SNP Links for Nucleotide (Select 937347221) - SNP

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Links from Nucleotide

Items: 1 to 20 of 46

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Select item 14602311031.

rs1460231103 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 6:53153864 (GRCh38)
6:53018662 (GRCh37)
Canonical SPDI:: NC_000006.12:53153863:C:T
Validated:: by frequency
MAF:: T=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.53153864C>T, NC_000006.11:g.53018662C>T, NG_044129.1:g.135G>A

Select item 14559734892.

rs1455973489 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 6:53153739 (GRCh38)
6:53018537 (GRCh37)
Canonical SPDI:: NC_000006.12:53153738: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_000006.12:g.53153739A>G, NC_000006.11:g.53018537A>G, NG_044129.1:g.260T>C

Select item 14557802503.

rs1455780250 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C [Show Flanks]
Chromosome:: 6:53153846 (GRCh38)
6:53018644 (GRCh37)
Canonical SPDI:: NC_000006.12:53153845:T:A,NC_000006.12:53153845:T:C
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000014/2 (GnomAD)
HGVS:: NC_000006.12:g.53153846T>A, NC_000006.12:g.53153846T>C, NC_000006.11:g.53018644T>A, NC_000006.11:g.53018644T>C, NG_044129.1:g.153A>T, NG_044129.1:g.153A>G

Select item 14353097414.

rs1435309741 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 6:53153721 (GRCh38)
6:53018519 (GRCh37)
Canonical SPDI:: NC_000006.12:53153720:T:G
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.00003/8 (TOPMED)
HGVS:: NC_000006.12:g.53153721T>G, NC_000006.11:g.53018519T>G, NG_044129.1:g.278A>C

Select item 14261173935.

rs1426117393 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 6:53153762 (GRCh38)
6:53018560 (GRCh37)
Canonical SPDI:: NC_000006.12:53153761:T:C
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000008/2 (TOPMED)
HGVS:: NC_000006.12:g.53153762T>C, NC_000006.11:g.53018560T>C, NG_044129.1:g.237A>G

Select item 13921657826.

rs1392165782 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 6:53153933 (GRCh38)
6:53018731 (GRCh37)
Canonical SPDI:: NC_000006.12:53153932:A:G
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
HGVS:: NC_000006.12:g.53153933A>G, NC_000006.11:g.53018731A>G, NG_044129.1:g.66T>C

Select item 13904028577.

rs1390402857 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 6:53153860 (GRCh38)
6:53018658 (GRCh37)
Canonical SPDI:: NC_000006.12:53153859:A:G
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000035/1 (TOMMO)
HGVS:: NC_000006.12:g.53153860A>G, NC_000006.11:g.53018658A>G, NG_044129.1:g.139T>C

Select item 13763136658.

rs1376313665 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 6:53153701 (GRCh38)
6:53018499 (GRCh37)
Canonical SPDI:: NC_000006.12:53153700:G:C
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000008/2 (TOPMED)
HGVS:: NC_000006.12:g.53153701G>C, NC_000006.11:g.53018499G>C, NG_044129.1:g.298C>G

Select item 13622050299.

rs1362205029 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 6:53153828 (GRCh38)
6:53018626 (GRCh37)
Canonical SPDI:: NC_000006.12:53153827:A:G
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000224/1 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000223/1 (Estonian)
HGVS:: NC_000006.12:g.53153828A>G, NC_000006.11:g.53018626A>G, NG_044129.1:g.171T>C

Select item 133705759710.

rs1337057597 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 6:53153886 (GRCh38)
6:53018684 (GRCh37)
Canonical SPDI:: NC_000006.12:53153885: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_000006.12:g.53153886C>T, NC_000006.11:g.53018684C>T, NG_044129.1:g.113G>A

Select item 132741790511.

rs1327417905 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 6:53153877 (GRCh38)
6:53018675 (GRCh37)
Canonical SPDI:: NC_000006.12:53153876:G:A
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000071/1 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.53153877G>A, NC_000006.11:g.53018675G>A, NG_044129.1:g.122C>T

