SNP Links for Nucleotide (Select 1112917097) - SNP

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Items: 1 to 20 of 546

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Select item 14904172691.

rs1490417269 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 4:8950444 (GRCh38)
4:8952170 (GRCh37)
Canonical SPDI:: NC_000004.12:8950443:T:C,NC_000004.12:8950443:T:G
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000016/2 (GnomAD_exomes)
HGVS:: NC_000004.12:g.8950444T>C, NC_000004.12:g.8950444T>G, NC_000004.11:g.8952170T>C, NC_000004.11:g.8952170T>G, NG_052560.1:g.941T>C, NG_052560.1:g.941T>G

Select item 14893016782.

rs1489301678 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 4:8950110 (GRCh38)
4:8951836 (GRCh37)
Canonical SPDI:: NC_000004.12:8950109:G:A,NC_000004.12:8950109:G:T
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
A=0.000006/1 (GnomAD_exomes)
HGVS:: NC_000004.12:g.8950110G>A, NC_000004.12:g.8950110G>T, NC_000004.11:g.8951836G>A, NC_000004.11:g.8951836G>T, NG_052560.1:g.607G>A, NG_052560.1:g.607G>T, NM_001040071.1:c.360G>A, NM_001040071.1:c.360G>T

Select item 14889535683.

rs1488953568 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 4:8950451 (GRCh38)
4:8952177 (GRCh37)
Canonical SPDI:: NC_000004.12:8950450:C:T
HGVS:: NC_000004.12:g.8950451C>T, NC_000004.11:g.8952177C>T, NG_052560.1:g.948C>T

Select item 14885665684.

rs1488566568 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 4:8950324 (GRCh38)
4:8952050 (GRCh37)
Canonical SPDI:: NC_000004.12:8950323:A:G
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
HGVS:: NC_000004.12:g.8950324A>G, NC_000004.11:g.8952050A>G, NG_052560.1:g.821A>G, NM_001040071.1:c.574A>G

Select item 14879682585.

rs1487968258 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 4:8950193 (GRCh38)
4:8951919 (GRCh37)
Canonical SPDI:: NC_000004.12:8950192:C:G
Validated:: by frequency
MAF:: G=0.000013/2 (GnomAD_exomes)
HGVS:: NC_000004.12:g.8950193C>G, NC_000004.11:g.8951919C>G, NG_052560.1:g.690C>G, NM_001040071.1:c.443C>G

Select item 14838792046.

rs1483879204 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 4:8950254 (GRCh38)
4:8951980 (GRCh37)
Canonical SPDI:: NC_000004.12:8950253:C:A,NC_000004.12:8950253:C:T
Validated:: by frequency
MAF:: A=0.000006/1 (GnomAD_exomes)
HGVS:: NC_000004.12:g.8950254C>A, NC_000004.12:g.8950254C>T, NC_000004.11:g.8951980C>A, NC_000004.11:g.8951980C>T, NG_052560.1:g.751C>A, NG_052560.1:g.751C>T, NM_001040071.1:c.504C>A, NM_001040071.1:c.504C>T

Select item 14830401507.

rs1483040150 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 4:8950518 (GRCh38)
4:8952244 (GRCh37)
Canonical SPDI:: NC_000004.12:8950517:C:A
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000208/3 (ALFA)
A=0.000108/15 (GnomAD)
A=0.00011/29 (TOPMED)
HGVS:: NC_000004.12:g.8950518C>A, NC_000004.11:g.8952244C>A, NG_052560.1:g.1015C>A

Select item 14805202828.

rs1480520282 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 4:8949693 (GRCh38)
4:8951419 (GRCh37)
Canonical SPDI:: NC_000004.12:8949692:A:C
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000071/1 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000011/3 (TOPMED)
HGVS:: NC_000004.12:g.8949693A>C, NC_000004.11:g.8951419A>C, NG_052560.1:g.190A>C

Select item 14797654709.

rs1479765470 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 4:8950125 (GRCh38)
4:8951851 (GRCh37)
Canonical SPDI:: NC_000004.12:8950124: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_000004.12:g.8950125G>A, NC_000004.11:g.8951851G>A, NG_052560.1:g.622G>A, NM_001040071.1:c.375G>A

Select item 147951997610.

rs1479519976 [Homo sapiens]

