SNP Links for Nucleotide (Select 239985536) - SNP

Links from Nucleotide

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Select item 14913945391.

rs1491394539 [Homo sapiens]

Variant type:: INS
Alleles:: ->A [Show Flanks]
Chromosome:: X:64434862 (GRCh38)
X:63654743 (GRCh37)
Canonical SPDI:: NC_000023.11:64434862::A
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.00001/1 (GnomAD)
A=0.000135/2 (TOMMO)
HGVS:: NC_000023.11:g.64434862_64434863insA, NC_000023.10:g.63654742_63654743insA, NG_001195.5:g.2780_2781insA

Select item 14911919302.

rs1491191930 [Homo sapiens]

Variant type:: DELINS
Alleles:: TG>- [Show Flanks]
Chromosome:: X:64434863 (GRCh38)
X:63654743 (GRCh37)
Canonical SPDI:: NC_000023.11:64434861:GTG:G
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
HGVS:: NC_000023.11:g.64434863_64434864del, NC_000023.10:g.63654743_63654744del, NG_001195.5:g.2781_2782del

Select item 14904987533.

rs1490498753 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: X:64434009 (GRCh38)
X:63653889 (GRCh37)
Canonical SPDI:: NC_000023.11:64434008:C:A
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000058/6 (GnomAD)
HGVS:: NC_000023.11:g.64434009C>A, NC_000023.10:g.63653889C>A, NG_001195.5:g.1927C>A

Select item 14902075124.

rs1490207512 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: X:64435366 (GRCh38)
X:63655246 (GRCh37)
Canonical SPDI:: NC_000023.11:64435365:G:C
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.64435366G>C, NC_000023.10:g.63655246G>C, NG_001195.5:g.3284G>C

Select item 14889864265.

rs1488986426 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: X:64434975 (GRCh38)
X:63654855 (GRCh37)
Canonical SPDI:: NC_000023.11:64434974:C:T
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000023.11:g.64434975C>T, NC_000023.10:g.63654855C>T, NG_001195.5:g.2893C>T

Select item 14889512906.

rs1488951290 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: X:64434242 (GRCh38)
X:63654122 (GRCh37)
Canonical SPDI:: NC_000023.11:64434241:G:A
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000023.11:g.64434242G>A, NC_000023.10:g.63654122G>A, NG_001195.5:g.2160G>A

Select item 14879999767.

rs1487999976 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: X:64433942 (GRCh38)
X:63653822 (GRCh37)
Canonical SPDI:: NC_000023.11:64433941:C:T
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.64433942C>T, NC_000023.10:g.63653822C>T, NG_001195.5:g.1860C>T

Select item 14878871878.

rs1487887187 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: X:64433852 (GRCh38)
X:63653732 (GRCh37)
Canonical SPDI:: NC_000023.11:64433851:G:A
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000011/3 (TOPMED)
A=0.000019/2 (GnomAD)
HGVS:: NC_000023.11:g.64433852G>A, NC_000023.10:g.63653732G>A, NG_001195.5:g.1770G>A

Select item 14874898979.

rs1487489897 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: X:64433746 (GRCh38)
X:63653626 (GRCh37)
Canonical SPDI:: NC_000023.11:64433745:A:G
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000023.11:g.64433746A>G, NC_000023.10:g.63653626A>G, NG_001195.5:g.1664A>G

Select item 148671274510.

rs1486712745 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: X:64433990 (GRCh38)
X:63653870 (GRCh37)
Canonical SPDI:: NC_000023.11:64433989:G:A,NC_000023.11:64433989:G:T
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000023.11:g.64433990G>A, NC_000023.11:g.64433990G>T, NC_000023.10:g.63653870G>A, NC_000023.10:g.63653870G>T, NG_001195.5:g.1908G>A, NG_001195.5:g.1908G>T

Select item 148559070811.

