SNP Links for Protein (Select 530361882) - SNP

Select item 14745224811.

rs1474522481 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:33298938 (GRCh38)
1:33764539 (GRCh37)
Canonical SPDI:: NC_000001.11:33298937:C:T
Gene:: ZNF362 (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=0.000008/2 (TOPMED)
T=0.000014/2 (GnomAD)
HGVS:: NC_000001.11:g.33298938C>T, NC_000001.10:g.33764539C>T, XM_005270508.6:c.1116C>T, XM_005270508.5:c.1116C>T, XM_005270508.4:c.1116C>T, XM_005270508.3:c.1116C>T, XM_005270508.2:c.1116C>T, XM_005270508.1:c.1116C>T, NM_152493.3:c.1155C>T, NM_152493.2:c.1155C>T, XM_005270507.3:c.1116C>T, XM_005270507.2:c.1116C>T, XM_005270507.1:c.1116C>T, XM_047447108.1:c.1209C>T, NM_001370212.1:c.1155C>T, XM_047447109.1:c.1155C>T, XM_047447107.1:c.1209C>T, XM_047447110.1:c.1071C>T

Select item 14728107352.

rs1472810735 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 1:33281604 (GRCh38)
1:33747205 (GRCh37)
Canonical SPDI:: NC_000001.11:33281603:T:G
Gene:: ZNF362 (Varview)
Functional Consequence:: missense_variant,coding_sequence_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_000001.11:g.33281604T>G, NC_000001.10:g.33747205T>G, XM_005270508.6:c.662T>G, XM_005270508.5:c.662T>G, XM_005270508.4:c.662T>G, XM_005270508.3:c.662T>G, XM_005270508.2:c.662T>G, XM_005270508.1:c.662T>G, NM_152493.3:c.701T>G, NM_152493.2:c.701T>G, XM_005270507.3:c.662T>G, XM_005270507.2:c.662T>G, XM_005270507.1:c.662T>G, XM_047447108.1:c.755T>G, NM_001370212.1:c.701T>G, XM_047447109.1:c.701T>G, XM_047447107.1:c.755T>G, XM_047447110.1:c.701T>G, XP_005270565.1:p.Leu221Arg, NP_689706.2:p.Leu234Arg, XP_005270564.1:p.Leu221Arg, XP_047303064.1:p.Leu252Arg, NP_001357141.1:p.Leu234Arg, XP_047303065.1:p.Leu234Arg, XP_047303063.1:p.Leu252Arg, XP_047303066.1:p.Leu234Arg

Select item 14684315963.

rs1468431596 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 1:33276412 (GRCh38)
1:33742013 (GRCh37)
Canonical SPDI:: NC_000001.11:33276411:C:G
Gene:: ZNF362 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
HGVS:: NC_000001.11:g.33276412C>G, NC_000001.10:g.33742013C>G, XM_005270508.6:c.128C>G, XM_005270508.5:c.128C>G, XM_005270508.4:c.128C>G, XM_005270508.3:c.128C>G, XM_005270508.2:c.128C>G, XM_005270508.1:c.128C>G, NM_152493.3:c.167C>G, NM_152493.2:c.167C>G, XM_005270507.3:c.128C>G, XM_005270507.2:c.128C>G, XM_005270507.1:c.128C>G, XM_047447108.1:c.221C>G, NM_001370212.1:c.167C>G, XM_047447109.1:c.167C>G, XM_047447107.1:c.221C>G, XM_047447110.1:c.167C>G, XP_005270565.1:p.Pro43Arg, NP_689706.2:p.Pro56Arg, XP_005270564.1:p.Pro43Arg, XP_047303064.1:p.Pro74Arg, NP_001357141.1:p.Pro56Arg, XP_047303065.1:p.Pro56Arg, XP_047303063.1:p.Pro74Arg, XP_047303066.1:p.Pro56Arg

Select item 14640691344.

