SNP Links for Nucleotide (Select 219521904) - SNP

Links from Nucleotide

Items: 1 to 20 of 1501

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Select item 14909904691.

rs1490990469 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTAC>- [Show Flanks]
Chromosome:: 16:46518276 (GRCh38)
16:46552188 (GRCh37)
Canonical SPDI:: NC_000016.10:46518273:ACTTAC:AC
Gene:: ANKRD26P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AC=0./0 (ALFA)
-=0.000034/9 (TOPMED)
-=0.000043/6 (GnomAD)
HGVS:: NC_000016.10:g.46518276_46518279del, NC_000016.9:g.46552188_46552191del, NR_026556.1:n.1176_1179del, NM_001004299.1:c.*28_*31del

Select item 14907515882.

rs1490751588 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 16:46471490 (GRCh38)
16:46505402 (GRCh37)
Canonical SPDI:: NC_000016.10:46471489:A:G
Gene:: ANKRD26P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000014/2 (GnomAD)
G=0.000015/4 (TOPMED)
HGVS:: NC_000016.10:g.46471490A>G, NC_000016.9:g.46505402A>G, NR_026556.1:n.3970T>C

Select item 14905885103.

rs1490588510 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 16:46471118 (GRCh38)
16:46505030 (GRCh37)
Canonical SPDI:: NC_000016.10:46471117:A:C
Gene:: ANKRD26P1 (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_000016.10:g.46471118A>C, NC_000016.9:g.46505030A>C, NR_026556.1:n.4342T>G

Select item 14904089144.

rs1490408914 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 16:46563870 (GRCh38)
16:46597782 (GRCh37)
Canonical SPDI:: NC_000016.10:46563869:T:C
Gene:: ANKRD26P1 (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)
C=0.000849/14 (TOMMO)
C=0.001092/2 (Korea1K)
HGVS:: NC_000016.10:g.46563870T>C, NC_000016.9:g.46597782T>C, NR_026556.1:n.703A>G, NM_001004299.1:c.521A>G

Select item 14897525895.

rs1489752589 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 16:46470688 (GRCh38)
16:46504600 (GRCh37)
Canonical SPDI:: NC_000016.10:46470687:C:A
Gene:: ANKRD26P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000016.10:g.46470688C>A, NC_000016.9:g.46504600C>A, NR_026556.1:n.4772G>T

Select item 14894688146.

rs1489468814 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 16:46518254 (GRCh38)
16:46552166 (GRCh37)
Canonical SPDI:: NC_000016.10:46518253:T:C
Gene:: ANKRD26P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
C=0.000014/2 (GnomAD)
C=0.000035/1 (TOMMO)
C=0.000546/1 (Korea1K)
HGVS:: NC_000016.10:g.46518254T>C, NC_000016.9:g.46552166T>C, NR_026556.1:n.1199A>G, NM_001004299.1:c.*51A>G

Select item 14886076747.

rs1488607674 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 16:46474257 (GRCh38)
16:46508169 (GRCh37)
Canonical SPDI:: NC_000016.10:46474256:A:C
Gene:: ANKRD26P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000016.10:g.46474257A>C, NC_000016.9:g.46508169A>C, NR_026556.1:n.3523T>G, NM_001004299.1:c.*2375T>G

Select item 14880898548.

rs1488089854 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 16:46470172 (GRCh38)
16:46504084 (GRCh37)
Canonical SPDI:: NC_000016.10:46470171:G:T
Gene:: ANKRD26P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000008/2 (TOPMED)
HGVS:: NC_000016.10:g.46470172G>T, NC_000016.9:g.46504084G>T, NR_026556.1:n.5288C>A

Select item 14870012849.

rs1487001284 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 16:46478402 (GRCh38)
16:46512314 (GRCh37)
Canonical SPDI:: NC_000016.10:46478401:C:G,NC_000016.10:46478401:C:T
Gene:: ANKRD26P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
G=0.000007/1 (GnomAD_exomes)
HGVS:: NC_000016.10:g.46478402C>G, NC_000016.10:g.46478402C>T, NC_000016.9:g.46512314C>G, NC_000016.9:g.46512314C>T, NR_026556.1:n.3148G>C, NR_026556.1:n.3148G>A, NM_001004299.1:c.*2000G>C, NM_001004299.1:c.*2000G>A

Select item 148528825710.

rs1485288257 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 16:46471023 (GRCh38)
16:46504935 (GRCh37)
Canonical SPDI:: NC_000016.10:46471022:T:C
Gene:: ANKRD26P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0.000071/1 (ALFA)
C=0.000008/2 (TOPMED)
HGVS:: NC_000016.10:g.46471023T>C, NC_000016.9:g.46504935T>C, NR_026556.1:n.4437A>G

Select item 148453984211.

