SNP Links for Protein (Select 4506027) - SNP

Links from Protein

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Select item 14904990851.

rs1490499085 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 16:30083486 (GRCh38)
16:30094807 (GRCh37)
Canonical SPDI:: NC_000016.10:30083485:C:T
Gene:: PPP4C (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000008/2 (TOPMED)
HGVS:: NC_000016.10:g.30083486C>T, NC_000016.9:g.30094807C>T, XM_006721061.5:c.294C>T, XM_006721061.4:c.294C>T, XM_006721061.3:c.294C>T, XM_006721061.2:c.294C>T, XM_006721061.1:c.294C>T, NM_002720.3:c.396C>T, NM_002720.2:c.396C>T, NM_002720.1:c.396C>T, NM_001303506.2:c.159C>T, NM_001303506.1:c.159C>T, NM_001303503.2:c.396C>T, NM_001303503.1:c.396C>T, NM_001303507.2:c.159C>T, NM_001303507.1:c.159C>T, NM_001303504.2:c.294C>T, NM_001303504.1:c.294C>T

Select item 14871551082.

rs1487155108 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 16:30084844 (GRCh38)
16:30096165 (GRCh37)
Canonical SPDI:: NC_000016.10:30084843:C:T
Gene:: PPP4C (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: T=0.000071/1 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000016.10:g.30084844C>T, NC_000016.9:g.30096165C>T, NG_023283.1:g.12041G>A, XM_006721061.5:c.681C>T, XM_006721061.4:c.681C>T, XM_006721061.3:c.681C>T, XM_006721061.2:c.681C>T, XM_006721061.1:c.681C>T, NM_002720.3:c.783C>T, NM_002720.2:c.783C>T, NM_002720.1:c.783C>T, NM_001303506.2:c.546C>T, NM_001303506.1:c.546C>T, NM_001303503.2:c.783C>T, NM_001303503.1:c.783C>T, NM_001303507.2:c.546C>T, NM_001303507.1:c.546C>T, NM_001303504.2:c.681C>T, NM_001303504.1:c.681C>T

Select item 14782166763.

rs1478216676 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 16:30076407 (GRCh38)
16:30087728 (GRCh37)
Canonical SPDI:: NC_000016.10:30076406:G:T
Gene:: PPP4C (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,5_prime_UTR_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000016.10:g.30076407G>T, NC_000016.9:g.30087728G>T, XM_006721061.5:c.30G>T, XM_006721061.4:c.30G>T, XM_006721061.3:c.30G>T, XM_006721061.2:c.30G>T, XM_006721061.1:c.30G>T, NM_002720.3:c.30G>T, NM_002720.2:c.30G>T, NM_002720.1:c.30G>T, NM_001303506.2:c.-267G>T, NM_001303506.1:c.-267G>T, NM_001303503.2:c.30G>T, NM_001303503.1:c.30G>T, NM_001303507.2:c.-156G>T, NM_001303507.1:c.-156G>T, NM_001303504.2:c.30G>T, NM_001303504.1:c.30G>T, XP_006721124.1:p.Gln10His, NP_002711.1:p.Gln10His, NP_001290432.1:p.Gln10His, NP_001290433.1:p.Gln10His

Select item 14777814654.

rs1477781465 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 16:30076390 (GRCh38)
16:30087711 (GRCh37)
Canonical SPDI:: NC_000016.10:30076389:A:G
Gene:: PPP4C (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,5_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000051/1 (ALFA)
G=0.000004/1 (GnomAD_exomes)
G=0.000014/2 (GnomAD)
HGVS:: NC_000016.10:g.30076390A>G, NC_000016.9:g.30087711A>G, XM_006721061.5:c.13A>G, XM_006721061.4:c.13A>G, XM_006721061.3:c.13A>G, XM_006721061.2:c.13A>G, XM_006721061.1:c.13A>G, NM_002720.3:c.13A>G, NM_002720.2:c.13A>G, NM_002720.1:c.13A>G, NM_001303506.2:c.-284A>G, NM_001303506.1:c.-284A>G, NM_001303503.2:c.13A>G, NM_001303503.1:c.13A>G, NM_001303507.2:c.-173A>G, NM_001303507.1:c.-173A>G, NM_001303504.2:c.13A>G, NM_001303504.1:c.13A>G, XP_006721124.1:p.Ser5Gly, NP_002711.1:p.Ser5Gly, NP_001290432.1:p.Ser5Gly, NP_001290433.1:p.Ser5Gly

