SNP Links for Nucleotide (Select 1034630227) - SNP

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Links from Nucleotide

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Select item 14907756721.

rs1490775672 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 22:24007994 (GRCh38)
22:24404440 (GRCh37)
Canonical SPDI:: NC_000022.11:24007993:C:T
Gene:: LOC105372959 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0.000084/1 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000022.11:g.24007994C>T, NG_047136.1:g.1803C>T, NT_187633.1:g.298615C>T, NC_000022.10:g.24404440C>T, XR_001755457.1:n.2319C>T, XR_007068704.1:n.2319C>T

Select item 14883001012.

rs1488300101 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 22:24007931 (GRCh38)
22:24404377 (GRCh37)
Canonical SPDI:: NC_000022.11:24007930:A:T
Gene:: LOC105372959 (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_000022.11:g.24007931A>T, NG_047136.1:g.1740A>T, NT_187633.1:g.298552A>T, NC_000022.10:g.24404377A>T, XR_001755457.1:n.2256A>T, XR_007068704.1:n.2256A>T

Select item 14872206083.

rs1487220608 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C [Show Flanks]
Chromosome:: 22:24006852 (GRCh38)
22:24403298 (GRCh37)
Canonical SPDI:: NC_000022.11:24006851:T:A,NC_000022.11:24006851:T:C
Gene:: GSTT4 (Varview), LOC105372959 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000043/6 (GnomAD)
HGVS:: NC_000022.11:g.24006852T>A, NC_000022.11:g.24006852T>C, NG_047136.1:g.661T>A, NG_047136.1:g.661T>C, NT_187633.1:g.297473T>A, NT_187633.1:g.297473T>C, NC_000022.10:g.24403298T>A, NC_000022.10:g.24403298T>C, XR_001755457.1:n.1177T>A, XR_001755457.1:n.1177T>C, XR_007068704.1:n.1177T>A, XR_007068704.1:n.1177T>C

Select item 14860641154.

rs1486064115 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 22:24008689 (GRCh38)
22:24405135 (GRCh37)
Canonical SPDI:: NC_000022.11:24008688:G:A
Gene:: LOC105372959 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000008/2 (TOPMED)
HGVS:: NC_000022.11:g.24008689G>A, NG_047136.1:g.2498G>A, NT_187633.1:g.299310G>A, NC_000022.10:g.24405135G>A, XR_001755457.1:n.3014G>A, XR_007068704.1:n.3014G>A

Select item 14857114315.

rs1485711431 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 22:24006212 (GRCh38)
22:24402658 (GRCh37)
Canonical SPDI:: NC_000022.11:24006211:G:T
Gene:: GSTT4 (Varview), LOC105372959 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000022.11:g.24006212G>T, NG_047136.1:g.21G>T, NT_187633.1:g.296833G>T, NC_000022.10:g.24402658G>T, XR_001755457.1:n.537G>T, XR_007068704.1:n.537G>T

Select item 14852232186.

rs1485223218 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 22:24006657 (GRCh38)
22:24403103 (GRCh37)
Canonical SPDI:: NC_000022.11:24006656:T:A
Gene:: GSTT4 (Varview), LOC105372959 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000022.11:g.24006657T>A, NG_047136.1:g.466T>A, NT_187633.1:g.297278T>A, NC_000022.10:g.24403103T>A, XR_001755457.1:n.982T>A, XR_007068704.1:n.982T>A

Select item 14850378847.

rs1485037884 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 22:24008151 (GRCh38)
22:24404597 (GRCh37)
Canonical SPDI:: NC_000022.11:24008150:G:A
Gene:: LOC105372959 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000084/1 (ALFA)
A=0.000008/2 (TOPMED)
A=0.000014/2 (GnomAD)
HGVS:: NC_000022.11:g.24008151G>A, NG_047136.1:g.1960G>A, NT_187633.1:g.298772G>A, NC_000022.10:g.24404597G>A, XR_001755457.1:n.2476G>A, XR_007068704.1:n.2476G>A

Select item 14841356828.

rs1484135682 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 22:24006643 (GRCh38)
22:24403089 (GRCh37)
Canonical SPDI:: NC_000022.11:24006642:G:A
Gene:: GSTT4 (Varview), LOC105372959 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0.000071/1 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000022.11:g.24006643G>A, NG_047136.1:g.452G>A, NT_187633.1:g.297264G>A, NC_000022.10:g.24403089G>A, XR_001755457.1:n.968G>A, XR_007068704.1:n.968G>A

Select item 14835856739.

rs1483585673 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G [Show Flanks]
Chromosome:: 22:24006941 (GRCh38)
22:24403387 (GRCh37)
Canonical SPDI:: NC_000022.11:24006940:A:C,NC_000022.11:24006940:A:G
Gene:: GSTT4 (Varview), LOC105372959 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_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)
G=0.000156/1 (1000Genomes)
HGVS:: NC_000022.11:g.24006941A>C, NC_000022.11:g.24006941A>G, NG_047136.1:g.750A>C, NG_047136.1:g.750A>G, NT_187633.1:g.297562A>C, NT_187633.1:g.297562A>G, NC_000022.10:g.24403387A>C, NC_000022.10:g.24403387A>G, XR_001755457.1:n.1266A>C, XR_001755457.1:n.1266A>G, XR_007068704.1:n.1266A>C, XR_007068704.1:n.1266A>G

Select item 148328205910.

rs1483282059 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 22:24006376 (GRCh38)
22:24402822 (GRCh37)
Canonical SPDI:: NC_000022.11:24006375:C:T
Gene:: GSTT4 (Varview), LOC105372959 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000022.11:g.24006376C>T, NG_047136.1:g.185C>T, NT_187633.1:g.296997C>T, NC_000022.10:g.24402822C>T, XR_001755457.1:n.701C>T, XR_007068704.1:n.701C>T

