SNP Links for Nucleotide (Select 214830808) - SNP

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Links from Nucleotide

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Select item 14905642431.

rs1490564243 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 19:21751892 (GRCh38)
19:21934694 (GRCh37)
Canonical SPDI:: NC_000019.10:21751891:T:C
Gene:: ZNF100 (Varview), CCNYL6 (Varview)
Functional Consequence:: non_coding_transcript_variant,upstream_transcript_variant,intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000019.10:g.21751892T>C, NC_000019.9:g.21934694T>C, NG_054926.1:g.20737A>G, NW_003315964.2:g.113082T>C, NR_024523.1:n.1148T>C

Select item 14902081542.

rs1490208154 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 19:21752449 (GRCh38)
19:21935251 (GRCh37)
Canonical SPDI:: NC_000019.10:21752448:C:A,NC_000019.10:21752448:C:T
Gene:: ZNF100 (Varview), CCNYL6 (Varview)
Functional Consequence:: non_coding_transcript_variant,upstream_transcript_variant,intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
HGVS:: NC_000019.10:g.21752449C>A, NC_000019.10:g.21752449C>T, NC_000019.9:g.21935251C>A, NC_000019.9:g.21935251C>T, NG_054926.1:g.20180G>T, NG_054926.1:g.20180G>A, NW_003315964.2:g.113639C>A, NW_003315964.2:g.113639C>T, NR_024523.1:n.1705C>A, NR_024523.1:n.1705C>T

Select item 14892809693.

rs1489280969 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 19:21751160 (GRCh38)
19:21933962 (GRCh37)
Canonical SPDI:: NC_000019.10:21751159:A:G
Gene:: ZNF100 (Varview), CCNYL6 (Varview)
Functional Consequence:: non_coding_transcript_variant,upstream_transcript_variant,intron_variant,genic_upstream_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_000019.10:g.21751160A>G, NC_000019.9:g.21933962A>G, NG_054926.1:g.21469T>C, NW_003315964.2:g.112350A>G, NR_024523.1:n.416A>G

Select item 14877879924.

rs1487787992 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 19:21752651 (GRCh38)
19:21935453 (GRCh37)
Canonical SPDI:: NC_000019.10:21752650:T:A
Gene:: ZNF100 (Varview), CCNYL6 (Varview)
Functional Consequence:: non_coding_transcript_variant,upstream_transcript_variant,intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000008/2 (TOPMED)
HGVS:: NC_000019.10:g.21752651T>A, NC_000019.9:g.21935453T>A, NG_054926.1:g.19978A>T, NW_003315964.2:g.113841T>A, NR_024523.1:n.1907T>A

Select item 14864536925.

rs1486453692 [Homo sapiens]

Variant type:: DELINS
Alleles:: CAAA>- [Show Flanks]
Chromosome:: 19:21752558 (GRCh38)
19:21935360 (GRCh37)
Canonical SPDI:: NC_000019.10:21752554:AAACAAA:AAA
Gene:: ZNF100 (Varview), CCNYL6 (Varview)
Functional Consequence:: non_coding_transcript_variant,upstream_transcript_variant,intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAA=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.000011/1 (GnomAD)
HGVS:: NC_000019.10:g.21752558_21752561del, NC_000019.9:g.21935360_21935363del, NG_054926.1:g.20071_20074del, NW_003315964.2:g.113748_113751del, NR_024523.1:n.1814_1817del

Select item 14858650976.

rs1485865097 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 19:21752419 (GRCh38)
19:21935221 (GRCh37)
Canonical SPDI:: NC_000019.10:21752418:G:C
Gene:: ZNF100 (Varview), CCNYL6 (Varview)
Functional Consequence:: non_coding_transcript_variant,upstream_transcript_variant,intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
HGVS:: NC_000019.10:g.21752419G>C, NC_000019.9:g.21935221G>C, NG_054926.1:g.20210C>G, NW_003315964.2:g.113609G>C, NR_024523.1:n.1675G>C

Select item 14848291667.

