SNP Links for Protein (Select 379317177) - SNP

Links from Protein

Items: 1 to 20 of 491

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Select item 14865171071.

rs1486517107 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 10:68967160 (GRCh38)
10:70726916 (GRCh37)
Canonical SPDI:: NC_000010.11:68967159:T:C
Gene:: DDX21 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
HGVS:: NC_000010.11:g.68967160T>C, NC_000010.10:g.70726916T>C, NM_004728.4:c.1047T>C, NM_004728.3:c.1047T>C, NM_001256910.2:c.843T>C, NM_001256910.1:c.843T>C, XM_011540336.2:c.1047T>C, NM_001410932.1:c.1047T>C

Select item 14855847682.

rs1485584768 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 10:68962130 (GRCh38)
10:70721886 (GRCh37)
Canonical SPDI:: NC_000010.11:68962129:T:A
Gene:: DDX21 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000010.11:g.68962130T>A, NC_000010.10:g.70721886T>A, NM_004728.4:c.580T>A, NM_004728.3:c.580T>A, NM_001256910.2:c.376T>A, NM_001256910.1:c.376T>A, XM_011540336.2:c.580T>A, NM_001410932.1:c.580T>A, NP_004719.2:p.Ser194Thr, NP_001243839.1:p.Ser126Thr, XP_011538638.1:p.Ser194Thr

Select item 14835921403.

rs1483592140 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 10:68963455 (GRCh38)
10:70723211 (GRCh37)
Canonical SPDI:: NC_000010.11:68963454:G:A
Gene:: DDX21 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000010.11:g.68963455G>A, NC_000010.10:g.70723211G>A, NM_004728.4:c.772G>A, NM_004728.3:c.772G>A, NM_001256910.2:c.568G>A, NM_001256910.1:c.568G>A, XM_011540336.2:c.772G>A, NM_001410932.1:c.772G>A, NP_004719.2:p.Gly258Ser, NP_001243839.1:p.Gly190Ser, XP_011538638.1:p.Gly258Ser

Select item 14834115114.

rs1483411511 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 10:68971937 (GRCh38)
10:70731693 (GRCh37)
Canonical SPDI:: NC_000010.11:68971936:T:G
Gene:: DDX21 (Varview)
Functional Consequence:: coding_sequence_variant,intron_variant,missense_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000010.11:g.68971937T>G, NC_000010.10:g.70731693T>G, NM_004728.4:c.1433T>G, NM_004728.3:c.1433T>G, NM_001256910.2:c.1229T>G, NM_001256910.1:c.1229T>G, NP_004719.2:p.Ile478Ser, NP_001243839.1:p.Ile410Ser

Select item 14822723795.

rs1482272379 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 10:68973577 (GRCh38)
10:70733333 (GRCh37)
Canonical SPDI:: NC_000010.11:68973576:G:A
Gene:: DDX21 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by cluster
MAF:: A=0.000004/1 (GnomAD_exomes)
A=0.000007/1 (GnomAD)
HGVS:: NC_000010.11:g.68973577G>A, NC_000010.10:g.70733333G>A, NM_004728.4:c.1581G>A, NM_004728.3:c.1581G>A, NM_001256910.2:c.1377G>A, NM_001256910.1:c.1377G>A, XM_011540336.2:c.1419G>A, NM_001410932.1:c.1419G>A

Select item 14737269736.

rs1473726973 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 10:68977682 (GRCh38)
10:70737438 (GRCh37)
Canonical SPDI:: NC_000010.11:68977681:A:T
Gene:: DDX21 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_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.68977682A>T, NC_000010.10:g.70737438A>T, NM_004728.4:c.1896A>T, NM_004728.3:c.1896A>T, NM_001256910.2:c.1692A>T, NM_001256910.1:c.1692A>T, XM_011540336.2:c.1734A>T, NM_001410932.1:c.1734A>T

Select item 14697385137.

rs1469738513 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 10:68960158 (GRCh38)
10:70719914 (GRCh37)
Canonical SPDI:: NC_000010.11:68960157:G:A
Gene:: DDX21 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000010.11:g.68960158G>A, NC_000010.10:g.70719914G>A, NM_004728.4:c.440G>A, NM_004728.3:c.440G>A, NM_001256910.2:c.236G>A, NM_001256910.1:c.236G>A, XM_011540336.2:c.440G>A, NM_001410932.1:c.440G>A, NP_004719.2:p.Ser147Asn, NP_001243839.1:p.Ser79Asn, XP_011538638.1:p.Ser147Asn

Select item 14666839828.

