SNP Links for Nucleotide (Select 302393533) - SNP

Links from Nucleotide

Items: 1 to 20 of 604

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Select item 14895231351.

rs1489523135 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->T [Show Flanks]
Chromosome:: 2:131403084 (GRCh38)
2:132160658 (GRCh37)
Canonical SPDI:: NC_000002.12:131403084:TTT:TTTT
Gene:: LINC01120 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTT=0.000162/3 (ALFA)
T=0.000014/2 (GnomAD)
T=0.000015/4 (TOPMED)
T=0.000106/3 (TOMMO)
T=0.000446/2 (Estonian)
HGVS:: NC_000002.12:g.131403087dup, NC_000002.11:g.132160660dup, NR_036499.1:n.187dup

Select item 14894086842.

rs1489408684 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 2:131405349 (GRCh38)
2:132162922 (GRCh37)
Canonical SPDI:: NC_000002.12:131405348:A:G
Gene:: LINC01120 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000002.12:g.131405349A>G, NC_000002.11:g.132162922A>G, NR_036499.1:n.488A>G

Select item 14886833923.

rs1488683392 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 2:131406489 (GRCh38)
2:132164062 (GRCh37)
Canonical SPDI:: NC_000002.12:131406488:G:A
Gene:: LINC01120 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000002.12:g.131406489G>A, NC_000002.11:g.132164062G>A, NR_036499.1:n.1628G>A

Select item 14884889044.

rs1488488904 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 2:131405876 (GRCh38)
2:132163449 (GRCh37)
Canonical SPDI:: NC_000002.12:131405875:T:C,NC_000002.12:131405875:T:G
Gene:: LINC01120 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
C=0.000014/2 (GnomAD)
HGVS:: NC_000002.12:g.131405876T>C, NC_000002.12:g.131405876T>G, NC_000002.11:g.132163449T>C, NC_000002.11:g.132163449T>G, NR_036499.1:n.1015T>C, NR_036499.1:n.1015T>G

Select item 14861690825.

rs1486169082 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 2:131406683 (GRCh38)
2:132164256 (GRCh37)
Canonical SPDI:: NC_000002.12:131406682:T:A
Gene:: LINC01120 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000002.12:g.131406683T>A, NC_000002.11:g.132164256T>A, NR_036499.1:n.1822T>A

Select item 14842009306.

rs1484200930 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 2:131405742 (GRCh38)
2:132163315 (GRCh37)
Canonical SPDI:: NC_000002.12:131405741:C:G
Gene:: LINC01120 (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_000002.12:g.131405742C>G, NC_000002.11:g.132163315C>G, NR_036499.1:n.881C>G

Select item 14838035507.

rs1483803550 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 2:131406250 (GRCh38)
2:132163823 (GRCh37)
Canonical SPDI:: NC_000002.12:131406249:G:A
Gene:: LINC01120 (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=0.000036/5 (GnomAD)
HGVS:: NC_000002.12:g.131406250G>A, NC_000002.11:g.132163823G>A, NR_036499.1:n.1389G>A

Select item 14830729778.

rs1483072977 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->G [Show Flanks]
Chromosome:: 2:131406594 (GRCh38)
2:132164168 (GRCh37)
Canonical SPDI:: NC_000002.12:131406594:G:GG
Gene:: LINC01120 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: GG=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000002.12:g.131406595dup, NC_000002.11:g.132164168dup, NR_036499.1:n.1734dup

Select item 14827167939.

rs1482716793 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 2:131407238 (GRCh38)
2:132164811 (GRCh37)
Canonical SPDI:: NC_000002.12:131407237:A:C
Gene:: LINC01120 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
C=0.000014/2 (GnomAD)
HGVS:: NC_000002.12:g.131407238A>C, NC_000002.11:g.132164811A>C, NR_036499.1:n.2377A>C

Select item 148085023110.

rs1480850231 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 2:131406333 (GRCh38)
2:132163906 (GRCh37)
Canonical SPDI:: NC_000002.12:131406332:C:G
Gene:: LINC01120 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000002.12:g.131406333C>G, NC_000002.11:g.132163906C>G, NR_036499.1:n.1472C>G

Select item 147720837511.

