SNP Links for Nucleotide (Select 300796183) - SNP

Links from Nucleotide

Items: 1 to 20 of 483

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Select item 14905027861.

rs1490502786 [Homo sapiens]

Variant type:: DELINS
Alleles:: C>- [Show Flanks]
Chromosome:: 11:115760064 (GRCh38)
11:115630782 (GRCh37)
Canonical SPDI:: NC_000011.10:115760063:CCC:CC
Gene:: LINC00900 (Varview), LINC02698 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: CC=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.115760066del, NC_000011.9:g.115630784del, NR_034148.1:n.137del

Select item 14890208272.

rs1489020827 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 11:115757184 (GRCh38)
11:115627902 (GRCh37)
Canonical SPDI:: NC_000011.10:115757183:G:C
Gene:: LINC00900 (Varview), LINC02698 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000071/1 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.115757184G>C, NC_000011.9:g.115627902G>C, NR_034148.1:n.392C>G

Select item 14878532443.

rs1487853244 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:115755665 (GRCh38)
11:115626383 (GRCh37)
Canonical SPDI:: NC_000011.10:115755664:G:A
Gene:: LINC00900 (Varview), LINC02698 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000011.10:g.115755665G>A, NC_000011.9:g.115626383G>A, NR_034148.1:n.1911C>T

Select item 14862681554.

rs1486268155 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:115756916 (GRCh38)
11:115627634 (GRCh37)
Canonical SPDI:: NC_000011.10:115756915:T:C
Gene:: LINC00900 (Varview), LINC02698 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency
MAF:: C=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.115756916T>C, NC_000011.9:g.115627634T>C, NR_034148.1:n.660A>G

Select item 14862387245.

rs1486238724 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:115756635 (GRCh38)
11:115627353 (GRCh37)
Canonical SPDI:: NC_000011.10:115756634:C:T
Gene:: LINC00900 (Varview), LINC02698 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000014/2 (GnomAD)
T=0.000019/5 (TOPMED)
HGVS:: NC_000011.10:g.115756635C>T, NC_000011.9:g.115627353C>T, NR_034148.1:n.941G>A

Select item 14861862536.

rs1486186253 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 11:115755526 (GRCh38)
11:115626244 (GRCh37)
Canonical SPDI:: NC_000011.10:115755525:C:A,NC_000011.10:115755525:C:T
Gene:: LINC00900 (Varview), LINC02698 (Varview)
Functional Consequence:: non_coding_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)
T=0.000035/1 (TOMMO)
HGVS:: NC_000011.10:g.115755526C>A, NC_000011.10:g.115755526C>T, NC_000011.9:g.115626244C>A, NC_000011.9:g.115626244C>T, NR_034148.1:n.2050G>T, NR_034148.1:n.2050G>A

Select item 14809344717.

rs1480934471 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:115760054 (GRCh38)
11:115630772 (GRCh37)
Canonical SPDI:: NC_000011.10:115760053:C:T
Gene:: LINC00900 (Varview), LINC02698 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by frequency,by cluster
MAF:: T=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.115760054C>T, NC_000011.9:g.115630772C>T, NR_034148.1:n.147G>A

Select item 14791104898.

rs1479110489 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:115756078 (GRCh38)
11:115626796 (GRCh37)
Canonical SPDI:: NC_000011.10:115756077:G:A
Gene:: LINC00900 (Varview), LINC02698 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000014/2 (GnomAD)
HGVS:: NC_000011.10:g.115756078G>A, NC_000011.9:g.115626796G>A, NR_034148.1:n.1498C>T

Select item 14781559919.

rs1478155991 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 11:115755734 (GRCh38)
11:115626452 (GRCh37)
Canonical SPDI:: NC_000011.10:115755733:G:C
Gene:: LINC00900 (Varview), LINC02698 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000054/1 (ALFA)
C=0.000015/4 (TOPMED)
C=0.000036/5 (GnomAD)
C=0.000223/1 (Estonian)
HGVS:: NC_000011.10:g.115755734G>C, NC_000011.9:g.115626452G>C, NR_034148.1:n.1842C>G

Select item 147811390710.

rs1478113907 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 11:115758233 (GRCh38)
11:115628951 (GRCh37)
Canonical SPDI:: NC_000011.10:115758232:T:A
Gene:: LINC00900 (Varview), LINC02698 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_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_000011.10:g.115758233T>A, NC_000011.9:g.115628951T>A, NR_034148.1:n.191A>T