rs1466683982 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 10:68970266 (GRCh38)
10:70730022 (GRCh37)
Canonical SPDI:: NC_000010.11:68970265:T:C
Gene:: DDX21 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000010.11:g.68970266T>C, NC_000010.10:g.70730022T>C, NM_004728.4:c.1302T>C, NM_004728.3:c.1302T>C, NM_001256910.2:c.1098T>C, NM_001256910.1:c.1098T>C, XM_011540336.2:c.1302T>C, NM_001410932.1:c.1302T>C

Select item 14630599559.

rs1463059955 [Homo sapiens]

Variant type:: INS
Alleles:: ->TTTTTGTCA [Show Flanks]
Chromosome:: 10:68960186 (GRCh38)
10:70719943 (GRCh37)
Canonical SPDI:: NC_000010.11:68960186::TTTTTGTCA
Gene:: DDX21 (Varview)
Functional Consequence:: coding_sequence_variant,inframe_insertion
Validated:: by frequency,by alfa,by cluster
MAF:: TTTTTGTCA=0.0001/1 (ALFA)
HGVS:: NC_000010.11:g.68960186_68960187insTTTTTGTCA, NC_000010.10:g.70719942_70719943insTTTTTGTCA, NM_004728.4:c.468_469insTTTTTGTCA, NM_004728.3:c.468_469insTTTTTGTCA, NM_001256910.2:c.264_265insTTTTTGTCA, NM_001256910.1:c.264_265insTTTTTGTCA, XM_011540336.2:c.468_469insTTTTTGTCA, NM_001410932.1:c.468_469insTTTTTGTCA, NP_004719.2:p.Pro157_Glu158insPheLeuSer, NP_001243839.1:p.Pro89_Glu90insPheLeuSer, XP_011538638.1:p.Pro157_Glu158insPheLeuSer

Select item 146107809310.

rs1461078093 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 10:68981556 (GRCh38)
10:70741312 (GRCh37)
Canonical SPDI:: NC_000010.11:68981555:C:T
Gene:: DDX21 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0./0 (Korea1K)
T=0.000008/2 (GnomAD_exomes)
T=0.000014/2 (GnomAD)
T=0.000035/1 (TOMMO)
HGVS:: NC_000010.11:g.68981556C>T, NC_000010.10:g.70741312C>T, NM_004728.4:c.2057C>T, NM_004728.3:c.2057C>T, NM_001256910.2:c.1853C>T, NM_001256910.1:c.1853C>T, XM_011540336.2:c.1895C>T, NM_001410932.1:c.1895C>T, NP_004719.2:p.Pro686Leu, NP_001243839.1:p.Pro618Leu, XP_011538638.1:p.Pro632Leu

Select item 145992080211.

rs1459920802 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 10:68963433 (GRCh38)
10:70723189 (GRCh37)
Canonical SPDI:: NC_000010.11:68963432:G:A
Gene:: DDX21 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000010.11:g.68963433G>A, NC_000010.10:g.70723189G>A, NM_004728.4:c.750G>A, NM_004728.3:c.750G>A, NM_001256910.2:c.546G>A, NM_001256910.1:c.546G>A, XM_011540336.2:c.750G>A, NM_001410932.1:c.750G>A

Select item 145759051712.

rs1457590517 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 10:68982743 (GRCh38)
10:70742499 (GRCh37)
Canonical SPDI:: NC_000010.11:68982742:T:C
Gene:: DDX21 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000010.11:g.68982743T>C, NC_000010.10:g.70742499T>C, NM_004728.4:c.2283T>C, NM_004728.3:c.2283T>C, NM_001256910.2:c.2079T>C, NM_001256910.1:c.2079T>C, XM_011540336.2:c.2121T>C, NM_001410932.1:c.2121T>C

Select item 145491366613.

rs1454913666 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 10:68967106 (GRCh38)
10:70726862 (GRCh37)
Canonical SPDI:: NC_000010.11:68967105:C:T
Gene:: DDX21 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000010.11:g.68967106C>T, NC_000010.10:g.70726862C>T, NM_004728.4:c.993C>T, NM_004728.3:c.993C>T, NM_001256910.2:c.789C>T, NM_001256910.1:c.789C>T, XM_011540336.2:c.993C>T, NM_001410932.1:c.993C>T

Select item 145326317414.

rs1453263174 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 10:68982627 (GRCh38)
10:70742383 (GRCh37)
Canonical SPDI:: NC_000010.11:68982626:G:A
Gene:: DDX21 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by cluster
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000010.11:g.68982627G>A, NC_000010.10:g.70742383G>A, NM_004728.4:c.2167G>A, NM_004728.3:c.2167G>A, NM_001256910.2:c.1963G>A, NM_001256910.1:c.1963G>A, XM_011540336.2:c.2005G>A, NM_001410932.1:c.2005G>A, NP_004719.2:p.Gly723Ser, NP_001243839.1:p.Gly655Ser, XP_011538638.1:p.Gly669Ser

