SNP Links for Nucleotide (Select 281183138) - SNP

Links from Nucleotide

Items: 1 to 20 of 166

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Select item 14835892701.

rs1483589270 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 7:64933253 (GRCh38)
7:64393631 (GRCh37)
Canonical SPDI:: NC_000007.14:64933252:G:A
Gene:: ZNF273 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000011/3 (TOPMED)
HGVS:: NC_000007.14:g.64933253G>A, NC_000007.13:g.64393631G>A, NG_015652.1:g.81G>A

Select item 14754607032.

rs1475460703 [Homo sapiens]

Variant type:: DEL
Alleles:: C>- [Show Flanks]
Chromosome:: 7:64933574 (GRCh38)
7:64393952 (GRCh37)
Canonical SPDI:: NC_000007.14:64933573:C:
Gene:: ZNF273 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.000014/2 (GnomAD)
-=0.000015/4 (TOPMED)
HGVS:: NC_000007.14:g.64933574del, NC_000007.13:g.64393952del, NG_015652.1:g.402del

Select item 14645565593.

rs1464556559 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 7:64933221 (GRCh38)
7:64393599 (GRCh37)
Canonical SPDI:: NC_000007.14:64933220:C:T
Gene:: ZNF273 (Varview)
Functional Consequence:: intron_variant,genic_downstream_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_000007.14:g.64933221C>T, NC_000007.13:g.64393599C>T, NG_015652.1:g.49C>T

Select item 14508179864.

rs1450817986 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 7:64933589 (GRCh38)
7:64393967 (GRCh37)
Canonical SPDI:: NC_000007.14:64933588:G:A
Gene:: ZNF273 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_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_000007.14:g.64933589G>A, NC_000007.13:g.64393967G>A, NG_015652.1:g.417G>A

Select item 14423976205.

rs1442397620 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 7:64933337 (GRCh38)
7:64393715 (GRCh37)
Canonical SPDI:: NC_000007.14:64933336:A:G
Gene:: ZNF273 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000014/2 (GnomAD)
G=0.000023/6 (TOPMED)
HGVS:: NC_000007.14:g.64933337A>G, NC_000007.13:g.64393715A>G, NG_015652.1:g.165A>G

Select item 14361093046.

rs1436109304 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 7:64933649 (GRCh38)
7:64394027 (GRCh37)
Canonical SPDI:: NC_000007.14:64933648:A:C
Gene:: ZNF273 (Varview)
Functional Consequence:: intron_variant,genic_downstream_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_000007.14:g.64933649A>C, NC_000007.13:g.64394027A>C, NG_015652.1:g.477A>C

Select item 14288957017.

rs1428895701 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: 7:64933209 (GRCh38)
7:64393587 (GRCh37)
Canonical SPDI:: NC_000007.14:64933208:A:G,NC_000007.14:64933208:A:T
Gene:: ZNF273 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000007.14:g.64933209A>G, NC_000007.14:g.64933209A>T, NC_000007.13:g.64393587A>G, NC_000007.13:g.64393587A>T, NG_015652.1:g.37A>G, NG_015652.1:g.37A>T

Select item 14284256968.

rs1428425696 [Homo sapiens]

Variant type:: DEL
Alleles:: C>- [Show Flanks]
Chromosome:: 7:64933568 (GRCh38)
7:64393946 (GRCh37)
Canonical SPDI:: NC_000007.14:64933567:C:
Gene:: ZNF273 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.000004/1 (TOPMED)
HGVS:: NC_000007.14:g.64933568del, NC_000007.13:g.64393946del, NG_015652.1:g.396del

Select item 14271571059.

rs1427157105 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 7:64933463 (GRCh38)
7:64393841 (GRCh37)
Canonical SPDI:: NC_000007.14:64933462:T:A
Gene:: ZNF273 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000021/3 (GnomAD)
HGVS:: NC_000007.14:g.64933463T>A, NC_000007.13:g.64393841T>A, NG_015652.1:g.291T>A

Select item 141344063710.

