SNP Links for Nucleotide (Select 1237938432) - SNP

Links from Nucleotide

Items: 1 to 20 of 1267

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Select item 14904070451.

rs1490407045 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 8:53515529 (GRCh38)
8:54428089 (GRCh37)
Canonical SPDI:: NC_000008.11:53515528:A:T
Gene:: LINC02984 (Varview), LOC124901947 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000011/3 (TOPMED)
T=0.000014/2 (GnomAD)
HGVS:: NC_000008.11:g.53515529A>T, NC_000008.10:g.54428089A>T, NR_149032.1:n.2063T>A

Select item 14901754002.

rs1490175400 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 8:53513789 (GRCh38)
8:54426349 (GRCh37)
Canonical SPDI:: NC_000008.11:53513788:T:C
Gene:: LINC02984 (Varview), LOC124901947 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000008.11:g.53513789T>C, NC_000008.10:g.54426349T>C, NR_149032.1:n.3803A>G

Select item 14897075493.

rs1489707549 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 8:53523953 (GRCh38)
8:54436513 (GRCh37)
Canonical SPDI:: NC_000008.11:53523952:A:G
Gene:: LINC02984 (Varview), LOC124901947 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_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_000008.11:g.53523953A>G, NC_000008.10:g.54436513A>G, NR_149032.1:n.13T>C

Select item 14890518864.

rs1489051886 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 8:53516457 (GRCh38)
8:54429017 (GRCh37)
Canonical SPDI:: NC_000008.11:53516456:T:C
Gene:: LINC02984 (Varview), LOC124901947 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_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_000008.11:g.53516457T>C, NC_000008.10:g.54429017T>C, NR_149032.1:n.1135A>G

Select item 14887277225.

rs1488727722 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 8:53516863 (GRCh38)
8:54429423 (GRCh37)
Canonical SPDI:: NC_000008.11:53516862:T:G
Gene:: LINC02984 (Varview), LOC124901947 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
HGVS:: NC_000008.11:g.53516863T>G, NC_000008.10:g.54429423T>G, NR_149032.1:n.729A>C

Select item 14887265796.

rs1488726579 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 8:53513633 (GRCh38)
8:54426193 (GRCh37)
Canonical SPDI:: NC_000008.11:53513632:T:C
Gene:: LINC02984 (Varview), LOC124901947 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
HGVS:: NC_000008.11:g.53513633T>C, NC_000008.10:g.54426193T>C, NR_149032.1:n.3959A>G

Select item 14886048817.

rs1488604881 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 8:53516555 (GRCh38)
8:54429115 (GRCh37)
Canonical SPDI:: NC_000008.11:53516554:A:G
Gene:: LINC02984 (Varview), LOC124901947 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000008.11:g.53516555A>G, NC_000008.10:g.54429115A>G, NR_149032.1:n.1037T>C

Select item 14879621208.

rs1487962120 [Homo sapiens]

Variant type:: DELINS
Alleles:: T>- [Show Flanks]
Chromosome:: 8:53515636 (GRCh38)
8:54428196 (GRCh37)
Canonical SPDI:: NC_000008.11:53515635:TT:T
Gene:: LINC02984 (Varview), LOC124901947 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: TT=0./0 (ALFA)
-=0.000004/1 (TOPMED)
HGVS:: NC_000008.11:g.53515637del, NC_000008.10:g.54428197del, NR_149032.1:n.1956del

Select item 14874989949.

rs1487498994 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 8:53523836 (GRCh38)
8:54436396 (GRCh37)
Canonical SPDI:: NC_000008.11:53523835:G:A
Gene:: LINC02984 (Varview), LOC124901947 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000008.11:g.53523836G>A, NC_000008.10:g.54436396G>A, NR_149032.1:n.130C>T

Select item 148680328910.

rs1486803289 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 8:53514555 (GRCh38)
8:54427115 (GRCh37)
Canonical SPDI:: NC_000008.11:53514554:A:T
Gene:: LINC02984 (Varview), LOC124901947 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000014/2 (GnomAD)
HGVS:: NC_000008.11:g.53514555A>T, NC_000008.10:g.54427115A>T, NR_149032.1:n.3037T>A

Select item 148554960711.

