SNP Links for Nucleotide (Select 224589130) - SNP

Links from Nucleotide

Items: 1 to 20 of 381

<< First< Prev

Page of 20

Next >Last >>

Select item 14874104721.

rs1487410472 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 17:68199028 (GRCh38)
17:66195169 (GRCh37)
Canonical SPDI:: NC_000017.11:68199027:G:A
Gene:: ARHGAP27P2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0.000071/1 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000017.11:g.68199028G>A, NC_000017.10:g.66195169G>A, NW_003871088.1:g.259039G>A, NR_027283.1:n.369G>A

Select item 14873588522.

rs1487358852 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 17:68199796 (GRCh38)
17:66195937 (GRCh37)
Canonical SPDI:: NC_000017.11:68199795:T:C,NC_000017.11:68199795:T:G
Gene:: ARHGAP27P2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
HGVS:: NC_000017.11:g.68199796T>C, NC_000017.11:g.68199796T>G, NC_000017.10:g.66195937T>C, NC_000017.10:g.66195937T>G, NW_003871088.1:g.259807T>C, NW_003871088.1:g.259807T>G, NR_027283.1:n.1137T>C, NR_027283.1:n.1137T>G

Select item 14851470163.

rs1485147016 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C,T [Show Flanks]
Chromosome:: 17:68200125 (GRCh38)
17:66196266 (GRCh37)
Canonical SPDI:: NC_000017.11:68200124:G:C,NC_000017.11:68200124:G:T
Gene:: ARHGAP27P2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
HGVS:: NC_000017.11:g.68200125G>C, NC_000017.11:g.68200125G>T, NC_000017.10:g.66196266G>C, NC_000017.10:g.66196266G>T, NW_003871088.1:g.260136G>C, NW_003871088.1:g.260136G>T, NR_027283.1:n.1466G>C, NR_027283.1:n.1466G>T

Select item 14845251704.

rs1484525170 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 17:68198795 (GRCh38)
17:66194936 (GRCh37)
Canonical SPDI:: NC_000017.11:68198794:A:C
Gene:: ARHGAP27P2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000017.11:g.68198795A>C, NC_000017.10:g.66194936A>C, NW_003871088.1:g.258806A>C, NR_027283.1:n.136A>C

Select item 14834992815.

rs1483499281 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 17:68199622 (GRCh38)
17:66195763 (GRCh37)
Canonical SPDI:: NC_000017.11:68199621:G:A,NC_000017.11:68199621:G:T
Gene:: ARHGAP27P2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.00002/3 (GnomAD_exomes)
HGVS:: NC_000017.11:g.68199622G>A, NC_000017.11:g.68199622G>T, NC_000017.10:g.66195763G>A, NC_000017.10:g.66195763G>T, NW_003871088.1:g.259633G>A, NW_003871088.1:g.259633G>T, NR_027283.1:n.963G>A, NR_027283.1:n.963G>T

Select item 14832692706.

rs1483269270 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 17:68199962 (GRCh38)
17:66196103 (GRCh37)
Canonical SPDI:: NC_000017.11:68199961:C:T
Gene:: ARHGAP27P2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000086/12 (GnomAD)
T=0.000227/60 (TOPMED)
HGVS:: NC_000017.11:g.68199962C>T, NC_000017.10:g.66196103C>T, NW_003871088.1:g.259973C>T, NR_027283.1:n.1303C>T

Select item 14828434917.

rs1482843491 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 17:68198885 (GRCh38)
17:66195026 (GRCh37)
Canonical SPDI:: NC_000017.11:68198884:C:T
Gene:: ARHGAP27P2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000017.11:g.68198885C>T, NC_000017.10:g.66195026C>T, NW_003871088.1:g.258896C>T, NR_027283.1:n.226C>T

Select item 14818605378.

rs1481860537 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 17:68199288 (GRCh38)
17:66195429 (GRCh37)
Canonical SPDI:: NC_000017.11:68199287:C:A,NC_000017.11:68199287:C:T
Gene:: ARHGAP27P2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000017.11:g.68199288C>A, NC_000017.11:g.68199288C>T, NC_000017.10:g.66195429C>A, NC_000017.10:g.66195429C>T, NW_003871088.1:g.259299C>A, NW_003871088.1:g.259299C>T, NR_027283.1:n.629C>A, NR_027283.1:n.629C>T

Select item 14788065109.

rs1478806510 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 17:68199421 (GRCh38)
17:66195562 (GRCh37)
Canonical SPDI:: NC_000017.11:68199420:G:A
Gene:: ARHGAP27P2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000008/2 (TOPMED)
HGVS:: NC_000017.11:g.68199421G>A, NC_000017.10:g.66195562G>A, NW_003871088.1:g.259432G>A, NR_027283.1:n.762G>A

Select item 147553421710.

rs1475534217 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 17:68198694 (GRCh38)
17:66194835 (GRCh37)
Canonical SPDI:: NC_000017.11:68198693:A:G
Gene:: ARHGAP27P2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000017.11:g.68198694A>G, NC_000017.10:g.66194835A>G, NW_003871088.1:g.258705A>G, NR_027283.1:n.35A>G

Select item 147457024611.

