SNP Links for Nucleotide (Select 299890815) - SNP

Links from Nucleotide

Items: 1 to 20 of 232

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Select item 14903625271.

rs1490362527 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 8:129216530 (GRCh38)
8:130228776 (GRCh37)
Canonical SPDI:: NC_000008.11:129216529:C:G
Gene:: LINC00977 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000224/1 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000223/1 (Estonian)
HGVS:: NC_000008.11:g.129216530C>G, NC_000008.10:g.130228776C>G, NR_033916.1:n.1090G>C

Select item 14888786512.

rs1488878651 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 8:129223243 (GRCh38)
8:130235489 (GRCh37)
Canonical SPDI:: NC_000008.11:129223242:A:G
Gene:: LINC00977 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000008.11:g.129223243A>G, NC_000008.10:g.130235489A>G, NR_033916.1:n.191T>C

Select item 14815744233.

rs1481574423 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->AAGCTCAAT [Show Flanks]
Chromosome:: 8:129217388 (GRCh38)
8:130229635 (GRCh37)
Canonical SPDI:: NC_000008.11:129217388:AAGCTCAAT:AAGCTCAATAAGCTCAAT
Gene:: LINC00977 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAGCTCAATAAGCTCAAT=0./0 (ALFA)
AAGCTCAAT=0.000004/1 (TOPMED)
AAGCTCAAT=0.000007/1 (GnomAD)
HGVS:: NC_000008.11:g.129217389_129217397dup, NC_000008.10:g.130229635_130229643dup, NR_033916.1:n.223_231dup

Select item 14774198694.

rs1477419869 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 8:129216510 (GRCh38)
8:130228756 (GRCh37)
Canonical SPDI:: NC_000008.11:129216509:A:T
Gene:: LINC00977 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000014/2 (GnomAD)
T=0.000023/6 (TOPMED)
HGVS:: NC_000008.11:g.129216510A>T, NC_000008.10:g.130228756A>T, NR_033916.1:n.1110T>A

Select item 14771220085.

rs1477122008 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 8:129217087 (GRCh38)
8:130229333 (GRCh37)
Canonical SPDI:: NC_000008.11:129217086:T:C
Gene:: LINC00977 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
HGVS:: NC_000008.11:g.129217087T>C, NC_000008.10:g.130229333T>C, NR_033916.1:n.533A>G

Select item 14762715306.

rs1476271530 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 8:129216580 (GRCh38)
8:130228826 (GRCh37)
Canonical SPDI:: NC_000008.11:129216579:G:T
Gene:: LINC00977 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
T=0.000021/3 (GnomAD)
HGVS:: NC_000008.11:g.129216580G>T, NC_000008.10:g.130228826G>T, NR_033916.1:n.1040C>A

Select item 14755660187.

rs1475566018 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 8:129217098 (GRCh38)
8:130229344 (GRCh37)
Canonical SPDI:: NC_000008.11:129217097:A:T
Gene:: LINC00977 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000008.11:g.129217098A>T, NC_000008.10:g.130229344A>T, NR_033916.1:n.522T>A

Select item 14711771018.

rs1471177101 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 8:129217249 (GRCh38)
8:130229495 (GRCh37)
Canonical SPDI:: NC_000008.11:129217248:T:C,NC_000008.11:129217248:T:G
Gene:: LINC00977 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000008.11:g.129217249T>C, NC_000008.11:g.129217249T>G, NC_000008.10:g.130229495T>C, NC_000008.10:g.130229495T>G, NR_033916.1:n.371A>G, NR_033916.1:n.371A>C

Select item 14645612219.

rs1464561221 [Homo sapiens]

Variant type:: DELINS
Alleles:: T>- [Show Flanks]
Chromosome:: 8:129217170 (GRCh38)
8:130229416 (GRCh37)
Canonical SPDI:: NC_000008.11:129217169:TT:T
Gene:: LINC00977 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TT=0.000071/1 (ALFA)
-=0.000007/1 (GnomAD)
-=0.000008/2 (TOPMED)
HGVS:: NC_000008.11:g.129217171del, NC_000008.10:g.130229417del, NR_033916.1:n.450del

Select item 145864445910.

rs1458644459 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 8:129216665 (GRCh38)
8:130228911 (GRCh37)
Canonical SPDI:: NC_000008.11:129216664:T:G
Gene:: LINC00977 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000008.11:g.129216665T>G, NC_000008.10:g.130228911T>G, NR_033916.1:n.955A>C