rs1484539842 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 16:46568740 (GRCh38)
16:46602652 (GRCh37)
Canonical SPDI:: NC_000016.10:46568739:C:T
Gene:: ANKRD26P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000224/1 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000156/1 (1000Genomes)
T=0.000223/1 (Estonian)
HGVS:: NC_000016.10:g.46568740C>T, NC_000016.9:g.46602652C>T, NR_026556.1:n.358G>A, NM_001004299.1:c.176G>A

Select item 148389090512.

rs1483890905 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 16:46479276 (GRCh38)
16:46513188 (GRCh37)
Canonical SPDI:: NC_000016.10:46479275:C:T
Gene:: ANKRD26P1 (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_000016.10:g.46479276C>T, NC_000016.9:g.46513188C>T, NR_026556.1:n.2862G>A, NM_001004299.1:c.*1714G>A

Select item 148388110813.

rs1483881108 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 16:46500361 (GRCh38)
16:46534273 (GRCh37)
Canonical SPDI:: NC_000016.10:46500360:G:C
Gene:: ANKRD26P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: C=0.000008/1 (GnomAD_exomes)
HGVS:: NC_000016.10:g.46500361G>C, NC_000016.9:g.46534273G>C, NR_026556.1:n.2146C>G, NM_001004299.1:c.*998C>G

Select item 148354795714.

rs1483547957 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C,T [Show Flanks]
Chromosome:: 16:46478522 (GRCh38)
16:46512434 (GRCh37)
Canonical SPDI:: NC_000016.10:46478521:G:C,NC_000016.10:46478521:G:T
Gene:: ANKRD26P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by cluster
MAF:: C=0.000007/1 (GnomAD_exomes)
HGVS:: NC_000016.10:g.46478522G>C, NC_000016.10:g.46478522G>T, NC_000016.9:g.46512434G>C, NC_000016.9:g.46512434G>T, NR_026556.1:n.3028C>G, NR_026556.1:n.3028C>A, NM_001004299.1:c.*1880C>G, NM_001004299.1:c.*1880C>A

Select item 148345474915.

rs1483454749 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 16:46470932 (GRCh38)
16:46504844 (GRCh37)
Canonical SPDI:: NC_000016.10:46470931:G:A
Gene:: ANKRD26P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000011/3 (TOPMED)
HGVS:: NC_000016.10:g.46470932G>A, NC_000016.9:g.46504844G>A, NR_026556.1:n.4528C>T

Select item 148331288316.

rs1483312883 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 16:46469345 (GRCh38)
16:46503257 (GRCh37)
Canonical SPDI:: NC_000016.10:46469344:G:C
Gene:: ANKRD26P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000016.10:g.46469345G>C, NC_000016.9:g.46503257G>C, NR_026556.1:n.6115C>G

Select item 148301140217.

rs1483011402 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 16:46475971 (GRCh38)
16:46509883 (GRCh37)
Canonical SPDI:: NC_000016.10:46475970:A:T
Gene:: ANKRD26P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0./0 (GnomAD)
T=0.000007/1 (GnomAD_exomes)
HGVS:: NC_000016.10:g.46475971A>T, NC_000016.9:g.46509883A>T, NR_026556.1:n.3245T>A, NM_001004299.1:c.*2097T>A

Select item 148270050118.

rs1482700501 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 16:46554026 (GRCh38)
16:46587938 (GRCh37)
Canonical SPDI:: NC_000016.10:46554025:T:G
Gene:: ANKRD26P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000014/2 (GnomAD)
G=0.00003/8 (TOPMED)
HGVS:: NC_000016.10:g.46554026T>G, NC_000016.9:g.46587938T>G, NR_026556.1:n.835A>C, NM_001004299.1:c.653A>C

Select item 148253283519.

rs1482532835 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 16:46469803 (GRCh38)
16:46503715 (GRCh37)
Canonical SPDI:: NC_000016.10:46469802:A:G
Gene:: ANKRD26P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000016.10:g.46469803A>G, NC_000016.9:g.46503715A>G, NR_026556.1:n.5657T>C

Select item 148191634320.

rs1481916343 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,G,T [Show Flanks]
Chromosome:: 16:46479220 (GRCh38)
16:46513132 (GRCh37)
Canonical SPDI:: NC_000016.10:46479219:C:A,NC_000016.10:46479219:C:G,NC_000016.10:46479219:C:T
Gene:: ANKRD26P1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by cluster
MAF:: G=0.000007/1 (GnomAD_exomes)
T=0.000035/1 (TOMMO)
HGVS:: NC_000016.10:g.46479220C>A, NC_000016.10:g.46479220C>G, NC_000016.10:g.46479220C>T, NC_000016.9:g.46513132C>A, NC_000016.9:g.46513132C>G, NC_000016.9:g.46513132C>T, NR_026556.1:n.2918G>T, NR_026556.1:n.2918G>C, NR_026556.1:n.2918G>A, NM_001004299.1:c.*1770G>T, NM_001004299.1:c.*1770G>C, NM_001004299.1:c.*1770G>A

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Items: 1 to 20 of 1501

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