SNP Links for Nucleotide (Select 300796644) - SNP

Links from Nucleotide

Items: 1 to 20 of 156

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Select item 14901184771.

rs1490118477 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:182407763 (GRCh38)
1:182376898 (GRCh37)
Canonical SPDI:: NC_000001.11:182407762:C:T
Gene:: LINC00272 (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=0.000034/9 (TOPMED)
HGVS:: NC_000001.11:g.182407763C>T, NC_000001.10:g.182376898C>T, NM_001010899.1:c.-144C>T, NR_034131.1:n.143C>T

Select item 14897925582.

rs1489792558 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 1:182409295 (GRCh38)
1:182378430 (GRCh37)
Canonical SPDI:: NC_000001.11:182409294:T:C
Gene:: LINC00272 (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=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.182409295T>C, NC_000001.10:g.182378430T>C, NM_001010899.1:c.259T>C, NR_034131.1:n.545T>C

Select item 14775926283.

rs1477592628 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:182407871 (GRCh38)
1:182377006 (GRCh37)
Canonical SPDI:: NC_000001.11:182407870:G:A
Gene:: LINC00272 (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=0.000014/2 (GnomAD)
HGVS:: NC_000001.11:g.182407871G>A, NC_000001.10:g.182377006G>A, NM_001010899.1:c.-36G>A, NR_034131.1:n.251G>A

Select item 14764524854.

rs1476452485 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 1:182407712 (GRCh38)
1:182376847 (GRCh37)
Canonical SPDI:: NC_000001.11:182407711:T:C
Gene:: LINC00272 (Varview)
Functional Consequence:: 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)
T=0.5/1 (SGDP_PRJ)
HGVS:: NC_000001.11:g.182407712T>C, NC_000001.10:g.182376847T>C, NM_001010899.1:c.-195T>C, NR_034131.1:n.92T>C

Select item 14695055075.

rs1469505507 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 1:182407731 (GRCh38)
1:182376866 (GRCh37)
Canonical SPDI:: NC_000001.11:182407730:C:A,NC_000001.11:182407730:C:T
Gene:: LINC00272 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.182407731C>A, NC_000001.11:g.182407731C>T, NC_000001.10:g.182376866C>A, NC_000001.10:g.182376866C>T, NM_001010899.1:c.-176C>A, NM_001010899.1:c.-176C>T, NR_034131.1:n.111C>A, NR_034131.1:n.111C>T

Select item 14683799006.

rs1468379900 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 1:182407969 (GRCh38)
1:182377104 (GRCh37)
Canonical SPDI:: NC_000001.11:182407968:T:C
Gene:: LINC00272 (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=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.182407969T>C, NC_000001.10:g.182377104T>C, NM_001010899.1:c.63T>C, NR_034131.1:n.349T>C

Select item 14564268797.

rs1456426879 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:182409353 (GRCh38)
1:182378488 (GRCh37)
Canonical SPDI:: NC_000001.11:182409352:G:A
Gene:: LINC00272 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.0002/1 (ALFA)
A=0.0002/1 (Estonian)
HGVS:: NC_000001.11:g.182409353G>A, NC_000001.10:g.182378488G>A, NM_001010899.1:c.*44G>A, NR_034131.1:n.603G>A

Select item 14557411078.

rs1455741107 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 1:182407870 (GRCh38)
1:182377005 (GRCh37)
Canonical SPDI:: NC_000001.11:182407869:T:A
Gene:: LINC00272 (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=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.182407870T>A, NC_000001.10:g.182377005T>A, NM_001010899.1:c.-37T>A, NR_034131.1:n.250T>A

Select item 14473830799.

rs1447383079 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 1:182408021 (GRCh38)
1:182377156 (GRCh37)
Canonical SPDI:: NC_000001.11:182408020:G:C
Gene:: LINC00272 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000071/1 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000008/2 (TOPMED)
HGVS:: NC_000001.11:g.182408021G>C, NC_000001.10:g.182377156G>C, NM_001010899.1:c.115G>C, NR_034131.1:n.401G>C

Select item 144585391510.

rs1445853915 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:182414752 (GRCh38)
1:182383887 (GRCh37)
Canonical SPDI:: NC_000001.11:182414751:G:A
Gene:: LINC00272 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000015/2 (GnomAD)
A=0.000015/4 (TOPMED)
HGVS:: NC_000001.11:g.182414752G>A, NC_000001.10:g.182383887G>A, NM_001010899.1:c.*118G>A, NR_034131.1:n.677G>A

