SNP Links for Protein (Select 225703077) - SNP

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Links from Protein

Items: 1 to 20 of 153

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Select item 14867061831.

rs1486706183 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: X:44844632 (GRCh38)
X:44703878 (GRCh37)
Canonical SPDI:: NC_000023.11:44844631:G:A
Gene:: DUSP21 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: A=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000023.11:g.44844632G>A, NC_000023.10:g.44703878G>A, NG_013231.1:g.5630G>A, NM_022076.4:c.500G>A, NM_022076.3:c.500G>A, NP_071359.3:p.Arg167His

Select item 14864684662.

rs1486468466 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: X:44844434 (GRCh38)
X:44703680 (GRCh37)
Canonical SPDI:: NC_000023.11:44844433:G:A,NC_000023.11:44844433:G:T
Gene:: DUSP21 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
A=0.000004/1 (TOPMED)
T=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.44844434G>A, NC_000023.11:g.44844434G>T, NC_000023.10:g.44703680G>A, NC_000023.10:g.44703680G>T, NG_013231.1:g.5432G>A, NG_013231.1:g.5432G>T, NM_022076.4:c.302G>A, NM_022076.4:c.302G>T, NM_022076.3:c.302G>A, NM_022076.3:c.302G>T, NP_071359.3:p.Arg101His, NP_071359.3:p.Arg101Leu

Select item 14857808233.

rs1485780823 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: X:44844704 (GRCh38)
X:44703950 (GRCh37)
Canonical SPDI:: NC_000023.11:44844703:A:G
Gene:: DUSP21 (Varview)
Functional Consequence:: terminator_codon_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: G=0.000142/2 (ALFA)
G=0.000008/2 (TOPMED)
HGVS:: NC_000023.11:g.44844704A>G, NC_000023.10:g.44703950A>G, NG_013231.1:g.5702A>G, NM_022076.4:c.572A>G, NM_022076.3:c.572A>G

Select item 14798575154.

rs1479857515 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: X:44844653 (GRCh38)
X:44703899 (GRCh37)
Canonical SPDI:: NC_000023.11:44844652:G:T
Gene:: DUSP21 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000006/1 (GnomAD_exomes)
T=0.000019/2 (GnomAD)
T=0.000034/9 (TOPMED)
HGVS:: NC_000023.11:g.44844653G>T, NC_000023.10:g.44703899G>T, NG_013231.1:g.5651G>T, NM_022076.4:c.521G>T, NM_022076.3:c.521G>T, NP_071359.3:p.Gly174Val

Select item 14797013465.

rs1479701346 [Homo sapiens]

Variant type:: DELINS
Alleles:: TCT>- [Show Flanks]
Chromosome:: X:44844258 (GRCh38)
X:44703504 (GRCh37)
Canonical SPDI:: NC_000023.11:44844255:CTTCT:CT
Gene:: DUSP21 (Varview)
Functional Consequence:: coding_sequence_variant,inframe_deletion
Validated:: by frequency,by cluster
MAF:: -=0.000005/1 (GnomAD_exomes)
-=0.000208/1 (1000Genomes)
HGVS:: NC_000023.11:g.44844258_44844260del, NC_000023.10:g.44703504_44703506del, NG_013231.1:g.5256_5258del, NM_022076.4:c.126_128del, NM_022076.3:c.126_128del, NP_071359.3:p.Leu43del

Select item 14764937886.

rs1476493788 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: X:44844551 (GRCh38)
X:44703797 (GRCh37)
Canonical SPDI:: NC_000023.11:44844550:G:A,NC_000023.11:44844550:G:C
Gene:: DUSP21 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000023.11:g.44844551G>A, NC_000023.11:g.44844551G>C, NC_000023.10:g.44703797G>A, NC_000023.10:g.44703797G>C, NG_013231.1:g.5549G>A, NG_013231.1:g.5549G>C, NM_022076.4:c.419G>A, NM_022076.4:c.419G>C, NM_022076.3:c.419G>A, NM_022076.3:c.419G>C, NP_071359.3:p.Arg140His, NP_071359.3:p.Arg140Pro

Select item 14722467997.

rs1472246799 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: X:44844138 (GRCh38)
X:44703384 (GRCh37)
Canonical SPDI:: NC_000023.11:44844137:A:G
Gene:: DUSP21 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000253/3 (ALFA)
G=0.000008/2 (TOPMED)
G=0.000011/2 (GnomAD_exomes)
HGVS:: NC_000023.11:g.44844138A>G, NC_000023.10:g.44703384A>G, NG_013231.1:g.5136A>G, NM_022076.4:c.6A>G, NM_022076.3:c.6A>G

Select item 14703971528.

rs1470397152 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: X:44844153 (GRCh38)
X:44703399 (GRCh37)
Canonical SPDI:: NC_000023.11:44844152:C:T
Gene:: DUSP21 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: T=0.000006/1 (GnomAD_exomes)
HGVS:: NC_000023.11:g.44844153C>T, NC_000023.10:g.44703399C>T, NG_013231.1:g.5151C>T, NM_022076.4:c.21C>T, NM_022076.3:c.21C>T

Select item 14696650339.

rs1469665033 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: X:44844371 (GRCh38)
X:44703617 (GRCh37)
Canonical SPDI:: NC_000023.11:44844370:G:A
Gene:: DUSP21 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: A=0.000011/2 (GnomAD_exomes)
HGVS:: NC_000023.11:g.44844371G>A, NC_000023.10:g.44703617G>A, NG_013231.1:g.5369G>A, NM_022076.4:c.239G>A, NM_022076.3:c.239G>A, NP_071359.3:p.Arg80His

