SNP Links for Nucleotide (Select 262205756) - SNP

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Links from Nucleotide

Items: 1 to 20 of 27

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Select item 14751064841.

rs1475106484 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 21:16539169 (GRCh38)
21:17911489 (GRCh37)
Canonical SPDI:: NC_000021.9:16539168:G:A
Gene:: MIR99AHG (Varview), MIRLET7C (Varview), MIR99A (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant,upstream_transcript_variant,non_coding_transcript_variant,2KB_upstream_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000021.9:g.16539169G>A, NC_000021.8:g.17911489G>A, NR_029514.1:n.81G>A

Select item 14730460242.

rs1473046024 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 21:16539162 (GRCh38)
21:17911482 (GRCh37)
Canonical SPDI:: NC_000021.9:16539161:T:A
Gene:: MIR99AHG (Varview), MIRLET7C (Varview), MIR99A (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant,upstream_transcript_variant,non_coding_transcript_variant,2KB_upstream_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000021.9:g.16539162T>A, NC_000021.8:g.17911482T>A, NR_029514.1:n.74T>A

Select item 14580851933.

rs1458085193 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 21:16539094 (GRCh38)
21:17911414 (GRCh37)
Canonical SPDI:: NC_000021.9:16539093:T:A
Gene:: MIR99AHG (Varview), MIRLET7C (Varview), MIR99A (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant,upstream_transcript_variant,non_coding_transcript_variant,2KB_upstream_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000021.9:g.16539094T>A, NC_000021.8:g.17911414T>A, NR_029514.1:n.6T>A

Select item 14460953264.

rs1446095326 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 21:16539103 (GRCh38)
21:17911423 (GRCh37)
Canonical SPDI:: NC_000021.9:16539102:C:T
Gene:: MIR99AHG (Varview), MIRLET7C (Varview), MIR99A (Varview)
Functional Consequence:: intron_variant,genic_upstream_transcript_variant,upstream_transcript_variant,non_coding_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000021.9:g.16539103C>T, NC_000021.8:g.17911423C>T, NR_029514.1:n.15C>T

Select item 14196169255.

rs1419616925 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 21:16539158 (GRCh38)
21:17911478 (GRCh37)
Canonical SPDI:: NC_000021.9:16539157:T:A
Gene:: MIR99AHG (Varview), MIRLET7C (Varview), MIR99A (Varview)
Functional Consequence:: non_coding_transcript_variant,genic_upstream_transcript_variant,upstream_transcript_variant,intron_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000011/3 (TOPMED)
HGVS:: NC_000021.9:g.16539158T>A, NC_000021.8:g.17911478T>A, NR_029514.1:n.70T>A

Select item 13928401076.

rs1392840107 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 21:16539112 (GRCh38)
21:17911432 (GRCh37)
Canonical SPDI:: NC_000021.9:16539111:C:A,NC_000021.9:16539111:C:T
Gene:: MIR99AHG (Varview), MIRLET7C (Varview), MIR99A (Varview)
Functional Consequence:: non_coding_transcript_variant,genic_upstream_transcript_variant,upstream_transcript_variant,intron_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000021.9:g.16539112C>A, NC_000021.9:g.16539112C>T, NC_000021.8:g.17911432C>A, NC_000021.8:g.17911432C>T, NR_029514.1:n.24C>A, NR_029514.1:n.24C>T

Select item 13635094587.

rs1363509458 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 21:16539089 (GRCh38)
21:17911409 (GRCh37)
Canonical SPDI:: NC_000021.9:16539088:C:T
Gene:: MIR99AHG (Varview), MIRLET7C (Varview), MIR99A (Varview)
Functional Consequence:: non_coding_transcript_variant,upstream_transcript_variant,genic_upstream_transcript_variant,2KB_upstream_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
T=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000021.9:g.16539089C>T, NC_000021.8:g.17911409C>T, NR_029514.1:n.1C>T

Select item 13058324908.

rs1305832490 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 21:16539132 (GRCh38)
21:17911452 (GRCh37)
Canonical SPDI:: NC_000021.9:16539131:A:G
Gene:: MIR99AHG (Varview), MIRLET7C (Varview), MIR99A (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant,non_coding_transcript_variant,genic_upstream_transcript_variant,intron_variant
Validated:: by frequency
MAF:: G=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000021.9:g.16539132A>G, NC_000021.8:g.17911452A>G, NR_029514.1:n.44A>G

Select item 13007936769.

rs1300793676 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 21:16539093 (GRCh38)
21:17911413 (GRCh37)
Canonical SPDI:: NC_000021.9:16539092:T:C
Gene:: MIR99AHG (Varview), MIRLET7C (Varview), MIR99A (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant,non_coding_transcript_variant,genic_upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000014/2 (GnomAD)
HGVS:: NC_000021.9:g.16539093T>C, NC_000021.8:g.17911413T>C, NR_029514.1:n.5T>C

Select item 127107042210.

rs1271070422 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 21:16539142 (GRCh38)
21:17911462 (GRCh37)
Canonical SPDI:: NC_000021.9:16539141:C:T
Gene:: MIR99AHG (Varview), MIRLET7C (Varview), MIR99A (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant,non_coding_transcript_variant,genic_upstream_transcript_variant,intron_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000021.9:g.16539142C>T, NC_000021.8:g.17911462C>T, NR_029514.1:n.54C>T

Select item 125001601011.

rs1250016010 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 21:16539160 (GRCh38)
21:17911480 (GRCh37)
Canonical SPDI:: NC_000021.9:16539159:T:A
Gene:: MIR99AHG (Varview), MIRLET7C (Varview), MIR99A (Varview)
Functional Consequence:: genic_upstream_transcript_variant,upstream_transcript_variant,2KB_upstream_variant,non_coding_transcript_variant,intron_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000021.9:g.16539160T>A, NC_000021.8:g.17911480T>A, NR_029514.1:n.72T>A

