SNP Links for Nucleotide (Select 333470725) - SNP

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Links from Nucleotide

Items: 1 to 20 of 1277

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Select item 14908131431.

rs1490813143 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 15:30770014 (GRCh38)
15:31062217 (GRCh37)
Canonical SPDI:: NC_000015.10:30770013:G:T
Gene:: LOC100288637 (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_000015.10:g.30770014G>T, NC_000015.9:g.31062217G>T, NW_011332701.1:g.2943292G>T, NT_187660.1:g.3055744G>T, NR_038253.1:n.2758G>T, NR_038254.1:n.2658G>T, NR_038255.1:n.2563G>T

Select item 14906472152.

rs1490647215 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 15:30748626 (GRCh38)
15:31040829 (GRCh37)
Canonical SPDI:: NC_000015.10:30748625:A:G
Gene:: LOC100288637 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000094/1 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000015.10:g.30748626A>G, NC_000015.9:g.31040829A>G, NW_011332701.1:g.2921894A>G, NT_187660.1:g.3034346A>G, NR_038253.1:n.402A>G, NR_038254.1:n.302A>G

Select item 14905415473.

rs1490541547 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 15:30768632 (GRCh38)
15:31060835 (GRCh37)
Canonical SPDI:: NC_000015.10:30768631:C:G
Gene:: LOC100288637 (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_000015.10:g.30768632C>G, NC_000015.9:g.31060835C>G, NW_011332701.1:g.2941911C>G, NT_187660.1:g.3054363C>G, NR_038253.1:n.1376C>G, NR_038254.1:n.1276C>G, NR_038255.1:n.1181C>G

Select item 14904971534.

rs1490497153 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C,G [Show Flanks]
Chromosome:: 15:30768504 (GRCh38)
15:31060707 (GRCh37)
Canonical SPDI:: NC_000015.10:30768503:T:A,NC_000015.10:30768503:T:C,NC_000015.10:30768503:T:G
Gene:: LOC100288637 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000011/3 (TOPMED)
HGVS:: NC_000015.10:g.30768504T>A, NC_000015.10:g.30768504T>C, NC_000015.10:g.30768504T>G, NC_000015.9:g.31060707T>A, NC_000015.9:g.31060707T>C, NC_000015.9:g.31060707T>G, NW_011332701.1:g.2941783T>A, NW_011332701.1:g.2941783T>C, NW_011332701.1:g.2941783T>G, NT_187660.1:g.3054235T>A, NT_187660.1:g.3054235T>C, NT_187660.1:g.3054235T>G, NR_038253.1:n.1248T>A, NR_038253.1:n.1248T>C, NR_038253.1:n.1248T>G, NR_038254.1:n.1148T>A, NR_038254.1:n.1148T>C, NR_038254.1:n.1148T>G, NR_038255.1:n.1053T>A, NR_038255.1:n.1053T>C, NR_038255.1:n.1053T>G

Select item 14904635335.

rs1490463533 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 15:30748650 (GRCh38)
15:31040853 (GRCh37)
Canonical SPDI:: NC_000015.10:30748649:A:C
Gene:: LOC100288637 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000015.10:g.30748650A>C, NC_000015.9:g.31040853A>C, NW_011332701.1:g.2921918A>C, NT_187660.1:g.3034370A>C, NR_038253.1:n.426A>C, NR_038254.1:n.326A>C

Select item 14898309006.

rs1489830900 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 15:30769144 (GRCh38)
15:31061347 (GRCh37)
Canonical SPDI:: NC_000015.10:30769143:C:T
Gene:: LOC100288637 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000015.10:g.30769144C>T, NC_000015.9:g.31061347C>T, NW_011332701.1:g.2942422C>T, NT_187660.1:g.3054874C>T, NR_038253.1:n.1888C>T, NR_038254.1:n.1788C>T, NR_038255.1:n.1693C>T

Select item 14895374177.

rs1489537417 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 15:30768740 (GRCh38)
15:31060943 (GRCh37)
Canonical SPDI:: NC_000015.10:30768739:T:C
Gene:: LOC100288637 (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_000015.10:g.30768740T>C, NC_000015.9:g.31060943T>C, NW_011332701.1:g.2942019T>C, NT_187660.1:g.3054471T>C, NR_038253.1:n.1484T>C, NR_038254.1:n.1384T>C, NR_038255.1:n.1289T>C