rs1474570246 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 17:68200188 (GRCh38)
17:66196329 (GRCh37)
Canonical SPDI:: NC_000017.11:68200187:A:G
Gene:: ARHGAP27P2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000017.11:g.68200188A>G, NC_000017.10:g.66196329A>G, NW_003871088.1:g.260199A>G, NR_027283.1:n.1529A>G

Select item 147226541712.

rs1472265417 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 17:68199011 (GRCh38)
17:66195152 (GRCh37)
Canonical SPDI:: NC_000017.11:68199010:C:T
Gene:: ARHGAP27P2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000008/1 (GnomAD_exomes)
HGVS:: NC_000017.11:g.68199011C>T, NC_000017.10:g.66195152C>T, NW_003871088.1:g.259022C>T, NR_027283.1:n.352C>T

Select item 147128748913.

rs1471287489 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 17:68199348 (GRCh38)
17:66195489 (GRCh37)
Canonical SPDI:: NC_000017.11:68199347:C:A,NC_000017.11:68199347:C:T
Gene:: ARHGAP27P2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000019/5 (TOPMED)
T=0.000042/3 (GnomAD_exomes)
HGVS:: NC_000017.11:g.68199348C>A, NC_000017.11:g.68199348C>T, NC_000017.10:g.66195489C>A, NC_000017.10:g.66195489C>T, NW_003871088.1:g.259359C>A, NW_003871088.1:g.259359C>T, NR_027283.1:n.689C>A, NR_027283.1:n.689C>T

Select item 146827122614.

rs1468271226 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 17:68200262 (GRCh38)
17:66196403 (GRCh37)
Canonical SPDI:: NC_000017.11:68200261:G:A
Gene:: ARHGAP27P2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000014/2 (GnomAD)
A=0.000019/5 (TOPMED)
HGVS:: NC_000017.11:g.68200262G>A, NC_000017.10:g.66196403G>A, NW_003871088.1:g.260273G>A, NR_027283.1:n.1603G>A

Select item 146812627815.

rs1468126278 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 17:68200288 (GRCh38)
17:66196429 (GRCh37)
Canonical SPDI:: NC_000017.11:68200287:C:T
Gene:: ARHGAP27P2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000017.11:g.68200288C>T, NC_000017.10:g.66196429C>T, NW_003871088.1:g.260299C>T, NR_027283.1:n.1629C>T

Select item 146603574716.

rs1466035747 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 17:68199135 (GRCh38)
17:66195276 (GRCh37)
Canonical SPDI:: NC_000017.11:68199134:A:G
Gene:: ARHGAP27P2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000017.11:g.68199135A>G, NC_000017.10:g.66195276A>G, NW_003871088.1:g.259146A>G, NR_027283.1:n.476A>G

Select item 146589460717.

rs1465894607 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 17:68199806 (GRCh38)
17:66195947 (GRCh37)
Canonical SPDI:: NC_000017.11:68199805:T:C
Gene:: ARHGAP27P2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000017.11:g.68199806T>C, NC_000017.10:g.66195947T>C, NW_003871088.1:g.259817T>C, NR_027283.1:n.1147T>C

Select item 146392386018.

rs1463923860 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 17:68199524 (GRCh38)
17:66195665 (GRCh37)
Canonical SPDI:: NC_000017.11:68199523:C:A
Gene:: ARHGAP27P2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000017.11:g.68199524C>A, NC_000017.10:g.66195665C>A, NW_003871088.1:g.259535C>A, NR_027283.1:n.865C>A

Select item 146376904319.

rs1463769043 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 17:68198701 (GRCh38)
17:66194842 (GRCh37)
Canonical SPDI:: NC_000017.11:68198700:C:G,NC_000017.11:68198700:C:T
Gene:: ARHGAP27P2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0./0 (GnomAD)
G=0.000008/2 (TOPMED)
HGVS:: NC_000017.11:g.68198701C>G, NC_000017.11:g.68198701C>T, NC_000017.10:g.66194842C>G, NC_000017.10:g.66194842C>T, NW_003871088.1:g.258712C>G, NW_003871088.1:g.258712C>T, NR_027283.1:n.42C>G, NR_027283.1:n.42C>T

Select item 146171206720.

rs1461712067 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->AGTC [Show Flanks]
Chromosome:: 17:68199205 (GRCh38)
17:66195347 (GRCh37)
Canonical SPDI:: NC_000017.11:68199205:CAGTC:CAGTCAGTC
Gene:: ARHGAP27P2 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: CAGTCAGTC=0.000071/1 (ALFA)
CAGT=0.000024/3 (GnomAD_exomes)
CAGT=0.000036/5 (GnomAD)
CAGT=0.000042/11 (TOPMED)
HGVS:: NC_000017.11:g.68199207_68199210dup, NC_000017.10:g.66195348_66195351dup, NW_003871088.1:g.259218_259221dup, NR_027283.1:n.548_551dup

dbSNP

Result Filters

Validation Status

Function Class

Variation Class

Annotation

Global MAF

Custom range

Additional filters

Display Settings:

Send to:

Links from Nucleotide

Items: 1 to 20 of 381

Display Settings:

Send to:

Supplemental Content

Find related data

Recent activity