SNP Links for Nucleotide (Select 224493888) - SNP

Links from Nucleotide

Items: 1 to 20 of 203

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Select item 14907179411.

rs1490717941 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:45772044 (GRCh38)
11:45793595 (GRCh37)
Canonical SPDI:: NC_000011.10:45772043:G:A
Gene:: LINC02716 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000087/2 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
A=0.000015/2 (GnomAD_exomes)
HGVS:: NC_000011.10:g.45772044G>A, NC_000011.9:g.45793595G>A, NR_027134.1:n.335G>A, NM_199137.1:c.182G>A

Select item 14897346952.

rs1489734695 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 11:45772111 (GRCh38)
11:45793662 (GRCh37)
Canonical SPDI:: NC_000011.10:45772110:G:T
Gene:: LINC02716 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: T=0.000007/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.45772111G>T, NC_000011.9:g.45793662G>T, NR_027134.1:n.402G>T, NM_199137.1:c.249G>T

Select item 14868278473.

rs1486827847 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 11:45772045 (GRCh38)
11:45793596 (GRCh37)
Canonical SPDI:: NC_000011.10:45772044:G:A,NC_000011.10:45772044:G:T
Gene:: LINC02716 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.45772045G>A, NC_000011.10:g.45772045G>T, NC_000011.9:g.45793596G>A, NC_000011.9:g.45793596G>T, NR_027134.1:n.336G>A, NR_027134.1:n.336G>T, NM_199137.1:c.183G>A, NM_199137.1:c.183G>T

Select item 14807466794.

rs1480746679 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 11:45772231 (GRCh38)
11:45793782 (GRCh37)
Canonical SPDI:: NC_000011.10:45772230:G:C
Gene:: LINC02716 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.45772231G>C, NC_000011.9:g.45793782G>C, NR_027134.1:n.522G>C, NM_199137.1:c.*6G>C

Select item 14796475015.

rs1479647501 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:45772055 (GRCh38)
11:45793606 (GRCh37)
Canonical SPDI:: NC_000011.10:45772054:C:T
Gene:: LINC02716 (Varview)
Functional Consequence:: non_coding_transcript_variant
HGVS:: NC_000011.10:g.45772055C>T, NC_000011.9:g.45793606C>T, NR_027134.1:n.346C>T, NM_199137.1:c.193C>T

Select item 14786911256.

rs1478691125 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 11:45772123 (GRCh38)
11:45793674 (GRCh37)
Canonical SPDI:: NC_000011.10:45772122:A:C
Gene:: LINC02716 (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_000011.10:g.45772123A>C, NC_000011.9:g.45793674A>C, NR_027134.1:n.414A>C, NM_199137.1:c.261A>C

Select item 14753306467.

rs1475330646 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:45772119 (GRCh38)
11:45793670 (GRCh37)
Canonical SPDI:: NC_000011.10:45772118:C:T
Gene:: LINC02716 (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_exomes)
HGVS:: NC_000011.10:g.45772119C>T, NC_000011.9:g.45793670C>T, NR_027134.1:n.410C>T, NM_199137.1:c.257C>T

Select item 14726290508.

rs1472629050 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 11:45772104 (GRCh38)
11:45793655 (GRCh37)
Canonical SPDI:: NC_000011.10:45772103:T:G
Gene:: LINC02716 (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_000011.10:g.45772104T>G, NC_000011.9:g.45793655T>G, NR_027134.1:n.395T>G, NM_199137.1:c.242T>G

Select item 14712379929.

rs1471237992 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:45772219 (GRCh38)
11:45793770 (GRCh37)
Canonical SPDI:: NC_000011.10:45772218:T:C
Gene:: LINC02716 (Varview)
Functional Consequence:: non_coding_transcript_variant
HGVS:: NC_000011.10:g.45772219T>C, NC_000011.9:g.45793770T>C, NR_027134.1:n.510T>C, NM_199137.1:c.357T>C

Select item 147036328610.

rs1470363286 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:45771520 (GRCh38)
11:45793071 (GRCh37)
Canonical SPDI:: NC_000011.10:45771519:G:A
Gene:: LINC02716 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: A=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.45771520G>A, NC_000011.9:g.45793071G>A, NR_027134.1:n.89G>A, NM_199137.1:c.-65G>A

