SNP Links for Protein (Select 46559763) - SNP

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Links from Protein

Items: 1 to 20 of 460

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Select item 14870976831.

rs1487097683 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 3:42915216 (GRCh38)
3:42956708 (GRCh37)
Canonical SPDI:: NC_000003.12:42915215:C:T
Gene:: ZNF662 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000003.12:g.42915216C>T, NC_000003.11:g.42956708C>T, NM_207404.4:c.1143C>T, NM_207404.3:c.1143C>T, NM_001134656.2:c.1221C>T, NM_001134656.1:c.1221C>T

Select item 14831782762.

rs1483178276 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 3:42908858 (GRCh38)
3:42950350 (GRCh37)
Canonical SPDI:: NC_000003.12:42908857:T:C
Gene:: ZNF662 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000071/1 (ALFA)
C=0.000004/1 (GnomAD_exomes)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000003.12:g.42908858T>C, NC_000003.11:g.42950350T>C, NM_207404.4:c.100T>C, NM_207404.3:c.100T>C, NM_001134656.2:c.280T>C, NM_001134656.1:c.280T>C, NP_997287.2:p.Ser34Pro, NP_001128128.1:p.Ser94Pro

Select item 14794053943.

rs1479405394 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 3:42914829 (GRCh38)
3:42956321 (GRCh37)
Canonical SPDI:: NC_000003.12:42914828:A:C
Gene:: ZNF662 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000003.12:g.42914829A>C, NC_000003.11:g.42956321A>C, NM_207404.4:c.756A>C, NM_207404.3:c.756A>C, NM_001134656.2:c.834A>C, NM_001134656.1:c.834A>C, NP_997287.2:p.Glu252Asp, NP_001128128.1:p.Glu278Asp

Select item 14768805964.

rs1476880596 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C,T [Show Flanks]
Chromosome:: 3:42915330 (GRCh38)
3:42956822 (GRCh37)
Canonical SPDI:: NC_000003.12:42915329:G:C,NC_000003.12:42915329:G:T
Gene:: ZNF662 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000084/1 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000003.12:g.42915330G>C, NC_000003.12:g.42915330G>T, NC_000003.11:g.42956822G>C, NC_000003.11:g.42956822G>T, NM_207404.4:c.1257G>C, NM_207404.4:c.1257G>T, NM_207404.3:c.1257G>C, NM_207404.3:c.1257G>T, NM_001134656.2:c.1335G>C, NM_001134656.2:c.1335G>T, NM_001134656.1:c.1335G>C, NM_001134656.1:c.1335G>T, NP_997287.2:p.Gln419His, NP_997287.2:p.Gln419His, NP_001128128.1:p.Gln445His, NP_001128128.1:p.Gln445His

Select item 14752005765.

rs1475200576 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 3:42914733 (GRCh38)
3:42956225 (GRCh37)
Canonical SPDI:: NC_000003.12:42914732:T:C
Gene:: ZNF662 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_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_000003.12:g.42914733T>C, NC_000003.11:g.42956225T>C, NM_207404.4:c.660T>C, NM_207404.3:c.660T>C, NM_001134656.2:c.738T>C, NM_001134656.1:c.738T>C

Select item 14727220626.

rs1472722062 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 3:42908797 (GRCh38)
3:42950289 (GRCh37)
Canonical SPDI:: NC_000003.12:42908796:A:G
Gene:: ZNF662 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000071/1 (ALFA)
G=0.000004/1 (GnomAD_exomes)
G=0.000007/1 (GnomAD)
G=0.000015/4 (TOPMED)
HGVS:: NC_000003.12:g.42908797A>G, NC_000003.11:g.42950289A>G, NM_207404.4:c.39A>G, NM_207404.3:c.39A>G, NM_001134656.2:c.219A>G, NM_001134656.1:c.219A>G

Select item 14717647817.