Select item 14760353005.

rs1476035300 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 16:30084951 (GRCh38)
16:30096272 (GRCh37)
Canonical SPDI:: NC_000016.10:30084950:C:T
Gene:: PPP4C (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000031/1 (ALFA)
T=0.000004/1 (GnomAD_exomes)
T=0.000004/1 (TOPMED)
HGVS:: NC_000016.10:g.30084951C>T, NC_000016.9:g.30096272C>T, NG_023283.1:g.11934G>A, XM_006721061.5:c.711C>T, XM_006721061.4:c.711C>T, XM_006721061.3:c.711C>T, XM_006721061.2:c.711C>T, XM_006721061.1:c.711C>T, NM_002720.3:c.813C>T, NM_002720.2:c.813C>T, NM_002720.1:c.813C>T, NM_001303506.2:c.576C>T, NM_001303506.1:c.576C>T, NM_001303503.2:c.813C>T, NM_001303503.1:c.813C>T, NM_001303507.2:c.576C>T, NM_001303507.1:c.576C>T, NM_001303504.2:c.711C>T, NM_001303504.1:c.711C>T

Select item 14709091916.

rs1470909191 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 16:30083561 (GRCh38)
16:30094882 (GRCh37)
Canonical SPDI:: NC_000016.10:30083560:T:C
Gene:: PPP4C (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000016.10:g.30083561T>C, NC_000016.9:g.30094882T>C, XM_006721061.5:c.369T>C, XM_006721061.4:c.369T>C, XM_006721061.3:c.369T>C, XM_006721061.2:c.369T>C, XM_006721061.1:c.369T>C, NM_002720.3:c.471T>C, NM_002720.2:c.471T>C, NM_002720.1:c.471T>C, NM_001303506.2:c.234T>C, NM_001303506.1:c.234T>C, NM_001303503.2:c.471T>C, NM_001303503.1:c.471T>C, NM_001303507.2:c.234T>C, NM_001303507.1:c.234T>C, NM_001303504.2:c.369T>C, NM_001303504.1:c.369T>C

Select item 14697232467.

rs1469723246 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 16:30082822 (GRCh38)
16:30094143 (GRCh37)
Canonical SPDI:: NC_000016.10:30082821:C:T
Gene:: PPP4C (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,intron_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000016.10:g.30082822C>T, NC_000016.9:g.30094143C>T, NM_002720.3:c.278C>T, NM_002720.2:c.278C>T, NM_002720.1:c.278C>T, NM_001303506.2:c.41C>T, NM_001303506.1:c.41C>T, NM_001303503.2:c.278C>T, NM_001303503.1:c.278C>T, NM_001303507.2:c.41C>T, NM_001303507.1:c.41C>T, NP_002711.1:p.Thr93Met, NP_001290435.1:p.Thr14Met, NP_001290432.1:p.Thr93Met, NP_001290436.1:p.Thr14Met

Select item 14616376758.

rs1461637675 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 16:30084668 (GRCh38)
16:30095989 (GRCh37)
Canonical SPDI:: NC_000016.10:30084667:A:G
Gene:: PPP4C (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000016.10:g.30084668A>G, NC_000016.9:g.30095989A>G, NG_023283.1:g.12217T>C, XM_006721061.5:c.505A>G, XM_006721061.4:c.505A>G, XM_006721061.3:c.505A>G, XM_006721061.2:c.505A>G, XM_006721061.1:c.505A>G, NM_002720.3:c.607A>G, NM_002720.2:c.607A>G, NM_002720.1:c.607A>G, NM_001303506.2:c.370A>G, NM_001303506.1:c.370A>G, NM_001303503.2:c.607A>G, NM_001303503.1:c.607A>G, NM_001303507.2:c.370A>G, NM_001303507.1:c.370A>G, NM_001303504.2:c.505A>G, NM_001303504.1:c.505A>G, XP_006721124.1:p.Thr169Ala, NP_002711.1:p.Thr203Ala, NP_001290435.1:p.Thr124Ala, NP_001290432.1:p.Thr203Ala, NP_001290436.1:p.Thr124Ala, NP_001290433.1:p.Thr169Ala

Select item 14523061929.

