SNP Links for Protein (Select 122937333) - SNP

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Links from Protein

Items: 1 to 20 of 743

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Select item 14907101621.

rs1490710162 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 1:119623325 (GRCh38)
1:120165948 (GRCh37)
Canonical SPDI:: NC_000001.11:119623324:C:A
Gene:: ZNF697 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000008/1 (GnomAD)
HGVS:: NC_000001.11:g.119623325C>A, NC_000001.10:g.120165948C>A, XM_005271315.4:c.1018G>T, XM_005271315.3:c.1018G>T, XM_005271315.2:c.1018G>T, XM_005271315.1:c.1018G>T, NM_001080470.2:c.1018G>T, NM_001080470.1:c.1018G>T, XM_047433849.1:c.1018G>T, NM_138366.1:c.-210G>T, XP_005271372.1:p.Ala340Ser, NP_001073939.1:p.Ala340Ser, XP_047289805.1:p.Ala340Ser

Select item 14900455322.

rs1490045532 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 1:119623304 (GRCh38)
1:120165927 (GRCh37)
Canonical SPDI:: NC_000001.11:119623303:C:A,NC_000001.11:119623303:C:T
Gene:: ZNF697 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.00003/4 (GnomAD)
HGVS:: NC_000001.11:g.119623304C>A, NC_000001.11:g.119623304C>T, NC_000001.10:g.120165927C>A, NC_000001.10:g.120165927C>T, XM_005271315.4:c.1039G>T, XM_005271315.4:c.1039G>A, XM_005271315.3:c.1039G>T, XM_005271315.3:c.1039G>A, XM_005271315.2:c.1039G>T, XM_005271315.2:c.1039G>A, XM_005271315.1:c.1039G>T, XM_005271315.1:c.1039G>A, NM_001080470.2:c.1039G>T, NM_001080470.2:c.1039G>A, NM_001080470.1:c.1039G>T, NM_001080470.1:c.1039G>A, XM_047433849.1:c.1039G>T, XM_047433849.1:c.1039G>A, NM_138366.1:c.-189G>T, NM_138366.1:c.-189G>A, XP_005271372.1:p.Ala347Ser, XP_005271372.1:p.Ala347Thr, NP_001073939.1:p.Ala347Ser, NP_001073939.1:p.Ala347Thr, XP_047289805.1:p.Ala347Ser, XP_047289805.1:p.Ala347Thr

Select item 14900156573.

rs1490015657 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 1:119622816 (GRCh38)
1:120165439 (GRCh37)
Canonical SPDI:: NC_000001.11:119622815:G:T
Gene:: ZNF697 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000001.11:g.119622816G>T, NC_000001.10:g.120165439G>T, XM_005271315.4:c.1527C>A, XM_005271315.3:c.1527C>A, XM_005271315.2:c.1527C>A, XM_005271315.1:c.1527C>A, NM_001080470.2:c.1527C>A, NM_001080470.1:c.1527C>A, XM_047433849.1:c.1527C>A, NM_138366.1:c.300C>A

Select item 14895135104.

rs1489513510 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:119623086 (GRCh38)
1:120165709 (GRCh37)
Canonical SPDI:: NC_000001.11:119623085:G:A
Gene:: ZNF697 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000001.11:g.119623086G>A, NC_000001.10:g.120165709G>A, XM_005271315.4:c.1257C>T, XM_005271315.3:c.1257C>T, XM_005271315.2:c.1257C>T, XM_005271315.1:c.1257C>T, NM_001080470.2:c.1257C>T, NM_001080470.1:c.1257C>T, XM_047433849.1:c.1257C>T, NM_138366.1:c.30C>T

Select item 14882882645.

rs1488288264 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:119623932 (GRCh38)
1:120166555 (GRCh37)
Canonical SPDI:: NC_000001.11:119623931:G:A
Gene:: ZNF697 (Varview)
Functional Consequence:: synonymous_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_000001.11:g.119623932G>A, NC_000001.10:g.120166555G>A, XM_005271315.4:c.411C>T, XM_005271315.3:c.411C>T, XM_005271315.2:c.411C>T, XM_005271315.1:c.411C>T, NM_001080470.2:c.411C>T, NM_001080470.1:c.411C>T, XM_047433849.1:c.411C>T

