SNP Links for Nucleotide (Select 385648246) - SNP

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Links from Nucleotide

Items: 1 to 20 of 626

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Select item 14907491271.

rs1490749127 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 14:101070548 (GRCh38)
14:101536885 (GRCh37)
Canonical SPDI:: NC_000014.9:101070547:T:C
Gene:: MEG9 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
HGVS:: NC_000014.9:g.101070548T>C, NC_000014.8:g.101536885T>C, NR_047664.1:n.252T>C

Select item 14904360112.

rs1490436011 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 14:101071097 (GRCh38)
14:101537434 (GRCh37)
Canonical SPDI:: NC_000014.9:101071096:G:A
Gene:: MEG9 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000045/12 (TOPMED)
A=0.000093/13 (GnomAD)
HGVS:: NC_000014.9:g.101071097G>A, NC_000014.8:g.101537434G>A, NR_047664.1:n.801G>A

Select item 14899319643.

rs1489931964 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 14:101071028 (GRCh38)
14:101537365 (GRCh37)
Canonical SPDI:: NC_000014.9:101071027:C:A
Gene:: MEG9 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000014.9:g.101071028C>A, NC_000014.8:g.101537365C>A, NR_047664.1:n.732C>A

Select item 14888078974.

rs1488807897 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 14:101072302 (GRCh38)
14:101538639 (GRCh37)
Canonical SPDI:: NC_000014.9:101072301:A:G
Gene:: MEG9 (Varview), LOC105370670 (Varview)
Functional Consequence:: non_coding_transcript_variant,genic_downstream_transcript_variant,downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000011/3 (TOPMED)
G=0.000021/3 (GnomAD)
HGVS:: NC_000014.9:g.101072302A>G, NC_000014.8:g.101538639A>G, XR_001750890.2:n.1035T>C, NR_047664.1:n.2006A>G

Select item 14859240605.

rs1485924060 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 14:101070450 (GRCh38)
14:101536787 (GRCh37)
Canonical SPDI:: NC_000014.9:101070449:A:G
Gene:: MEG9 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
G=0.000014/2 (GnomAD)
HGVS:: NC_000014.9:g.101070450A>G, NC_000014.8:g.101536787A>G, NR_047664.1:n.154A>G

Select item 14853736896.

rs1485373689 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 14:101072221 (GRCh38)
14:101538558 (GRCh37)
Canonical SPDI:: NC_000014.9:101072220:G:A
Gene:: MEG9 (Varview), LOC105370670 (Varview)
Functional Consequence:: non_coding_transcript_variant,genic_downstream_transcript_variant,downstream_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_000014.9:g.101072221G>A, NC_000014.8:g.101538558G>A, XR_001750890.2:n.1116C>T, NR_047664.1:n.1925G>A

Select item 14811427947.

rs1481142794 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 14:101070658 (GRCh38)
14:101536995 (GRCh37)
Canonical SPDI:: NC_000014.9:101070657:C:G,NC_000014.9:101070657:C:T
Gene:: MEG9 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
G=0./0 (GnomAD)
T=0.000011/3 (TOPMED)
T=0.000342/1 (KOREAN)
C=0.5/1 (SGDP_PRJ)
HGVS:: NC_000014.9:g.101070658C>G, NC_000014.9:g.101070658C>T, NC_000014.8:g.101536995C>G, NC_000014.8:g.101536995C>T, NR_047664.1:n.362C>G, NR_047664.1:n.362C>T

Select item 14796823058.

rs1479682305 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 14:101072446 (GRCh38)
14:101538783 (GRCh37)
Canonical SPDI:: NC_000014.9:101072445:A:G
Gene:: MEG9 (Varview), LOC105370670 (Varview)
Functional Consequence:: non_coding_transcript_variant,genic_downstream_transcript_variant,downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000035/1 (TOMMO)
G=0.00005/7 (GnomAD)
G=0.000064/17 (TOPMED)
HGVS:: NC_000014.9:g.101072446A>G, NC_000014.8:g.101538783A>G, XR_001750890.2:n.891T>C, NR_047664.1:n.2150A>G

Select item 14796019449.

rs1479601944 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 14:101071954 (GRCh38)
14:101538291 (GRCh37)
Canonical SPDI:: NC_000014.9:101071953:G:A
Gene:: MEG9 (Varview), LOC105370670 (Varview)
Functional Consequence:: non_coding_transcript_variant,500B_downstream_variant,downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000023/6 (TOPMED)
HGVS:: NC_000014.9:g.101071954G>A, NC_000014.8:g.101538291G>A, NR_047664.1:n.1658G>A

Select item 147896028610.

rs1478960286 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 14:101072725 (GRCh38)
14:101539062 (GRCh37)
Canonical SPDI:: NC_000014.9:101072724:T:A
Gene:: MEG9 (Varview), LOC105370670 (Varview)
Functional Consequence:: non_coding_transcript_variant,genic_downstream_transcript_variant,downstream_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_000014.9:g.101072725T>A, NC_000014.8:g.101539062T>A, XR_001750890.2:n.612A>T, NR_047664.1:n.2429T>A, XR_007064340.1:n.1259A>T