rs1413440637 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C [Show Flanks]
Chromosome:: 7:64933749 (GRCh38)
7:64394127 (GRCh37)
Canonical SPDI:: NC_000007.14:64933748:T:A,NC_000007.14:64933748:T:C
Gene:: ZNF273 (Varview)
Functional Consequence:: intron_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
HGVS:: NC_000007.14:g.64933749T>A, NC_000007.14:g.64933749T>C, NC_000007.13:g.64394127T>A, NC_000007.13:g.64394127T>C, NG_015652.1:g.577T>A, NG_015652.1:g.577T>C

Select item 140994612311.

rs1409946123 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 7:64933313 (GRCh38)
7:64393691 (GRCh37)
Canonical SPDI:: NC_000007.14:64933312:A:T
Gene:: ZNF273 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_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_000007.14:g.64933313A>T, NC_000007.13:g.64393691A>T, NG_015652.1:g.141A>T

Select item 140624122512.

rs1406241225 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 7:64933831 (GRCh38)
7:64394209 (GRCh37)
Canonical SPDI:: NC_000007.14:64933830:A:G
Gene:: ZNF273 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000007.14:g.64933831A>G, NC_000007.13:g.64394209A>G, NG_015652.1:g.659A>G

Select item 140507292013.

rs1405072920 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 7:64933560 (GRCh38)
7:64393938 (GRCh37)
Canonical SPDI:: NC_000007.14:64933559:C:G,NC_000007.14:64933559:C:T
Gene:: ZNF273 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
HGVS:: NC_000007.14:g.64933560C>G, NC_000007.14:g.64933560C>T, NC_000007.13:g.64393938C>G, NC_000007.13:g.64393938C>T, NG_015652.1:g.388C>G, NG_015652.1:g.388C>T

Select item 140350151314.

rs1403501513 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 7:64933281 (GRCh38)
7:64393659 (GRCh37)
Canonical SPDI:: NC_000007.14:64933280:C:A
Gene:: ZNF273 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency
MAF:: A=0.000007/1 (GnomAD)
HGVS:: NC_000007.14:g.64933281C>A, NC_000007.13:g.64393659C>A, NG_015652.1:g.109C>A

Select item 140156021315.

rs1401560213 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 7:64933300 (GRCh38)
7:64393678 (GRCh37)
Canonical SPDI:: NC_000007.14:64933299:G:A
Gene:: ZNF273 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000014/2 (GnomAD)
A=0.000015/4 (TOPMED)
HGVS:: NC_000007.14:g.64933300G>A, NC_000007.13:g.64393678G>A, NG_015652.1:g.128G>A

Select item 140017246416.

rs1400172464 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 7:64933310 (GRCh38)
7:64393688 (GRCh37)
Canonical SPDI:: NC_000007.14:64933309:T:C
Gene:: ZNF273 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000142/2 (ALFA)
C=0.000014/2 (GnomAD)
C=0.00003/8 (TOPMED)
HGVS:: NC_000007.14:g.64933310T>C, NC_000007.13:g.64393688T>C, NG_015652.1:g.138T>C

Select item 139426299017.

rs1394262990 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 7:64933292 (GRCh38)
7:64393670 (GRCh37)
Canonical SPDI:: NC_000007.14:64933291:T:G
Gene:: ZNF273 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000011/3 (TOPMED)
HGVS:: NC_000007.14:g.64933292T>G, NC_000007.13:g.64393670T>G, NG_015652.1:g.120T>G

Select item 139390932818.

rs1393909328 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 7:64933562 (GRCh38)
7:64393940 (GRCh37)
Canonical SPDI:: NC_000007.14:64933561:A:G
Gene:: ZNF273 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000019/5 (TOPMED)
G=0.000029/4 (GnomAD)
HGVS:: NC_000007.14:g.64933562A>G, NC_000007.13:g.64393940A>G, NG_015652.1:g.390A>G

Select item 138705957519.

rs1387059575 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 7:64933206 (GRCh38)
7:64393584 (GRCh37)
Canonical SPDI:: NC_000007.14:64933205:C:T
Gene:: ZNF273 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_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_000007.14:g.64933206C>T, NC_000007.13:g.64393584C>T, NG_015652.1:g.34C>T

Select item 138662245520.

rs1386622455 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 7:64933395 (GRCh38)
7:64393773 (GRCh37)
Canonical SPDI:: NC_000007.14:64933394:A:G
Gene:: ZNF273 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_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_000007.14:g.64933395A>G, NC_000007.13:g.64393773A>G, NG_015652.1:g.223A>G

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