SNP Links for Nucleotide (Select 224493794) - SNP

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Links from Nucleotide

Items: 1 to 20 of 153

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Select item 14878617141.

rs1487861714 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 13:21094268 (GRCh38)
13:21668407 (GRCh37)
Canonical SPDI:: NC_000013.11:21094267:T:C
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
HGVS:: NC_000013.11:g.21094268T>C, NC_000013.10:g.21668407T>C, NG_010945.1:g.628A>G

Select item 14830804082.

rs1483080408 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 13:21094565 (GRCh38)
13:21668704 (GRCh37)
Canonical SPDI:: NC_000013.11:21094564:A:G
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
HGVS:: NC_000013.11:g.21094565A>G, NC_000013.10:g.21668704A>G, NG_010945.1:g.331T>C

Select item 14764482973.

rs1476448297 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 13:21094860 (GRCh38)
13:21668999 (GRCh37)
Canonical SPDI:: NC_000013.11:21094859:C:T
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000013.11:g.21094860C>T, NC_000013.10:g.21668999C>T, NG_010945.1:g.36G>A

Select item 14675690704.

rs1467569070 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 13:21094863 (GRCh38)
13:21669002 (GRCh37)
Canonical SPDI:: NC_000013.11:21094862:C:T
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000071/1 (ALFA)
T=0.000015/4 (TOPMED)
HGVS:: NC_000013.11:g.21094863C>T, NC_000013.10:g.21669002C>T, NG_010945.1:g.33G>A

Select item 14668329585.

rs1466832958 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 13:21094224 (GRCh38)
13:21668363 (GRCh37)
Canonical SPDI:: NC_000013.11:21094223:T:G
Validated:: by frequency,by alfa
MAF:: G=0.0002/1 (ALFA)
G=0.0002/1 (Estonian)
HGVS:: NC_000013.11:g.21094224T>G, NC_000013.10:g.21668363T>G, NG_010945.1:g.672A>C

Select item 14605716416.

rs1460571641 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 13:21094639 (GRCh38)
13:21668778 (GRCh37)
Canonical SPDI:: NC_000013.11:21094638:G: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_000013.11:g.21094639G>A, NC_000013.10:g.21668778G>A, NG_010945.1:g.257C>T

Select item 14589062837.

rs1458906283 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 13:21094390 (GRCh38)
13:21668529 (GRCh37)
Canonical SPDI:: NC_000013.11:21094389:C:T
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000013.11:g.21094390C>T, NC_000013.10:g.21668529C>T, NG_010945.1:g.506G>A

Select item 14575810618.

rs1457581061 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 13:21094869 (GRCh38)
13:21669008 (GRCh37)
Canonical SPDI:: NC_000013.11:21094868:T:C
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000011/3 (TOPMED)
HGVS:: NC_000013.11:g.21094869T>C, NC_000013.10:g.21669008T>C, NG_010945.1:g.27A>G

Select item 14552293039.

rs1455229303 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 13:21094652 (GRCh38)
13:21668791 (GRCh37)
Canonical SPDI:: NC_000013.11:21094651:C:T
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000015/4 (TOPMED)
T=0.000021/3 (GnomAD)
HGVS:: NC_000013.11:g.21094652C>T, NC_000013.10:g.21668791C>T, NG_010945.1:g.244G>A

Select item 145430584710.

rs1454305847 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 13:21094497 (GRCh38)
13:21668636 (GRCh37)
Canonical SPDI:: NC_000013.11:21094496:T:A
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000013.11:g.21094497T>A, NC_000013.10:g.21668636T>A, NG_010945.1:g.399A>T

Select item 145417378611.

rs1454173786 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 13:21094289 (GRCh38)
13:21668428 (GRCh37)
Canonical SPDI:: NC_000013.11:21094288:T:C
Validated:: by frequency
MAF:: C=0.000029/4 (GnomAD)
HGVS:: NC_000013.11:g.21094289T>C, NC_000013.10:g.21668428T>C, NG_010945.1:g.607A>G

Select item 144580848212.

rs1445808482 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 13:21094895 (GRCh38)
13:21669034 (GRCh37)
Canonical SPDI:: NC_000013.11:21094894:T:C
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000013.11:g.21094895T>C, NC_000013.10:g.21669034T>C, NG_010945.1:g.1A>G

Select item 144048490113.

rs1440484901 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 13:21094325 (GRCh38)
13:21668464 (GRCh37)
Canonical SPDI:: NC_000013.11:21094324: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_000013.11:g.21094325C>T, NC_000013.10:g.21668464C>T, NG_010945.1:g.571G>A

Select item 143212605114.

rs1432126051 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 13:21094372 (GRCh38)
13:21668511 (GRCh37)
Canonical SPDI:: NC_000013.11:21094371: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_000013.11:g.21094372C>T, NC_000013.10:g.21668511C>T, NG_010945.1:g.524G>A

Select item 143156263215.

rs1431562632 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 13:21094230 (GRCh38)
13:21668369 (GRCh37)
Canonical SPDI:: NC_000013.11:21094229:A:C
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000013.11:g.21094230A>C, NC_000013.10:g.21668369A>C, NG_010945.1:g.666T>G

Select item 142324768916.

rs1423247689 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 13:21094827 (GRCh38)
13:21668966 (GRCh37)
Canonical SPDI:: NC_000013.11:21094826:G:A
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000019/5 (TOPMED)
A=0.000021/3 (GnomAD)
HGVS:: NC_000013.11:g.21094827G>A, NC_000013.10:g.21668966G>A, NG_010945.1:g.69C>T

Select item 142034348917.

rs1420343489 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 13:21094845 (GRCh38)
13:21668984 (GRCh37)
Canonical SPDI:: NC_000013.11:21094844:A:G
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000014/2 (GnomAD)
HGVS:: NC_000013.11:g.21094845A>G, NC_000013.10:g.21668984A>G, NG_010945.1:g.51T>C

Select item 141494317018.

rs1414943170 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 13:21094722 (GRCh38)
13:21668861 (GRCh37)
Canonical SPDI:: NC_000013.11:21094721:G:A,NC_000013.11:21094721:G:T
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000064/9 (GnomAD)
HGVS:: NC_000013.11:g.21094722G>A, NC_000013.11:g.21094722G>T, NC_000013.10:g.21668861G>A, NC_000013.10:g.21668861G>T, NG_010945.1:g.174C>T, NG_010945.1:g.174C>A

Select item 139956637519.

rs1399566375 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 13:21094207 (GRCh38)
13:21668346 (GRCh37)
Canonical SPDI:: NC_000013.11:21094206:T:C
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000013.11:g.21094207T>C, NC_000013.10:g.21668346T>C, NG_010945.1:g.689A>G

Select item 139694231320.

rs1396942313 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 13:21094636 (GRCh38)
13:21668775 (GRCh37)
Canonical SPDI:: NC_000013.11:21094635:T:G
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000021/3 (GnomAD)
HGVS:: NC_000013.11:g.21094636T>G, NC_000013.10:g.21668775T>G, NG_010945.1:g.260A>C