rs1484829166 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 19:21752275 (GRCh38)
19:21935077 (GRCh37)
Canonical SPDI:: NC_000019.10:21752274:A:G
Gene:: ZNF100 (Varview), CCNYL6 (Varview)
Functional Consequence:: non_coding_transcript_variant,upstream_transcript_variant,intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000019/5 (TOPMED)
HGVS:: NC_000019.10:g.21752275A>G, NC_000019.9:g.21935077A>G, NG_054926.1:g.20354T>C, NW_003315964.2:g.113465A>G, NR_024523.1:n.1531A>G

Select item 14842467848.

rs1484246784 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 19:21753337 (GRCh38)
19:21936139 (GRCh37)
Canonical SPDI:: NC_000019.10:21753336:G:A
Gene:: ZNF100 (Varview), CCNYL6 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000011/3 (TOPMED)
A=0.000014/2 (GnomAD)
HGVS:: NC_000019.10:g.21753337G>A, NC_000019.9:g.21936139G>A, NG_054926.1:g.19292C>T, NW_003315964.2:g.114527G>A, NR_024523.1:n.2593G>A

Select item 14811847699.

rs1481184769 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 19:21752388 (GRCh38)
19:21935190 (GRCh37)
Canonical SPDI:: NC_000019.10:21752387:G:A
Gene:: ZNF100 (Varview), CCNYL6 (Varview)
Functional Consequence:: non_coding_transcript_variant,upstream_transcript_variant,intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000019.10:g.21752388G>A, NC_000019.9:g.21935190G>A, NG_054926.1:g.20241C>T, NW_003315964.2:g.113578G>A, NR_024523.1:n.1644G>A

Select item 148090784410.

rs1480907844 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 19:21751960 (GRCh38)
19:21934762 (GRCh37)
Canonical SPDI:: NC_000019.10:21751959:T:C
Gene:: ZNF100 (Varview), CCNYL6 (Varview)
Functional Consequence:: non_coding_transcript_variant,upstream_transcript_variant,intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000019.10:g.21751960T>C, NC_000019.9:g.21934762T>C, NG_054926.1:g.20669A>G, NW_003315964.2:g.113150T>C, NR_024523.1:n.1216T>C

Select item 147895291111.

rs1478952911 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 19:21750951 (GRCh38)
19:21933753 (GRCh37)
Canonical SPDI:: NC_000019.10:21750950:C:A,NC_000019.10:21750950:C:T
Gene:: ZNF100 (Varview), CCNYL6 (Varview)
Functional Consequence:: non_coding_transcript_variant,upstream_transcript_variant,intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000019.10:g.21750951C>A, NC_000019.10:g.21750951C>T, NC_000019.9:g.21933753C>A, NC_000019.9:g.21933753C>T, NG_054926.1:g.21678G>T, NG_054926.1:g.21678G>A, NW_003315964.2:g.112141C>A, NW_003315964.2:g.112141C>T, NR_024523.1:n.207C>A, NR_024523.1:n.207C>T

Select item 147868106712.

rs1478681067 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 19:21751507 (GRCh38)
19:21934309 (GRCh37)
Canonical SPDI:: NC_000019.10:21751506:T:A
Gene:: ZNF100 (Varview), CCNYL6 (Varview)
Functional Consequence:: non_coding_transcript_variant,upstream_transcript_variant,intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0.000224/1 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000019.10:g.21751507T>A, NC_000019.9:g.21934309T>A, NG_054926.1:g.21122A>T, NW_003315964.2:g.112697T>A, NR_024523.1:n.763T>A

Select item 147834274113.

rs1478342741 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 19:21751232 (GRCh38)
19:21934034 (GRCh37)
Canonical SPDI:: NC_000019.10:21751231:A:G
Gene:: ZNF100 (Varview), CCNYL6 (Varview)
Functional Consequence:: non_coding_transcript_variant,upstream_transcript_variant,intron_variant,genic_upstream_transcript_variant
Validated:: by frequency
MAF:: G=0.000007/1 (GnomAD)
HGVS:: NC_000019.10:g.21751232A>G, NC_000019.9:g.21934034A>G, NG_054926.1:g.21397T>C, NW_003315964.2:g.112422A>G, NR_024523.1:n.488A>G

Select item 147794257314.