rs1464069134 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 1:33276561 (GRCh38)
1:33742162 (GRCh37)
Canonical SPDI:: NC_000001.11:33276560:C:A
Gene:: ZNF362 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
HGVS:: NC_000001.11:g.33276561C>A, NC_000001.10:g.33742162C>A, XM_005270508.6:c.277C>A, XM_005270508.5:c.277C>A, XM_005270508.4:c.277C>A, XM_005270508.3:c.277C>A, XM_005270508.2:c.277C>A, XM_005270508.1:c.277C>A, NM_152493.3:c.316C>A, NM_152493.2:c.316C>A, XM_005270507.3:c.277C>A, XM_005270507.2:c.277C>A, XM_005270507.1:c.277C>A, XM_047447108.1:c.370C>A, NM_001370212.1:c.316C>A, XM_047447109.1:c.316C>A, XM_047447107.1:c.370C>A, XM_047447110.1:c.316C>A, XP_005270565.1:p.Leu93Met, NP_689706.2:p.Leu106Met, XP_005270564.1:p.Leu93Met, XP_047303064.1:p.Leu124Met, NP_001357141.1:p.Leu106Met, XP_047303065.1:p.Leu106Met, XP_047303063.1:p.Leu124Met, XP_047303066.1:p.Leu106Met

Select item 14634752275.

rs1463475227 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 1:33276499 (GRCh38)
1:33742100 (GRCh37)
Canonical SPDI:: NC_000001.11:33276498:T:C
Gene:: ZNF362 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000001.11:g.33276499T>C, NC_000001.10:g.33742100T>C, XM_005270508.6:c.215T>C, XM_005270508.5:c.215T>C, XM_005270508.4:c.215T>C, XM_005270508.3:c.215T>C, XM_005270508.2:c.215T>C, XM_005270508.1:c.215T>C, NM_152493.3:c.254T>C, NM_152493.2:c.254T>C, XM_005270507.3:c.215T>C, XM_005270507.2:c.215T>C, XM_005270507.1:c.215T>C, XM_047447108.1:c.308T>C, NM_001370212.1:c.254T>C, XM_047447109.1:c.254T>C, XM_047447107.1:c.308T>C, XM_047447110.1:c.254T>C, XP_005270565.1:p.Leu72Pro, NP_689706.2:p.Leu85Pro, XP_005270564.1:p.Leu72Pro, XP_047303064.1:p.Leu103Pro, NP_001357141.1:p.Leu85Pro, XP_047303065.1:p.Leu85Pro, XP_047303063.1:p.Leu103Pro, XP_047303066.1:p.Leu85Pro

Select item 14626923036.

rs1462692303 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:33280309 (GRCh38)
1:33745910 (GRCh37)
Canonical SPDI:: NC_000001.11:33280308:A:G
Gene:: ZNF362 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (GnomAD_exomes)
G=0.000004/1 (TOPMED)
G=0.000035/1 (TOMMO)
HGVS:: NC_000001.11:g.33280309A>G, NC_000001.10:g.33745910A>G, XM_005270508.6:c.496A>G, XM_005270508.5:c.496A>G, XM_005270508.4:c.496A>G, XM_005270508.3:c.496A>G, XM_005270508.2:c.496A>G, XM_005270508.1:c.496A>G, NM_152493.3:c.535A>G, NM_152493.2:c.535A>G, XM_005270507.3:c.496A>G, XM_005270507.2:c.496A>G, XM_005270507.1:c.496A>G, XM_047447108.1:c.589A>G, NM_001370212.1:c.535A>G, XM_047447109.1:c.535A>G, XM_047447107.1:c.589A>G, XM_047447110.1:c.535A>G, XP_005270565.1:p.Ile166Val, NP_689706.2:p.Ile179Val, XP_005270564.1:p.Ile166Val, XP_047303064.1:p.Ile197Val, NP_001357141.1:p.Ile179Val, XP_047303065.1:p.Ile179Val, XP_047303063.1:p.Ile197Val, XP_047303066.1:p.Ile179Val

Select item 14522917387.