Select item 14893460708.

rs1489346070 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 15:30716295 (GRCh38)
15:31008498 (GRCh37)
Canonical SPDI:: NC_000015.10:30716294:G:A
Gene:: LOC100288637 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000015.10:g.30716295G>A, NC_000015.9:g.31008498G>A, NG_044985.1:g.19657G>A, NW_011332701.1:g.2889561G>A, NT_187660.1:g.3002013G>A, NR_038253.1:n.304G>A, NR_038254.1:n.204G>A, NR_038255.1:n.204G>A

Select item 14893408949.

rs1489340894 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,G [Show Flanks]
Chromosome:: 15:30768468 (GRCh38)
15:31060671 (GRCh37)
Canonical SPDI:: NC_000015.10:30768467:C:A,NC_000015.10:30768467:C:G
Gene:: LOC100288637 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000034/9 (TOPMED)
HGVS:: NC_000015.10:g.30768468C>A, NC_000015.10:g.30768468C>G, NC_000015.9:g.31060671C>A, NC_000015.9:g.31060671C>G, NW_011332701.1:g.2941747C>A, NW_011332701.1:g.2941747C>G, NT_187660.1:g.3054199C>A, NT_187660.1:g.3054199C>G, NR_038253.1:n.1212C>A, NR_038253.1:n.1212C>G, NR_038254.1:n.1112C>A, NR_038254.1:n.1112C>G, NR_038255.1:n.1017C>A, NR_038255.1:n.1017C>G

Select item 148931060910.

rs1489310609 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 15:30770374 (GRCh38)
15:31062577 (GRCh37)
Canonical SPDI:: NC_000015.10:30770373:C:A
Gene:: LOC100288637 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000015.10:g.30770374C>A, NC_000015.9:g.31062577C>A, NW_011332701.1:g.2943652C>A, NT_187660.1:g.3056104C>A, NR_038253.1:n.3118C>A, NR_038254.1:n.3018C>A, NR_038255.1:n.2923C>A

Select item 148820621711.

rs1488206217 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 15:30748664 (GRCh38)
15:31040867 (GRCh37)
Canonical SPDI:: NC_000015.10:30748663:A:G
Gene:: LOC100288637 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000057/15 (TOPMED)
HGVS:: NC_000015.10:g.30748664A>G, NC_000015.9:g.31040867A>G, NW_011332701.1:g.2921932A>G, NT_187660.1:g.3034384A>G, NR_038253.1:n.440A>G, NR_038254.1:n.340A>G

Select item 148705468912.

rs1487054689 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 15:30769649 (GRCh38)
15:31061852 (GRCh37)
Canonical SPDI:: NC_000015.10:30769648:A:C
Gene:: LOC100288637 (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_000015.10:g.30769649A>C, NC_000015.9:g.31061852A>C, NW_011332701.1:g.2942927A>C, NT_187660.1:g.3055379A>C, NR_038253.1:n.2393A>C, NR_038254.1:n.2293A>C, NR_038255.1:n.2198A>C

Select item 148693132113.

rs1486931321 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 15:30772973 (GRCh38)
15:31065176 (GRCh37)
Canonical SPDI:: NC_000015.10:30772972:G:A
Gene:: LOC100288637 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000015.10:g.30772973G>A, NC_000015.9:g.31065176G>A, NW_011332701.1:g.2946251G>A, NT_187660.1:g.3058703G>A, NR_038253.1:n.5717G>A, NR_038254.1:n.5617G>A, NR_038255.1:n.5522G>A

Select item 148680274314.

rs1486802743 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 15:30748665 (GRCh38)
15:31040868 (GRCh37)
Canonical SPDI:: NC_000015.10:30748664:C:A,NC_000015.10:30748664:C:T
Gene:: LOC100288637 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
A=0.000019/5 (TOPMED)
HGVS:: NC_000015.10:g.30748665C>A, NC_000015.10:g.30748665C>T, NC_000015.9:g.31040868C>A, NC_000015.9:g.31040868C>T, NW_011332701.1:g.2921933C>A, NW_011332701.1:g.2921933C>T, NT_187660.1:g.3034385C>A, NT_187660.1:g.3034385C>T, NR_038253.1:n.441C>A, NR_038253.1:n.441C>T, NR_038254.1:n.341C>A, NR_038254.1:n.341C>T

