SNP Links for Nucleotide (Select 589908509) - SNP

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Links from Nucleotide

Items: 1 to 20 of 159

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Select item 14873317431.

rs1487331743 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 7:143047861 (GRCh38)
7:142744962 (GRCh37)
Canonical SPDI:: NC_000007.14:143047860:T:A
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000015/4 (TOPMED)
HGVS:: NC_000007.14:g.143047861T>A, NC_000007.13:g.142744962T>A, NG_004257.5:g.12A>T, NT_187562.1:g.1070928T>A, NW_003571040.1:g.1250622T>A

Select item 14870733182.

rs1487073318 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 7:143047585 (GRCh38)
7:142744686 (GRCh37)
Canonical SPDI:: NC_000007.14:143047584:C:G,NC_000007.14:143047584:C:T
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000007.14:g.143047585C>G, NC_000007.14:g.143047585C>T, NC_000007.13:g.142744686C>G, NC_000007.13:g.142744686C>T, NG_004257.5:g.288G>C, NG_004257.5:g.288G>A, NT_187562.1:g.1070652C>G, NT_187562.1:g.1070652C>T, NW_003571040.1:g.1250346C>G, NW_003571040.1:g.1250346C>T

Select item 14833031503.

rs1483303150 [Homo sapiens]

Variant type:: DEL
Alleles:: GAGTTGACGCTACATATTTATTAAGG>- [Show Flanks]
Chromosome:: 7:143047739 (GRCh38)
7:142744840 (GRCh37)
Canonical SPDI:: NC_000007.14:143047738:GAGTTGACGCTACATATTTATTAAGG:
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.000014/2 (GnomAD)
HGVS:: NC_000007.14:g.143047739_143047764del, NC_000007.13:g.142744840_142744865del, NG_004257.5:g.109_134del, NT_187562.1:g.1070806_1070831del, NW_003571040.1:g.1250500_1250525del

Select item 14824587184.

rs1482458718 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 7:143047752 (GRCh38)
7:142744853 (GRCh37)
Canonical SPDI:: NC_000007.14:143047751:A:G
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
HGVS:: NC_000007.14:g.143047752A>G, NC_000007.13:g.142744853A>G, NG_004257.5:g.121T>C, NT_187562.1:g.1070819A>G, NW_003571040.1:g.1250513A>G

Select item 14722298995.

rs1472229899 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 7:143047093 (GRCh38)
7:142744194 (GRCh37)
Canonical SPDI:: NC_000007.14:143047092:G:A
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000014/2 (GnomAD)
A=0.000019/5 (TOPMED)
HGVS:: NC_000007.14:g.143047093G>A, NC_000007.13:g.142744194G>A, NG_004257.5:g.780C>T, NT_187562.1:g.1070160G>A, NW_003571040.1:g.1249854G>A

Select item 14715924316.

rs1471592431 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 7:143047100 (GRCh38)
7:142744201 (GRCh37)
Canonical SPDI:: NC_000007.14:143047099: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_000007.14:g.143047100C>T, NC_000007.13:g.142744201C>T, NG_004257.5:g.773G>A, NT_187562.1:g.1070167C>T, NW_003571040.1:g.1249861C>T

Select item 14710874947.

rs1471087494 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 7:143047302 (GRCh38)
7:142744403 (GRCh37)
Canonical SPDI:: NC_000007.14:143047301:T:C
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000011/3 (TOPMED)
HGVS:: NC_000007.14:g.143047302T>C, NC_000007.13:g.142744403T>C, NG_004257.5:g.571A>G, NT_187562.1:g.1070369T>C, NW_003571040.1:g.1250063T>C

Select item 14512872548.

rs1451287254 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 7:143047316 (GRCh38)
7:142744417 (GRCh37)
Canonical SPDI:: NC_000007.14:143047315:G:A,NC_000007.14:143047315:G:C
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
HGVS:: NC_000007.14:g.143047316G>A, NC_000007.14:g.143047316G>C, NC_000007.13:g.142744417G>A, NC_000007.13:g.142744417G>C, NG_004257.5:g.557C>T, NG_004257.5:g.557C>G, NT_187562.1:g.1070383G>A, NT_187562.1:g.1070383G>C, NW_003571040.1:g.1250077G>A, NW_003571040.1:g.1250077G>C

Select item 14350988489.

rs1435098848 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 7:143047372 (GRCh38)
7:142744473 (GRCh37)
Canonical SPDI:: NC_000007.14:143047371:C:G
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000023/6 (TOPMED)
G=0.000029/4 (GnomAD)
HGVS:: NC_000007.14:g.143047372C>G, NC_000007.13:g.142744473C>G, NG_004257.5:g.501G>C, NT_187562.1:g.1070439C>G, NW_003571040.1:g.1250133C>G