rs1452291738 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: 1:33280198 (GRCh38)
1:33745799 (GRCh37)
Canonical SPDI:: NC_000001.11:33280197:A:G,NC_000001.11:33280197:A:T
Gene:: ZNF362 (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)
A=0.5/1 (SGDP_PRJ)
HGVS:: NC_000001.11:g.33280198A>G, NC_000001.11:g.33280198A>T, NC_000001.10:g.33745799A>G, NC_000001.10:g.33745799A>T, XM_005270508.6:c.385A>G, XM_005270508.6:c.385A>T, XM_005270508.5:c.385A>G, XM_005270508.5:c.385A>T, XM_005270508.4:c.385A>G, XM_005270508.4:c.385A>T, XM_005270508.3:c.385A>G, XM_005270508.3:c.385A>T, XM_005270508.2:c.385A>G, XM_005270508.2:c.385A>T, XM_005270508.1:c.385A>G, XM_005270508.1:c.385A>T, NM_152493.3:c.424A>G, NM_152493.3:c.424A>T, NM_152493.2:c.424A>G, NM_152493.2:c.424A>T, XM_005270507.3:c.385A>G, XM_005270507.3:c.385A>T, XM_005270507.2:c.385A>G, XM_005270507.2:c.385A>T, XM_005270507.1:c.385A>G, XM_005270507.1:c.385A>T, XM_047447108.1:c.478A>G, XM_047447108.1:c.478A>T, NM_001370212.1:c.424A>G, NM_001370212.1:c.424A>T, XM_047447109.1:c.424A>G, XM_047447109.1:c.424A>T, XM_047447107.1:c.478A>G, XM_047447107.1:c.478A>T, XM_047447110.1:c.424A>G, XM_047447110.1:c.424A>T, XP_005270565.1:p.Thr129Ala, XP_005270565.1:p.Thr129Ser, NP_689706.2:p.Thr142Ala, NP_689706.2:p.Thr142Ser, XP_005270564.1:p.Thr129Ala, XP_005270564.1:p.Thr129Ser, XP_047303064.1:p.Thr160Ala, XP_047303064.1:p.Thr160Ser, NP_001357141.1:p.Thr142Ala, NP_001357141.1:p.Thr142Ser, XP_047303065.1:p.Thr142Ala, XP_047303065.1:p.Thr142Ser, XP_047303063.1:p.Thr160Ala, XP_047303063.1:p.Thr160Ser, XP_047303066.1:p.Thr142Ala, XP_047303066.1:p.Thr142Ser

Select item 14519524518.

rs1451952451 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 1:33276570 (GRCh38)
1:33742171 (GRCh37)
Canonical SPDI:: NC_000001.11:33276569:C:A
Gene:: ZNF362 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
HGVS:: NC_000001.11:g.33276570C>A, NC_000001.10:g.33742171C>A, XM_005270508.6:c.286C>A, XM_005270508.5:c.286C>A, XM_005270508.4:c.286C>A, XM_005270508.3:c.286C>A, XM_005270508.2:c.286C>A, XM_005270508.1:c.286C>A, NM_152493.3:c.325C>A, NM_152493.2:c.325C>A, XM_005270507.3:c.286C>A, XM_005270507.2:c.286C>A, XM_005270507.1:c.286C>A, XM_047447108.1:c.379C>A, NM_001370212.1:c.325C>A, XM_047447109.1:c.325C>A, XM_047447107.1:c.379C>A, XM_047447110.1:c.325C>A

Select item 14481356679.

rs1448135667 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:33276531 (GRCh38)
1:33742132 (GRCh37)
Canonical SPDI:: NC_000001.11:33276530:C:T
Gene:: ZNF362 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
HGVS:: NC_000001.11:g.33276531C>T, NC_000001.10:g.33742132C>T, XM_005270508.6:c.247C>T, XM_005270508.5:c.247C>T, XM_005270508.4:c.247C>T, XM_005270508.3:c.247C>T, XM_005270508.2:c.247C>T, XM_005270508.1:c.247C>T, NM_152493.3:c.286C>T, NM_152493.2:c.286C>T, XM_005270507.3:c.247C>T, XM_005270507.2:c.247C>T, XM_005270507.1:c.247C>T, XM_047447108.1:c.340C>T, NM_001370212.1:c.286C>T, XM_047447109.1:c.286C>T, XM_047447107.1:c.340C>T, XM_047447110.1:c.286C>T, XP_005270565.1:p.Pro83Ser, NP_689706.2:p.Pro96Ser, XP_005270564.1:p.Pro83Ser, XP_047303064.1:p.Pro114Ser, NP_001357141.1:p.Pro96Ser, XP_047303065.1:p.Pro96Ser, XP_047303063.1:p.Pro114Ser, XP_047303066.1:p.Pro96Ser