Variant type:: DEL
Alleles:: TGCACAGTTGGATTGTGTTACAATT>- [Show Flanks]
Chromosome:: 4:8950124 (GRCh38)
4:8951850 (GRCh37)
Canonical SPDI:: NC_000004.12:8950123:TGCACAGTTGGATTGTGTTACAATT:
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.000013/2 (GnomAD_exomes)
-=0.000019/5 (TOPMED)
-=0.000036/5 (GnomAD)
HGVS:: NC_000004.12:g.8950124_8950148del, NC_000004.11:g.8951850_8951874del, NG_052560.1:g.621_645del, NM_001040071.1:c.374_398del

Select item 147809072911.

rs1478090729 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 4:8950389 (GRCh38)
4:8952115 (GRCh37)
Canonical SPDI:: NC_000004.12:8950388:A:T
HGVS:: NC_000004.12:g.8950389A>T, NC_000004.11:g.8952115A>T, NG_052560.1:g.886A>T, NM_001040071.1:c.639A>T

Select item 147779810112.

rs1477798101 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 4:8950131 (GRCh38)
4:8951857 (GRCh37)
Canonical SPDI:: NC_000004.12:8950130:T:C
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000071/1 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000015/4 (TOPMED)
C=0.000052/8 (GnomAD_exomes)
HGVS:: NC_000004.12:g.8950131T>C, NC_000004.11:g.8951857T>C, NG_052560.1:g.628T>C, NM_001040071.1:c.381T>C

Select item 147313071813.

rs1473130718 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 4:8949802 (GRCh38)
4:8951528 (GRCh37)
Canonical SPDI:: NC_000004.12:8949801:T:C
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000004.12:g.8949802T>C, NC_000004.11:g.8951528T>C, NG_052560.1:g.299T>C, NM_001040071.1:c.52T>C

Select item 147251511814.

rs1472515118 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 4:8949694 (GRCh38)
4:8951420 (GRCh37)
Canonical SPDI:: NC_000004.12:8949693:C:T
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000224/1 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000004.12:g.8949694C>T, NC_000004.11:g.8951420C>T, NG_052560.1:g.191C>T

Select item 147236586015.

rs1472365860 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 4:8949972 (GRCh38)
4:8951698 (GRCh37)
Canonical SPDI:: NC_000004.12:8949971:T:G
Validated:: by frequency,by cluster
MAF:: G=0.000006/1 (GnomAD_exomes)
G=0.00463/1 (Vietnamese)
HGVS:: NC_000004.12:g.8949972T>G, NC_000004.11:g.8951698T>G, NG_052560.1:g.469T>G, NM_001040071.1:c.222T>G

Select item 147164583316.

rs1471645833 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: 4:8950307 (GRCh38)
4:8952033 (GRCh37)
Canonical SPDI:: NC_000004.12:8950306:A:G,NC_000004.12:8950306:A:T
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000071/1 (TOMMO)
HGVS:: NC_000004.12:g.8950307A>G, NC_000004.12:g.8950307A>T, NC_000004.11:g.8952033A>G, NC_000004.11:g.8952033A>T, NG_052560.1:g.804A>G, NG_052560.1:g.804A>T, NM_001040071.1:c.557A>G, NM_001040071.1:c.557A>T

Select item 147071826217.

rs1470718262 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 4:8949523 (GRCh38)
4:8951249 (GRCh37)
Canonical SPDI:: NC_000004.12:8949522:C: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_000004.12:g.8949523C>A, NC_000004.11:g.8951249C>A, NG_052560.1:g.20C>A

Select item 146933589218.

rs1469335892 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 4:8950337 (GRCh38)
4:8952063 (GRCh37)
Canonical SPDI:: NC_000004.12:8950336:C:A
HGVS:: NC_000004.12:g.8950337C>A, NC_000004.11:g.8952063C>A, NG_052560.1:g.834C>A, NM_001040071.1:c.587C>A

Select item 146743379419.

rs1467433794 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 4:8950161 (GRCh38)
4:8951887 (GRCh37)
Canonical SPDI:: NC_000004.12:8950160:G: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_000004.12:g.8950161G>C, NC_000004.11:g.8951887G>C, NG_052560.1:g.658G>C, NM_001040071.1:c.411G>C

Select item 146703339820.

rs1467033398 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 4:8950361 (GRCh38)
4:8952087 (GRCh37)
Canonical SPDI:: NC_000004.12:8950360:C:G
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
G=0.000007/1 (GnomAD_exomes)
HGVS:: NC_000004.12:g.8950361C>G, NC_000004.11:g.8952087C>G, NG_052560.1:g.858C>G, NM_001040071.1:c.611C>G

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