SNP Links for Gene (Select 1847) - SNP

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Select item 14915868041.

rs1491586804 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->T [Show Flanks]
Chromosome:: 10:110507440 (GRCh38)
10:112267199 (GRCh37)
Canonical SPDI:: NC_000010.11:110507440:T:TT
Gene:: DUSP5 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: TT=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000010.11:g.110507441dup, NC_000010.10:g.112267199dup

Select item 14911085392.

rs1491108539 [Homo sapiens]

Variant type:: DELINS
Alleles:: GT>- [Show Flanks]
Chromosome:: 10:110507442 (GRCh38)
10:112267200 (GRCh37)
Canonical SPDI:: NC_000010.11:110507439:GTGT:GT
Gene:: DUSP5 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: GTGT=0./0 (ALFA)
-=0.000007/1 (GnomAD)
HGVS:: NC_000010.11:g.110507440GT[1], NC_000010.10:g.112267198GT[1]

Select item 14911062493.

rs1491106249 [Homo sapiens]

Variant type:: DEL
Alleles:: TG>- [Show Flanks]
Chromosome:: 10:110501965 (GRCh38)
10:112261723 (GRCh37)
Canonical SPDI:: NC_000010.11:110501964:TG:
Gene:: DUSP5 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0./0 (ALFA)
-=0.000268/33 (GnomAD)
HGVS:: NC_000010.11:g.110501965_110501966del, NC_000010.10:g.112261723_112261724del

Select item 14908314604.

rs1490831460 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 10:110501272 (GRCh38)
10:112261030 (GRCh37)
Canonical SPDI:: NC_000010.11:110501271:C:T
Gene:: DUSP5 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0./0 (KOREAN)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000010.11:g.110501272C>T, NC_000010.10:g.112261030C>T

Select item 14908154855.

rs1490815485 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 10:110503943 (GRCh38)
10:112263701 (GRCh37)
Canonical SPDI:: NC_000010.11:110503942:A:G
Gene:: DUSP5 (Varview)
Functional Consequence:: intron_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_000010.11:g.110503943A>G, NC_000010.10:g.112263701A>G

Select item 14905688346.

rs1490568834 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 10:110504753 (GRCh38)
10:112264511 (GRCh37)
Canonical SPDI:: NC_000010.11:110504752:C:G
Gene:: DUSP5 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
HGVS:: NC_000010.11:g.110504753C>G, NC_000010.10:g.112264511C>G

Select item 14904793797.

rs1490479379 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->A [Show Flanks]
Chromosome:: 10:110511145 (GRCh38)
10:112270904 (GRCh37)
Canonical SPDI:: NC_000010.11:110511145:AAAA:AAAAA
Gene:: DUSP5 (Varview)
Functional Consequence:: 3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAA=0./0 (ALFA)
A=0.000014/2 (GnomAD)
A=0.000034/9 (TOPMED)
HGVS:: NC_000010.11:g.110511149dup, NC_000010.10:g.112270907dup, NM_004419.4:c.*723dup, NM_004419.3:c.*723dup

Select item 14904726988.

rs1490472698 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C,T [Show Flanks]
Chromosome:: 10:110498484 (GRCh38)
10:112258242 (GRCh37)
Canonical SPDI:: NC_000010.11:110498483:G:C,NC_000010.11:110498483:G:T
Gene:: DUSP5 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
HGVS:: NC_000010.11:g.110498484G>C, NC_000010.11:g.110498484G>T, NC_000010.10:g.112258242G>C, NC_000010.10:g.112258242G>T, NM_004419.4:c.363G>C, NM_004419.4:c.363G>T, NM_004419.3:c.363G>C, NM_004419.3:c.363G>T

Select item 14904584899.

rs1490458489 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 10:110497924 (GRCh38)
10:112257682 (GRCh37)
Canonical SPDI:: NC_000010.11:110497923:G:A
Gene:: DUSP5 (Varview)
Functional Consequence:: 5_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
A=0.000014/2 (GnomAD)
HGVS:: NC_000010.11:g.110497924G>A, NC_000010.10:g.112257682G>A, NM_004419.4:c.-198G>A, NM_004419.3:c.-198G>A

