SNP Links for Protein (Select 28626521) - SNP

Links from Protein

Items: 1 to 20 of 1612

<< First< Prev

Page of 81

Next >Last >>

Select item 14907905491.

rs1490790549 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 20:49260529 (GRCh38)
20:47877066 (GRCh37)
Canonical SPDI:: NC_000020.11:49260528:C:G
Gene:: ZNFX1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000224/1 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000223/1 (Estonian)
HGVS:: NC_000020.11:g.49260529C>G, NC_000020.10:g.47877066C>G, NM_021035.3:c.2350G>C, NM_021035.2:c.2350G>C, NP_066363.1:p.Glu784Gln

Select item 14907663572.

rs1490766357 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 20:49252741 (GRCh38)
20:47869278 (GRCh37)
Canonical SPDI:: NC_000020.11:49252740:G:C
Gene:: ZNFX1 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: C=0.000012/3 (GnomAD_exomes)
HGVS:: NC_000020.11:g.49252741G>C, NC_000020.10:g.47869278G>C, NM_021035.3:c.3195C>G, NM_021035.2:c.3195C>G

Select item 14903022043.

rs1490302204 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 20:49253757 (GRCh38)
20:47870294 (GRCh37)
Canonical SPDI:: NC_000020.11:49253756:A:G
Gene:: ZNFX1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000020.11:g.49253757A>G, NC_000020.10:g.47870294A>G, NM_021035.3:c.3014T>C, NM_021035.2:c.3014T>C, NP_066363.1:p.Val1005Ala

Select item 14892950284.

rs1489295028 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 20:49263434 (GRCh38)
20:47879971 (GRCh37)
Canonical SPDI:: NC_000020.11:49263433:T:C
Gene:: ZNFX1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000020.11:g.49263434T>C, NC_000020.10:g.47879971T>C, NM_021035.3:c.2201A>G, NM_021035.2:c.2201A>G, NP_066363.1:p.Lys734Arg

Select item 14886720155.

rs1488672015 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 20:49271093 (GRCh38)
20:47887630 (GRCh37)
Canonical SPDI:: NC_000020.11:49271092:T:C
Gene:: ZNFX1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_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_000020.11:g.49271093T>C, NC_000020.10:g.47887630T>C, NM_021035.3:c.719A>G, NM_021035.2:c.719A>G, NP_066363.1:p.Tyr240Cys

Select item 14885072366.

rs1488507236 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 20:49263366 (GRCh38)
20:47879903 (GRCh37)
Canonical SPDI:: NC_000020.11:49263365:G:A
Gene:: ZNFX1 (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=0.000007/1 (GnomAD)
HGVS:: NC_000020.11:g.49263366G>A, NC_000020.10:g.47879903G>A, NM_021035.3:c.2269C>T, NM_021035.2:c.2269C>T, NP_066363.1:p.His757Tyr

Select item 14883558557.

rs1488355855 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 20:49247639 (GRCh38)
20:47864176 (GRCh37)
Canonical SPDI:: NC_000020.11:49247638:A:G
Gene:: ZNFX1 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
G=0.000014/2 (GnomAD)
HGVS:: NC_000020.11:g.49247639A>G, NC_000020.10:g.47864176A>G, NM_021035.3:c.5385T>C, NM_021035.2:c.5385T>C

Select item 14883250248.

rs1488325024 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 20:49270092 (GRCh38)
20:47886629 (GRCh37)
Canonical SPDI:: NC_000020.11:49270091:C:A
Gene:: ZNFX1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000020.11:g.49270092C>A, NC_000020.10:g.47886629C>A, NM_021035.3:c.1720G>T, NM_021035.2:c.1720G>T, NP_066363.1:p.Val574Phe

Select item 14880101949.

rs1488010194 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 20:49270904 (GRCh38)
20:47887441 (GRCh37)
Canonical SPDI:: NC_000020.11:49270903:T:G
Gene:: ZNFX1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
HGVS:: NC_000020.11:g.49270904T>G, NC_000020.10:g.47887441T>G, NM_021035.3:c.908A>C, NM_021035.2:c.908A>C, NP_066363.1:p.Glu303Ala

Select item 148785801210.

rs1487858012 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 20:49270086 (GRCh38)
20:47886623 (GRCh37)
Canonical SPDI:: NC_000020.11:49270085:C:T
Gene:: ZNFX1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
T=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000020.11:g.49270086C>T, NC_000020.10:g.47886623C>T, NM_021035.3:c.1726G>A, NM_021035.2:c.1726G>A, NP_066363.1:p.Gly576Ser

Select item 148770470611.

rs1487704706 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 20:49248851 (GRCh38)
20:47865388 (GRCh37)
Canonical SPDI:: NC_000020.11:49248850:A:G
Gene:: ZNFX1 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000020.11:g.49248851A>G, NC_000020.10:g.47865388A>G, NM_021035.3:c.4173T>C, NM_021035.2:c.4173T>C

Select item 148767387012.

