SNP Links for Gene (Select 100422982) - SNP

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Select item 14898716141.

rs1489871614 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: 8:10666779 (GRCh38)
8:10524289 (GRCh37)
Canonical SPDI:: NC_000008.11:10666778:A:G,NC_000008.11:10666778:A:T
Gene:: MIR4286 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_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_000008.11:g.10666779A>G, NC_000008.11:g.10666779A>T, NC_000008.10:g.10524289A>G, NC_000008.10:g.10524289A>T, NW_018654717.1:g.2680322T>C, NW_018654717.1:g.2680322T>A

Select item 14893908462.

rs1489390846 [Homo sapiens]

Variant type:: DEL
Alleles:: A>- [Show Flanks]
Chromosome:: 8:10666474 (GRCh38)
8:10523984 (GRCh37)
Canonical SPDI:: NC_000008.11:10666473:A:
Gene:: MIR4286 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.000007/1 (GnomAD)
-=0.000008/2 (TOPMED)
HGVS:: NC_000008.11:g.10666474del, NC_000008.10:g.10523984del, NW_018654717.1:g.2680603del

Select item 14890287413.

rs1489028741 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 8:10665538 (GRCh38)
8:10523048 (GRCh37)
Canonical SPDI:: NC_000008.11:10665537:C:T
Gene:: MIR4286 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency
MAF:: T=0.000007/1 (GnomAD)
HGVS:: NC_000008.11:g.10665538C>T, NC_000008.10:g.10523048C>T, NW_018654717.1:g.2681539G>A

Select item 14854327854.

rs1485432785 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 8:10666291 (GRCh38)
8:10523801 (GRCh37)
Canonical SPDI:: NC_000008.11:10666290:T:C,NC_000008.11:10666290:T:G
Gene:: MIR4286 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000008.11:g.10666291T>C, NC_000008.11:g.10666291T>G, NC_000008.10:g.10523801T>C, NC_000008.10:g.10523801T>G, NW_018654717.1:g.2680786A>G, NW_018654717.1:g.2680786A>C

Select item 14844902285.

rs1484490228 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 8:10665802 (GRCh38)
8:10523312 (GRCh37)
Canonical SPDI:: NC_000008.11:10665801:A:G
Gene:: MIR4286 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: G=0.000071/1 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000008.11:g.10665802A>G, NC_000008.10:g.10523312A>G, NW_018654717.1:g.2681275T>C

Select item 14837653806.

rs1483765380 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 8:10666116 (GRCh38)
8:10523626 (GRCh37)
Canonical SPDI:: NC_000008.11:10666115:A:G
Gene:: MIR4286 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000008.11:g.10666116A>G, NC_000008.10:g.10523626A>G, NW_018654717.1:g.2680961T>C

Select item 14834715507.

rs1483471550 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,T [Show Flanks]
Chromosome:: 8:10666686 (GRCh38)
8:10524196 (GRCh37)
Canonical SPDI:: NC_000008.11:10666685:A:C,NC_000008.11:10666685:A:T
Gene:: MIR4286 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000008/1 (GnomAD)
T=0.000008/2 (TOPMED)
HGVS:: NC_000008.11:g.10666686A>C, NC_000008.11:g.10666686A>T, NC_000008.10:g.10524196A>C, NC_000008.10:g.10524196A>T, NW_018654717.1:g.2680415T>G, NW_018654717.1:g.2680415T>A

Select item 14818606838.

rs1481860683 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 8:10665355 (GRCh38)
8:10522865 (GRCh37)
Canonical SPDI:: NC_000008.11:10665354:G:C
Gene:: MIR4286 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000008.11:g.10665355G>C, NC_000008.10:g.10522865G>C, NW_018654717.1:g.2681722C>G

Select item 14812151599.

rs1481215159 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 8:10666460 (GRCh38)
8:10523970 (GRCh37)
Canonical SPDI:: NC_000008.11:10666459:C:A
Gene:: MIR4286 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000071/1 (ALFA)
A=0.000014/2 (GnomAD)
A=0.000015/4 (TOPMED)
HGVS:: NC_000008.11:g.10666460C>A, NC_000008.10:g.10523970C>A, NW_018654717.1:g.2680617G>T

Select item 148098472710.

rs1480984727 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 8:10666081 (GRCh38)
8:10523591 (GRCh37)
Canonical SPDI:: NC_000008.11:10666080:G:C
Gene:: MIR4286 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_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_000008.11:g.10666081G>C, NC_000008.10:g.10523591G>C, NW_018654717.1:g.2680996C>G

Select item 148055921911.

rs1480559219 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 8:10666865 (GRCh38)
8:10524375 (GRCh37)
Canonical SPDI:: NC_000008.11:10666864:G:C
Gene:: MIR4286 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000071/1 (ALFA)
C=0.000015/4 (TOPMED)
C=0.000036/5 (GnomAD)
HGVS:: NC_000008.11:g.10666865G>C, NC_000008.10:g.10524375G>C, NW_018654717.1:g.2680236C>G