Select item 144684790610.

rs1446847906 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 1:33280260 (GRCh38)
1:33745861 (GRCh37)
Canonical SPDI:: NC_000001.11:33280259:C:A,NC_000001.11:33280259:C:T
Gene:: ZNF362 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_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_000001.11:g.33280260C>A, NC_000001.11:g.33280260C>T, NC_000001.10:g.33745861C>A, NC_000001.10:g.33745861C>T, XM_005270508.6:c.447C>A, XM_005270508.6:c.447C>T, XM_005270508.5:c.447C>A, XM_005270508.5:c.447C>T, XM_005270508.4:c.447C>A, XM_005270508.4:c.447C>T, XM_005270508.3:c.447C>A, XM_005270508.3:c.447C>T, XM_005270508.2:c.447C>A, XM_005270508.2:c.447C>T, XM_005270508.1:c.447C>A, XM_005270508.1:c.447C>T, NM_152493.3:c.486C>A, NM_152493.3:c.486C>T, NM_152493.2:c.486C>A, NM_152493.2:c.486C>T, XM_005270507.3:c.447C>A, XM_005270507.3:c.447C>T, XM_005270507.2:c.447C>A, XM_005270507.2:c.447C>T, XM_005270507.1:c.447C>A, XM_005270507.1:c.447C>T, XM_047447108.1:c.540C>A, XM_047447108.1:c.540C>T, NM_001370212.1:c.486C>A, NM_001370212.1:c.486C>T, XM_047447109.1:c.486C>A, XM_047447109.1:c.486C>T, XM_047447107.1:c.540C>A, XM_047447107.1:c.540C>T, XM_047447110.1:c.486C>A, XM_047447110.1:c.486C>T

Select item 144653002411.

rs1446530024 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:33295157 (GRCh38)
1:33760758 (GRCh37)
Canonical SPDI:: NC_000001.11:33295156:G:A
Gene:: ZNF362 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.33295157G>A, NC_000001.10:g.33760758G>A, XM_005270508.6:c.959G>A, XM_005270508.5:c.959G>A, XM_005270508.4:c.959G>A, XM_005270508.3:c.959G>A, XM_005270508.2:c.959G>A, XM_005270508.1:c.959G>A, NM_152493.3:c.998G>A, NM_152493.2:c.998G>A, XM_005270507.3:c.959G>A, XM_005270507.2:c.959G>A, XM_005270507.1:c.959G>A, XM_047447108.1:c.1052G>A, NM_001370212.1:c.998G>A, XM_047447109.1:c.998G>A, XM_047447107.1:c.1052G>A, XP_005270565.1:p.Arg320His, NP_689706.2:p.Arg333His, XP_005270564.1:p.Arg320His, XP_047303064.1:p.Arg351His, NP_001357141.1:p.Arg333His, XP_047303065.1:p.Arg333His, XP_047303063.1:p.Arg351His

Select item 144444546112.

rs1444445461 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 1:33280446 (GRCh38)
1:33746047 (GRCh37)
Canonical SPDI:: NC_000001.11:33280445:C:G
Gene:: ZNF362 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
G=0.000071/1 (TOMMO)
HGVS:: NC_000001.11:g.33280446C>G, NC_000001.10:g.33746047C>G, XM_005270508.6:c.633C>G, XM_005270508.5:c.633C>G, XM_005270508.4:c.633C>G, XM_005270508.3:c.633C>G, XM_005270508.2:c.633C>G, XM_005270508.1:c.633C>G, NM_152493.3:c.672C>G, NM_152493.2:c.672C>G, XM_005270507.3:c.633C>G, XM_005270507.2:c.633C>G, XM_005270507.1:c.633C>G, XM_047447108.1:c.726C>G, NM_001370212.1:c.672C>G, XM_047447109.1:c.672C>G, XM_047447107.1:c.726C>G, XM_047447110.1:c.672C>G

