SNP Links for Nucleotide (Select 1184495202) - SNP

Links from Nucleotide

Items: 1 to 20 of 212

<< First< Prev

Page of 11

Next >Last >>

Select item 14875614781.

rs1487561478 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 1:170174691 (GRCh38)
1:170143832 (GRCh37)
Canonical SPDI:: NC_000001.11:170174690:A:C
Gene:: LINC01681 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.170174691A>C, NC_000001.10:g.170143832A>C, NR_146891.1:n.313A>C

Select item 14873056532.

rs1487305653 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 1:170240284 (GRCh38)
1:170209425 (GRCh37)
Canonical SPDI:: NC_000001.11:170240283:T:C,NC_000001.11:170240283:T:G
Gene:: LINC01681 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.170240284T>C, NC_000001.11:g.170240284T>G, NC_000001.10:g.170209425T>C, NC_000001.10:g.170209425T>G, NR_146891.1:n.523T>C, NR_146891.1:n.523T>G

Select item 14835517983.

rs1483551798 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 1:170241150 (GRCh38)
1:170210291 (GRCh37)
Canonical SPDI:: NC_000001.11:170241149:G:T
Gene:: LINC01681 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000071/1 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.170241150G>T, NC_000001.10:g.170210291G>T, NR_146891.1:n.647G>T

Select item 14819723744.

rs1481972374 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 1:170174384 (GRCh38)
1:170143525 (GRCh37)
Canonical SPDI:: NC_000001.11:170174383:T:C
Gene:: LINC01681 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.00015/21 (GnomAD)
HGVS:: NC_000001.11:g.170174384T>C, NC_000001.10:g.170143525T>C, NR_146891.1:n.6T>C

Select item 14693898025.

rs1469389802 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 1:170241116 (GRCh38)
1:170210257 (GRCh37)
Canonical SPDI:: NC_000001.11:170241115:C:G,NC_000001.11:170241115:C:T
Gene:: LINC01681 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
HGVS:: NC_000001.11:g.170241116C>G, NC_000001.11:g.170241116C>T, NC_000001.10:g.170210257C>G, NC_000001.10:g.170210257C>T, NR_146891.1:n.613C>G, NR_146891.1:n.613C>T

Select item 14608227266.

rs1460822726 [Homo sapiens]

Variant type:: DELINS
Alleles:: TG>- [Show Flanks]
Chromosome:: 1:170241268 (GRCh38)
1:170210409 (GRCh37)
Canonical SPDI:: NC_000001.11:170241265:TGTG:TG
Gene:: LINC01681 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TGTG=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.170241266TG[1], NC_000001.10:g.170210407TG[1], NR_146891.1:n.763TG[1]

Select item 14607254957.

rs1460725495 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 1:170174559 (GRCh38)
1:170143700 (GRCh37)
Canonical SPDI:: NC_000001.11:170174558:G:T
Gene:: LINC01681 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: T=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.170174559G>T, NC_000001.10:g.170143700G>T, NR_146891.1:n.181G>T

Select item 14583600888.

rs1458360088 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:170241481 (GRCh38)
1:170210622 (GRCh37)
Canonical SPDI:: NC_000001.11:170241480:A:G
Gene:: LINC01681 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000071/1 (ALFA)
G=0./0 (GnomAD)
G=0.000008/2 (TOPMED)
HGVS:: NC_000001.11:g.170241481A>G, NC_000001.10:g.170210622A>G, NR_146891.1:n.878A>G

Select item 14566010339.

rs1456601033 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 1:170240231 (GRCh38)
1:170209372 (GRCh37)
Canonical SPDI:: NC_000001.11:170240230:G:T
Gene:: LINC01681 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000001.11:g.170240231G>T, NC_000001.10:g.170209372G>T, NR_146891.1:n.470G>T

Select item 145106770910.

rs1451067709 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:170174477 (GRCh38)
1:170143618 (GRCh37)
Canonical SPDI:: NC_000001.11:170174476:G:A
Gene:: LINC01681 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000011/3 (TOPMED)
A=0.000029/4 (GnomAD)
HGVS:: NC_000001.11:g.170174477G>A, NC_000001.10:g.170143618G>A, NR_146891.1:n.99G>A

