SNP Links for Nucleotide (Select 522838296) - SNP

Links from Nucleotide

Items: 1 to 20 of 761

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Select item 14908088931.

rs1490808893 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 10:42408870 (GRCh38)
10:42904318 (GRCh37)
Canonical SPDI:: NC_000010.11:42408869:C:G
Gene:: CCNYL2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000010.11:g.42408870C>G, NC_000010.10:g.42904318C>G, NR_103829.1:n.2609G>C

Select item 14906447572.

rs1490644757 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 10:42408297 (GRCh38)
10:42903745 (GRCh37)
Canonical SPDI:: NC_000010.11:42408296:G:C
Gene:: CCNYL2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000010.11:g.42408297G>C, NC_000010.10:g.42903745G>C, NR_103829.1:n.3182C>G

Select item 14903821083.

rs1490382108 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 10:42410138 (GRCh38)
10:42905586 (GRCh37)
Canonical SPDI:: NC_000010.11:42410137:G:A,NC_000010.11:42410137:G:T
Gene:: CCNYL2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
A=0.000007/1 (GnomAD_exomes)
HGVS:: NC_000010.11:g.42410138G>A, NC_000010.11:g.42410138G>T, NC_000010.10:g.42905586G>A, NC_000010.10:g.42905586G>T, NR_103829.1:n.1341C>T, NR_103829.1:n.1341C>A

Select item 14897508474.

rs1489750847 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 10:42433326 (GRCh38)
10:42928774 (GRCh37)
Canonical SPDI:: NC_000010.11:42433325:T:C
Gene:: CCNYL2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000010.11:g.42433326T>C, NC_000010.10:g.42928774T>C, NR_103829.1:n.727A>G

Select item 14892725795.

rs1489272579 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 10:42472096 (GRCh38)
10:42967544 (GRCh37)
Canonical SPDI:: NC_000010.11:42472095:A:C
Gene:: CCNYL2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000010.11:g.42472096A>C, NC_000010.10:g.42967544A>C, NR_103829.1:n.145T>G

Select item 14885352926.

rs1488535292 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 10:42409817 (GRCh38)
10:42905265 (GRCh37)
Canonical SPDI:: NC_000010.11:42409816:C:T
Gene:: CCNYL2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000019/5 (TOPMED)
T=0.000043/6 (GnomAD)
HGVS:: NC_000010.11:g.42409817C>T, NC_000010.10:g.42905265C>T, NR_103829.1:n.1662G>A

Select item 14877359317.

rs1487735931 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 10:42425423 (GRCh38)
10:42920871 (GRCh37)
Canonical SPDI:: NC_000010.11:42425422:C:A
Gene:: CCNYL2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0.00005/1 (ALFA)
HGVS:: NC_000010.11:g.42425423C>A, NC_000010.10:g.42920871C>A, NR_103829.1:n.850G>T

Select item 14863245268.

rs1486324526 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 10:42411813 (GRCh38)
10:42907261 (GRCh37)
Canonical SPDI:: NC_000010.11:42411812:G:A
Gene:: CCNYL2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: A=0.000007/1 (GnomAD_exomes)
HGVS:: NC_000010.11:g.42411813G>A, NC_000010.10:g.42907261G>A, NR_103829.1:n.1171C>T

Select item 14860674939.

rs1486067493 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 10:42471987 (GRCh38)
10:42967435 (GRCh37)
Canonical SPDI:: NC_000010.11:42471986:T:C
Gene:: CCNYL2 (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_000010.11:g.42471987T>C, NC_000010.10:g.42967435T>C, NR_103829.1:n.254A>G

Select item 148438510510.

rs1484385105 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 10:42409231 (GRCh38)
10:42904679 (GRCh37)
Canonical SPDI:: NC_000010.11:42409230:A:C
Gene:: CCNYL2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000019/5 (TOPMED)
C=0.000029/4 (GnomAD)
HGVS:: NC_000010.11:g.42409231A>C, NC_000010.10:g.42904679A>C, NR_103829.1:n.2248T>G

Select item 148339908611.

rs1483399086 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 10:42451665 (GRCh38)
10:42947113 (GRCh37)
Canonical SPDI:: NC_000010.11:42451664:T:G
Gene:: CCNYL2 (Varview)
Functional Consequence:: non_coding_transcript_variant
HGVS:: NC_000010.11:g.42451665T>G, NC_000010.10:g.42947113T>G, NR_103829.1:n.642A>C