rs1452306192 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 16:30084707 (GRCh38)
16:30096028 (GRCh37)
Canonical SPDI:: NC_000016.10:30084706:C:G
Gene:: PPP4C (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)
HGVS:: NC_000016.10:g.30084707C>G, NC_000016.9:g.30096028C>G, NG_023283.1:g.12178G>C, XM_006721061.5:c.544C>G, XM_006721061.4:c.544C>G, XM_006721061.3:c.544C>G, XM_006721061.2:c.544C>G, XM_006721061.1:c.544C>G, NM_002720.3:c.646C>G, NM_002720.2:c.646C>G, NM_002720.1:c.646C>G, NM_001303506.2:c.409C>G, NM_001303506.1:c.409C>G, NM_001303503.2:c.646C>G, NM_001303503.1:c.646C>G, NM_001303507.2:c.409C>G, NM_001303507.1:c.409C>G, NM_001303504.2:c.544C>G, NM_001303504.1:c.544C>G, XP_006721124.1:p.Leu182Val, NP_002711.1:p.Leu216Val, NP_001290435.1:p.Leu137Val, NP_001290432.1:p.Leu216Val, NP_001290436.1:p.Leu137Val, NP_001290433.1:p.Leu182Val

Select item 144727112910.

rs1447271129 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 16:30084973 (GRCh38)
16:30096294 (GRCh37)
Canonical SPDI:: NC_000016.10:30084972:C:G
Gene:: PPP4C (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000016.10:g.30084973C>G, NC_000016.9:g.30096294C>G, NG_023283.1:g.11912G>C, XM_006721061.5:c.733C>G, XM_006721061.4:c.733C>G, XM_006721061.3:c.733C>G, XM_006721061.2:c.733C>G, XM_006721061.1:c.733C>G, NM_002720.3:c.835C>G, NM_002720.2:c.835C>G, NM_002720.1:c.835C>G, NM_001303506.2:c.598C>G, NM_001303506.1:c.598C>G, NM_001303503.2:c.835C>G, NM_001303503.1:c.835C>G, NM_001303507.2:c.598C>G, NM_001303507.1:c.598C>G, NM_001303504.2:c.733C>G, NM_001303504.1:c.733C>G, XP_006721124.1:p.Leu245Val, NP_002711.1:p.Leu279Val, NP_001290435.1:p.Leu200Val, NP_001290432.1:p.Leu279Val, NP_001290436.1:p.Leu200Val, NP_001290433.1:p.Leu245Val

Select item 144188113811.

rs1441881138 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 16:30083672 (GRCh38)
16:30094993 (GRCh37)
Canonical SPDI:: NC_000016.10:30083671:G:T
Gene:: PPP4C (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=0.000007/1 (GnomAD)
HGVS:: NC_000016.10:g.30083672G>T, NC_000016.9:g.30094993G>T, XM_006721061.5:c.393G>T, XM_006721061.4:c.393G>T, XM_006721061.3:c.393G>T, XM_006721061.2:c.393G>T, XM_006721061.1:c.393G>T, NM_002720.3:c.495G>T, NM_002720.2:c.495G>T, NM_002720.1:c.495G>T, NM_001303506.2:c.258G>T, NM_001303506.1:c.258G>T, NM_001303503.2:c.495G>T, NM_001303503.1:c.495G>T, NM_001303507.2:c.258G>T, NM_001303507.1:c.258G>T, NM_001303504.2:c.393G>T, NM_001303504.1:c.393G>T

Select item 144135600112.

rs1441356001 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 16:30082793 (GRCh38)
16:30094114 (GRCh37)
Canonical SPDI:: NC_000016.10:30082792:T:C
Gene:: PPP4C (Varview)
Functional Consequence:: synonymous_variant,intron_variant,coding_sequence_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000016.10:g.30082793T>C, NC_000016.9:g.30094114T>C, NM_002720.3:c.249T>C, NM_002720.2:c.249T>C, NM_002720.1:c.249T>C, NM_001303506.2:c.12T>C, NM_001303506.1:c.12T>C, NM_001303503.2:c.249T>C, NM_001303503.1:c.249T>C, NM_001303507.2:c.12T>C, NM_001303507.1:c.12T>C

Select item 143657545013.