rs1485549607 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 8:53514048 (GRCh38)
8:54426608 (GRCh37)
Canonical SPDI:: NC_000008.11:53514047:A:G
Gene:: LINC02984 (Varview), LOC124901947 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000011/3 (TOPMED)
G=0.000014/2 (GnomAD)
HGVS:: NC_000008.11:g.53514048A>G, NC_000008.10:g.54426608A>G, NR_149032.1:n.3544T>C

Select item 148433817512.

rs1484338175 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 8:53513282 (GRCh38)
8:54425842 (GRCh37)
Canonical SPDI:: NC_000008.11:53513281:T:C
Gene:: LINC02984 (Varview), LOC124901947 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000008.11:g.53513282T>C, NC_000008.10:g.54425842T>C, NR_149032.1:n.4310A>G

Select item 148415501413.

rs1484155014 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 8:53514278 (GRCh38)
8:54426838 (GRCh37)
Canonical SPDI:: NC_000008.11:53514277:C:T
Gene:: LINC02984 (Varview), LOC124901947 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000026/7 (TOPMED)
HGVS:: NC_000008.11:g.53514278C>T, NC_000008.10:g.54426838C>T, NR_149032.1:n.3314G>A

Select item 148401931814.

rs1484019318 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 8:53515687 (GRCh38)
8:54428247 (GRCh37)
Canonical SPDI:: NC_000008.11:53515686:C:A,NC_000008.11:53515686:C:T
Gene:: LINC02984 (Varview), LOC124901947 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000015/4 (TOPMED)
HGVS:: NC_000008.11:g.53515687C>A, NC_000008.11:g.53515687C>T, NC_000008.10:g.54428247C>A, NC_000008.10:g.54428247C>T, NR_149032.1:n.1905G>T, NR_149032.1:n.1905G>A

Select item 148399357615.

rs1483993576 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G [Show Flanks]
Chromosome:: 8:53512900 (GRCh38)
8:54425460 (GRCh37)
Canonical SPDI:: NC_000008.11:53512899:A:C,NC_000008.11:53512899:A:G
Gene:: LINC02984 (Varview), LOC124901947 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000008.11:g.53512900A>C, NC_000008.11:g.53512900A>G, NC_000008.10:g.54425460A>C, NC_000008.10:g.54425460A>G, NR_149032.1:n.4692T>G, NR_149032.1:n.4692T>C

Select item 148387632816.

rs1483876328 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,G,T [Show Flanks]
Chromosome:: 8:53513732 (GRCh38)
8:54426292 (GRCh37)
Canonical SPDI:: NC_000008.11:53513731:C:A,NC_000008.11:53513731:C:G,NC_000008.11:53513731:C:T
Gene:: LINC02984 (Varview), LOC124901947 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
HGVS:: NC_000008.11:g.53513732C>A, NC_000008.11:g.53513732C>G, NC_000008.11:g.53513732C>T, NC_000008.10:g.54426292C>A, NC_000008.10:g.54426292C>G, NC_000008.10:g.54426292C>T, NR_149032.1:n.3860G>T, NR_149032.1:n.3860G>C, NR_149032.1:n.3860G>A

Select item 148238660617.

rs1482386606 [Homo sapiens]

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

Select item 148066529818.

rs1480665298 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 8:53515617 (GRCh38)
8:54428177 (GRCh37)
Canonical SPDI:: NC_000008.11:53515616:G:T
Gene:: LINC02984 (Varview), LOC124901947 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000011/3 (TOPMED)
HGVS:: NC_000008.11:g.53515617G>T, NC_000008.10:g.54428177G>T, NR_149032.1:n.1975C>A

Select item 148003092919.

rs1480030929 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 8:53513914 (GRCh38)
8:54426474 (GRCh37)
Canonical SPDI:: NC_000008.11:53513913:A:G
Gene:: LINC02984 (Varview), LOC124901947 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000015/4 (TOPMED)
G=0.000142/2 (TOMMO)
HGVS:: NC_000008.11:g.53513914A>G, NC_000008.10:g.54426474A>G, NR_149032.1:n.3678T>C

Select item 147975396420.

rs1479753964 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 8:53514261 (GRCh38)
8:54426821 (GRCh37)
Canonical SPDI:: NC_000008.11:53514260:C:T
Gene:: LINC02984 (Varview), LOC124901947 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000014/2 (GnomAD)
HGVS:: NC_000008.11:g.53514261C>T, NC_000008.10:g.54426821C>T, NR_149032.1:n.3331G>A

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