SNP Links for Nucleotide (Select 641451072) - SNP

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Links from Nucleotide

Items: 1 to 20 of 433

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Select item 14861163491.

rs1486116349 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:8062080 (GRCh38)
11:8083627 (GRCh37)
Canonical SPDI:: NC_000011.10:8062079:G:A
Gene:: TUB (Varview), TUB-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant,genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000011/3 (TOPMED)
HGVS:: NC_000011.10:g.8062080G>A, NC_000011.9:g.8083627G>A, NG_029912.1:g.28448G>A, NR_120537.1:n.49G>A, NR_120538.1:n.49G>A

Select item 14858204122.

rs1485820412 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:8068906 (GRCh38)
11:8090453 (GRCh37)
Canonical SPDI:: NC_000011.10:8068905:C:T
Gene:: TUB (Varview), TUB-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant,genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: T=0.000071/1 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.8068906C>T, NC_000011.9:g.8090453C>T, NG_029912.1:g.35274C>T, NR_120537.1:n.1554C>T, NR_120538.1:n.1497C>T

Select item 14848729953.

rs1484872995 [Homo sapiens]

Variant type:: DELINS
Alleles:: GG>- [Show Flanks]
Chromosome:: 11:8068870 (GRCh38)
11:8090417 (GRCh37)
Canonical SPDI:: NC_000011.10:8068867:GGGG:GG
Gene:: TUB (Varview), TUB-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant,genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GGGG=0./0 (ALFA)
-=0.000008/2 (TOPMED)
HGVS:: NC_000011.10:g.8068870_8068871del, NC_000011.9:g.8090417_8090418del, NG_029912.1:g.35238_35239del, NR_120537.1:n.1518_1519del, NR_120538.1:n.1461_1462del

Select item 14843457314.

rs1484345731 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:8068987 (GRCh38)
11:8090534 (GRCh37)
Canonical SPDI:: NC_000011.10:8068986:G:A
Gene:: TUB (Varview), TUB-AS1 (Varview)
Functional Consequence:: non_coding_transcript_variant,genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000023/6 (TOPMED)
HGVS:: NC_000011.10:g.8068987G>A, NC_000011.9:g.8090534G>A, NG_029912.1:g.35355G>A, NR_120537.1:n.1635G>A, NR_120538.1:n.1578G>A

Select item 14841446905.

rs1484144690 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:8068605 (GRCh38)
11:8090152 (GRCh37)
Canonical SPDI:: NC_000011.10:8068604:C:T
Gene:: TUB (Varview), TUB-AS1 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant,non_coding_transcript_variant
Validated:: by frequency
MAF:: T=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.8068605C>T, NC_000011.9:g.8090152C>T, NG_029912.1:g.34973C>T, NR_120537.1:n.1253C>T, NR_120538.1:n.1196C>T

Select item 14809595686.

rs1480959568 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 11:8067965 (GRCh38)
11:8089512 (GRCh37)
Canonical SPDI:: NC_000011.10:8067964:C:G
Gene:: TUB (Varview), TUB-AS1 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000019/5 (TOPMED)
HGVS:: NC_000011.10:g.8067965C>G, NC_000011.9:g.8089512C>G, NG_029912.1:g.34333C>G, NR_120537.1:n.613C>G, NR_120538.1:n.556C>G

Select item 14809072677.

rs1480907267 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:8068888 (GRCh38)
11:8090435 (GRCh37)
Canonical SPDI:: NC_000011.10:8068887:C:T
Gene:: TUB (Varview), TUB-AS1 (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=0.000011/3 (TOPMED)
T=0.000014/2 (GnomAD)
HGVS:: NC_000011.10:g.8068888C>T, NC_000011.9:g.8090435C>T, NG_029912.1:g.35256C>T, NR_120537.1:n.1536C>T, NR_120538.1:n.1479C>T

Select item 14768278828.

rs1476827882 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:8069128 (GRCh38)
11:8090675 (GRCh37)
Canonical SPDI:: NC_000011.10:8069127:T:C
Gene:: TUB (Varview), TUB-AS1 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.8069128T>C, NC_000011.9:g.8090675T>C, NG_029912.1:g.35496T>C, NR_120537.1:n.1776T>C, NR_120538.1:n.1719T>C

Select item 14761477899.

rs1476147789 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 11:8067740 (GRCh38)
11:8089287 (GRCh37)
Canonical SPDI:: NC_000011.10:8067739:T:G
Gene:: TUB (Varview), TUB-AS1 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000071/1 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.8067740T>G, NC_000011.9:g.8089287T>G, NG_029912.1:g.34108T>G, NR_120537.1:n.388T>G, NR_120538.1:n.331T>G

Select item 147491412910.

rs1474914129 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:8068676 (GRCh38)
11:8090223 (GRCh37)
Canonical SPDI:: NC_000011.10:8068675:C:T
Gene:: TUB (Varview), TUB-AS1 (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=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.8068676C>T, NC_000011.9:g.8090223C>T, NG_029912.1:g.35044C>T, NR_120537.1:n.1324C>T, NR_120538.1:n.1267C>T

Select item 147148003711.