rs1436575450 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 16:30082502 (GRCh38)
16:30093823 (GRCh37)
Canonical SPDI:: NC_000016.10:30082501:G:A
Gene:: PPP4C (Varview)
Functional Consequence:: 5_prime_UTR_variant,coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000016.10:g.30082502G>A, NC_000016.9:g.30093823G>A, XM_006721061.5:c.169G>A, XM_006721061.4:c.169G>A, XM_006721061.3:c.169G>A, XM_006721061.2:c.169G>A, XM_006721061.1:c.169G>A, NM_002720.3:c.169G>A, NM_002720.2:c.169G>A, NM_002720.1:c.169G>A, NM_001303506.2:c.-69G>A, NM_001303506.1:c.-69G>A, NM_001303503.2:c.169G>A, NM_001303503.1:c.169G>A, NM_001303507.2:c.-69G>A, NM_001303507.1:c.-69G>A, NM_001303504.2:c.169G>A, NM_001303504.1:c.169G>A, XP_006721124.1:p.Gly57Arg, NP_002711.1:p.Gly57Arg, NP_001290432.1:p.Gly57Arg, NP_001290433.1:p.Gly57Arg

Select item 143529432214.

rs1435294322 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 16:30076437 (GRCh38)
16:30087758 (GRCh37)
Canonical SPDI:: NC_000016.10:30076436:C:T
Gene:: PPP4C (Varview)
Functional Consequence:: 5_prime_UTR_variant,synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000016.10:g.30076437C>T, NC_000016.9:g.30087758C>T, XM_006721061.5:c.60C>T, XM_006721061.4:c.60C>T, XM_006721061.3:c.60C>T, XM_006721061.2:c.60C>T, XM_006721061.1:c.60C>T, NM_002720.3:c.60C>T, NM_002720.2:c.60C>T, NM_002720.1:c.60C>T, NM_001303506.2:c.-237C>T, NM_001303506.1:c.-237C>T, NM_001303503.2:c.60C>T, NM_001303503.1:c.60C>T, NM_001303507.2:c.-126C>T, NM_001303507.1:c.-126C>T, NM_001303504.2:c.60C>T, NM_001303504.1:c.60C>T

Select item 142726369015.

rs1427263690 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 16:30076404 (GRCh38)
16:30087725 (GRCh37)
Canonical SPDI:: NC_000016.10:30076403:G:T
Gene:: PPP4C (Varview)
Functional Consequence:: 5_prime_UTR_variant,synonymous_variant,coding_sequence_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_000016.10:g.30076404G>T, NC_000016.9:g.30087725G>T, XM_006721061.5:c.27G>T, XM_006721061.4:c.27G>T, XM_006721061.3:c.27G>T, XM_006721061.2:c.27G>T, XM_006721061.1:c.27G>T, NM_002720.3:c.27G>T, NM_002720.2:c.27G>T, NM_002720.1:c.27G>T, NM_001303506.2:c.-270G>T, NM_001303506.1:c.-270G>T, NM_001303503.2:c.27G>T, NM_001303503.1:c.27G>T, NM_001303507.2:c.-159G>T, NM_001303507.1:c.-159G>T, NM_001303504.2:c.27G>T, NM_001303504.1:c.27G>T

Select item 142666370516.

rs1426663705 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 16:30076400 (GRCh38)
16:30087721 (GRCh37)
Canonical SPDI:: NC_000016.10:30076399:A:T
Gene:: PPP4C (Varview)
Functional Consequence:: 5_prime_UTR_variant,coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000016.10:g.30076400A>T, NC_000016.9:g.30087721A>T, XM_006721061.5:c.23A>T, XM_006721061.4:c.23A>T, XM_006721061.3:c.23A>T, XM_006721061.2:c.23A>T, XM_006721061.1:c.23A>T, NM_002720.3:c.23A>T, NM_002720.2:c.23A>T, NM_002720.1:c.23A>T, NM_001303506.2:c.-274A>T, NM_001303506.1:c.-274A>T, NM_001303503.2:c.23A>T, NM_001303503.1:c.23A>T, NM_001303507.2:c.-163A>T, NM_001303507.1:c.-163A>T, NM_001303504.2:c.23A>T, NM_001303504.1:c.23A>T, XP_006721124.1:p.Asp8Val, NP_002711.1:p.Asp8Val, NP_001290432.1:p.Asp8Val, NP_001290433.1:p.Asp8Val

Select item 142358725417.