Select item 146787164311.

rs1467871643 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 11:45771668 (GRCh38)
11:45793219 (GRCh37)
Canonical SPDI:: NC_000011.10:45771667:G:C
Gene:: LINC02716 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000007/1 (GnomAD_exomes)
C=0.000011/3 (TOPMED)
HGVS:: NC_000011.10:g.45771668G>C, NC_000011.9:g.45793219G>C, NR_027134.1:n.237G>C, NM_199137.1:c.84G>C

Select item 146736353212.

rs1467363532 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:45771604 (GRCh38)
11:45793155 (GRCh37)
Canonical SPDI:: NC_000011.10:45771603:C:T
Gene:: LINC02716 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by cluster
MAF:: T=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.45771604C>T, NC_000011.9:g.45793155C>T, NR_027134.1:n.173C>T, NM_199137.1:c.20C>T

Select item 146420318213.

rs1464203182 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 11:45772220 (GRCh38)
11:45793771 (GRCh37)
Canonical SPDI:: NC_000011.10:45772219:G:C
Gene:: LINC02716 (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=0.000023/6 (TOPMED)
HGVS:: NC_000011.10:g.45772220G>C, NC_000011.9:g.45793771G>C, NR_027134.1:n.511G>C, NM_199137.1:c.358G>C

Select item 146262853914.

rs1462628539 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:45771529 (GRCh38)
11:45793080 (GRCh37)
Canonical SPDI:: NC_000011.10:45771528:C:T
Gene:: LINC02716 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.45771529C>T, NC_000011.9:g.45793080C>T, NR_027134.1:n.98C>T, NM_199137.1:c.-56C>T

Select item 146242856915.

rs1462428569 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:45771463 (GRCh38)
11:45793014 (GRCh37)
Canonical SPDI:: NC_000011.10:45771462:G:A
Gene:: LINC02716 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000011/3 (TOPMED)
HGVS:: NC_000011.10:g.45771463G>A, NC_000011.9:g.45793014G>A, NR_027134.1:n.32G>A, NM_199137.1:c.-122G>A

Select item 146083666216.

rs1460836662 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 11:45771655 (GRCh38)
11:45793206 (GRCh37)
Canonical SPDI:: NC_000011.10:45771654:G:T
Gene:: LINC02716 (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=0.000015/2 (GnomAD_exomes)
T=0.000015/4 (TOPMED)
HGVS:: NC_000011.10:g.45771655G>T, NC_000011.9:g.45793206G>T, NR_027134.1:n.224G>T, NM_199137.1:c.71G>T

Select item 145586846817.

rs1455868468 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:45772014 (GRCh38)
11:45793565 (GRCh37)
Canonical SPDI:: NC_000011.10:45772013:G:A
Gene:: LINC02716 (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_000011.10:g.45772014G>A, NC_000011.9:g.45793565G>A, NR_027134.1:n.305G>A, NM_199137.1:c.152G>A

Select item 145400818818.

rs1454008188 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 11:45771588 (GRCh38)
11:45793139 (GRCh37)
Canonical SPDI:: NC_000011.10:45771587:G:C
Gene:: LINC02716 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000043/1 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000015/2 (GnomAD_exomes)
C=0.000015/4 (TOPMED)
HGVS:: NC_000011.10:g.45771588G>C, NC_000011.9:g.45793139G>C, NR_027134.1:n.157G>C, NM_199137.1:c.4G>C

Select item 145329675519.

rs1453296755 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:45772229 (GRCh38)
11:45793780 (GRCh37)
Canonical SPDI:: NC_000011.10:45772228:T:C
Gene:: LINC02716 (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=0.000015/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.45772229T>C, NC_000011.9:g.45793780T>C, NR_027134.1:n.520T>C, NM_199137.1:c.*4T>C

Select item 145110845320.

rs1451108453 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:45771682 (GRCh38)
11:45793233 (GRCh37)
Canonical SPDI:: NC_000011.10:45771681:G:A
Gene:: LINC02716 (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_exomes)
HGVS:: NC_000011.10:g.45771682G>A, NC_000011.9:g.45793233G>A, NR_027134.1:n.251G>A, NM_199137.1:c.98G>A

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Links from Nucleotide

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