Select item 146508986810.

rs1465089868 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: X:44844593 (GRCh38)
X:44703839 (GRCh37)
Canonical SPDI:: NC_000023.11:44844592:T:C
Gene:: DUSP21 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000005/1 (GnomAD_exomes)
C=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.44844593T>C, NC_000023.10:g.44703839T>C, NG_013231.1:g.5591T>C, NM_022076.4:c.461T>C, NM_022076.3:c.461T>C, NP_071359.3:p.Ile154Thr

Select item 145733894511.

rs1457338945 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: X:44844553 (GRCh38)
X:44703799 (GRCh37)
Canonical SPDI:: NC_000023.11:44844552:C:T
Gene:: DUSP21 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
T=0.000029/3 (GnomAD)
HGVS:: NC_000023.11:g.44844553C>T, NC_000023.10:g.44703799C>T, NG_013231.1:g.5551C>T, NM_022076.4:c.421C>T, NM_022076.3:c.421C>T, NP_071359.3:p.Pro141Ser

Select item 144356912312.

rs1443569123 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: X:44844422 (GRCh38)
X:44703668 (GRCh37)
Canonical SPDI:: NC_000023.11:44844421:T:A
Gene:: DUSP21 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000023.11:g.44844422T>A, NC_000023.10:g.44703668T>A, NG_013231.1:g.5420T>A, NM_022076.4:c.290T>A, NM_022076.3:c.290T>A, NP_071359.3:p.Met97Lys

Select item 142919403413.

rs1429194034 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: X:44844290 (GRCh38)
X:44703536 (GRCh37)
Canonical SPDI:: NC_000023.11:44844289:A:G
Gene:: DUSP21 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: G=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000023.11:g.44844290A>G, NC_000023.10:g.44703536A>G, NG_013231.1:g.5288A>G, NM_022076.4:c.158A>G, NM_022076.3:c.158A>G, NP_071359.3:p.Asn53Ser

Select item 141459435914.

rs1414594359 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: X:44844312 (GRCh38)
X:44703558 (GRCh37)
Canonical SPDI:: NC_000023.11:44844311:C:T
Gene:: DUSP21 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.44844312C>T, NC_000023.10:g.44703558C>T, NG_013231.1:g.5310C>T, NM_022076.4:c.180C>T, NM_022076.3:c.180C>T

Select item 141281712015.

rs1412817120 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: X:44844159 (GRCh38)
X:44703405 (GRCh37)
Canonical SPDI:: NC_000023.11:44844158:A:T
Gene:: DUSP21 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000006/1 (GnomAD_exomes)
T=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.44844159A>T, NC_000023.10:g.44703405A>T, NG_013231.1:g.5157A>T, NM_022076.4:c.27A>T, NM_022076.3:c.27A>T

Select item 140237321816.

rs1402373218 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: X:44844515 (GRCh38)
X:44703761 (GRCh37)
Canonical SPDI:: NC_000023.11:44844514:C:A
Gene:: DUSP21 (Varview)
Functional Consequence:: coding_sequence_variant,stop_gained
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.00001/1 (GnomAD)
HGVS:: NC_000023.11:g.44844515C>A, NC_000023.10:g.44703761C>A, NG_013231.1:g.5513C>A, NM_022076.4:c.383C>A, NM_022076.3:c.383C>A, NP_071359.3:p.Ser128Ter

Select item 140184734817.

rs1401847348 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: X:44844157 (GRCh38)
X:44703403 (GRCh37)
Canonical SPDI:: NC_000023.11:44844156:T:G
Gene:: DUSP21 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: G=0.000006/1 (GnomAD_exomes)
HGVS:: NC_000023.11:g.44844157T>G, NC_000023.10:g.44703403T>G, NG_013231.1:g.5155T>G, NM_022076.4:c.25T>G, NM_022076.3:c.25T>G, NP_071359.3:p.Ser9Ala

Select item 139933385118.

rs1399333851 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: X:44844299 (GRCh38)
X:44703545 (GRCh37)
Canonical SPDI:: NC_000023.11:44844298:T:G
Gene:: DUSP21 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: G=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000023.11:g.44844299T>G, NC_000023.10:g.44703545T>G, NG_013231.1:g.5297T>G, NM_022076.4:c.167T>G, NM_022076.3:c.167T>G, NP_071359.3:p.Val56Gly

Select item 139630274919.

rs1396302749 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: X:44844685 (GRCh38)
X:44703931 (GRCh37)
Canonical SPDI:: NC_000023.11:44844684:C:A,NC_000023.11:44844684:C:T
Gene:: DUSP21 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000019/2 (GnomAD)
HGVS:: NC_000023.11:g.44844685C>A, NC_000023.11:g.44844685C>T, NC_000023.10:g.44703931C>A, NC_000023.10:g.44703931C>T, NG_013231.1:g.5683C>A, NG_013231.1:g.5683C>T, NM_022076.4:c.553C>A, NM_022076.4:c.553C>T, NM_022076.3:c.553C>A, NM_022076.3:c.553C>T, NP_071359.3:p.Arg185Ser, NP_071359.3:p.Arg185Cys

Select item 139230998120.

rs1392309981 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: X:44844301 (GRCh38)
X:44703547 (GRCh37)
Canonical SPDI:: NC_000023.11:44844300:G:C
Gene:: DUSP21 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: C=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000023.11:g.44844301G>C, NC_000023.10:g.44703547G>C, NG_013231.1:g.5299G>C, NM_022076.4:c.169G>C, NM_022076.3:c.169G>C, NP_071359.3:p.Glu57Gln