SNP Links for Nucleotide (Select 985701217) - SNP

Links from Nucleotide

Items: 1 to 20 of 104

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Select item 14896240351.

rs1489624035 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 1:150181130 (GRCh38)
1:150153365 (GRCh37)
Canonical SPDI:: NC_000001.11:150181129:C:A
Gene:: LINC02988 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.150181130C>A, NW_003871055.3:g.6996543C>A, NC_000001.10:g.150153365C>A, NR_135098.1:n.494C>A

Select item 14880167942.

rs1488016794 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 1:150160808 (GRCh38)
1:150133006 (GRCh37)
Canonical SPDI:: NC_000001.11:150160807:G:C
Gene:: LINC02988 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.150160808G>C, NW_003871055.3:g.6976221G>C, NC_000001.10:g.150133006G>C, NR_135098.1:n.81G>C

Select item 14848096673.

rs1484809667 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:150160731 (GRCh38)
1:150132929 (GRCh37)
Canonical SPDI:: NC_000001.11:150160730:A:G
Gene:: LINC02988 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000071/1 (ALFA)
G=0.000053/14 (TOPMED)
G=0.000057/8 (GnomAD)
HGVS:: NC_000001.11:g.150160731A>G, NW_003871055.3:g.6976144A>G, NC_000001.10:g.150132929A>G, NR_135098.1:n.4A>G

Select item 14759112624.

rs1475911262 [Homo sapiens]

Variant type:: DELINS
Alleles:: CCT>- [Show Flanks]
Chromosome:: 1:150164278 (GRCh38)
1:150136474 (GRCh37)
Canonical SPDI:: NC_000001.11:150164275:CTCCT:CT
Gene:: LINC02988 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: CT=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.150164278_150164280del, NW_003871055.3:g.6979691_6979693del, NC_000001.10:g.150136474_150136476del, NR_135098.1:n.166_168del

Select item 14636935965.

rs1463693596 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 1:150173769 (GRCh38)
1:150145989 (GRCh37)
Canonical SPDI:: NC_000001.11:150173768:G:T
Gene:: LINC02988 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000008/2 (TOPMED)
HGVS:: NC_000001.11:g.150173769G>T, NW_003871055.3:g.6989182G>T, NC_000001.10:g.150145989G>T, NR_135098.1:n.230G>T

Select item 14591319376.

rs1459131937 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 1:150181052 (GRCh38)
1:150153287 (GRCh37)
Canonical SPDI:: NC_000001.11:150181051:C:G
Gene:: LINC02988 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.150181052C>G, NW_003871055.3:g.6996465C>G, NC_000001.10:g.150153287C>G, NR_135098.1:n.416C>G

Select item 14580559457.

rs1458055945 [Homo sapiens]

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

Select item 14532774138.

rs1453277413 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:150164239 (GRCh38)
1:150136435 (GRCh37)
Canonical SPDI:: NC_000001.11:150164238:C:T
Gene:: LINC02988 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000019/5 (TOPMED)
HGVS:: NC_000001.11:g.150164239C>T, NW_003871055.3:g.6979652C>T, NC_000001.10:g.150136435C>T, NR_135098.1:n.127C>T

Select item 14505913629.

rs1450591362 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->GTCACACTT [Show Flanks]
Chromosome:: 1:150181090 (GRCh38)
1:150153326 (GRCh37)
Canonical SPDI:: NC_000001.11:150181090:TGTCACACTT:TGTCACACTTGTCACACTT
Gene:: LINC02988 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: TGTCACACTTGTCACACTT=0./0 (ALFA)
HGVS:: NC_000001.11:g.150181092_150181100dup, NW_003871055.3:g.6996505_6996513dup, NC_000001.10:g.150153327_150153335dup, NR_135098.1:n.456_464dup

Select item 143950256510.

rs1439502565 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:150181208 (GRCh38)
1:150153443 (GRCh37)
Canonical SPDI:: NC_000001.11:150181207:A:G
Gene:: LINC02988 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000008/2 (TOPMED)
HGVS:: NC_000001.11:g.150181208A>G, NW_003871055.3:g.6996621A>G, NC_000001.10:g.150153443A>G, NR_135098.1:n.572A>G

Select item 143097083311.

rs1430970833 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 1:150181227 (GRCh38)
1:150153462 (GRCh37)
Canonical SPDI:: NC_000001.11:150181226:T:C
Gene:: LINC02988 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000008/2 (TOPMED)
HGVS:: NC_000001.11:g.150181227T>C, NW_003871055.3:g.6996640T>C, NC_000001.10:g.150153462T>C, NR_135098.1:n.591T>C

Select item 142563374912.