rs1477942573 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 19:21752884 (GRCh38)
19:21935686 (GRCh37)
Canonical SPDI:: NC_000019.10:21752883:G:A
Gene:: ZNF100 (Varview), CCNYL6 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000019.10:g.21752884G>A, NC_000019.9:g.21935686G>A, NG_054926.1:g.19745C>T, NW_003315964.2:g.114074G>A, NR_024523.1:n.2140G>A

Select item 147770252815.

rs1477702528 [Homo sapiens]

Variant type:: SNV:
Alleles:: T>A
Chromosome:: no mapping
Canonical SPDI:

Select item 147768590016.

rs1477685900 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 19:21753336 (GRCh38)
19:21936138 (GRCh37)
Canonical SPDI:: NC_000019.10:21753335:G:A
Gene:: ZNF100 (Varview), CCNYL6 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000019.10:g.21753336G>A, NC_000019.9:g.21936138G>A, NG_054926.1:g.19293C>T, NW_003315964.2:g.114526G>A, NR_024523.1:n.2592G>A

Select item 147666416417.

rs1476664164 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 19:21751432 (GRCh38)
19:21934234 (GRCh37)
Canonical SPDI:: NC_000019.10:21751431:T:C,NC_000019.10:21751431:T:G
Gene:: ZNF100 (Varview), CCNYL6 (Varview)
Functional Consequence:: non_coding_transcript_variant,upstream_transcript_variant,intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
HGVS:: NC_000019.10:g.21751432T>C, NC_000019.10:g.21751432T>G, NC_000019.9:g.21934234T>C, NC_000019.9:g.21934234T>G, NG_054926.1:g.21197A>G, NG_054926.1:g.21197A>C, NW_003315964.2:g.112622T>C, NW_003315964.2:g.112622T>G, NR_024523.1:n.688T>C, NR_024523.1:n.688T>G

Select item 147627646618.

rs1476276466 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 19:21751991 (GRCh38)
19:21934793 (GRCh37)
Canonical SPDI:: NC_000019.10:21751990:C:A,NC_000019.10:21751990:C:T
Gene:: ZNF100 (Varview), CCNYL6 (Varview)
Functional Consequence:: non_coding_transcript_variant,upstream_transcript_variant,intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
A=0.000011/3 (TOPMED)
HGVS:: NC_000019.10:g.21751991C>A, NC_000019.10:g.21751991C>T, NC_000019.9:g.21934793C>A, NC_000019.9:g.21934793C>T, NG_054926.1:g.20638G>T, NG_054926.1:g.20638G>A, NW_003315964.2:g.113181C>A, NW_003315964.2:g.113181C>T, NR_024523.1:n.1247C>A, NR_024523.1:n.1247C>T

Select item 147500143019.

rs1475001430 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 19:21751803 (GRCh38)
19:21934605 (GRCh37)
Canonical SPDI:: NC_000019.10:21751802:T:C
Gene:: ZNF100 (Varview), CCNYL6 (Varview)
Functional Consequence:: non_coding_transcript_variant,upstream_transcript_variant,intron_variant,genic_upstream_transcript_variant
Validated:: by frequency
MAF:: C=0.000007/1 (GnomAD)
HGVS:: NC_000019.10:g.21751803T>C, NC_000019.9:g.21934605T>C, NG_054926.1:g.20826A>G, NW_003315964.2:g.112993T>C, NR_024523.1:n.1059T>C

Select item 147357023220.

rs1473570232 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 19:21750761 (GRCh38)
19:21933563 (GRCh37)
Canonical SPDI:: NC_000019.10:21750760:T:C,NC_000019.10:21750760:T:G
Gene:: ZNF100 (Varview), CCNYL6 (Varview)
Functional Consequence:: non_coding_transcript_variant,upstream_transcript_variant,intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
C=0.000008/2 (TOPMED)
C=0.000029/4 (GnomAD)
G=0.000035/1 (TOMMO)
HGVS:: NC_000019.10:g.21750761T>C, NC_000019.10:g.21750761T>G, NC_000019.9:g.21933563T>C, NC_000019.9:g.21933563T>G, NG_054926.1:g.21868A>G, NG_054926.1:g.21868A>C, NW_003315964.2:g.111951T>C, NW_003315964.2:g.111951T>G, NR_024523.1:n.17T>C, NR_024523.1:n.17T>G