rs1471764781 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 3:42915161 (GRCh38)
3:42956653 (GRCh37)
Canonical SPDI:: NC_000003.12:42915160:C:T
Gene:: ZNF662 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000011/3 (TOPMED)
HGVS:: NC_000003.12:g.42915161C>T, NC_000003.11:g.42956653C>T, NM_207404.4:c.1088C>T, NM_207404.3:c.1088C>T, NM_001134656.2:c.1166C>T, NM_001134656.1:c.1166C>T, NP_997287.2:p.Thr363Ile, NP_001128128.1:p.Thr389Ile

Select item 14715874838.

rs1471587483 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 3:42914850 (GRCh38)
3:42956342 (GRCh37)
Canonical SPDI:: NC_000003.12:42914849:G:A
Gene:: ZNF662 (Varview)
Functional Consequence:: stop_gained,coding_sequence_variant
HGVS:: NC_000003.12:g.42914850G>A, NC_000003.11:g.42956342G>A, NM_207404.4:c.777G>A, NM_207404.3:c.777G>A, NM_001134656.2:c.855G>A, NM_001134656.1:c.855G>A, NP_997287.2:p.Trp259Ter, NP_001128128.1:p.Trp285Ter

Select item 14708066209.

rs1470806620 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 3:42914737 (GRCh38)
3:42956229 (GRCh37)
Canonical SPDI:: NC_000003.12:42914736:T:A
Gene:: ZNF662 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000003.12:g.42914737T>A, NC_000003.11:g.42956229T>A, NM_207404.4:c.664T>A, NM_207404.3:c.664T>A, NM_001134656.2:c.742T>A, NM_001134656.1:c.742T>A, NP_997287.2:p.Cys222Ser, NP_001128128.1:p.Cys248Ser

Select item 147069503910.

rs1470695039 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 3:42914612 (GRCh38)
3:42956104 (GRCh37)
Canonical SPDI:: NC_000003.12:42914611:G:A,NC_000003.12:42914611:G:C
Gene:: ZNF662 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
C=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000003.12:g.42914612G>A, NC_000003.12:g.42914612G>C, NC_000003.11:g.42956104G>A, NC_000003.11:g.42956104G>C, NM_207404.4:c.539G>A, NM_207404.4:c.539G>C, NM_207404.3:c.539G>A, NM_207404.3:c.539G>C, NM_001134656.2:c.617G>A, NM_001134656.2:c.617G>C, NM_001134656.1:c.617G>A, NM_001134656.1:c.617G>C, NP_997287.2:p.Gly180Asp, NP_997287.2:p.Gly180Ala, NP_001128128.1:p.Gly206Asp, NP_001128128.1:p.Gly206Ala

Select item 146957382911.

rs1469573829 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 3:42914448 (GRCh38)
3:42955940 (GRCh37)
Canonical SPDI:: NC_000003.12:42914447:T:G
Gene:: ZNF662 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000003.12:g.42914448T>G, NC_000003.11:g.42955940T>G, NM_207404.4:c.375T>G, NM_207404.3:c.375T>G, NM_001134656.2:c.453T>G, NM_001134656.1:c.453T>G, NP_997287.2:p.Phe125Leu, NP_001128128.1:p.Phe151Leu

Select item 146956507512.

rs1469565075 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 3:42914913 (GRCh38)
3:42956405 (GRCh37)
Canonical SPDI:: NC_000003.12:42914912:A:G
Gene:: ZNF662 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000003.12:g.42914913A>G, NC_000003.11:g.42956405A>G, NM_207404.4:c.840A>G, NM_207404.3:c.840A>G, NM_001134656.2:c.918A>G, NM_001134656.1:c.918A>G

Select item 146823264513.

rs1468232645 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 3:42914752 (GRCh38)
3:42956244 (GRCh37)
Canonical SPDI:: NC_000003.12:42914751:A:G
Gene:: ZNF662 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000003.12:g.42914752A>G, NC_000003.11:g.42956244A>G, NM_207404.4:c.679A>G, NM_207404.3:c.679A>G, NM_001134656.2:c.757A>G, NM_001134656.1:c.757A>G, NP_997287.2:p.Lys227Glu, NP_001128128.1:p.Lys253Glu