rs1477208375 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: 2:131405923 (GRCh38)
2:132163496 (GRCh37)
Canonical SPDI:: NC_000002.12:131405922:A:G,NC_000002.12:131405922:A:T
Gene:: LINC01120 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
G=0.000008/2 (TOPMED)
HGVS:: NC_000002.12:g.131405923A>G, NC_000002.12:g.131405923A>T, NC_000002.11:g.132163496A>G, NC_000002.11:g.132163496A>T, NR_036499.1:n.1062A>G, NR_036499.1:n.1062A>T

Select item 147596995812.

rs1475969958 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 2:131402926 (GRCh38)
2:132160499 (GRCh37)
Canonical SPDI:: NC_000002.12:131402925:A:G
Gene:: LINC01120 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000071/1 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000014/2 (GnomAD)
G=0.000035/1 (TOMMO)
HGVS:: NC_000002.12:g.131402926A>G, NC_000002.11:g.132160499A>G, NR_036499.1:n.26A>G

Select item 147373763413.

rs1473737634 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 2:131406986 (GRCh38)
2:132164559 (GRCh37)
Canonical SPDI:: NC_000002.12:131406985:G:A
Gene:: LINC01120 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000002.12:g.131406986G>A, NC_000002.11:g.132164559G>A, NR_036499.1:n.2125G>A

Select item 147274736214.

rs1472747362 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 2:131405337 (GRCh38)
2:132162910 (GRCh37)
Canonical SPDI:: NC_000002.12:131405336:A:G
Gene:: LINC01120 (Varview)
Functional Consequence:: non_coding_transcript_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_000002.12:g.131405337A>G, NC_000002.11:g.132162910A>G, NR_036499.1:n.476A>G

Select item 147159171915.

rs1471591719 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->TT [Show Flanks]
Chromosome:: 2:131406243 (GRCh38)
2:132163817 (GRCh37)
Canonical SPDI:: NC_000002.12:131406243:TT:TTTT
Gene:: LINC01120 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TTTT=0./0 (ALFA)
TT=0.000004/1 (TOPMED)
TT=0.000007/1 (GnomAD)
HGVS:: NC_000002.12:g.131406244_131406245dup, NC_000002.11:g.132163817_132163818dup, NR_036499.1:n.1383_1384dup

Select item 146929012216.

rs1469290122 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 2:131405216 (GRCh38)
2:132162789 (GRCh37)
Canonical SPDI:: NC_000002.12:131405215:G:A
Gene:: LINC01120 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000002.12:g.131405216G>A, NC_000002.11:g.132162789G>A, NR_036499.1:n.355G>A

Select item 146645051517.

rs1466450515 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 2:131405983 (GRCh38)
2:132163556 (GRCh37)
Canonical SPDI:: NC_000002.12:131405982:C:A
Gene:: LINC01120 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: A=0.000007/1 (GnomAD)
HGVS:: NC_000002.12:g.131405983C>A, NC_000002.11:g.132163556C>A, NR_036499.1:n.1122C>A

Select item 146578344018.

rs1465783440 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 2:131408157 (GRCh38)
2:132165730 (GRCh37)
Canonical SPDI:: NC_000002.12:131408156:A:G
Gene:: LINC01120 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000014/2 (GnomAD)
G=0.000015/4 (TOPMED)
HGVS:: NC_000002.12:g.131408157A>G, NC_000002.11:g.132165730A>G, NR_036499.1:n.2984A>G

Select item 146520465419.

rs1465204654 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 2:131402984 (GRCh38)
2:132160557 (GRCh37)
Canonical SPDI:: NC_000002.12:131402983:G:A
Gene:: LINC01120 (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=0.000684/2 (KOREAN)
HGVS:: NC_000002.12:g.131402984G>A, NC_000002.11:g.132160557G>A, NR_036499.1:n.84G>A

Select item 146487737120.

rs1464877371 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 2:131407095 (GRCh38)
2:132164668 (GRCh37)
Canonical SPDI:: NC_000002.12:131407094:G:A,NC_000002.12:131407094:G:C
Gene:: LINC01120 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
HGVS:: NC_000002.12:g.131407095G>A, NC_000002.12:g.131407095G>C, NC_000002.11:g.132164668G>A, NC_000002.11:g.132164668G>C, NR_036499.1:n.2234G>A, NR_036499.1:n.2234G>C

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