rs1485590708 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: X:64432867 (GRCh38)
X:63652747 (GRCh37)
Canonical SPDI:: NC_000023.11:64432866:G:A
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000011/3 (TOPMED)
HGVS:: NC_000023.11:g.64432867G>A, NC_000023.10:g.63652747G>A, NG_001195.5:g.785G>A

Select item 148553949812.

rs1485539498 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: X:64433113 (GRCh38)
X:63652993 (GRCh37)
Canonical SPDI:: NC_000023.11:64433112:C:T
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.64433113C>T, NC_000023.10:g.63652993C>T, NG_001195.5:g.1031C>T

Select item 148535117913.

rs1485351179 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: X:64433436 (GRCh38)
X:63653316 (GRCh37)
Canonical SPDI:: NC_000023.11:64433435:G:A
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000142/2 (ALFA)
A=0.000048/5 (GnomAD)
A=0.000083/22 (TOPMED)
HGVS:: NC_000023.11:g.64433436G>A, NC_000023.10:g.63653316G>A, NG_001195.5:g.1354G>A

Select item 148395891314.

rs1483958913 [Homo sapiens]

Variant type:: DEL
Alleles:: A>- [Show Flanks]
Chromosome:: X:64432493 (GRCh38)
X:63652373 (GRCh37)
Canonical SPDI:: NC_000023.11:64432492:A:
Validated:: by frequency,by alfa
MAF:: -=0.000142/2 (ALFA)
-=0.000008/2 (TOPMED)
HGVS:: NC_000023.11:g.64432493del, NC_000023.10:g.63652373del, NG_001195.5:g.411del

Select item 148274894115.

rs1482748941 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: X:64434454 (GRCh38)
X:63654334 (GRCh37)
Canonical SPDI:: NC_000023.11:64434453:G:A
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000011/3 (TOPMED)
HGVS:: NC_000023.11:g.64434454G>A, NC_000023.10:g.63654334G>A, NG_001195.5:g.2372G>A

Select item 148120154916.

rs1481201549 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: X:64434732 (GRCh38)
X:63654612 (GRCh37)
Canonical SPDI:: NC_000023.11:64434731:C:A,NC_000023.11:64434731:C:T
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.00001/1 (GnomAD)
T=0.000315/4 (TOMMO)
T=0.000685/2 (KOREAN)
HGVS:: NC_000023.11:g.64434732C>A, NC_000023.11:g.64434732C>T, NC_000023.10:g.63654612C>A, NC_000023.10:g.63654612C>T, NG_001195.5:g.2650C>A, NG_001195.5:g.2650C>T

Select item 148066047817.

rs1480660478 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: X:64432946 (GRCh38)
X:63652826 (GRCh37)
Canonical SPDI:: NC_000023.11:64432945:A:T
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.64432946A>T, NC_000023.10:g.63652826A>T, NG_001195.5:g.864A>T

Select item 148043803418.

rs1480438034 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: X:64433754 (GRCh38)
X:63653634 (GRCh37)
Canonical SPDI:: NC_000023.11:64433753:C:G,NC_000023.11:64433753:C:T
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
G=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.64433754C>G, NC_000023.11:g.64433754C>T, NC_000023.10:g.63653634C>G, NC_000023.10:g.63653634C>T, NG_001195.5:g.1672C>G, NG_001195.5:g.1672C>T

Select item 148004750819.

rs1480047508 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: X:64432648 (GRCh38)
X:63652528 (GRCh37)
Canonical SPDI:: NC_000023.11:64432647:A:T
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000023.11:g.64432648A>T, NC_000023.10:g.63652528A>T, NG_001195.5:g.566A>T

Select item 147908084520.

rs1479080845 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: X:64435024 (GRCh38)
X:63654904 (GRCh37)
Canonical SPDI:: NC_000023.11:64435023:T:C
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.00001/1 (GnomAD)
C=0.000011/3 (TOPMED)
HGVS:: NC_000023.11:g.64435024T>C, NC_000023.10:g.63654904T>C, NG_001195.5:g.2942T>C

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