Select item 146074660614.

rs1460746606 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 3:42915094 (GRCh38)
3:42956586 (GRCh37)
Canonical SPDI:: NC_000003.12:42915093:T:A
Gene:: ZNF662 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000003.12:g.42915094T>A, NC_000003.11:g.42956586T>A, NM_207404.4:c.1021T>A, NM_207404.3:c.1021T>A, NM_001134656.2:c.1099T>A, NM_001134656.1:c.1099T>A, NP_997287.2:p.Phe341Ile, NP_001128128.1:p.Phe367Ile

Select item 146015251415.

rs1460152514 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 3:42914379 (GRCh38)
3:42955871 (GRCh37)
Canonical SPDI:: NC_000003.12:42914378:T:C
Gene:: ZNF662 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000003.12:g.42914379T>C, NC_000003.11:g.42955871T>C, NM_207404.4:c.306T>C, NM_207404.3:c.306T>C, NM_001134656.2:c.384T>C, NM_001134656.1:c.384T>C

Select item 145543403016.

rs1455434030 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 3:42915140 (GRCh38)
3:42956632 (GRCh37)
Canonical SPDI:: NC_000003.12:42915139:G:C
Gene:: ZNF662 (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=0.000007/1 (GnomAD)
HGVS:: NC_000003.12:g.42915140G>C, NC_000003.11:g.42956632G>C, NM_207404.4:c.1067G>C, NM_207404.3:c.1067G>C, NM_001134656.2:c.1145G>C, NM_001134656.1:c.1145G>C, NP_997287.2:p.Gly356Ala, NP_001128128.1:p.Gly382Ala

Select item 145294956017.

rs1452949560 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 3:42913291 (GRCh38)
3:42954783 (GRCh37)
Canonical SPDI:: NC_000003.12:42913290:T:C
Gene:: ZNF662 (Varview)
Functional Consequence:: coding_sequence_variant,intron_variant,missense_variant
HGVS:: NC_000003.12:g.42913291T>C, NC_000003.11:g.42954783T>C, NM_207404.4:c.242T>C, NM_207404.3:c.242T>C, NP_997287.2:p.Leu81Pro

Select item 145293122918.

rs1452931229 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 3:42908816 (GRCh38)
3:42950308 (GRCh37)
Canonical SPDI:: NC_000003.12:42908815:G:T
Gene:: ZNF662 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000003.12:g.42908816G>T, NC_000003.11:g.42950308G>T, NM_207404.4:c.58G>T, NM_207404.3:c.58G>T, NM_001134656.2:c.238G>T, NM_001134656.1:c.238G>T, NP_997287.2:p.Ala20Ser, NP_001128128.1:p.Ala80Ser

Select item 145251713119.

rs1452517131 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 3:42914392 (GRCh38)
3:42955884 (GRCh37)
Canonical SPDI:: NC_000003.12:42914391:G:A
Gene:: ZNF662 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000003.12:g.42914392G>A, NC_000003.11:g.42955884G>A, NM_207404.4:c.319G>A, NM_207404.3:c.319G>A, NM_001134656.2:c.397G>A, NM_001134656.1:c.397G>A, NP_997287.2:p.Asp107Asn, NP_001128128.1:p.Asp133Asn

Select item 145229740320.

rs1452297403 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 3:42913273 (GRCh38)
3:42954765 (GRCh37)
Canonical SPDI:: NC_000003.12:42913272:A:C
Gene:: ZNF662 (Varview)
Functional Consequence:: coding_sequence_variant,intron_variant,missense_variant
Validated:: by frequency
MAF:: C=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000003.12:g.42913273A>C, NC_000003.11:g.42954765A>C, NM_207404.4:c.224A>C, NM_207404.3:c.224A>C, NP_997287.2:p.Gln75Pro