Select item 149034200510.

rs1490342005 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 10:110502423 (GRCh38)
10:112262181 (GRCh37)
Canonical SPDI:: NC_000010.11:110502422:T:C
Gene:: DUSP5 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
C=0.000014/2 (GnomAD)
HGVS:: NC_000010.11:g.110502423T>C, NC_000010.10:g.112262181T>C

Select item 149031022811.

rs1490310228 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 10:110498786 (GRCh38)
10:112258544 (GRCh37)
Canonical SPDI:: NC_000010.11:110498785:C:T
Gene:: DUSP5 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000071/1 (ALFA)
T=0.000014/2 (GnomAD)
T=0.000015/4 (TOPMED)
HGVS:: NC_000010.11:g.110498786C>T, NC_000010.10:g.112258544C>T

Select item 149011482112.

rs1490114821 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 10:110505853 (GRCh38)
10:112265611 (GRCh37)
Canonical SPDI:: NC_000010.11:110505852:G:A
Gene:: DUSP5 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0.000071/1 (ALFA)
A=0.000011/3 (TOPMED)
HGVS:: NC_000010.11:g.110505853G>A, NC_000010.10:g.112265611G>A

Select item 148983682113.

rs1489836821 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 10:110505975 (GRCh38)
10:112265733 (GRCh37)
Canonical SPDI:: NC_000010.11:110505974:T:C
Gene:: DUSP5 (Varview)
Functional Consequence:: intron_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_000010.11:g.110505975T>C, NC_000010.10:g.112265733T>C

Select item 148910599514.

rs1489105995 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 10:110502638 (GRCh38)
10:112262396 (GRCh37)
Canonical SPDI:: NC_000010.11:110502637:A:G
Gene:: DUSP5 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
HGVS:: NC_000010.11:g.110502638A>G, NC_000010.10:g.112262396A>G

Select item 148880707415.

rs1488807074 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 10:110498710 (GRCh38)
10:112258468 (GRCh37)
Canonical SPDI:: NC_000010.11:110498709:G:C
Gene:: DUSP5 (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_000010.11:g.110498710G>C, NC_000010.10:g.112258468G>C

Select item 148847124116.

rs1488471241 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 10:110506704 (GRCh38)
10:112266462 (GRCh37)
Canonical SPDI:: NC_000010.11:110506703:C:T
Gene:: DUSP5 (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_000010.11:g.110506704C>T, NC_000010.10:g.112266462C>T

Select item 148804406317.

rs1488044063 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 10:110506861 (GRCh38)
10:112266619 (GRCh37)
Canonical SPDI:: NC_000010.11:110506860:G:A
Gene:: DUSP5 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000071/1 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000008/2 (TOPMED)
HGVS:: NC_000010.11:g.110506861G>A, NC_000010.10:g.112266619G>A

Select item 148790366618.

rs1487903666 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 10:110508030 (GRCh38)
10:112267788 (GRCh37)
Canonical SPDI:: NC_000010.11:110508029:G:A,NC_000010.11:110508029:G:T
Gene:: DUSP5 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000066/1 (ALFA)
A=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
T=0.000223/1 (Estonian)
HGVS:: NC_000010.11:g.110508030G>A, NC_000010.11:g.110508030G>T, NC_000010.10:g.112267788G>A, NC_000010.10:g.112267788G>T

Select item 148745573519.

rs1487455735 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 10:110507579 (GRCh38)
10:112267337 (GRCh37)
Canonical SPDI:: NC_000010.11:110507578:C:T
Gene:: DUSP5 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
T=0.00006/1 (TOMMO)
HGVS:: NC_000010.11:g.110507579C>T, NC_000010.10:g.112267337C>T

Select item 148727576720.

rs1487275767 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 10:110499727 (GRCh38)
10:112259485 (GRCh37)
Canonical SPDI:: NC_000010.11:110499726:C:A
Gene:: DUSP5 (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: A=0.000071/1 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000010.11:g.110499727C>A, NC_000010.10:g.112259485C>A

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