Select item 14850556686.

rs1485055668 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:119623138 (GRCh38)
1:120165761 (GRCh37)
Canonical SPDI:: NC_000001.11:119623137:A:G
Gene:: ZNF697 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000005/1 (GnomAD_exomes)
G=0.000072/10 (GnomAD)
HGVS:: NC_000001.11:g.119623138A>G, NC_000001.10:g.120165761A>G, XM_005271315.4:c.1205T>C, XM_005271315.3:c.1205T>C, XM_005271315.2:c.1205T>C, XM_005271315.1:c.1205T>C, NM_001080470.2:c.1205T>C, NM_001080470.1:c.1205T>C, XM_047433849.1:c.1205T>C, NM_138366.1:c.-23T>C, XP_005271372.1:p.Val402Ala, NP_001073939.1:p.Val402Ala, XP_047289805.1:p.Val402Ala

Select item 14838539007.

rs1483853900 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:119623738 (GRCh38)
1:120166361 (GRCh37)
Canonical SPDI:: NC_000001.11:119623737:G:A
Gene:: ZNF697 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: A=0.000015/2 (GnomAD_exomes)
HGVS:: NC_000001.11:g.119623738G>A, NC_000001.10:g.120166361G>A, XM_005271315.4:c.605C>T, XM_005271315.3:c.605C>T, XM_005271315.2:c.605C>T, XM_005271315.1:c.605C>T, NM_001080470.2:c.605C>T, NM_001080470.1:c.605C>T, XM_047433849.1:c.605C>T, XP_005271372.1:p.Ala202Val, NP_001073939.1:p.Ala202Val, XP_047289805.1:p.Ala202Val

Select item 14830385618.

rs1483038561 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:119622859 (GRCh38)
1:120165482 (GRCh37)
Canonical SPDI:: NC_000001.11:119622858:C:T
Gene:: ZNF697 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: T=0.000071/1 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.119622859C>T, NC_000001.10:g.120165482C>T, XM_005271315.4:c.1484G>A, XM_005271315.3:c.1484G>A, XM_005271315.2:c.1484G>A, XM_005271315.1:c.1484G>A, NM_001080470.2:c.1484G>A, NM_001080470.1:c.1484G>A, XM_047433849.1:c.1484G>A, NM_138366.1:c.257G>A, XP_005271372.1:p.Cys495Tyr, NP_001073939.1:p.Cys495Tyr, XP_047289805.1:p.Cys495Tyr

Select item 14827885439.

rs1482788543 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:119624024 (GRCh38)
1:120166647 (GRCh37)
Canonical SPDI:: NC_000001.11:119624023:A:G
Gene:: ZNF697 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: G=0.000016/4 (GnomAD_exomes)
HGVS:: NC_000001.11:g.119624024A>G, NC_000001.10:g.120166647A>G, XM_005271315.4:c.319T>C, XM_005271315.3:c.319T>C, XM_005271315.2:c.319T>C, XM_005271315.1:c.319T>C, NM_001080470.2:c.319T>C, NM_001080470.1:c.319T>C, XM_047433849.1:c.319T>C, XP_005271372.1:p.Ser107Pro, NP_001073939.1:p.Ser107Pro, XP_047289805.1:p.Ser107Pro

Select item 148178244310.

rs1481782443 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 1:119625959 (GRCh38)
1:120168582 (GRCh37)
Canonical SPDI:: NC_000001.11:119625958:T:C
Gene:: ZNF697 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000001.11:g.119625959T>C, NC_000001.10:g.120168582T>C, XM_005271315.4:c.142A>G, XM_005271315.3:c.142A>G, XM_005271315.2:c.142A>G, XM_005271315.1:c.142A>G, NM_001080470.2:c.142A>G, NM_001080470.1:c.142A>G, XM_047433849.1:c.142A>G, XP_005271372.1:p.Lys48Glu, NP_001073939.1:p.Lys48Glu, XP_047289805.1:p.Lys48Glu

Select item 148019724111.