Select item 145642375111.

rs1456423751 [Homo sapiens]

Variant type:: DEL
Alleles:: A>- [Show Flanks]
Chromosome:: 8:129217245 (GRCh38)
8:130229491 (GRCh37)
Canonical SPDI:: NC_000008.11:129217244:A:
Gene:: LINC00977 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.000007/1 (GnomAD)
-=0.000008/2 (TOPMED)
HGVS:: NC_000008.11:g.129217245del, NC_000008.10:g.130229491del, NR_033916.1:n.375del

Select item 145573739412.

rs1455737394 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 8:129216658 (GRCh38)
8:130228904 (GRCh37)
Canonical SPDI:: NC_000008.11:129216657:G:A
Gene:: LINC00977 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0./0 (GnomAD)
HGVS:: NC_000008.11:g.129216658G>A, NC_000008.10:g.130228904G>A, NR_033916.1:n.962C>T

Select item 145437293113.

rs1454372931 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 8:129217183 (GRCh38)
8:130229429 (GRCh37)
Canonical SPDI:: NC_000008.11:129217182:A:G
Gene:: LINC00977 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000008.11:g.129217183A>G, NC_000008.10:g.130229429A>G, NR_033916.1:n.437T>C

Select item 145340758214.

rs1453407582 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 8:129217217 (GRCh38)
8:130229463 (GRCh37)
Canonical SPDI:: NC_000008.11:129217216:T:C
Gene:: LINC00977 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000071/1 (ALFA)
C=0.000014/2 (GnomAD)
C=0.000038/10 (TOPMED)
HGVS:: NC_000008.11:g.129217217T>C, NC_000008.10:g.130229463T>C, NR_033916.1:n.403A>G

Select item 145082475015.

rs1450824750 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 8:129217105 (GRCh38)
8:130229351 (GRCh37)
Canonical SPDI:: NC_000008.11:129217104:T:C
Gene:: LINC00977 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000008.11:g.129217105T>C, NC_000008.10:g.130229351T>C, NR_033916.1:n.515A>G

Select item 144573926516.

rs1445739265 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 8:129216742 (GRCh38)
8:130228988 (GRCh37)
Canonical SPDI:: NC_000008.11:129216741:A:G
Gene:: LINC00977 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
G=0.000014/2 (GnomAD)
HGVS:: NC_000008.11:g.129216742A>G, NC_000008.10:g.130228988A>G, NR_033916.1:n.878T>C

Select item 144491855517.

rs1444918555 [Homo sapiens]

Variant type:: DEL
Alleles:: A>- [Show Flanks]
Chromosome:: 8:129217350 (GRCh38)
8:130229596 (GRCh37)
Canonical SPDI:: NC_000008.11:129217349:A:
Gene:: LINC00977 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.000008/2 (TOPMED)
HGVS:: NC_000008.11:g.129217350del, NC_000008.10:g.130229596del, NR_033916.1:n.270del

Select item 144253864118.

rs1442538641 [Homo sapiens]

Variant type:: DELINS
Alleles:: TAAACTC>- [Show Flanks]
Chromosome:: 8:129216865 (GRCh38)
8:130229111 (GRCh37)
Canonical SPDI:: NC_000008.11:129216862:TCTAAACTC:TC
Gene:: LINC00977 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: TC=0.000071/1 (ALFA)
-=0.000007/1 (GnomAD)
HGVS:: NC_000008.11:g.129216865_129216871del, NC_000008.10:g.130229111_130229117del, NR_033916.1:n.751_757del

Select item 144109887819.

rs1441098878 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 8:129216604 (GRCh38)
8:130228850 (GRCh37)
Canonical SPDI:: NC_000008.11:129216603:G:T
Gene:: LINC00977 (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_000008.11:g.129216604G>T, NC_000008.10:g.130228850G>T, NR_033916.1:n.1016C>A

Select item 144028658720.

rs1440286587 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 8:129241195 (GRCh38)
8:130253441 (GRCh37)
Canonical SPDI:: NC_000008.11:129241194:G:T
Gene:: LINC00977 (Varview), LOC124902022 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000008.11:g.129241195G>T, NC_000008.10:g.130253441G>T, XR_007061109.1:n.303G>T, NR_033916.1:n.46C>A

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