Select item 148251491112.

rs1482514911 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 10:42409308 (GRCh38)
10:42904756 (GRCh37)
Canonical SPDI:: NC_000010.11:42409307:C:T
Gene:: CCNYL2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
T=0.000014/2 (GnomAD)
HGVS:: NC_000010.11:g.42409308C>T, NC_000010.10:g.42904756C>T, NR_103829.1:n.2171G>A

Select item 148089586313.

rs1480895863 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 10:42420848 (GRCh38)
10:42916296 (GRCh37)
Canonical SPDI:: NC_000010.11:42420847:G:A,NC_000010.11:42420847:G:T
Gene:: CCNYL2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000028/1 (ALFA)
T=0.000013/2 (GnomAD_exomes)
T=0.000014/2 (GnomAD)
HGVS:: NC_000010.11:g.42420848G>A, NC_000010.11:g.42420848G>T, NC_000010.10:g.42916296G>A, NC_000010.10:g.42916296G>T, NR_103829.1:n.1037C>T, NR_103829.1:n.1037C>A

Select item 148047332614.

rs1480473326 [Homo sapiens]

Variant type:: DELINS
Alleles:: GGGTTCAG>- [Show Flanks]
Chromosome:: 10:42410048 (GRCh38)
10:42905496 (GRCh37)
Canonical SPDI:: NC_000010.11:42410045:AGGGGTTCAG:AG
Gene:: CCNYL2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AG=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.000007/1 (GnomAD)
-=0.000008/1 (GnomAD_exomes)
HGVS:: NC_000010.11:g.42410048_42410055del, NC_000010.10:g.42905496_42905503del, NR_103829.1:n.1426_1433del

Select item 147950409415.

rs1479504094 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 10:42471982 (GRCh38)
10:42967430 (GRCh37)
Canonical SPDI:: NC_000010.11:42471981:C:T
Gene:: CCNYL2 (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_000010.11:g.42471982C>T, NC_000010.10:g.42967430C>T, NR_103829.1:n.259G>A

Select item 147885523716.

rs1478855237 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 10:42472168 (GRCh38)
10:42967616 (GRCh37)
Canonical SPDI:: NC_000010.11:42472167:C:T
Gene:: CCNYL2 (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_000010.11:g.42472168C>T, NC_000010.10:g.42967616C>T, NR_103829.1:n.73G>A

Select item 147862722717.

rs1478627227 [Homo sapiens]

Variant type:: DELINS
Alleles:: CT>- [Show Flanks]
Chromosome:: 10:42409857 (GRCh38)
10:42905305 (GRCh37)
Canonical SPDI:: NC_000010.11:42409854:CTCT:CT
Gene:: CCNYL2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: CTCT=0./0 (ALFA)
-=0.000019/5 (TOPMED)
-=0.000036/5 (GnomAD)
HGVS:: NC_000010.11:g.42409855CT[1], NC_000010.10:g.42905303CT[1], NR_103829.1:n.1621AG[1]

Select item 147844252418.

rs1478442524 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 10:42420804 (GRCh38)
10:42916252 (GRCh37)
Canonical SPDI:: NC_000010.11:42420803:C:T
Gene:: CCNYL2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0.000056/2 (ALFA)
T=0.000011/3 (TOPMED)
HGVS:: NC_000010.11:g.42420804C>T, NC_000010.10:g.42916252C>T, NR_103829.1:n.1081G>A

Select item 147829342419.

rs1478293424 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 10:42408626 (GRCh38)
10:42904074 (GRCh37)
Canonical SPDI:: NC_000010.11:42408625:A:G
Gene:: CCNYL2 (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=0.000021/3 (GnomAD)
HGVS:: NC_000010.11:g.42408626A>G, NC_000010.10:g.42904074A>G, NR_103829.1:n.2853T>C

Select item 147803522920.

rs1478035229 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 10:42471847 (GRCh38)
10:42967295 (GRCh37)
Canonical SPDI:: NC_000010.11:42471846:A:G
Gene:: CCNYL2 (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_000010.11:g.42471847A>G, NC_000010.10:g.42967295A>G, NR_103829.1:n.394T>C

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