rs1480197241 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:119623017 (GRCh38)
1:120165640 (GRCh37)
Canonical SPDI:: NC_000001.11:119623016:G:A
Gene:: ZNF697 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
HGVS:: NC_000001.11:g.119623017G>A, NC_000001.10:g.120165640G>A, XM_005271315.4:c.1326C>T, XM_005271315.3:c.1326C>T, XM_005271315.2:c.1326C>T, XM_005271315.1:c.1326C>T, NM_001080470.2:c.1326C>T, NM_001080470.1:c.1326C>T, XM_047433849.1:c.1326C>T, NM_138366.1:c.99C>T

Select item 147994342912.

rs1479943429 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:119623268 (GRCh38)
1:120165891 (GRCh37)
Canonical SPDI:: NC_000001.11:119623267:C:T
Gene:: ZNF697 (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=0.000016/2 (GnomAD_exomes)
HGVS:: NC_000001.11:g.119623268C>T, NC_000001.10:g.120165891C>T, XM_005271315.4:c.1075G>A, XM_005271315.3:c.1075G>A, XM_005271315.2:c.1075G>A, XM_005271315.1:c.1075G>A, NM_001080470.2:c.1075G>A, NM_001080470.1:c.1075G>A, XM_047433849.1:c.1075G>A, NM_138366.1:c.-153G>A, XP_005271372.1:p.Gly359Ser, NP_001073939.1:p.Gly359Ser, XP_047289805.1:p.Gly359Ser

Select item 147983003313.

rs1479830033 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:119622723 (GRCh38)
1:120165346 (GRCh37)
Canonical SPDI:: NC_000001.11:119622722:C:T
Gene:: ZNF697 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
HGVS:: NC_000001.11:g.119622723C>T, NC_000001.10:g.120165346C>T, XM_005271315.4:c.1620G>A, XM_005271315.3:c.1620G>A, XM_005271315.2:c.1620G>A, XM_005271315.1:c.1620G>A, NM_001080470.2:c.1620G>A, NM_001080470.1:c.1620G>A, XM_047433849.1:c.1620G>A, NM_138366.1:c.393G>A

Select item 147928265914.

rs1479282659 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:119622729 (GRCh38)
1:120165352 (GRCh37)
Canonical SPDI:: NC_000001.11:119622728:C:T
Gene:: ZNF697 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.119622729C>T, NC_000001.10:g.120165352C>T, XM_005271315.4:c.1614G>A, XM_005271315.3:c.1614G>A, XM_005271315.2:c.1614G>A, XM_005271315.1:c.1614G>A, NM_001080470.2:c.1614G>A, NM_001080470.1:c.1614G>A, XM_047433849.1:c.1614G>A, NM_138366.1:c.387G>A

Select item 147886799415.

rs1478867994 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 1:119626054 (GRCh38)
1:120168677 (GRCh37)
Canonical SPDI:: NC_000001.11:119626053:T:C
Gene:: ZNF697 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000008/2 (TOPMED)
HGVS:: NC_000001.11:g.119626054T>C, NC_000001.10:g.120168677T>C, XM_005271315.4:c.47A>G, XM_005271315.3:c.47A>G, XM_005271315.2:c.47A>G, XM_005271315.1:c.47A>G, NM_001080470.2:c.47A>G, NM_001080470.1:c.47A>G, XM_047433849.1:c.47A>G, XP_005271372.1:p.Glu16Gly, NP_001073939.1:p.Glu16Gly, XP_047289805.1:p.Glu16Gly

Select item 147814167716.

rs1478141677 [Homo sapiens]

Variant type:: DELINS
Alleles:: CTGGCCGCCGCGTGCGCGCGCCG>- [Show Flanks]
Chromosome:: 1:119623315 (GRCh38)
1:120165938 (GRCh37)
Canonical SPDI:: NC_000001.11:119623307:CGCGCCGCTGGCCGCCGCGTGCGCGCGCCG:CGCGCCG
Gene:: ZNF697 (Varview)
Functional Consequence:: coding_sequence_variant,frameshift_variant
Validated:: by frequency,by cluster
MAF:: -=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.119623315_119623337del, NC_000001.10:g.120165938_120165960del, XM_005271315.4:c.1013_1035del, XM_005271315.3:c.1013_1035del, XM_005271315.2:c.1013_1035del, XM_005271315.1:c.1013_1035del, NM_001080470.2:c.1013_1035del, NM_001080470.1:c.1013_1035del, XM_047433849.1:c.1013_1035del, NM_138366.1:c.-215_-193del, XP_005271372.1:p.Ala338fs, NP_001073939.1:p.Ala338fs, XP_047289805.1:p.Ala338fs

