SNP Links for Nucleotide (Select 586597958) - SNP

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Links from Nucleotide

Items: 1 to 20 of 548

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Select item 14893799931.

rs1489379993 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 22:18651420 (GRCh38)
22:20501287 (GRCh37)
Canonical SPDI:: NC_000022.11:18651419:C:G,NC_000022.11:18651419:C:T
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
HGVS:: NC_000022.11:g.18651420C>G, NC_000022.11:g.18651420C>T, NC_000022.10:g.20501287C>G, NC_000022.10:g.20501287C>T, NG_022867.2:g.2395G>C, NG_022867.2:g.2395G>A

Select item 14886815152.

rs1488681515 [Homo sapiens]

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

Select item 14874692503.

rs1487469250 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 22:18651663 (GRCh38)
22:20501530 (GRCh37)
Canonical SPDI:: NC_000022.11:18651662:G:A
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
G=0./0 (SGDP_PRJ)
A=0.00047/7 (TOMMO)
A=0.00242/6 (KOREAN)
HGVS:: NC_000022.11:g.18651663G>A, NC_000022.10:g.20501530G>A, NG_022867.2:g.2152C>T

Select item 14867790004.

rs1486779000 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 22:18651689 (GRCh38)
22:20501556 (GRCh37)
Canonical SPDI:: NC_000022.11:18651688:C:A,NC_000022.11:18651688:C:T
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000022.11:g.18651689C>A, NC_000022.11:g.18651689C>T, NC_000022.10:g.20501556C>A, NC_000022.10:g.20501556C>T, NG_022867.2:g.2126G>T, NG_022867.2:g.2126G>A

Select item 14859607215.

rs1485960721 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 22:18652471 (GRCh38)
22:20502338 (GRCh37)
Canonical SPDI:: NC_000022.11:18652470:C:T
HGVS:: NC_000022.11:g.18652471C>T, NC_000022.10:g.20502338C>T, NG_022867.2:g.1344G>A

Select item 14851559976.

rs1485155997 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 22:18653784 (GRCh38)
22:20503651 (GRCh37)
Canonical SPDI:: NC_000022.11:18653783:C:G
HGVS:: NC_000022.11:g.18653784C>G, NC_000022.10:g.20503651C>G, NG_022867.2:g.31G>C

Select item 14848679677.

rs1484867967 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 22:18652436 (GRCh38)
22:20502303 (GRCh37)
Canonical SPDI:: NC_000022.11:18652435:C:G
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000022.11:g.18652436C>G, NC_000022.10:g.20502303C>G, NG_022867.2:g.1379G>C

Select item 14836113558.

rs1483611355 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 22:18652742 (GRCh38)
22:20502609 (GRCh37)
Canonical SPDI:: NC_000022.11:18652741:C:A
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000022.11:g.18652742C>A, NC_000022.10:g.20502609C>A, NG_022867.2:g.1073G>T

Select item 14832320149.

rs1483232014 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 22:18651232 (GRCh38)
22:20501099 (GRCh37)
Canonical SPDI:: NC_000022.11:18651231:G:T
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000022.11:g.18651232G>T, NC_000022.10:g.20501099G>T, NG_022867.2:g.2583C>A

Select item 148315095210.

rs1483150952 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 22:18652164 (GRCh38)
22:20502031 (GRCh37)
Canonical SPDI:: NC_000022.11:18652163:C:T
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.0032/38 (ALFA)
C=0.5/1 (SGDP_PRJ)
HGVS:: NC_000022.11:g.18652164C>T, NC_000022.10:g.20502031C>T, NG_022867.2:g.1651G>A

Select item 148300344511.

rs1483003445 [Homo sapiens]

Variant type:: DELINS
Alleles:: CT>- [Show Flanks]
Chromosome:: 22:18651228 (GRCh38)
22:20501095 (GRCh37)
Canonical SPDI:: NC_000022.11:18651223:CTCTCT:CTCT
Validated:: by frequency,by alfa
MAF:: CTCT=0./0 (ALFA)
-=0.000004/1 (TOPMED)
HGVS:: NC_000022.11:g.18651224CT[2], NC_000022.10:g.20501091CT[2], NG_022867.2:g.2586AG[2]

Select item 148216767112.

rs1482167671 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 22:18651465 (GRCh38)
22:20501332 (GRCh37)
Canonical SPDI:: NC_000022.11:18651464:G:C
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.00002/1 (GnomAD)
C=0.00072/2 (KOREAN)
HGVS:: NC_000022.11:g.18651465G>C, NC_000022.10:g.20501332G>C, NG_022867.2:g.2350C>G

Select item 148166306613.

rs1481663066 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 22:18651158 (GRCh38)
22:20501025 (GRCh37)
Canonical SPDI:: NC_000022.11:18651157:A:G
Validated:: by frequency
MAF:: G=0.00013/2 (TOMMO)
HGVS:: NC_000022.11:g.18651158A>G, NC_000022.10:g.20501025A>G, NG_022867.2:g.2657T>C

Select item 148150871914.

rs1481508719 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 22:18649872 (GRCh38)
22:20499739 (GRCh37)
Canonical SPDI:: NC_000022.11:18649871:T:C
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.00001/1 (GnomAD)
HGVS:: NC_000022.11:g.18649872T>C, NC_000022.10:g.20499739T>C, NG_022867.2:g.3943A>G

Select item 148124205815.

rs1481242058 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 22:18649888 (GRCh38)
22:20499755 (GRCh37)
Canonical SPDI:: NC_000022.11:18649887:C:T
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.00211/25 (ALFA)
C=0./0 (SGDP_PRJ)
T=0.00734/47 (1000Genomes)
HGVS:: NC_000022.11:g.18649888C>T, NC_000022.10:g.20499755C>T, NG_022867.2:g.3927G>A

Select item 147735151416.

rs1477351514 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 22:18652307 (GRCh38)
22:20502174 (GRCh37)
Canonical SPDI:: NC_000022.11:18652306:A:G
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.00006/1 (ALFA)
G=0.00008/1 (GnomAD)
G=0.00176/26 (TOMMO)
G=0.00238/6 (KOREAN)
G=0.00245/3 (Korea1K)
HGVS:: NC_000022.11:g.18652307A>G, NC_000022.10:g.20502174A>G, NG_022867.2:g.1508T>C

Select item 147729978517.

rs1477299785 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 22:18649930 (GRCh38)
22:20499797 (GRCh37)
Canonical SPDI:: NC_000022.11:18649929:A:G
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.00004/3 (GnomAD)
HGVS:: NC_000022.11:g.18649930A>G, NC_000022.10:g.20499797A>G, NG_022867.2:g.3885T>C

Select item 147372214618.

rs1473722146 [Homo sapiens]

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

Select item 147310529519.

rs1473105295 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 22:18650066 (GRCh38)
22:20499933 (GRCh37)
Canonical SPDI:: NC_000022.11:18650065:C:G
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
HGVS:: NC_000022.11:g.18650066C>G, NC_000022.10:g.20499933C>G, NG_022867.2:g.3749G>C

Select item 147304272620.

rs1473042726 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 22:18651407 (GRCh38)
22:20501274 (GRCh37)
Canonical SPDI:: NC_000022.11:18651406:A:T
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000022.11:g.18651407A>T, NC_000022.10:g.20501274A>T, NG_022867.2:g.2408T>A