Select item 144774586611.

rs1447745866 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 1:170174562 (GRCh38)
1:170143703 (GRCh37)
Canonical SPDI:: NC_000001.11:170174561:C:G
Gene:: LINC01681 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.170174562C>G, NC_000001.10:g.170143703C>G, NR_146891.1:n.184C>G

Select item 144501294212.

rs1445012942 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 1:170240266 (GRCh38)
1:170209407 (GRCh37)
Canonical SPDI:: NC_000001.11:170240265:C:G
Gene:: LINC01681 (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_000001.11:g.170240266C>G, NC_000001.10:g.170209407C>G, NR_146891.1:n.505C>G

Select item 144465348013.

rs1444653480 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 1:170174662 (GRCh38)
1:170143803 (GRCh37)
Canonical SPDI:: NC_000001.11:170174661:C:G
Gene:: LINC01681 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: G=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.170174662C>G, NC_000001.10:g.170143803C>G, NR_146891.1:n.284C>G

Select item 144381483414.

rs1443814834 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 1:170227048 (GRCh38)
1:170196189 (GRCh37)
Canonical SPDI:: NC_000001.11:170227047:T:G
Gene:: LINC01681 (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=0.000011/3 (TOPMED)
HGVS:: NC_000001.11:g.170227048T>G, NC_000001.10:g.170196189T>G, NR_146891.1:n.458T>G

Select item 144157502315.

rs1441575023 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 1:170174445 (GRCh38)
1:170143586 (GRCh37)
Canonical SPDI:: NC_000001.11:170174444:T:G
Gene:: LINC01681 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.170174445T>G, NC_000001.10:g.170143586T>G, NR_146891.1:n.67T>G

Select item 143986152516.

rs1439861525 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:170174603 (GRCh38)
1:170143744 (GRCh37)
Canonical SPDI:: NC_000001.11:170174602:A:G
Gene:: LINC01681 (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_000001.11:g.170174603A>G, NC_000001.10:g.170143744A>G, NR_146891.1:n.225A>G

Select item 143525207117.

rs1435252071 [Homo sapiens]

Variant type:: DELINS
Alleles:: GT>- [Show Flanks]
Chromosome:: 1:170174686 (GRCh38)
1:170143827 (GRCh37)
Canonical SPDI:: NC_000001.11:170174684:TGT:T
Gene:: LINC01681 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
-=0.000007/1 (GnomAD)
-=0.000008/2 (TOPMED)
HGVS:: NC_000001.11:g.170174686_170174687del, NC_000001.10:g.170143827_170143828del, NR_146891.1:n.308_309del

Select item 143329772018.

rs1433297720 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:170241240 (GRCh38)
1:170210381 (GRCh37)
Canonical SPDI:: NC_000001.11:170241239:A:G
Gene:: LINC01681 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000447/2 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000446/2 (Estonian)
HGVS:: NC_000001.11:g.170241240A>G, NC_000001.10:g.170210381A>G, NR_146891.1:n.737A>G

Select item 143168818819.

rs1431688188 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 1:170227026 (GRCh38)
1:170196167 (GRCh37)
Canonical SPDI:: NC_000001.11:170227025:T:C
Gene:: LINC01681 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.170227026T>C, NC_000001.10:g.170196167T>C, NR_146891.1:n.436T>C

Select item 142732620420.

rs1427326204 [Homo sapiens]

Variant type:: DELINS
Alleles:: GT>- [Show Flanks]
Chromosome:: 1:170241120 (GRCh38)
1:170210261 (GRCh37)
Canonical SPDI:: NC_000001.11:170241118:TGT:T
Gene:: LINC01681 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
-=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.170241120_170241121del, NC_000001.10:g.170210261_170210262del, NR_146891.1:n.617_618del

dbSNP

Result Filters

Validation Status

Function Class

Variation Class

Annotation

Global MAF

Custom range

Additional filters

Display Settings:

Send to:

Links from Nucleotide

Items: 1 to 20 of 212

Display Settings:

Send to:

Supplemental Content

Find related data

Recent activity