Select item 148038554512.

rs1480385545 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C,T [Show Flanks]
Chromosome:: 8:10666160 (GRCh38)
8:10523670 (GRCh37)
Canonical SPDI:: NC_000008.11:10666159:G:C,NC_000008.11:10666159:G:T
Gene:: MIR4286 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_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_000008.11:g.10666160G>C, NC_000008.11:g.10666160G>T, NC_000008.10:g.10523670G>C, NC_000008.10:g.10523670G>T, NW_018654717.1:g.2680917C>G, NW_018654717.1:g.2680917C>A

Select item 147961253013.

rs1479612530 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 8:10666853 (GRCh38)
8:10524363 (GRCh37)
Canonical SPDI:: NC_000008.11:10666852:C:T
Gene:: MIR4286 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000008.11:g.10666853C>T, NC_000008.10:g.10524363C>T, NW_018654717.1:g.2680248G>A

Select item 147896543514.

rs1478965435 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 8:10667493 (GRCh38)
8:10525003 (GRCh37)
Canonical SPDI:: NC_000008.11:10667492:G:A
Gene:: MIR4286 (Varview)
Functional Consequence:: 500B_downstream_variant,downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000014/2 (GnomAD)
HGVS:: NC_000008.11:g.10667493G>A, NC_000008.10:g.10525003G>A, NW_018654717.1:g.2679608C>T

Select item 147870915215.

rs1478709152 has merged into rs141601742 [Homo sapiens]

Variant type:: DELINS
Alleles:: A>-,AA [Show Flanks]
Chromosome:: 8:10667252 (GRCh38)
8:10524762 (GRCh37)
Canonical SPDI:: NC_000008.11:10667251:AAAAAAA:AAAAAA,NC_000008.11:10667251:AAAAAAA:AAAAAAAA
Gene:: MIR4286 (Varview)
Functional Consequence:: 500B_downstream_variant,downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAA=0./0 (ALFA)
-=0.006402/32 (1000Genomes)
-=0.006751/1787 (TOPMED)
HGVS:: NC_000008.11:g.10667258del, NC_000008.11:g.10667258dup, NC_000008.10:g.10524768del, NC_000008.10:g.10524768dup, NW_018654717.1:g.2679849del, NW_018654717.1:g.2679849dup

Select item 147866933116.

rs1478669331 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 8:10665329 (GRCh38)
8:10522839 (GRCh37)
Canonical SPDI:: NC_000008.11:10665328:G:A,NC_000008.11:10665328:G:T
Gene:: MIR4286 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000011/3 (TOPMED)
HGVS:: NC_000008.11:g.10665329G>A, NC_000008.11:g.10665329G>T, NC_000008.10:g.10522839G>A, NC_000008.10:g.10522839G>T, NW_018654717.1:g.2681748C>T, NW_018654717.1:g.2681748C>A

Select item 147861068817.

rs1478610688 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C,T [Show Flanks]
Chromosome:: 8:10665358 (GRCh38)
8:10522868 (GRCh37)
Canonical SPDI:: NC_000008.11:10665357:G:A,NC_000008.11:10665357:G:C,NC_000008.11:10665357:G:T
Gene:: MIR4286 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
HGVS:: NC_000008.11:g.10665358G>A, NC_000008.11:g.10665358G>C, NC_000008.11:g.10665358G>T, NC_000008.10:g.10522868G>A, NC_000008.10:g.10522868G>C, NC_000008.10:g.10522868G>T, NW_018654717.1:g.2681719C>T, NW_018654717.1:g.2681719C>G, NW_018654717.1:g.2681719C>A

Select item 147855092018.

rs1478550920 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 8:10666905 (GRCh38)
8:10524415 (GRCh37)
Canonical SPDI:: NC_000008.11:10666904:C:T
Gene:: MIR4286 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000071/1 (ALFA)
T=0.000011/3 (TOPMED)
T=0.000014/2 (GnomAD)
HGVS:: NC_000008.11:g.10666905C>T, NC_000008.10:g.10524415C>T, NW_018654717.1:g.2680196G>A

Select item 147797611619.

rs1477976116 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 8:10667198 (GRCh38)
8:10524708 (GRCh37)
Canonical SPDI:: NC_000008.11:10667197:T:C
Gene:: MIR4286 (Varview)
Functional Consequence:: 500B_downstream_variant,downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000011/3 (TOPMED)
HGVS:: NC_000008.11:g.10667198T>C, NC_000008.10:g.10524708T>C, NW_018654717.1:g.2679903A>G

Select item 147537654920.

rs1475376549 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 8:10667235 (GRCh38)
8:10524745 (GRCh37)
Canonical SPDI:: NC_000008.11:10667234:G:T
Gene:: MIR4286 (Varview)
Functional Consequence:: 500B_downstream_variant,downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000143/20 (GnomAD)
HGVS:: NC_000008.11:g.10667235G>T, NC_000008.10:g.10524745G>T, NW_018654717.1:g.2679866C>A

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