Select item 143046294510.

rs1430462945 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 7:143047715 (GRCh38)
7:142744816 (GRCh37)
Canonical SPDI:: NC_000007.14:143047714:G:A
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000008/2 (TOPMED)
HGVS:: NC_000007.14:g.143047715G>A, NC_000007.13:g.142744816G>A, NG_004257.5:g.158C>T, NT_187562.1:g.1070782G>A, NW_003571040.1:g.1250476G>A

Select item 142959078411.

rs1429590784 [Homo sapiens]

Variant type:: SNV:
Alleles:: C>G
Chromosome:: no mapping
Canonical SPDI:

Select item 142508839512.

rs1425088395 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 7:143047763 (GRCh38)
7:142744864 (GRCh37)
Canonical SPDI:: NC_000007.14:143047762:G:A
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000007.14:g.143047763G>A, NC_000007.13:g.142744864G>A, NG_004257.5:g.110C>T, NT_187562.1:g.1070830G>A, NW_003571040.1:g.1250524G>A

Select item 142098347313.

rs1420983473 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 7:143047073 (GRCh38)
7:142744174 (GRCh37)
Canonical SPDI:: NC_000007.14:143047072:A:G
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
HGVS:: NC_000007.14:g.143047073A>G, NC_000007.13:g.142744174A>G, NG_004257.5:g.800T>C, NT_187562.1:g.1070140A>G, NW_003571040.1:g.1249834A>G

Select item 141722368214.

rs1417223682 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 7:143047046 (GRCh38)
7:142744147 (GRCh37)
Canonical SPDI:: NC_000007.14:143047045:G:T
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.143047046G>T, NC_000007.13:g.142744147G>T, NG_004257.5:g.827C>A, NT_187562.1:g.1070113G>T, NW_003571040.1:g.1249807G>T

Select item 141539818515.

rs1415398185 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 7:143047665 (GRCh38)
7:142744766 (GRCh37)
Canonical SPDI:: NC_000007.14:143047664:C:T
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000019/5 (TOPMED)
T=0.000342/1 (KOREAN)
HGVS:: NC_000007.14:g.143047665C>T, NC_000007.13:g.142744766C>T, NG_004257.5:g.208G>A, NT_187562.1:g.1070732C>T, NW_003571040.1:g.1250426C>T

Select item 141097921616.

rs1410979216 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 7:143047646 (GRCh38)
7:142744747 (GRCh37)
Canonical SPDI:: NC_000007.14:143047645:C:T
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000094/1 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000008/2 (TOPMED)
HGVS:: NC_000007.14:g.143047646C>T, NC_000007.13:g.142744747C>T, NG_004257.5:g.227G>A, NT_187562.1:g.1070713C>T, NW_003571040.1:g.1250407C>T

Select item 140446912617.

rs1404469126 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 7:143047248 (GRCh38)
7:142744349 (GRCh37)
Canonical SPDI:: NC_000007.14:143047247:A:G
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000007.14:g.143047248A>G, NC_000007.13:g.142744349A>G, NG_004257.5:g.625T>C, NT_187562.1:g.1070315A>G, NW_003571040.1:g.1250009A>G

Select item 140244307818.

rs1402443078 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 7:143047415 (GRCh38)
7:142744516 (GRCh37)
Canonical SPDI:: NC_000007.14:143047414:G:A,NC_000007.14:143047414:G:C
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000007.14:g.143047415G>A, NC_000007.14:g.143047415G>C, NC_000007.13:g.142744516G>A, NC_000007.13:g.142744516G>C, NG_004257.5:g.458C>T, NG_004257.5:g.458C>G, NT_187562.1:g.1070482G>A, NT_187562.1:g.1070482G>C, NW_003571040.1:g.1250176G>A, NW_003571040.1:g.1250176G>C

Select item 139583441919.

rs1395834419 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 7:143047575 (GRCh38)
7:142744676 (GRCh37)
Canonical SPDI:: NC_000007.14:143047574:G:A
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000011/3 (TOPMED)
HGVS:: NC_000007.14:g.143047575G>A, NC_000007.13:g.142744676G>A, NG_004257.5:g.298C>T, NT_187562.1:g.1070642G>A, NW_003571040.1:g.1250336G>A

Select item 138923035820.

rs1389230358 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 7:143047834 (GRCh38)
7:142744935 (GRCh37)
Canonical SPDI:: NC_000007.14:143047833:T:C
Validated:: by frequency,by alfa
MAF:: C=0.000071/1 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000007.14:g.143047834T>C, NC_000007.13:g.142744935T>C, NG_004257.5:g.39A>G, NT_187562.1:g.1070901T>C, NW_003571040.1:g.1250595T>C

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