Select item 144788946015.

rs1447889460 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 10:68973660 (GRCh38)
10:70733416 (GRCh37)
Canonical SPDI:: NC_000010.11:68973659:A:G
Gene:: DDX21 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: G=0.000071/1 (ALFA)
G=0.000011/3 (TOPMED)
HGVS:: NC_000010.11:g.68973660A>G, NC_000010.10:g.70733416A>G, NM_004728.4:c.1664A>G, NM_004728.3:c.1664A>G, NM_001256910.2:c.1460A>G, NM_001256910.1:c.1460A>G, XM_011540336.2:c.1502A>G, NM_001410932.1:c.1502A>G, NP_004719.2:p.Lys555Arg, NP_001243839.1:p.Lys487Arg, XP_011538638.1:p.Lys501Arg

Select item 144454857516.

rs1444548575 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 10:68969054 (GRCh38)
10:70728810 (GRCh37)
Canonical SPDI:: NC_000010.11:68969053:T:C
Gene:: DDX21 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (GnomAD_exomes)
C=0.000004/1 (TOPMED)
HGVS:: NC_000010.11:g.68969054T>C, NC_000010.10:g.70728810T>C, NM_004728.4:c.1169T>C, NM_004728.3:c.1169T>C, NM_001256910.2:c.965T>C, NM_001256910.1:c.965T>C, XM_011540336.2:c.1169T>C, NM_001410932.1:c.1169T>C, NP_004719.2:p.Met390Thr, NP_001243839.1:p.Met322Thr, XP_011538638.1:p.Met390Thr

Select item 144343014217.

rs1443430142 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 10:68977635 (GRCh38)
10:70737391 (GRCh37)
Canonical SPDI:: NC_000010.11:68977634:C:T
Gene:: DDX21 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (GnomAD_exomes)
T=0.000004/1 (TOPMED)
HGVS:: NC_000010.11:g.68977635C>T, NC_000010.10:g.70737391C>T, NM_004728.4:c.1849C>T, NM_004728.3:c.1849C>T, NM_001256910.2:c.1645C>T, NM_001256910.1:c.1645C>T, XM_011540336.2:c.1687C>T, NM_001410932.1:c.1687C>T, NP_004719.2:p.His617Tyr, NP_001243839.1:p.His549Tyr, XP_011538638.1:p.His563Tyr

Select item 144289402218.

rs1442894022 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 10:68970326 (GRCh38)
10:70730082 (GRCh37)
Canonical SPDI:: NC_000010.11:68970325:G:A,NC_000010.11:68970325:G:C
Gene:: DDX21 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by cluster
HGVS:: NC_000010.11:g.68970326G>A, NC_000010.11:g.68970326G>C, NC_000010.10:g.70730082G>A, NC_000010.10:g.70730082G>C, NM_004728.4:c.1362G>A, NM_004728.4:c.1362G>C, NM_004728.3:c.1362G>A, NM_004728.3:c.1362G>C, NM_001256910.2:c.1158G>A, NM_001256910.2:c.1158G>C, NM_001256910.1:c.1158G>A, NM_001256910.1:c.1158G>C, XM_011540336.2:c.1362G>A, XM_011540336.2:c.1362G>C, NM_001410932.1:c.1362G>A, NM_001410932.1:c.1362G>C

Select item 144062796619.

rs1440627966 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 10:68978925 (GRCh38)
10:70738681 (GRCh37)
Canonical SPDI:: NC_000010.11:68978924:C:T
Gene:: DDX21 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: T=0.000028/1 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000010.11:g.68978925C>T, NC_000010.10:g.70738681C>T, NM_004728.4:c.1986C>T, NM_004728.3:c.1986C>T, NM_001256910.2:c.1782C>T, NM_001256910.1:c.1782C>T, XM_011540336.2:c.1824C>T, NM_001410932.1:c.1824C>T

Select item 144040493720.

rs1440404937 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 10:68963324 (GRCh38)
10:70723080 (GRCh37)
Canonical SPDI:: NC_000010.11:68963323:C:T
Gene:: DDX21 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000010.11:g.68963324C>T, NC_000010.10:g.70723080C>T, NM_004728.4:c.641C>T, NM_004728.3:c.641C>T, NM_001256910.2:c.437C>T, NM_001256910.1:c.437C>T, XM_011540336.2:c.641C>T, NM_001410932.1:c.641C>T, NP_004719.2:p.Ala214Val, NP_001243839.1:p.Ala146Val, XP_011538638.1:p.Ala214Val

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