Select item 130179197112.

rs1301791971 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 6:53153704 (GRCh38)
6:53018502 (GRCh37)
Canonical SPDI:: NC_000006.12:53153703:G:A,NC_000006.12:53153703:G:T
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
A=0.00667/4 (NorthernSweden)
HGVS:: NC_000006.12:g.53153704G>A, NC_000006.12:g.53153704G>T, NC_000006.11:g.53018502G>A, NC_000006.11:g.53018502G>T, NG_044129.1:g.295C>T, NG_044129.1:g.295C>A

Select item 129094509313.

rs1290945093 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 6:53153985 (GRCh38)
6:53018783 (GRCh37)
Canonical SPDI:: NC_000006.12:53153984:T:G
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000006.12:g.53153985T>G, NC_000006.11:g.53018783T>G, NG_044129.1:g.14A>C

Select item 128356013614.

rs1283560136 [Homo sapiens]

Variant type:: DELINS
Alleles:: TTA>- [Show Flanks]
Chromosome:: 6:53153907 (GRCh38)
6:53018705 (GRCh37)
Canonical SPDI:: NC_000006.12:53153901:TATTATTA:TATTA
Validated:: by frequency,by alfa,by cluster
MAF:: TATTA=0.000142/2 (ALFA)
-=0.000043/6 (GnomAD)
-=0.000053/14 (TOPMED)
HGVS:: NC_000006.12:g.53153904TTA[1], NC_000006.11:g.53018702TTA[1], NG_044129.1:g.92ATA[1]

Select item 125513063715.

rs1255130637 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 6:53153755 (GRCh38)
6:53018553 (GRCh37)
Canonical SPDI:: NC_000006.12:53153754:T:C
Validated:: by frequency
MAF:: C=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.53153755T>C, NC_000006.11:g.53018553T>C, NG_044129.1:g.244A>G

Select item 125013861316.

rs1250138613 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 6:53153773 (GRCh38)
6:53018571 (GRCh37)
Canonical SPDI:: NC_000006.12:53153772:C:G
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000006.12:g.53153773C>G, NC_000006.11:g.53018571C>G, NG_044129.1:g.226G>C

Select item 124848529917.

rs1248485299 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 6:53153966 (GRCh38)
6:53018764 (GRCh37)
Canonical SPDI:: NC_000006.12:53153965:C:A
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000014/2 (GnomAD)
A=0.000177/3 (TOMMO)
HGVS:: NC_000006.12:g.53153966C>A, NC_000006.11:g.53018764C>A, NG_044129.1:g.33G>T

Select item 123965062218.

rs1239650622 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 6:53153897 (GRCh38)
6:53018695 (GRCh37)
Canonical SPDI:: NC_000006.12:53153896:A:G
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000071/1 (ALFA)
G=0.000011/3 (TOPMED)
G=0.000014/2 (GnomAD)
HGVS:: NC_000006.12:g.53153897A>G, NC_000006.11:g.53018695A>G, NG_044129.1:g.102T>C

Select item 122913172219.

rs1229131722 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 6:53153995 (GRCh38)
6:53018793 (GRCh37)
Canonical SPDI:: NC_000006.12:53153994:C:T
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000006.12:g.53153995C>T, NC_000006.11:g.53018793C>T, NG_044129.1:g.4G>A

Select item 119194243520.

rs1191942435 [Homo sapiens]

Variant type:: DEL
Alleles:: A>- [Show Flanks]
Chromosome:: 6:53153729 (GRCh38)
6:53018527 (GRCh37)
Canonical SPDI:: NC_000006.12:53153728:A:
Validated:: by frequency,by alfa
MAF:: -=0.00007/1 (ALFA)
HGVS:: NC_000006.12:g.53153729del, NC_000006.11:g.53018527del, NG_044129.1:g.270del