rs1423587254 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 16:30083425 (GRCh38)
16:30094746 (GRCh37)
Canonical SPDI:: NC_000016.10:30083424:G:A
Gene:: PPP4C (Varview)
Functional Consequence:: missense_variant,coding_sequence_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_000016.10:g.30083425G>A, NC_000016.9:g.30094746G>A, XM_006721061.5:c.233G>A, XM_006721061.4:c.233G>A, XM_006721061.3:c.233G>A, XM_006721061.2:c.233G>A, XM_006721061.1:c.233G>A, NM_002720.3:c.335G>A, NM_002720.2:c.335G>A, NM_002720.1:c.335G>A, NM_001303506.2:c.98G>A, NM_001303506.1:c.98G>A, NM_001303503.2:c.335G>A, NM_001303503.1:c.335G>A, NM_001303507.2:c.98G>A, NM_001303507.1:c.98G>A, NM_001303504.2:c.233G>A, NM_001303504.1:c.233G>A, XP_006721124.1:p.Arg78Gln, NP_002711.1:p.Arg112Gln, NP_001290435.1:p.Arg33Gln, NP_001290432.1:p.Arg112Gln, NP_001290436.1:p.Arg33Gln, NP_001290433.1:p.Arg78Gln

Select item 141794234018.

rs1417942340 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 16:30076417 (GRCh38)
16:30087738 (GRCh37)
Canonical SPDI:: NC_000016.10:30076416:C:T
Gene:: PPP4C (Varview)
Functional Consequence:: 5_prime_UTR_variant,synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
T=0.000012/3 (GnomAD_exomes)
T=0.000014/2 (GnomAD)
HGVS:: NC_000016.10:g.30076417C>T, NC_000016.9:g.30087738C>T, XM_006721061.5:c.40C>T, XM_006721061.4:c.40C>T, XM_006721061.3:c.40C>T, XM_006721061.2:c.40C>T, XM_006721061.1:c.40C>T, NM_002720.3:c.40C>T, NM_002720.2:c.40C>T, NM_002720.1:c.40C>T, NM_001303506.2:c.-257C>T, NM_001303506.1:c.-257C>T, NM_001303503.2:c.40C>T, NM_001303503.1:c.40C>T, NM_001303507.2:c.-146C>T, NM_001303507.1:c.-146C>T, NM_001303504.2:c.40C>T, NM_001303504.1:c.40C>T

Select item 140552248219.

rs1405522482 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 16:30083729 (GRCh38)
16:30095050 (GRCh37)
Canonical SPDI:: NC_000016.10:30083728:A:G
Gene:: PPP4C (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.00006/1 (TOMMO)
HGVS:: NC_000016.10:g.30083729A>G, NC_000016.9:g.30095050A>G, XM_006721061.5:c.450A>G, XM_006721061.4:c.450A>G, XM_006721061.3:c.450A>G, XM_006721061.2:c.450A>G, XM_006721061.1:c.450A>G, NM_002720.3:c.552A>G, NM_002720.2:c.552A>G, NM_002720.1:c.552A>G, NM_001303506.2:c.315A>G, NM_001303506.1:c.315A>G, NM_001303503.2:c.552A>G, NM_001303503.1:c.552A>G, NM_001303507.2:c.315A>G, NM_001303507.1:c.315A>G, NM_001303504.2:c.450A>G, NM_001303504.1:c.450A>G

Select item 140498088620.

rs1404980886 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 16:30083554 (GRCh38)
16:30094875 (GRCh37)
Canonical SPDI:: NC_000016.10:30083553:T:C
Gene:: PPP4C (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000016.10:g.30083554T>C, NC_000016.9:g.30094875T>C, XM_006721061.5:c.362T>C, XM_006721061.4:c.362T>C, XM_006721061.3:c.362T>C, XM_006721061.2:c.362T>C, XM_006721061.1:c.362T>C, NM_002720.3:c.464T>C, NM_002720.2:c.464T>C, NM_002720.1:c.464T>C, NM_001303506.2:c.227T>C, NM_001303506.1:c.227T>C, NM_001303503.2:c.464T>C, NM_001303503.1:c.464T>C, NM_001303507.2:c.227T>C, NM_001303507.1:c.227T>C, NM_001303504.2:c.362T>C, NM_001303504.1:c.362T>C, XP_006721124.1:p.Ile121Thr, NP_002711.1:p.Ile155Thr, NP_001290435.1:p.Ile76Thr, NP_001290432.1:p.Ile155Thr, NP_001290436.1:p.Ile76Thr, NP_001290433.1:p.Ile121Thr

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