Select item 148661314815.

rs1486613148 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 15:30770539 (GRCh38)
15:31062742 (GRCh37)
Canonical SPDI:: NC_000015.10:30770538:C:A
Gene:: LOC100288637 (Varview)
Functional Consequence:: 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_000015.10:g.30770539C>A, NC_000015.9:g.31062742C>A, NW_011332701.1:g.2943817C>A, NT_187660.1:g.3056269C>A, NR_038253.1:n.3283C>A, NR_038254.1:n.3183C>A, NR_038255.1:n.3088C>A

Select item 148550109916.

rs1485501099 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 15:30768287 (GRCh38)
15:31060490 (GRCh37)
Canonical SPDI:: NC_000015.10:30768286:C:T
Gene:: LOC100288637 (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)
T=0.00039/7 (TOMMO)
HGVS:: NC_000015.10:g.30768287C>T, NC_000015.9:g.31060490C>T, NW_011332701.1:g.2941566C>T, NT_187660.1:g.3054018C>T, NR_038253.1:n.1031C>T, NR_038254.1:n.931C>T, NR_038255.1:n.836C>T

Select item 148520818017.

rs1485208180 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 15:30772384 (GRCh38)
15:31064587 (GRCh37)
Canonical SPDI:: NC_000015.10:30772383:T:G
Gene:: LOC100288637 (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=0.000015/4 (TOPMED)
HGVS:: NC_000015.10:g.30772384T>G, NC_000015.9:g.31064587T>G, NW_011332701.1:g.2945662T>G, NT_187660.1:g.3058114T>G, NR_038253.1:n.5128T>G, NR_038254.1:n.5028T>G, NR_038255.1:n.4933T>G

Select item 148501781618.

rs1485017816 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 15:30771056 (GRCh38)
15:31063259 (GRCh37)
Canonical SPDI:: NC_000015.10:30771055:T:C
Gene:: LOC100288637 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000014/2 (GnomAD)
C=0.000015/4 (TOPMED)
HGVS:: NC_000015.10:g.30771056T>C, NC_000015.9:g.31063259T>C, NW_011332701.1:g.2944334T>C, NT_187660.1:g.3056786T>C, NR_038253.1:n.3800T>C, NR_038254.1:n.3700T>C, NR_038255.1:n.3605T>C

Select item 148488351319.

rs1484883513 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 15:30771915 (GRCh38)
15:31064118 (GRCh37)
Canonical SPDI:: NC_000015.10:30771914:C:G,NC_000015.10:30771914:C:T
Gene:: LOC100288637 (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)
T=0.000071/1 (TOMMO)
HGVS:: NC_000015.10:g.30771915C>G, NC_000015.10:g.30771915C>T, NC_000015.9:g.31064118C>G, NC_000015.9:g.31064118C>T, NW_011332701.1:g.2945193C>G, NW_011332701.1:g.2945193C>T, NT_187660.1:g.3057645C>G, NT_187660.1:g.3057645C>T, NR_038253.1:n.4659C>G, NR_038253.1:n.4659C>T, NR_038254.1:n.4559C>G, NR_038254.1:n.4559C>T, NR_038255.1:n.4464C>G, NR_038255.1:n.4464C>T

Select item 148455084620.

rs1484550846 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 15:30770755 (GRCh38)
15:31062958 (GRCh37)
Canonical SPDI:: NC_000015.10:30770754:T:C
Gene:: LOC100288637 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0.000447/2 (ALFA)
C=0.000014/2 (GnomAD)
HGVS:: NC_000015.10:g.30770755T>C, NC_000015.9:g.31062958T>C, NW_011332701.1:g.2944033T>C, NT_187660.1:g.3056485T>C, NR_038253.1:n.3499T>C, NR_038254.1:n.3399T>C, NR_038255.1:n.3304T>C

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