Select item 147498109511.

rs1474981095 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTCAGCTG>- [Show Flanks]
Chromosome:: 11:115756606 (GRCh38)
11:115627324 (GRCh37)
Canonical SPDI:: NC_000011.10:115756603:TGTTCAGCTG:TG
Gene:: LINC00900 (Varview), LINC02698 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: TG=0./0 (ALFA)
HGVS:: NC_000011.10:g.115756606_115756613del, NC_000011.9:g.115627324_115627331del, NR_034148.1:n.965_972del

Select item 147495632512.

rs1474956325 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 11:115755427 (GRCh38)
11:115626145 (GRCh37)
Canonical SPDI:: NC_000011.10:115755426:A:T
Gene:: LINC00900 (Varview), LINC02698 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.115755427A>T, NC_000011.9:g.115626145A>T, NR_034148.1:n.2149T>A

Select item 147413509413.

rs1474135094 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:115757251 (GRCh38)
11:115627969 (GRCh37)
Canonical SPDI:: NC_000011.10:115757250:A:G
Gene:: LINC00900 (Varview), LINC02698 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000011/3 (TOPMED)
HGVS:: NC_000011.10:g.115757251A>G, NC_000011.9:g.115627969A>G, NR_034148.1:n.325T>C

Select item 147399349614.

rs1473993496 [Homo sapiens]

Variant type:: DEL
Alleles:: GACTA>- [Show Flanks]
Chromosome:: 11:115756100 (GRCh38)
11:115626818 (GRCh37)
Canonical SPDI:: NC_000011.10:115756099:GACTA:
Gene:: LINC00900 (Varview), LINC02698 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.000008/2 (TOPMED)
HGVS:: NC_000011.10:g.115756100_115756104del, NC_000011.9:g.115626818_115626822del, NR_034148.1:n.1472_1476del

Select item 147093844915.

rs1470938449 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 11:115757216 (GRCh38)
11:115627934 (GRCh37)
Canonical SPDI:: NC_000011.10:115757215:G:C
Gene:: LINC00900 (Varview), LINC02698 (Varview)
Functional Consequence:: intron_variant,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_000011.10:g.115757216G>C, NC_000011.9:g.115627934G>C, NR_034148.1:n.360C>G

Select item 146858135716.

rs1468581357 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:115755764 (GRCh38)
11:115626482 (GRCh37)
Canonical SPDI:: NC_000011.10:115755763:G:A
Gene:: LINC00900 (Varview), LINC02698 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000011.10:g.115755764G>A, NC_000011.9:g.115626482G>A, NR_034148.1:n.1812C>T

Select item 146729087217.

rs1467290872 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:115756532 (GRCh38)
11:115627250 (GRCh37)
Canonical SPDI:: NC_000011.10:115756531:A:G
Gene:: LINC00900 (Varview), LINC02698 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.115756532A>G, NC_000011.9:g.115627250A>G, NR_034148.1:n.1044T>C

Select item 146486063318.

rs1464860633 [Homo sapiens]

Variant type:: DELINS
Alleles:: GA>- [Show Flanks]
Chromosome:: 11:115755866 (GRCh38)
11:115626584 (GRCh37)
Canonical SPDI:: NC_000011.10:115755864:AGA:A
Gene:: LINC00900 (Varview), LINC02698 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
-=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.115755866_115755867del, NC_000011.9:g.115626584_115626585del, NR_034148.1:n.1710_1711del

Select item 146386194819.

rs1463861948 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 11:115756900 (GRCh38)
11:115627618 (GRCh37)
Canonical SPDI:: NC_000011.10:115756899:C:A
Gene:: LINC00900 (Varview), LINC02698 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.115756900C>A, NC_000011.9:g.115627618C>A, NR_034148.1:n.676G>T

Select item 146222287020.

rs1462222870 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:115755343 (GRCh38)
11:115626061 (GRCh37)
Canonical SPDI:: NC_000011.10:115755342:C:T
Gene:: LINC00900 (Varview), LINC02698 (Varview)
Functional Consequence:: intron_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.115755343C>T, NC_000011.9:g.115626061C>T, NR_034148.1:n.2233G>A

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