SNP Links for Gene (Select 642006) - SNP

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Items: 1 to 20 of 4450

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Select item 14912384611.

rs1491238461 [Homo sapiens]

Variant type:: DEL
Alleles:: CA>- [Show Flanks]
Chromosome:: 7:57166956 (GRCh38)
7:57234663 (GRCh37)
Canonical SPDI:: NC_000007.14:57166955:CA:
Gene:: GUSBP10 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: -=0.01197/142 (ALFA)
HGVS:: NC_000007.14:g.57166956_57166957del, NC_000007.13:g.57234663_57234664del

Select item 14910034472.

rs1491003447 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 7:57169769 (GRCh38)
7:57237476 (GRCh37)
Canonical SPDI:: NC_000007.14:57169768:T:G
Gene:: GUSBP10 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
HGVS:: NC_000007.14:g.57169769T>G, NC_000007.13:g.57237476T>G, NG_032459.1:g.1200A>C

Select item 14906814033.

rs1490681403 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 7:57169058 (GRCh38)
7:57236765 (GRCh37)
Canonical SPDI:: NC_000007.14:57169057:G:A
Gene:: GUSBP10 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000071/1 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000015/4 (TOPMED)
HGVS:: NC_000007.14:g.57169058G>A, NC_000007.13:g.57236765G>A, NG_068471.1:g.16G>A

Select item 14905775574.

rs1490577557 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 7:57175752 (GRCh38)
7:57243459 (GRCh37)
Canonical SPDI:: NC_000007.14:57175751:A:G
Gene:: GUSBP10 (Varview)
Functional Consequence:: intron_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_000007.14:g.57175752A>G, NC_000007.13:g.57243459A>G

Select item 14905338765.

rs1490533876 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 7:57171762 (GRCh38)
7:57239469 (GRCh37)
Canonical SPDI:: NC_000007.14:57171761:T:C
Gene:: GUSBP10 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000007.14:g.57171762T>C, NC_000007.13:g.57239469T>C, NG_032485.1:g.870T>C

Select item 14905194406.

rs1490519440 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 7:57169823 (GRCh38)
7:57237530 (GRCh37)
Canonical SPDI:: NC_000007.14:57169822:C:A
Gene:: GUSBP10 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000011/3 (TOPMED)
A=0.000014/2 (GnomAD)
HGVS:: NC_000007.14:g.57169823C>A, NC_000007.13:g.57237530C>A, NG_032459.1:g.1146G>T

Select item 14905125177.

rs1490512517 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 7:57170156 (GRCh38)
7:57237863 (GRCh37)
Canonical SPDI:: NC_000007.14:57170155:C:G
Gene:: GUSBP10 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000007.14:g.57170156C>G, NC_000007.13:g.57237863C>G, NG_032459.1:g.813G>C

Select item 14900859478.

rs1490085947 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 7:57176131 (GRCh38)
7:57243838 (GRCh37)
Canonical SPDI:: NC_000007.14:57176130:C:A
Gene:: GUSBP10 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000007.14:g.57176131C>A, NC_000007.13:g.57243838C>A

Select item 14896349879.

rs1489634987 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 7:57172638 (GRCh38)
7:57240345 (GRCh37)
Canonical SPDI:: NC_000007.14:57172637:T:G
Gene:: GUSBP10 (Varview)
Functional Consequence:: intron_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_000007.14:g.57172638T>G, NC_000007.13:g.57240345T>G, NG_032485.1:g.1746T>G

Select item 148948645510.

rs1489486455 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 7:57178254 (GRCh38)
7:57245961 (GRCh37)
Canonical SPDI:: NC_000007.14:57178253:G:A
Gene:: GUSBP10 (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=0.000156/1 (1000Genomes)
HGVS:: NC_000007.14:g.57178254G>A, NC_000007.13:g.57245961G>A, NR_030766.1:n.421C>T

Select item 148945401111.