Select item 144524337211.

rs1445243372 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:182414713 (GRCh38)
1:182383848 (GRCh37)
Canonical SPDI:: NC_000001.11:182414712:C:T
Gene:: LINC00272 (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_000001.11:g.182414713C>T, NC_000001.10:g.182383848C>T, NM_001010899.1:c.*79C>T, NR_034131.1:n.638C>T

Select item 144377076412.

rs1443770764 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 1:182408534 (GRCh38)
1:182377669 (GRCh37)
Canonical SPDI:: NC_000001.11:182408533:G:T
Gene:: LINC00272 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000224/1 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000223/1 (Estonian)
HGVS:: NC_000001.11:g.182408534G>T, NC_000001.10:g.182377669G>T, NM_001010899.1:c.133G>T, NR_034131.1:n.419G>T

Select item 143767070813.

rs1437670708 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 1:182414765 (GRCh38)
1:182383900 (GRCh37)
Canonical SPDI:: NC_000001.11:182414764:C:G
Gene:: LINC00272 (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.182414765C>G, NC_000001.10:g.182383900C>G, NM_001010899.1:c.*131C>G, NR_034131.1:n.690C>G

Select item 143553668614.

rs1435536686 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 1:182407900 (GRCh38)
1:182377035 (GRCh37)
Canonical SPDI:: NC_000001.11:182407899:G:A,NC_000001.11:182407899:G:T
Gene:: LINC00272 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000071/1 (ALFA)
T=0.000008/2 (TOPMED)
A=0.000014/2 (GnomAD)
G=0.5/1 (SGDP_PRJ)
HGVS:: NC_000001.11:g.182407900G>A, NC_000001.11:g.182407900G>T, NC_000001.10:g.182377035G>A, NC_000001.10:g.182377035G>T, NM_001010899.1:c.-7G>A, NM_001010899.1:c.-7G>T, NR_034131.1:n.280G>A, NR_034131.1:n.280G>T

Select item 143178064415.

rs1431780644 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:182407867 (GRCh38)
1:182377002 (GRCh37)
Canonical SPDI:: NC_000001.11:182407866:C:T
Gene:: LINC00272 (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_000001.11:g.182407867C>T, NC_000001.10:g.182377002C>T, NM_001010899.1:c.-40C>T, NR_034131.1:n.247C>T

Select item 142310091816.

rs1423100918 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 1:182407699 (GRCh38)
1:182376834 (GRCh37)
Canonical SPDI:: NC_000001.11:182407698:G:A,NC_000001.11:182407698:G:T
Gene:: LINC00272 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
HGVS:: NC_000001.11:g.182407699G>A, NC_000001.11:g.182407699G>T, NC_000001.10:g.182376834G>A, NC_000001.10:g.182376834G>T, NM_001010899.1:c.-208G>A, NM_001010899.1:c.-208G>T, NR_034131.1:n.79G>A, NR_034131.1:n.79G>T

Select item 142016512117.

rs1420165121 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:182407858 (GRCh38)
1:182376993 (GRCh37)
Canonical SPDI:: NC_000001.11:182407857:A:G
Gene:: LINC00272 (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.182407858A>G, NC_000001.10:g.182376993A>G, NM_001010899.1:c.-49A>G, NR_034131.1:n.238A>G

Select item 141944439018.

rs1419444390 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:182408601 (GRCh38)
1:182377736 (GRCh37)
Canonical SPDI:: NC_000001.11:182408600:G:A
Gene:: LINC00272 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000001.11:g.182408601G>A, NC_000001.10:g.182377736G>A, NM_001010899.1:c.200G>A, NR_034131.1:n.486G>A

Select item 141406361519.

rs1414063615 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 1:182407941 (GRCh38)
1:182377076 (GRCh37)
Canonical SPDI:: NC_000001.11:182407940:T:C
Gene:: LINC00272 (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.182407941T>C, NC_000001.10:g.182377076T>C, NM_001010899.1:c.35T>C, NR_034131.1:n.321T>C

Select item 141001419020.

rs1410014190 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 1:182409279 (GRCh38)
1:182378414 (GRCh37)
Canonical SPDI:: NC_000001.11:182409278:A:T
Gene:: LINC00272 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000015/4 (TOPMED)
HGVS:: NC_000001.11:g.182409279A>T, NC_000001.10:g.182378414A>T, NM_001010899.1:c.243A>T, NR_034131.1:n.529A>T

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