Select item 147834771711.

rs1478347717 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 14:101072789 (GRCh38)
14:101539126 (GRCh37)
Canonical SPDI:: NC_000014.9:101072788:T:C
Gene:: MEG9 (Varview), LOC105370670 (Varview)
Functional Consequence:: non_coding_transcript_variant,genic_downstream_transcript_variant,downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000015/4 (TOPMED)
HGVS:: NC_000014.9:g.101072789T>C, NC_000014.8:g.101539126T>C, XR_001750890.2:n.548A>G, NR_047664.1:n.2493T>C, XR_007064340.1:n.1195A>G

Select item 147644901412.

rs1476449014 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 14:101071866 (GRCh38)
14:101538203 (GRCh37)
Canonical SPDI:: NC_000014.9:101071865:A:G
Gene:: MEG9 (Varview), LOC105370670 (Varview)
Functional Consequence:: non_coding_transcript_variant,500B_downstream_variant,downstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
HGVS:: NC_000014.9:g.101071866A>G, NC_000014.8:g.101538203A>G, NR_047664.1:n.1570A>G

Select item 147639772213.

rs1476397722 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 14:101071006 (GRCh38)
14:101537343 (GRCh37)
Canonical SPDI:: NC_000014.9:101071005:A:G
Gene:: MEG9 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
HGVS:: NC_000014.9:g.101071006A>G, NC_000014.8:g.101537343A>G, NR_047664.1:n.710A>G

Select item 147316723914.

rs1473167239 [Homo sapiens]

Variant type:: INS
Alleles:: ->G [Show Flanks]
Chromosome:: 14:101072668 (GRCh38)
14:101539006 (GRCh37)
Canonical SPDI:: NC_000014.9:101072668::G
Gene:: MEG9 (Varview), LOC105370670 (Varview)
Functional Consequence:: non_coding_transcript_variant,genic_downstream_transcript_variant,downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000084/1 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000035/1 (TOMMO)
HGVS:: NC_000014.9:g.101072668_101072669insG, NC_000014.8:g.101539005_101539006insG, XR_001750890.2:n.668_669insC, NR_047664.1:n.2372_2373insG

Select item 147284023715.

rs1472840237 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 14:101072076 (GRCh38)
14:101538413 (GRCh37)
Canonical SPDI:: NC_000014.9:101072075:C:T
Gene:: MEG9 (Varview), LOC105370670 (Varview)
Functional Consequence:: non_coding_transcript_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
T=0.000177/3 (TOMMO)
HGVS:: NC_000014.9:g.101072076C>T, NC_000014.8:g.101538413C>T, XR_001750890.2:n.1261G>A, NR_047664.1:n.1780C>T

Select item 147135293116.

rs1471352931 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 14:101072354 (GRCh38)
14:101538691 (GRCh37)
Canonical SPDI:: NC_000014.9:101072353:T:G
Gene:: MEG9 (Varview), LOC105370670 (Varview)
Functional Consequence:: non_coding_transcript_variant,genic_downstream_transcript_variant,downstream_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_000014.9:g.101072354T>G, NC_000014.8:g.101538691T>G, XR_001750890.2:n.983A>C, NR_047664.1:n.2058T>G

Select item 147068212217.

rs1470682122 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 14:101071632 (GRCh38)
14:101537969 (GRCh37)
Canonical SPDI:: NC_000014.9:101071631:G:A
Gene:: MEG9 (Varview), LOC105370670 (Varview)
Functional Consequence:: non_coding_transcript_variant,500B_downstream_variant,downstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000015/4 (TOPMED)
HGVS:: NC_000014.9:g.101071632G>A, NC_000014.8:g.101537969G>A, NR_047664.1:n.1336G>A

Select item 146823882418.

rs1468238824 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 14:101071146 (GRCh38)
14:101537483 (GRCh37)
Canonical SPDI:: NC_000014.9:101071145:G:A
Gene:: MEG9 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000014.9:g.101071146G>A, NC_000014.8:g.101537483G>A, NR_047664.1:n.850G>A

Select item 146788324619.

rs1467883246 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 14:101072520 (GRCh38)
14:101538857 (GRCh37)
Canonical SPDI:: NC_000014.9:101072519:G:A
Gene:: MEG9 (Varview), LOC105370670 (Varview)
Functional Consequence:: non_coding_transcript_variant,genic_downstream_transcript_variant,downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000015/4 (TOPMED)
A=0.000021/3 (GnomAD)
HGVS:: NC_000014.9:g.101072520G>A, NC_000014.8:g.101538857G>A, XR_001750890.2:n.817C>T, NR_047664.1:n.2224G>A

Select item 146569844220.

rs1465698442 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 14:101072504 (GRCh38)
14:101538841 (GRCh37)
Canonical SPDI:: NC_000014.9:101072503:G:A
Gene:: MEG9 (Varview), LOC105370670 (Varview)
Functional Consequence:: non_coding_transcript_variant,genic_downstream_transcript_variant,downstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000014.9:g.101072504G>A, NC_000014.8:g.101538841G>A, XR_001750890.2:n.833C>T, NR_047664.1:n.2208G>A