SNP Links for Nucleotide (Select 589908414) - SNP

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Links from Nucleotide

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Select item 14904178501.

rs1490417850 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 20:23772925 (GRCh38)
20:23753562 (GRCh37)
Canonical SPDI:: NC_000020.11:23772924:T:C
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
HGVS:: NC_000020.11:g.23772925T>C, NC_000020.10:g.23753562T>C, NG_029332.2:g.3345A>G

Select item 14893033052.

rs1489303305 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 20:23773329 (GRCh38)
20:23753966 (GRCh37)
Canonical SPDI:: NC_000020.11:23773328:T:G
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000020.11:g.23773329T>G, NC_000020.10:g.23753966T>G, NG_029332.2:g.2941A>C

Select item 14892610893.

rs1489261089 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 20:23774385 (GRCh38)
20:23755022 (GRCh37)
Canonical SPDI:: NC_000020.11:23774384:A:G
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000011/3 (TOPMED)
G=0.000014/2 (GnomAD)
HGVS:: NC_000020.11:g.23774385A>G, NC_000020.10:g.23755022A>G, NG_029332.2:g.1885T>C

Select item 14881711874.

rs1488171187 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 20:23776051 (GRCh38)
20:23756688 (GRCh37)
Canonical SPDI:: NC_000020.11:23776050:C:T
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000014/2 (GnomAD)
HGVS:: NC_000020.11:g.23776051C>T, NC_000020.10:g.23756688C>T, NG_029332.2:g.219G>A

Select item 14875119915.

rs1487511991 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 20:23773089 (GRCh38)
20:23753726 (GRCh37)
Canonical SPDI:: NC_000020.11:23773088:T:C
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000020.11:g.23773089T>C, NC_000020.10:g.23753726T>C, NG_029332.2:g.3181A>G

Select item 14873619906.

rs1487361990 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G [Show Flanks]
Chromosome:: 20:23776246 (GRCh38)
20:23756883 (GRCh37)
Canonical SPDI:: NC_000020.11:23776245:A:C,NC_000020.11:23776245:A:G
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000020.11:g.23776246A>C, NC_000020.11:g.23776246A>G, NC_000020.10:g.23756883A>C, NC_000020.10:g.23756883A>G, NG_029332.2:g.24T>G, NG_029332.2:g.24T>C

Select item 14868015707.

rs1486801570 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 20:23774780 (GRCh38)
20:23755417 (GRCh37)
Canonical SPDI:: NC_000020.11:23774779:T:G
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000020.11:g.23774780T>G, NC_000020.10:g.23755417T>G, NG_029332.2:g.1490A>C

Select item 14860207038.

rs1486020703 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 20:23776027 (GRCh38)
20:23756664 (GRCh37)
Canonical SPDI:: NC_000020.11:23776026:G:A
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000020.11:g.23776027G>A, NC_000020.10:g.23756664G>A, NG_029332.2:g.243C>T

Select item 14856282489.

rs1485628248 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 20:23773393 (GRCh38)
20:23754030 (GRCh37)
Canonical SPDI:: NC_000020.11:23773392:A:G
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000020.11:g.23773393A>G, NC_000020.10:g.23754030A>G, NG_029332.2:g.2877T>C

Select item 148551541810.

rs1485515418 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 20:23773545 (GRCh38)
20:23754182 (GRCh37)
Canonical SPDI:: NC_000020.11:23773544:A:G
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000054/1 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000014/2 (GnomAD)
HGVS:: NC_000020.11:g.23773545A>G, NC_000020.10:g.23754182A>G, NG_029332.2:g.2725T>C

Select item 148467669911.

rs1484676699 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 20:23776215 (GRCh38)
20:23756852 (GRCh37)
Canonical SPDI:: NC_000020.11:23776214:G:A
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000036/5 (GnomAD)
HGVS:: NC_000020.11:g.23776215G>A, NC_000020.10:g.23756852G>A, NG_029332.2:g.55C>T