Select item 144247156213.

rs1442471562 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:33281623 (GRCh38)
1:33747224 (GRCh37)
Canonical SPDI:: NC_000001.11:33281622:A:G
Gene:: ZNF362 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.33281623A>G, NC_000001.10:g.33747224A>G, XM_005270508.6:c.681A>G, XM_005270508.5:c.681A>G, XM_005270508.4:c.681A>G, XM_005270508.3:c.681A>G, XM_005270508.2:c.681A>G, XM_005270508.1:c.681A>G, NM_152493.3:c.720A>G, NM_152493.2:c.720A>G, XM_005270507.3:c.681A>G, XM_005270507.2:c.681A>G, XM_005270507.1:c.681A>G, XM_047447108.1:c.774A>G, NM_001370212.1:c.720A>G, XM_047447109.1:c.720A>G, XM_047447107.1:c.774A>G, XM_047447110.1:c.720A>G

Select item 143993587514.

rs1439935875 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 1:33276590 (GRCh38)
1:33742191 (GRCh37)
Canonical SPDI:: NC_000001.11:33276589:C:G
Gene:: ZNF362 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000015/4 (TOPMED)
G=0.000021/3 (GnomAD)
HGVS:: NC_000001.11:g.33276590C>G, NC_000001.10:g.33742191C>G, XM_005270508.6:c.306C>G, XM_005270508.5:c.306C>G, XM_005270508.4:c.306C>G, XM_005270508.3:c.306C>G, XM_005270508.2:c.306C>G, XM_005270508.1:c.306C>G, NM_152493.3:c.345C>G, NM_152493.2:c.345C>G, XM_005270507.3:c.306C>G, XM_005270507.2:c.306C>G, XM_005270507.1:c.306C>G, XM_047447108.1:c.399C>G, NM_001370212.1:c.345C>G, XM_047447109.1:c.345C>G, XM_047447107.1:c.399C>G, XM_047447110.1:c.345C>G

Select item 143640631415.

rs1436406314 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 1:33276359 (GRCh38)
1:33741960 (GRCh37)
Canonical SPDI:: NC_000001.11:33276358:G:T
Gene:: ZNF362 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: T=0.00005/1 (ALFA)
HGVS:: NC_000001.11:g.33276359G>T, NC_000001.10:g.33741960G>T, XM_005270508.6:c.75G>T, XM_005270508.5:c.75G>T, XM_005270508.4:c.75G>T, XM_005270508.3:c.75G>T, XM_005270508.2:c.75G>T, XM_005270508.1:c.75G>T, NM_152493.3:c.114G>T, NM_152493.2:c.114G>T, XM_005270507.3:c.75G>T, XM_005270507.2:c.75G>T, XM_005270507.1:c.75G>T, XM_047447108.1:c.168G>T, NM_001370212.1:c.114G>T, XM_047447109.1:c.114G>T, XM_047447107.1:c.168G>T, XM_047447110.1:c.114G>T

Select item 143605151116.