Select item 148308438211.

rs1483084382 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 22:24005944 (GRCh38)
22:24402390 (GRCh37)
Canonical SPDI:: NC_000022.11:24005943:G:C
Gene:: GSTT4 (Varview), LOC105372959 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000011/3 (TOPMED)
HGVS:: NC_000022.11:g.24005944G>C, NT_187633.1:g.296565G>C, NC_000022.10:g.24402390G>C, XR_001755457.1:n.269G>C, XR_007068704.1:n.269G>C

Select item 148292924412.

rs1482929244 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C [Show Flanks]
Chromosome:: 22:24007689 (GRCh38)
22:24404135 (GRCh37)
Canonical SPDI:: NC_000022.11:24007688:T:A,NC_000022.11:24007688:T:C
Gene:: LOC105372959 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000022.11:g.24007689T>A, NC_000022.11:g.24007689T>C, NG_047136.1:g.1498T>A, NG_047136.1:g.1498T>C, NT_187633.1:g.298310T>A, NT_187633.1:g.298310T>C, NC_000022.10:g.24404135T>A, NC_000022.10:g.24404135T>C, XR_001755457.1:n.2014T>A, XR_001755457.1:n.2014T>C, XR_007068704.1:n.2014T>A, XR_007068704.1:n.2014T>C

Select item 148095900713.

rs1480959007 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 22:24007808 (GRCh38)
22:24404254 (GRCh37)
Canonical SPDI:: NC_000022.11:24007807:C:T
Gene:: LOC105372959 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000022.11:g.24007808C>T, NG_047136.1:g.1617C>T, NT_187633.1:g.298429C>T, NC_000022.10:g.24404254C>T, XR_001755457.1:n.2133C>T, XR_007068704.1:n.2133C>T

Select item 148091188714.

rs1480911887 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 22:24008077 (GRCh38)
22:24404523 (GRCh37)
Canonical SPDI:: NC_000022.11:24008076:G:A
Gene:: LOC105372959 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000036/5 (GnomAD)
HGVS:: NC_000022.11:g.24008077G>A, NG_047136.1:g.1886G>A, NT_187633.1:g.298698G>A, NC_000022.10:g.24404523G>A, XR_001755457.1:n.2402G>A, XR_007068704.1:n.2402G>A

Select item 148091037315.

rs1480910373 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 22:24005802 (GRCh38)
22:24402248 (GRCh37)
Canonical SPDI:: NC_000022.11:24005801:G:T
Gene:: GSTT4 (Varview), LOC105372959 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000022.11:g.24005802G>T, NT_187633.1:g.296423G>T, NC_000022.10:g.24402248G>T, XR_001755457.1:n.127G>T, XR_007068704.1:n.127G>T

Select item 148026334816.

rs1480263348 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 22:24006327 (GRCh38)
22:24402773 (GRCh37)
Canonical SPDI:: NC_000022.11:24006326:T:C,NC_000022.11:24006326:T:G
Gene:: GSTT4 (Varview), LOC105372959 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000008/2 (TOPMED)
C=0.000531/15 (TOMMO)
HGVS:: NC_000022.11:g.24006327T>C, NC_000022.11:g.24006327T>G, NG_047136.1:g.136T>C, NG_047136.1:g.136T>G, NT_187633.1:g.296948T>C, NT_187633.1:g.296948T>G, NC_000022.10:g.24402773T>C, NC_000022.10:g.24402773T>G, XR_001755457.1:n.652T>C, XR_001755457.1:n.652T>G, XR_007068704.1:n.652T>C, XR_007068704.1:n.652T>G

Select item 148008208317.

rs1480082083 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 22:24006930 (GRCh38)
22:24403376 (GRCh37)
Canonical SPDI:: NC_000022.11:24006929:G:A
Gene:: GSTT4 (Varview), LOC105372959 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_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_000022.11:g.24006930G>A, NG_047136.1:g.739G>A, NT_187633.1:g.297551G>A, NC_000022.10:g.24403376G>A, XR_001755457.1:n.1255G>A, XR_007068704.1:n.1255G>A

Select item 147867724018.

rs1478677240 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 22:24006625 (GRCh38)
22:24403071 (GRCh37)
Canonical SPDI:: NC_000022.11:24006624:A:T
Gene:: GSTT4 (Varview), LOC105372959 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_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_000022.11:g.24006625A>T, NG_047136.1:g.434A>T, NT_187633.1:g.297246A>T, NC_000022.10:g.24403071A>T, XR_001755457.1:n.950A>T, XR_007068704.1:n.950A>T

Select item 147840090819.

rs1478400908 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 22:24007341 (GRCh38)
22:24403787 (GRCh37)
Canonical SPDI:: NC_000022.11:24007340:C:T
Gene:: GSTT4 (Varview), LOC105372959 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000014/2 (GnomAD)
HGVS:: NC_000022.11:g.24007341C>T, NG_047136.1:g.1150C>T, NT_187633.1:g.297962C>T, NC_000022.10:g.24403787C>T, XR_001755457.1:n.1666C>T, XR_007068704.1:n.1666C>T

Select item 147801748820.

rs1478017488 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 22:24007233 (GRCh38)
22:24403679 (GRCh37)
Canonical SPDI:: NC_000022.11:24007232:G:C
Gene:: GSTT4 (Varview), LOC105372959 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000022.11:g.24007233G>C, NG_047136.1:g.1042G>C, NT_187633.1:g.297854G>C, NC_000022.10:g.24403679G>C, XR_001755457.1:n.1558G>C, XR_007068704.1:n.1558G>C

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