SNP Links for Nucleotide (Select 951234120) - SNP

Warning: The NCBI web site requires JavaScript to function. more...

Links from Nucleotide

Items: 1 to 20 of 102

<< First< Prev

Page of 6

Next >Last >>

Select item 14845678621.

rs1484567862 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 2:127170044 (GRCh38)
2:127927620 (GRCh37)
Canonical SPDI:: NC_000002.12:127170043:G:T
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000002.12:g.127170044G>T, NC_000002.11:g.127927620G>T, NG_045146.1:g.134G>T

Select item 14825993862.

rs1482599386 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 2:127170129 (GRCh38)
2:127927705 (GRCh37)
Canonical SPDI:: NC_000002.12:127170128:G:T
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000002.12:g.127170129G>T, NC_000002.11:g.127927705G>T, NG_045146.1:g.219G>T

Select item 14698692113.

rs1469869211 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 2:127170179 (GRCh38)
2:127927755 (GRCh37)
Canonical SPDI:: NC_000002.12:127170178: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_000002.12:g.127170179T>C, NC_000002.11:g.127927755T>C, NG_045146.1:g.269T>C

Select item 14645361584.

rs1464536158 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 2:127170090 (GRCh38)
2:127927666 (GRCh37)
Canonical SPDI:: NC_000002.12:127170089:A:G
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
HGVS:: NC_000002.12:g.127170090A>G, NC_000002.11:g.127927666A>G, NG_045146.1:g.180A>G

Select item 14558133305.

rs1455813330 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 2:127170319 (GRCh38)
2:127927895 (GRCh37)
Canonical SPDI:: NC_000002.12:127170318:C:T
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000002.12:g.127170319C>T, NC_000002.11:g.127927895C>T, NG_045146.1:g.409C>T

Select item 14474390766.

rs1447439076 [Homo sapiens]

Variant type:: DEL
Alleles:: AT>- [Show Flanks]
Chromosome:: 2:127169950 (GRCh38)
2:127927526 (GRCh37)
Canonical SPDI:: NC_000002.12:127169949:AT:
Validated:: by frequency
MAF:: -=0.000007/1 (GnomAD)
HGVS:: NC_000002.12:g.127169950_127169951del, NC_000002.11:g.127927526_127927527del, NG_045146.1:g.40_41del

Select item 14470535477.

rs1447053547 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 2:127170052 (GRCh38)
2:127927628 (GRCh37)
Canonical SPDI:: NC_000002.12:127170051:G:A
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000002.12:g.127170052G>A, NC_000002.11:g.127927628G>A, NG_045146.1:g.142G>A

Select item 14422365248.

rs1442236524 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 2:127170016 (GRCh38)
2:127927592 (GRCh37)
Canonical SPDI:: NC_000002.12:127170015:T:C
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.001566/7 (ALFA)
C=0.00005/7 (GnomAD)
C=0.001339/6 (Estonian)
HGVS:: NC_000002.12:g.127170016T>C, NC_000002.11:g.127927592T>C, NG_045146.1:g.106T>C

Select item 14372457849.

rs1437245784 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 2:127170115 (GRCh38)
2:127927691 (GRCh37)
Canonical SPDI:: NC_000002.12:127170114:C:A
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000002.12:g.127170115C>A, NC_000002.11:g.127927691C>A, NG_045146.1:g.205C>A

Select item 142414949010.

rs1424149490 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 2:127170096 (GRCh38)
2:127927672 (GRCh37)
Canonical SPDI:: NC_000002.12:127170095:G:A,NC_000002.12:127170095:G:C
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
HGVS:: NC_000002.12:g.127170096G>A, NC_000002.12:g.127170096G>C, NC_000002.11:g.127927672G>A, NC_000002.11:g.127927672G>C, NG_045146.1:g.186G>A, NG_045146.1:g.186G>C

Select item 142255683611.

rs1422556836 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 2:127170186 (GRCh38)
2:127927762 (GRCh37)
Canonical SPDI:: NC_000002.12:127170185:G:A
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000019/5 (TOPMED)
HGVS:: NC_000002.12:g.127170186G>A, NC_000002.11:g.127927762G>A, NG_045146.1:g.276G>A

Select item 142124795012.

rs1421247950 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 2:127170166 (GRCh38)
2:127927742 (GRCh37)
Canonical SPDI:: NC_000002.12:127170165:G:A
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000002.12:g.127170166G>A, NC_000002.11:g.127927742G>A, NG_045146.1:g.256G>A

Select item 140230664113.

rs1402306641 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 2:127170066 (GRCh38)
2:127927642 (GRCh37)
Canonical SPDI:: NC_000002.12:127170065:G:A
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000002.12:g.127170066G>A, NC_000002.11:g.127927642G>A, NG_045146.1:g.156G>A

Select item 138168959114.

rs1381689591 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 2:127169973 (GRCh38)
2:127927549 (GRCh37)
Canonical SPDI:: NC_000002.12:127169972:G:A
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000011/3 (TOPMED)
A=0.000036/5 (GnomAD)
HGVS:: NC_000002.12:g.127169973G>A, NC_000002.11:g.127927549G>A, NG_045146.1:g.63G>A

Select item 137817818815.

rs1378178188 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 2:127169989 (GRCh38)
2:127927565 (GRCh37)
Canonical SPDI:: NC_000002.12:127169988: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_000002.12:g.127169989A>G, NC_000002.11:g.127927565A>G, NG_045146.1:g.79A>G

Select item 136912255216.

rs1369122552 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 2:127170180 (GRCh38)
2:127927756 (GRCh37)
Canonical SPDI:: NC_000002.12:127170179:G:A,NC_000002.12:127170179:G:C
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000021/3 (GnomAD)
C=0.000042/11 (TOPMED)
HGVS:: NC_000002.12:g.127170180G>A, NC_000002.12:g.127170180G>C, NC_000002.11:g.127927756G>A, NC_000002.11:g.127927756G>C, NG_045146.1:g.270G>A, NG_045146.1:g.270G>C

Select item 136596802817.

rs1365968028 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 2:127169961 (GRCh38)
2:127927537 (GRCh37)
Canonical SPDI:: NC_000002.12:127169960:C:T
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000014/2 (GnomAD)
T=0.000015/4 (TOPMED)
T=0.000035/1 (TOMMO)
HGVS:: NC_000002.12:g.127169961C>T, NC_000002.11:g.127927537C>T, NG_045146.1:g.51C>T

Select item 135846106018.

rs1358461060 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 2:127169937 (GRCh38)
2:127927513 (GRCh37)
Canonical SPDI:: NC_000002.12:127169936:A:T
Validated:: by frequency
MAF:: T=0.000007/1 (GnomAD)
HGVS:: NC_000002.12:g.127169937A>T, NC_000002.11:g.127927513A>T, NG_045146.1:g.27A>T

Select item 135631737419.

rs1356317374 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 2:127170136 (GRCh38)
2:127927712 (GRCh37)
Canonical SPDI:: NC_000002.12:127170135:T:C
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000002.12:g.127170136T>C, NC_000002.11:g.127927712T>C, NG_045146.1:g.226T>C

Select item 135430599920.

rs1354305999 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 2:127170235 (GRCh38)
2:127927811 (GRCh37)
Canonical SPDI:: NC_000002.12:127170234:T:G
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
HGVS:: NC_000002.12:g.127170235T>G, NC_000002.11:g.127927811T>G, NG_045146.1:g.325T>G