)
A=0.000057/8 (GnomAD)
A=0.000331/4 (ExAC)
HGVS:: NC_000011.10:g.75335145G>A, NC_000011.10:g.75335145G>T, NC_000011.9:g.75046189G>A, NC_000011.9:g.75046189G>T, NG_028118.1:g.21687C>T, NG_028118.1:g.21687C>A, NR_029891.1:n.42C>T, NR_029891.1:n.42C>A

Select item 74808041618.

rs748080416 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:75335099 (GRCh38)
11:75046143 (GRCh37)
Canonical SPDI:: NC_000011.10:75335098:G:A
Gene:: ARRB1 (Varview), MIR326 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000071/1 (ALFA)
A=0./0 (TWINSUK)
A=0.000026/7 (TOPMED)
A=0.000043/6 (GnomAD)
A=0.000259/1 (ALSPAC)
HGVS:: NC_000011.10:g.75335099G>A, NC_000011.9:g.75046143G>A, NG_028118.1:g.21733C>T, NR_029891.1:n.88C>T

Select item 57533978719.

rs575339787 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 11:75335104 (GRCh38)
11:75046148 (GRCh37)
Canonical SPDI:: NC_000011.10:75335103:G:A,NC_000011.10:75335103:G:T
Gene:: ARRB1 (Varview), MIR326 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0./0 (ExAC)
A=0.000008/2 (TOPMED)
A=0.000021/3 (GnomAD)
T=0.000035/1 (GnomAD_exomes)
A=0.001002/1 (GoNL)
HGVS:: NC_000011.10:g.75335104G>A, NC_000011.10:g.75335104G>T, NC_000011.9:g.75046148G>A, NC_000011.9:g.75046148G>T, NG_028118.1:g.21728C>T, NG_028118.1:g.21728C>A, NR_029891.1:n.83C>T, NR_029891.1:n.83C>A

Select item 53040489520.

rs530404895 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:75335140 (GRCh38)
11:75046184 (GRCh37)
Canonical SPDI:: NC_000011.10:75335139:C:T
Gene:: ARRB1 (Varview), MIR326 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000021/3 (GnomAD)
T=0.000064/17 (TOPMED)
T=0.000091/1 (ExAC)
T=0.000312/2 (1000Genomes)
T=0.000342/1 (KOREAN)
T=0.00092/15 (TOMMO)
T=0.001638/3 (Korea1K)
HGVS:: NC_000011.10:g.75335140C>T, NC_000011.9:g.75046184C>T, NG_028118.1:g.21692G>A, NR_029891.1:n.47G>A