rs1436051511 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 1:33276460 (GRCh38)
1:33742061 (GRCh37)
Canonical SPDI:: NC_000001.11:33276459:C:A,NC_000001.11:33276459:C:T
Gene:: ZNF362 (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=0.000007/1 (GnomAD_exomes)
T=0.001667/1 (NorthernSweden)
HGVS:: NC_000001.11:g.33276460C>A, NC_000001.11:g.33276460C>T, NC_000001.10:g.33742061C>A, NC_000001.10:g.33742061C>T, XM_005270508.6:c.176C>A, XM_005270508.6:c.176C>T, XM_005270508.5:c.176C>A, XM_005270508.5:c.176C>T, XM_005270508.4:c.176C>A, XM_005270508.4:c.176C>T, XM_005270508.3:c.176C>A, XM_005270508.3:c.176C>T, XM_005270508.2:c.176C>A, XM_005270508.2:c.176C>T, XM_005270508.1:c.176C>A, XM_005270508.1:c.176C>T, NM_152493.3:c.215C>A, NM_152493.3:c.215C>T, NM_152493.2:c.215C>A, NM_152493.2:c.215C>T, XM_005270507.3:c.176C>A, XM_005270507.3:c.176C>T, XM_005270507.2:c.176C>A, XM_005270507.2:c.176C>T, XM_005270507.1:c.176C>A, XM_005270507.1:c.176C>T, XM_047447108.1:c.269C>A, XM_047447108.1:c.269C>T, NM_001370212.1:c.215C>A, NM_001370212.1:c.215C>T, XM_047447109.1:c.215C>A, XM_047447109.1:c.215C>T, XM_047447107.1:c.269C>A, XM_047447107.1:c.269C>T, XM_047447110.1:c.215C>A, XM_047447110.1:c.215C>T, XP_005270565.1:p.Pro59Gln, XP_005270565.1:p.Pro59Leu, NP_689706.2:p.Pro72Gln, NP_689706.2:p.Pro72Leu, XP_005270564.1:p.Pro59Gln, XP_005270564.1:p.Pro59Leu, XP_047303064.1:p.Pro90Gln, XP_047303064.1:p.Pro90Leu, NP_001357141.1:p.Pro72Gln, NP_001357141.1:p.Pro72Leu, XP_047303065.1:p.Pro72Gln, XP_047303065.1:p.Pro72Leu, XP_047303063.1:p.Pro90Gln, XP_047303063.1:p.Pro90Leu, XP_047303066.1:p.Pro72Gln, XP_047303066.1:p.Pro72Leu

Select item 143421384517.

rs1434213845 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 1:33276549 (GRCh38)
1:33742150 (GRCh37)
Canonical SPDI:: NC_000001.11:33276548:C:G
Gene:: ZNF362 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
HGVS:: NC_000001.11:g.33276549C>G, NC_000001.10:g.33742150C>G, XM_005270508.6:c.265C>G, XM_005270508.5:c.265C>G, XM_005270508.4:c.265C>G, XM_005270508.3:c.265C>G, XM_005270508.2:c.265C>G, XM_005270508.1:c.265C>G, NM_152493.3:c.304C>G, NM_152493.2:c.304C>G, XM_005270507.3:c.265C>G, XM_005270507.2:c.265C>G, XM_005270507.1:c.265C>G, XM_047447108.1:c.358C>G, NM_001370212.1:c.304C>G, XM_047447109.1:c.304C>G, XM_047447107.1:c.358C>G, XM_047447110.1:c.304C>G, XP_005270565.1:p.Pro89Ala, NP_689706.2:p.Pro102Ala, XP_005270564.1:p.Pro89Ala, XP_047303064.1:p.Pro120Ala, NP_001357141.1:p.Pro102Ala, XP_047303065.1:p.Pro102Ala, XP_047303063.1:p.Pro120Ala, XP_047303066.1:p.Pro102Ala

Select item 143199369118.

rs1431993691 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:33276537 (GRCh38)
1:33742138 (GRCh37)
Canonical SPDI:: NC_000001.11:33276536:G:A
Gene:: ZNF362 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: A=0.000008/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.33276537G>A, NC_000001.10:g.33742138G>A, XM_005270508.6:c.253G>A, XM_005270508.5:c.253G>A, XM_005270508.4:c.253G>A, XM_005270508.3:c.253G>A, XM_005270508.2:c.253G>A, XM_005270508.1:c.253G>A, NM_152493.3:c.292G>A, NM_152493.2:c.292G>A, XM_005270507.3:c.253G>A, XM_005270507.2:c.253G>A, XM_005270507.1:c.253G>A, XM_047447108.1:c.346G>A, NM_001370212.1:c.292G>A, XM_047447109.1:c.292G>A, XM_047447107.1:c.346G>A, XM_047447110.1:c.292G>A, XP_005270565.1:p.Ala85Thr, NP_689706.2:p.Ala98Thr, XP_005270564.1:p.Ala85Thr, XP_047303064.1:p.Ala116Thr, NP_001357141.1:p.Ala98Thr, XP_047303065.1:p.Ala98Thr, XP_047303063.1:p.Ala116Thr, XP_047303066.1:p.Ala98Thr

Select item 143097431319.