rs1489454011 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C,T [Show Flanks]
Chromosome:: 7:57181268 (GRCh38)
7:57248975 (GRCh37)
Canonical SPDI:: NC_000007.14:57181267:G:A,NC_000007.14:57181267:G:C,NC_000007.14:57181267:G:T
Gene:: GUSBP10 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000019/5 (TOPMED)
A=0.000071/2 (TOMMO)
HGVS:: NC_000007.14:g.57181268G>A, NC_000007.14:g.57181268G>C, NC_000007.14:g.57181268G>T, NC_000007.13:g.57248975G>A, NC_000007.13:g.57248975G>C, NC_000007.13:g.57248975G>T

Select item 148939460712.

rs1489394607 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 7:57176456 (GRCh38)
7:57244163 (GRCh37)
Canonical SPDI:: NC_000007.14:57176455:A:T
Gene:: GUSBP10 (Varview)
Functional Consequence:: intron_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_000007.14:g.57176456A>T, NC_000007.13:g.57244163A>T

Select item 148926587513.

rs1489265875 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 7:57170936 (GRCh38)
7:57238643 (GRCh37)
Canonical SPDI:: NC_000007.14:57170935:T:C
Gene:: GUSBP10 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: C=0.000071/1 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000007.14:g.57170936T>C, NC_000007.13:g.57238643T>C, NG_032485.1:g.44T>C, NG_032459.1:g.33A>G

Select item 148909963714.

rs1489099637 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 7:57177198 (GRCh38)
7:57244905 (GRCh37)
Canonical SPDI:: NC_000007.14:57177197:C:A
Gene:: GUSBP10 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000007.14:g.57177198C>A, NC_000007.13:g.57244905C>A

Select item 148908362515.

rs1489083625 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 7:57165189 (GRCh38)
7:57232896 (GRCh37)
Canonical SPDI:: NC_000007.14:57165188:T:A
Gene:: GUSBP10 (Varview)
Functional Consequence:: downstream_transcript_variant,500B_downstream_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000007.14:g.57165189T>A, NC_000007.13:g.57232896T>A

Select item 148901629316.

rs1489016293 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 7:57167579 (GRCh38)
7:57235286 (GRCh37)
Canonical SPDI:: NC_000007.14:57167578:A:G
Gene:: GUSBP10 (Varview)
Functional Consequence:: intron_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_000007.14:g.57167579A>G, NC_000007.13:g.57235286A>G, NG_046637.1:g.480A>G

Select item 148883515917.

rs1488835159 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 7:57174027 (GRCh38)
7:57241734 (GRCh37)
Canonical SPDI:: NC_000007.14:57174026:A:G
Gene:: GUSBP10 (Varview)
Functional Consequence:: intron_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_000007.14:g.57174027A>G, NC_000007.13:g.57241734A>G, NG_046507.1:g.771A>G

Select item 148870283318.

rs1488702833 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 7:57180441 (GRCh38)
7:57248148 (GRCh37)
Canonical SPDI:: NC_000007.14:57180440:G:A
Gene:: GUSBP10 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000011/3 (TOPMED)
HGVS:: NC_000007.14:g.57180441G>A, NC_000007.13:g.57248148G>A

Select item 148866226519.

rs1488662265 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 7:57171797 (GRCh38)
7:57239504 (GRCh37)
Canonical SPDI:: NC_000007.14:57171796:T:C
Gene:: GUSBP10 (Varview)
Functional Consequence:: 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_000007.14:g.57171797T>C, NC_000007.13:g.57239504T>C, NG_032485.1:g.905T>C

Select item 148856460820.

rs1488564608 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 7:57165297 (GRCh38)
7:57233004 (GRCh37)
Canonical SPDI:: NC_000007.14:57165296:C:T
Gene:: GUSBP10 (Varview)
Functional Consequence:: downstream_transcript_variant,500B_downstream_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_000007.14:g.57165297C>T, NC_000007.13:g.57233004C>T

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