rs1487673870 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 20:49270837 (GRCh38)
20:47887374 (GRCh37)
Canonical SPDI:: NC_000020.11:49270836:C:T
Gene:: ZNFX1 (Varview)
Functional Consequence:: synonymous_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)
T=0.000007/1 (GnomAD)
HGVS:: NC_000020.11:g.49270837C>T, NC_000020.10:g.47887374C>T, NM_021035.3:c.975G>A, NM_021035.2:c.975G>A

Select item 148733948713.

rs1487339487 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 20:49270405 (GRCh38)
20:47886942 (GRCh37)
Canonical SPDI:: NC_000020.11:49270404:T:C
Gene:: ZNFX1 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: C=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000020.11:g.49270405T>C, NC_000020.10:g.47886942T>C, NM_021035.3:c.1407A>G, NM_021035.2:c.1407A>G

Select item 148669074914.

rs1486690749 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 20:49271247 (GRCh38)
20:47887784 (GRCh37)
Canonical SPDI:: NC_000020.11:49271246:G:A,NC_000020.11:49271246:G:C
Gene:: ZNFX1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,stop_gained
Validated:: by frequency,by cluster
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000020.11:g.49271247G>A, NC_000020.11:g.49271247G>C, NC_000020.10:g.47887784G>A, NC_000020.10:g.47887784G>C, NM_021035.3:c.565C>T, NM_021035.3:c.565C>G, NM_021035.2:c.565C>T, NM_021035.2:c.565C>G, NP_066363.1:p.Gln189Ter, NP_066363.1:p.Gln189Glu

Select item 148663591315.

rs1486635913 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 20:49247767 (GRCh38)
20:47864304 (GRCh37)
Canonical SPDI:: NC_000020.11:49247766:G:C
Gene:: ZNFX1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by cluster
MAF:: C=0.000004/1 (GnomAD_exomes)
C=0.000035/1 (TOMMO)
C=0.000342/1 (KOREAN)
HGVS:: NC_000020.11:g.49247767G>C, NC_000020.10:g.47864304G>C, NM_021035.3:c.5257C>G, NM_021035.2:c.5257C>G, NP_066363.1:p.Leu1753Val

Select item 148563220116.

rs1485632201 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 20:49270880 (GRCh38)
20:47887417 (GRCh37)
Canonical SPDI:: NC_000020.11:49270879:T:C
Gene:: ZNFX1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_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_000020.11:g.49270880T>C, NC_000020.10:g.47887417T>C, NM_021035.3:c.932A>G, NM_021035.2:c.932A>G, NP_066363.1:p.Glu311Gly

Select item 148529961717.

rs1485299617 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 20:49247671 (GRCh38)
20:47864208 (GRCh37)
Canonical SPDI:: NC_000020.11:49247670:C:T
Gene:: ZNFX1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000020.11:g.49247671C>T, NC_000020.10:g.47864208C>T, NM_021035.3:c.5353G>A, NM_021035.2:c.5353G>A, NP_066363.1:p.Ala1785Thr

Select item 148521791418.

rs1485217914 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 20:49253772 (GRCh38)
20:47870309 (GRCh37)
Canonical SPDI:: NC_000020.11:49253771:G:A
Gene:: ZNFX1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by cluster
MAF:: A=0.000004/1 (GnomAD_exomes)
A=0.000035/1 (TOMMO)
HGVS:: NC_000020.11:g.49253772G>A, NC_000020.10:g.47870309G>A, NM_021035.3:c.2999C>T, NM_021035.2:c.2999C>T, NP_066363.1:p.Pro1000Leu

Select item 148506630219.

rs1485066302 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 20:49257638 (GRCh38)
20:47874175 (GRCh37)
Canonical SPDI:: NC_000020.11:49257637:C:T
Gene:: ZNFX1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000020.11:g.49257638C>T, NC_000020.10:g.47874175C>T, NM_021035.3:c.2443G>A, NM_021035.2:c.2443G>A, NP_066363.1:p.Glu815Lys

Select item 148446006520.

rs1484460065 [Homo sapiens]

Variant type:: DEL
Alleles:: CT>- [Show Flanks]
Chromosome:: 20:49270397 (GRCh38)
20:47886934 (GRCh37)
Canonical SPDI:: NC_000020.11:49270396:CT:
Gene:: ZNFX1 (Varview)
Functional Consequence:: coding_sequence_variant,frameshift_variant
Validated:: by frequency
MAF:: -=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000020.11:g.49270397_49270398del, NC_000020.10:g.47886934_47886935del, NM_021035.3:c.1414_1415del, NM_021035.2:c.1414_1415del, NP_066363.1:p.Arg472fs

dbSNP

Result Filters

Clinical Significance

Validation Status

Publication

Function Class

Variation Class

Annotation

Global MAF

Custom range

Additional filters

Display Settings:

Send to:

Links from Protein

Items: 1 to 20 of 1612

Display Settings:

Send to:

Supplemental Content

Find related data

Recent activity