Select item 147767572417.

rs1477675724 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 1:119623301 (GRCh38)
1:120165924 (GRCh37)
Canonical SPDI:: NC_000001.11:119623300:C:A,NC_000001.11:119623300:C:T
Gene:: ZNF697 (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=0.000008/1 (GnomAD)
A=0.00006/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.119623301C>A, NC_000001.11:g.119623301C>T, NC_000001.10:g.120165924C>A, NC_000001.10:g.120165924C>T, XM_005271315.4:c.1042G>T, XM_005271315.4:c.1042G>A, XM_005271315.3:c.1042G>T, XM_005271315.3:c.1042G>A, XM_005271315.2:c.1042G>T, XM_005271315.2:c.1042G>A, XM_005271315.1:c.1042G>T, XM_005271315.1:c.1042G>A, NM_001080470.2:c.1042G>T, NM_001080470.2:c.1042G>A, NM_001080470.1:c.1042G>T, NM_001080470.1:c.1042G>A, XM_047433849.1:c.1042G>T, XM_047433849.1:c.1042G>A, NM_138366.1:c.-186G>T, NM_138366.1:c.-186G>A, XP_005271372.1:p.Ala348Ser, XP_005271372.1:p.Ala348Thr, NP_001073939.1:p.Ala348Ser, NP_001073939.1:p.Ala348Thr, XP_047289805.1:p.Ala348Ser, XP_047289805.1:p.Ala348Thr

Select item 147747887218.

rs1477478872 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 1:119623819 (GRCh38)
1:120166442 (GRCh37)
Canonical SPDI:: NC_000001.11:119623818:C:G
Gene:: ZNF697 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: G=0.000007/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.119623819C>G, NC_000001.10:g.120166442C>G, XM_005271315.4:c.524G>C, XM_005271315.3:c.524G>C, XM_005271315.2:c.524G>C, XM_005271315.1:c.524G>C, NM_001080470.2:c.524G>C, NM_001080470.1:c.524G>C, XM_047433849.1:c.524G>C, XP_005271372.1:p.Gly175Ala, NP_001073939.1:p.Gly175Ala, XP_047289805.1:p.Gly175Ala

Select item 147616109619.

rs1476161096 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:119622837 (GRCh38)
1:120165460 (GRCh37)
Canonical SPDI:: NC_000001.11:119622836:A:G
Gene:: ZNF697 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by cluster
MAF:: G=0.00025/4 (TOMMO)
HGVS:: NC_000001.11:g.119622837A>G, NC_000001.10:g.120165460A>G, XM_005271315.4:c.1506T>C, XM_005271315.3:c.1506T>C, XM_005271315.2:c.1506T>C, XM_005271315.1:c.1506T>C, NM_001080470.2:c.1506T>C, NM_001080470.1:c.1506T>C, XM_047433849.1:c.1506T>C, NM_138366.1:c.279T>C

Select item 147606634720.

rs1476066347 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 1:119624083 (GRCh38)
1:120166706 (GRCh37)
Canonical SPDI:: NC_000001.11:119624082:A:C
Gene:: ZNF697 (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_000001.11:g.119624083A>C, NC_000001.10:g.120166706A>C, XM_005271315.4:c.260T>G, XM_005271315.3:c.260T>G, XM_005271315.2:c.260T>G, XM_005271315.1:c.260T>G, NM_001080470.2:c.260T>G, NM_001080470.1:c.260T>G, XM_047433849.1:c.260T>G, XP_005271372.1:p.Val87Gly, NP_001073939.1:p.Val87Gly, XP_047289805.1:p.Val87Gly

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