Select item 121805371112.

rs1218053711 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 21:16539090 (GRCh38)
21:17911410 (GRCh37)
Canonical SPDI:: NC_000021.9:16539089:C:G
Gene:: MIR99AHG (Varview), MIRLET7C (Varview), MIR99A (Varview)
Functional Consequence:: genic_upstream_transcript_variant,upstream_transcript_variant,2KB_upstream_variant,non_coding_transcript_variant,intron_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_000021.9:g.16539090C>G, NC_000021.8:g.17911410C>G, NR_029514.1:n.2C>G

Select item 121422291613.

rs1214222916 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 21:16539147 (GRCh38)
21:17911467 (GRCh37)
Canonical SPDI:: NC_000021.9:16539146:T:C
Gene:: MIR99AHG (Varview), MIRLET7C (Varview), MIR99A (Varview)
Functional Consequence:: genic_upstream_transcript_variant,upstream_transcript_variant,2KB_upstream_variant,non_coding_transcript_variant,intron_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000021.9:g.16539147T>C, NC_000021.8:g.17911467T>C, NR_029514.1:n.59T>C

Select item 95038250714.

rs950382507 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 21:16539154 (GRCh38)
21:17911474 (GRCh37)
Canonical SPDI:: NC_000021.9:16539153:G:A
Gene:: MIR99AHG (Varview), MIRLET7C (Varview), MIR99A (Varview)
Functional Consequence:: upstream_transcript_variant,intron_variant,2KB_upstream_variant,non_coding_transcript_variant,genic_upstream_transcript_variant
HGVS:: NC_000021.9:g.16539154G>A, NC_000021.8:g.17911474G>A, NR_029514.1:n.66G>A

Select item 91339700115.

rs913397001 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 21:16539145 (GRCh38)
21:17911465 (GRCh37)
Canonical SPDI:: NC_000021.9:16539144:G:A
Gene:: MIR99AHG (Varview), MIRLET7C (Varview), MIR99A (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant,genic_upstream_transcript_variant,non_coding_transcript_variant,intron_variant
Validated:: by frequency,by cluster
MAF:: A=0.0002/1 (1000Genomes)
HGVS:: NC_000021.9:g.16539145G>A, NC_000021.8:g.17911465G>A, NR_029514.1:n.57G>A

Select item 77873892116.

rs778738921 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 21:16539100 (GRCh38)
21:17911420 (GRCh37)
Canonical SPDI:: NC_000021.9:16539099:A:G
Gene:: MIR99AHG (Varview), MIRLET7C (Varview), MIR99A (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant,upstream_transcript_variant,2KB_upstream_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (GnomAD_exomes)
G=0.000004/1 (TOPMED)
G=0.000009/1 (ExAC)
G=0.000035/1 (TOMMO)
HGVS:: NC_000021.9:g.16539100A>G, NC_000021.8:g.17911420A>G, NR_029514.1:n.12A>G

Select item 77474868817.

rs774748688 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 21:16539159 (GRCh38)
21:17911479 (GRCh37)
Canonical SPDI:: NC_000021.9:16539158:G:C
Gene:: MIR99AHG (Varview), MIRLET7C (Varview), MIR99A (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant,upstream_transcript_variant,2KB_upstream_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (GnomAD_exomes)
C=0.000009/1 (ExAC)
HGVS:: NC_000021.9:g.16539159G>C, NC_000021.8:g.17911479G>C, NR_029514.1:n.71G>C

Select item 76781908218.

rs767819082 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C,T [Show Flanks]
Chromosome:: 21:16539165 (GRCh38)
21:17911485 (GRCh37)
Canonical SPDI:: NC_000021.9:16539164:G:C,NC_000021.9:16539164:G:T
Gene:: MIR99AHG (Varview), MIRLET7C (Varview), MIR99A (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant,upstream_transcript_variant,2KB_upstream_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
C=0.000012/3 (GnomAD_exomes)
C=0.000026/3 (ExAC)
HGVS:: NC_000021.9:g.16539165G>C, NC_000021.9:g.16539165G>T, NC_000021.8:g.17911485G>C, NC_000021.8:g.17911485G>T, NR_029514.1:n.77G>C, NR_029514.1:n.77G>T

Select item 76642866419.

rs766428664 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 21:16539153 (GRCh38)
21:17911473 (GRCh37)
Canonical SPDI:: NC_000021.9:16539152:G:A
Gene:: MIR99AHG (Varview), MIRLET7C (Varview), MIR99A (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant,upstream_transcript_variant,2KB_upstream_variant,non_coding_transcript_variant
Validated:: by frequency,by cluster
MAF:: A=0.000004/1 (GnomAD_exomes)
A=0.000009/1 (ExAC)
HGVS:: NC_000021.9:g.16539153G>A, NC_000021.8:g.17911473G>A, NR_029514.1:n.65G>A

Select item 76313426220.

rs763134262 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 21:16539151 (GRCh38)
21:17911471 (GRCh37)
Canonical SPDI:: NC_000021.9:16539150:A:G
Gene:: MIR99AHG (Varview), MIRLET7C (Varview), MIR99A (Varview)
Functional Consequence:: genic_upstream_transcript_variant,intron_variant,upstream_transcript_variant,2KB_upstream_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000071/1 (ALFA)
G=0.000008/2 (GnomAD_exomes)
G=0.000009/1 (ExAC)
G=0.000021/3 (GnomAD)
G=0.000023/6 (TOPMED)
HGVS:: NC_000021.9:g.16539151A>G, NC_000021.8:g.17911471A>G, NR_029514.1:n.63A>G