rs1471480037 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:8068566 (GRCh38)
11:8090113 (GRCh37)
Canonical SPDI:: NC_000011.10:8068565:C:T
Gene:: TUB (Varview), TUB-AS1 (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)
T=0.000008/2 (TOPMED)
HGVS:: NC_000011.10:g.8068566C>T, NC_000011.9:g.8090113C>T, NG_029912.1:g.34934C>T, NR_120537.1:n.1214C>T, NR_120538.1:n.1157C>T

Select item 147078718112.

rs1470787181 [Homo sapiens]

Variant type:: DELINS
Alleles:: TATT>- [Show Flanks]
Chromosome:: 11:8068059 (GRCh38)
11:8089606 (GRCh37)
Canonical SPDI:: NC_000011.10:8068052:TTTATTTATT:TTTATT
Gene:: TUB (Varview), TUB-AS1 (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTATT=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.8068055TATT[1], NC_000011.9:g.8089602TATT[1], NG_029912.1:g.34423TATT[1], NR_120537.1:n.703TATT[1], NR_120538.1:n.646TATT[1]

Select item 146723629113.

rs1467236291 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 11:8068960 (GRCh38)
11:8090507 (GRCh37)
Canonical SPDI:: NC_000011.10:8068959:C:A
Gene:: TUB (Varview), TUB-AS1 (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=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.8068960C>A, NC_000011.9:g.8090507C>A, NG_029912.1:g.35328C>A, NR_120537.1:n.1608C>A, NR_120538.1:n.1551C>A

Select item 146488605414.

rs1464886054 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:8068042 (GRCh38)
11:8089589 (GRCh37)
Canonical SPDI:: NC_000011.10:8068041:T:C
Gene:: TUB (Varview), TUB-AS1 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000071/1 (ALFA)
C=0.000036/5 (GnomAD)
C=0.000049/13 (TOPMED)
HGVS:: NC_000011.10:g.8068042T>C, NC_000011.9:g.8089589T>C, NG_029912.1:g.34410T>C, NR_120537.1:n.690T>C, NR_120538.1:n.633T>C

Select item 146468165715.

rs1464681657 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:8067716 (GRCh38)
11:8089263 (GRCh37)
Canonical SPDI:: NC_000011.10:8067715:T:C
Gene:: TUB (Varview), TUB-AS1 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000011/3 (TOPMED)
C=0.000021/3 (GnomAD)
HGVS:: NC_000011.10:g.8067716T>C, NC_000011.9:g.8089263T>C, NG_029912.1:g.34084T>C, NR_120537.1:n.364T>C, NR_120538.1:n.307T>C

Select item 146333187416.

rs1463331874 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:8068184 (GRCh38)
11:8089731 (GRCh37)
Canonical SPDI:: NC_000011.10:8068183:C:T
Gene:: TUB (Varview), TUB-AS1 (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=0.000014/2 (GnomAD)
T=0.000026/7 (TOPMED)
HGVS:: NC_000011.10:g.8068184C>T, NC_000011.9:g.8089731C>T, NG_029912.1:g.34552C>T, NR_120537.1:n.832C>T, NR_120538.1:n.775C>T

Select item 146213385117.

rs1462133851 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 11:8067628 (GRCh38)
11:8089175 (GRCh37)
Canonical SPDI:: NC_000011.10:8067627:G:A,NC_000011.10:8067627:G:C
Gene:: TUB (Varview), TUB-AS1 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000014/2 (GnomAD)
HGVS:: NC_000011.10:g.8067628G>A, NC_000011.10:g.8067628G>C, NC_000011.9:g.8089175G>A, NC_000011.9:g.8089175G>C, NG_029912.1:g.33996G>A, NG_029912.1:g.33996G>C, NR_120537.1:n.276G>A, NR_120537.1:n.276G>C, NR_120538.1:n.219G>A, NR_120538.1:n.219G>C

Select item 146033690418.

rs1460336904 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 11:8068477 (GRCh38)
11:8090024 (GRCh37)
Canonical SPDI:: NC_000011.10:8068476:C:G
Gene:: TUB (Varview), TUB-AS1 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
HGVS:: NC_000011.10:g.8068477C>G, NC_000011.9:g.8090024C>G, NG_029912.1:g.34845C>G, NR_120537.1:n.1125C>G, NR_120538.1:n.1068C>G

Select item 146023458519.

rs1460234585 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 11:8069263 (GRCh38)
11:8090810 (GRCh37)
Canonical SPDI:: NC_000011.10:8069262:T:G
Gene:: TUB (Varview), TUB-AS1 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000071/1 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000011/3 (TOPMED)
HGVS:: NC_000011.10:g.8069263T>G, NC_000011.9:g.8090810T>G, NG_029912.1:g.35631T>G, NR_120537.1:n.1911T>G, NR_120538.1:n.1854T>G

Select item 145907112220.

rs1459071122 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:8062135 (GRCh38)
11:8083682 (GRCh37)
Canonical SPDI:: NC_000011.10:8062134:C:T
Gene:: TUB (Varview), TUB-AS1 (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=0.000026/7 (TOPMED)
HGVS:: NC_000011.10:g.8062135C>T, NC_000011.9:g.8083682C>T, NG_029912.1:g.28503C>T, NR_120537.1:n.104C>T, NR_120538.1:n.104C>T

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