Select item 148451004612.

rs1484510046 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 20:23774347 (GRCh38)
20:23754984 (GRCh37)
Canonical SPDI:: NC_000020.11:23774346:C:A,NC_000020.11:23774346:C:T
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
A=0.000007/1 (GnomAD)
T=0.000342/1 (KOREAN)
HGVS:: NC_000020.11:g.23774347C>A, NC_000020.11:g.23774347C>T, NC_000020.10:g.23754984C>A, NC_000020.10:g.23754984C>T, NG_029332.2:g.1923G>T, NG_029332.2:g.1923G>A

Select item 148259530113.

rs1482595301 [Homo sapiens]

Variant type:: DELINS
Alleles:: TGCC>- [Show Flanks]
Chromosome:: 20:23776122 (GRCh38)
20:23756759 (GRCh37)
Canonical SPDI:: NC_000020.11:23776120:CTGCC:C
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
-=0.000011/3 (TOPMED)
-=0.000021/3 (GnomAD)
HGVS:: NC_000020.11:g.23776122_23776125del, NC_000020.10:g.23756759_23756762del, NG_029332.2:g.146_149del

Select item 148206563314.

rs1482065633 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 20:23773500 (GRCh38)
20:23754137 (GRCh37)
Canonical SPDI:: NC_000020.11:23773499:C:G,NC_000020.11:23773499:C:T
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000020.11:g.23773500C>G, NC_000020.11:g.23773500C>T, NC_000020.10:g.23754137C>G, NC_000020.10:g.23754137C>T, NG_029332.2:g.2770G>C, NG_029332.2:g.2770G>A

Select item 148011859915.

rs1480118599 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 20:23774119 (GRCh38)
20:23754756 (GRCh37)
Canonical SPDI:: NC_000020.11:23774118:T:G
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000014/2 (GnomAD)
HGVS:: NC_000020.11:g.23774119T>G, NC_000020.10:g.23754756T>G, NG_029332.2:g.2151A>C

Select item 147896319816.

rs1478963198 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,G [Show Flanks]
Chromosome:: 20:23774147 (GRCh38)
20:23754784 (GRCh37)
Canonical SPDI:: NC_000020.11:23774146:T:A,NC_000020.11:23774146:T:G
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000020.11:g.23774147T>A, NC_000020.11:g.23774147T>G, NC_000020.10:g.23754784T>A, NC_000020.10:g.23754784T>G, NG_029332.2:g.2123A>T, NG_029332.2:g.2123A>C

Select item 147880097717.

rs1478800977 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 20:23773622 (GRCh38)
20:23754259 (GRCh37)
Canonical SPDI:: NC_000020.11:23773621:C:A
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000020.11:g.23773622C>A, NC_000020.10:g.23754259C>A, NG_029332.2:g.2648G>T

Select item 147816840218.

rs1478168402 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 20:23774189 (GRCh38)
20:23754826 (GRCh37)
Canonical SPDI:: NC_000020.11:23774188:C:T
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000020.11:g.23774189C>T, NC_000020.10:g.23754826C>T, NG_029332.2:g.2081G>A

Select item 147771027419.

rs1477710274 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 20:23775639 (GRCh38)
20:23756276 (GRCh37)
Canonical SPDI:: NC_000020.11:23775638:C:A
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000011/3 (TOPMED)
A=0.000014/2 (GnomAD)
HGVS:: NC_000020.11:g.23775639C>A, NC_000020.10:g.23756276C>A, NG_029332.2:g.631G>T

Select item 147457288120.

rs1474572881 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 20:23775172 (GRCh38)
20:23755809 (GRCh37)
Canonical SPDI:: NC_000020.11:23775171:C:A
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000020.11:g.23775172C>A, NC_000020.10:g.23755809C>A, NG_029332.2:g.1098G>T