rs1430974313 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 1:33280383 (GRCh38)
1:33745984 (GRCh37)
Canonical SPDI:: NC_000001.11:33280382:G:A,NC_000001.11:33280382:G:T
Gene:: ZNF362 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.33280383G>A, NC_000001.11:g.33280383G>T, NC_000001.10:g.33745984G>A, NC_000001.10:g.33745984G>T, XM_005270508.6:c.570G>A, XM_005270508.6:c.570G>T, XM_005270508.5:c.570G>A, XM_005270508.5:c.570G>T, XM_005270508.4:c.570G>A, XM_005270508.4:c.570G>T, XM_005270508.3:c.570G>A, XM_005270508.3:c.570G>T, XM_005270508.2:c.570G>A, XM_005270508.2:c.570G>T, XM_005270508.1:c.570G>A, XM_005270508.1:c.570G>T, NM_152493.3:c.609G>A, NM_152493.3:c.609G>T, NM_152493.2:c.609G>A, NM_152493.2:c.609G>T, XM_005270507.3:c.570G>A, XM_005270507.3:c.570G>T, XM_005270507.2:c.570G>A, XM_005270507.2:c.570G>T, XM_005270507.1:c.570G>A, XM_005270507.1:c.570G>T, XM_047447108.1:c.663G>A, XM_047447108.1:c.663G>T, NM_001370212.1:c.609G>A, NM_001370212.1:c.609G>T, XM_047447109.1:c.609G>A, XM_047447109.1:c.609G>T, XM_047447107.1:c.663G>A, XM_047447107.1:c.663G>T, XM_047447110.1:c.609G>A, XM_047447110.1:c.609G>T

Select item 141804449520.

rs1418044495 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 1:33280322 (GRCh38)
1:33745923 (GRCh37)
Canonical SPDI:: NC_000001.11:33280321:G:A,NC_000001.11:33280321:G:C
Gene:: ZNF362 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.33280322G>A, NC_000001.11:g.33280322G>C, NC_000001.10:g.33745923G>A, NC_000001.10:g.33745923G>C, XM_005270508.6:c.509G>A, XM_005270508.6:c.509G>C, XM_005270508.5:c.509G>A, XM_005270508.5:c.509G>C, XM_005270508.4:c.509G>A, XM_005270508.4:c.509G>C, XM_005270508.3:c.509G>A, XM_005270508.3:c.509G>C, XM_005270508.2:c.509G>A, XM_005270508.2:c.509G>C, XM_005270508.1:c.509G>A, XM_005270508.1:c.509G>C, NM_152493.3:c.548G>A, NM_152493.3:c.548G>C, NM_152493.2:c.548G>A, NM_152493.2:c.548G>C, XM_005270507.3:c.509G>A, XM_005270507.3:c.509G>C, XM_005270507.2:c.509G>A, XM_005270507.2:c.509G>C, XM_005270507.1:c.509G>A, XM_005270507.1:c.509G>C, XM_047447108.1:c.602G>A, XM_047447108.1:c.602G>C, NM_001370212.1:c.548G>A, NM_001370212.1:c.548G>C, XM_047447109.1:c.548G>A, XM_047447109.1:c.548G>C, XM_047447107.1:c.602G>A, XM_047447107.1:c.602G>C, XM_047447110.1:c.548G>A, XM_047447110.1:c.548G>C, XP_005270565.1:p.Gly170Asp, XP_005270565.1:p.Gly170Ala, NP_689706.2:p.Gly183Asp, NP_689706.2:p.Gly183Ala, XP_005270564.1:p.Gly170Asp, XP_005270564.1:p.Gly170Ala, XP_047303064.1:p.Gly201Asp, XP_047303064.1:p.Gly201Ala, NP_001357141.1:p.Gly183Asp, NP_001357141.1:p.Gly183Ala, XP_047303065.1:p.Gly183Asp, XP_047303065.1:p.Gly183Ala, XP_047303063.1:p.Gly201Asp, XP_047303063.1:p.Gly201Ala, XP_047303066.1:p.Gly183Asp, XP_047303066.1:p.Gly183Ala

dbSNP

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Result Filters

Validation Status

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Global MAF

Custom range

Additional filters

Display Settings:

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Items: 1 to 20 of 361

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