rs1425633749 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 1:150173762 (GRCh38)
1:150145982 (GRCh37)
Canonical SPDI:: NC_000001.11:150173761:C:A,NC_000001.11:150173761:C:T
Gene:: LINC02988 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000014/2 (GnomAD)
T=0.000023/6 (TOPMED)
HGVS:: NC_000001.11:g.150173762C>A, NC_000001.11:g.150173762C>T, NW_003871055.3:g.6989175C>A, NW_003871055.3:g.6989175C>T, NC_000001.10:g.150145982C>A, NC_000001.10:g.150145982C>T, NR_135098.1:n.223C>A, NR_135098.1:n.223C>T

Select item 141641483413.

rs1416414834 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:150180948 (GRCh38)
1:150153183 (GRCh37)
Canonical SPDI:: NC_000001.11:150180947:G:A
Gene:: LINC02988 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000162/3 (ALFA)
A=0.000015/4 (TOPMED)
A=0.000021/3 (GnomAD)
A=0.00067/3 (Estonian)
HGVS:: NC_000001.11:g.150180948G>A, NW_003871055.3:g.6996361G>A, NC_000001.10:g.150153183G>A, NR_135098.1:n.312G>A

Select item 141462193914.

rs1414621939 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:150173763 (GRCh38)
1:150145983 (GRCh37)
Canonical SPDI:: NC_000001.11:150173762:G:A
Gene:: LINC02988 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000142/2 (ALFA)
A=0.000035/1 (TOMMO)
A=0.000083/22 (TOPMED)
A=0.000086/12 (GnomAD)
HGVS:: NC_000001.11:g.150173763G>A, NW_003871055.3:g.6989176G>A, NC_000001.10:g.150145983G>A, NR_135098.1:n.224G>A

Select item 140971837115.

rs1409718371 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 1:150181066 (GRCh38)
1:150153301 (GRCh37)
Canonical SPDI:: NC_000001.11:150181065:C:G
Gene:: LINC02988 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000011/3 (TOPMED)
HGVS:: NC_000001.11:g.150181066C>G, NW_003871055.3:g.6996479C>G, NC_000001.10:g.150153301C>G, NR_135098.1:n.430C>G

Select item 138800493416.

rs1388004934 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->T [Show Flanks]
Chromosome:: 1:150181196 (GRCh38)
1:150153432 (GRCh37)
Canonical SPDI:: NC_000001.11:150181196:T:TT
Gene:: LINC02988 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TT=0.000071/1 (ALFA)
T=0.000014/2 (GnomAD)
T=0.000053/14 (TOPMED)
HGVS:: NC_000001.11:g.150181197dup, NW_003871055.3:g.6996610dup, NC_000001.10:g.150153432dup, NR_135098.1:n.561dup

Select item 138593892217.

rs1385938922 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 1:150160782 (GRCh38)
1:150132980 (GRCh37)
Canonical SPDI:: NC_000001.11:150160781:T:C
Gene:: LINC02988 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.150160782T>C, NW_003871055.3:g.6976195T>C, NC_000001.10:g.150132980T>C, NR_135098.1:n.55T>C

Select item 138326439618.

rs1383264396 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 1:150160755 (GRCh38)
1:150132953 (GRCh37)
Canonical SPDI:: NC_000001.11:150160754:C:G
Gene:: LINC02988 (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=0.000014/2 (GnomAD)
HGVS:: NC_000001.11:g.150160755C>G, NW_003871055.3:g.6976168C>G, NC_000001.10:g.150132953C>G, NR_135098.1:n.28C>G

Select item 138285853919.

rs1382858539 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:150160753 (GRCh38)
1:150132951 (GRCh37)
Canonical SPDI:: NC_000001.11:150160752:G:A
Gene:: LINC02988 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000021/3 (GnomAD)
A=0.000026/7 (TOPMED)
HGVS:: NC_000001.11:g.150160753G>A, NW_003871055.3:g.6976166G>A, NC_000001.10:g.150132951G>A, NR_135098.1:n.26G>A

Select item 137918966020.

rs1379189660 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C,T [Show Flanks]
Chromosome:: 1:150173733 (GRCh38)
1:150145953 (GRCh37)
Canonical SPDI:: NC_000001.11:150173732:G:C,NC_000001.11:150173732:G:T
Gene:: LINC02988 (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_000001.11:g.150173733G>C, NC_000001.11:g.150173733G>T, NW_003871055.3:g.6989146G>C, NW_003871055.3:g.6989146G>T, NG_076441.1:g.485G>C, NG_076441.1:g.485G>T, NC_000001.10:g.150145953G>C, NC_000001.10:g.150145953G>T, NR_135098.1:n.194G>C, NR_135098.1:n.194G>T

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