SNP Links for Protein (Select 1034562228) - SNP

Links from Protein

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Select item 14908924381.

rs1490892438 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:1333040 (GRCh38)
1:1268420 (GRCh37)
Canonical SPDI:: NC_000001.11:1333039:G:A
Gene:: TAS1R3 (Varview)
Functional Consequence:: synonymous_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_000001.11:g.1333040G>A, NC_000001.10:g.1268420G>A, NM_152228.3:c.1395G>A, NM_152228.2:c.1395G>A, NM_152228.1:c.1395G>A, XM_017002435.2:c.1395G>A, XM_017002435.1:c.1395G>A, XM_017002436.2:c.1395G>A, XM_017002436.1:c.1395G>A, XM_047431571.1:c.1395G>A

Select item 14901729072.

rs1490172907 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:1332389 (GRCh38)
1:1267769 (GRCh37)
Canonical SPDI:: NC_000001.11:1332388:C:T
Gene:: TAS1R3 (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_000001.11:g.1332389C>T, NC_000001.10:g.1267769C>T, NM_152228.3:c.858C>T, NM_152228.2:c.858C>T, NM_152228.1:c.858C>T, XM_017002435.2:c.858C>T, XM_017002435.1:c.858C>T, XM_017002436.2:c.858C>T, XM_017002436.1:c.858C>T, XM_047431571.1:c.858C>T

Select item 14894449713.

rs1489444971 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 1:1331804 (GRCh38)
1:1267184 (GRCh37)
Canonical SPDI:: NC_000001.11:1331803:G:A,NC_000001.11:1331803:G:T
Gene:: TAS1R3 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.00014/2 (TOMMO)
HGVS:: NC_000001.11:g.1331804G>A, NC_000001.11:g.1331804G>T, NC_000001.10:g.1267184G>A, NC_000001.10:g.1267184G>T, NM_152228.3:c.358G>A, NM_152228.3:c.358G>T, NM_152228.2:c.358G>A, NM_152228.2:c.358G>T, NM_152228.1:c.358G>A, NM_152228.1:c.358G>T, XM_017002435.2:c.358G>A, XM_017002435.2:c.358G>T, XM_017002435.1:c.358G>A, XM_017002435.1:c.358G>T, XM_017002436.2:c.358G>A, XM_017002436.2:c.358G>T, XM_017002436.1:c.358G>A, XM_017002436.1:c.358G>T, XM_047431571.1:c.358G>A, XM_047431571.1:c.358G>T, NP_689414.2:p.Ala120Thr, NP_689414.2:p.Ala120Ser, XP_016857924.1:p.Ala120Thr, XP_016857924.1:p.Ala120Ser, XP_016857925.1:p.Ala120Thr, XP_016857925.1:p.Ala120Ser, XP_047287527.1:p.Ala120Thr, XP_047287527.1:p.Ala120Ser

Select item 14893930894.

rs1489393089 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 1:1332220 (GRCh38)
1:1267600 (GRCh37)
Canonical SPDI:: NC_000001.11:1332219:C:G,NC_000001.11:1332219:C:T
Gene:: TAS1R3 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by cluster
MAF:: T=0.00004/1 (TOMMO)
HGVS:: NC_000001.11:g.1332220C>G, NC_000001.11:g.1332220C>T, NC_000001.10:g.1267600C>G, NC_000001.10:g.1267600C>T, NM_152228.3:c.689C>G, NM_152228.3:c.689C>T, NM_152228.2:c.689C>G, NM_152228.2:c.689C>T, NM_152228.1:c.689C>G, NM_152228.1:c.689C>T, XM_017002435.2:c.689C>G, XM_017002435.2:c.689C>T, XM_017002435.1:c.689C>G, XM_017002435.1:c.689C>T, XM_017002436.2:c.689C>G, XM_017002436.2:c.689C>T, XM_017002436.1:c.689C>G, XM_017002436.1:c.689C>T, XM_047431571.1:c.689C>G, XM_047431571.1:c.689C>T, NP_689414.2:p.Ala230Gly, NP_689414.2:p.Ala230Val, XP_016857924.1:p.Ala230Gly, XP_016857924.1:p.Ala230Val, XP_016857925.1:p.Ala230Gly, XP_016857925.1:p.Ala230Val, XP_047287527.1:p.Ala230Gly, XP_047287527.1:p.Ala230Val

Select item 14887125705.

rs1488712570 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 1:1332464 (GRCh38)
1:1267844 (GRCh37)
Canonical SPDI:: NC_000001.11:1332463:G:T
Gene:: TAS1R3 (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_000001.11:g.1332464G>T, NC_000001.10:g.1267844G>T, NM_152228.3:c.933G>T, NM_152228.2:c.933G>T, NM_152228.1:c.933G>T, XM_017002435.2:c.933G>T, XM_017002435.1:c.933G>T, XM_017002436.2:c.933G>T, XM_017002436.1:c.933G>T, XM_047431571.1:c.933G>T

Select item 14881407816.

rs1488140781 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:1334197 (GRCh38)
1:1269577 (GRCh37)
Canonical SPDI:: NC_000001.11:1334196:C:T
Gene:: TAS1R3 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
HGVS:: NC_000001.11:g.1334197C>T, NC_000001.10:g.1269577C>T, NG_008048.2:g.19916G>A, NM_152228.3:c.2292C>T, NM_152228.2:c.2292C>T, NM_152228.1:c.2292C>T, XM_017002435.2:c.2418C>T, XM_017002435.1:c.2418C>T, XM_017002436.2:c.2415C>T, XM_017002436.1:c.2415C>T, XM_047431571.1:c.2289C>T

Select item 14878752757.

rs1487875275 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 1:1332356 (GRCh38)
1:1267736 (GRCh37)
Canonical SPDI:: NC_000001.11:1332355:C:G,NC_000001.11:1332355:C:T
Gene:: TAS1R3 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000062/2 (ALFA)
T=0.000008/2 (TOPMED)
T=0.000018/4 (GnomAD_exomes)
HGVS:: NC_000001.11:g.1332356C>G, NC_000001.11:g.1332356C>T, NC_000001.10:g.1267736C>G, NC_000001.10:g.1267736C>T, NM_152228.3:c.825C>G, NM_152228.3:c.825C>T, NM_152228.2:c.825C>G, NM_152228.2:c.825C>T, NM_152228.1:c.825C>G, NM_152228.1:c.825C>T, XM_017002435.2:c.825C>G, XM_017002435.2:c.825C>T, XM_017002435.1:c.825C>G, XM_017002435.1:c.825C>T, XM_017002436.2:c.825C>G, XM_017002436.2:c.825C>T, XM_017002436.1:c.825C>G, XM_017002436.1:c.825C>T, XM_047431571.1:c.825C>G, XM_047431571.1:c.825C>T

Select item 14865046758.

rs1486504675 [Homo sapiens]

Variant type:: DELINS
Alleles:: C>- [Show Flanks]
Chromosome:: 1:1334404 (GRCh38)
1:1269784 (GRCh37)
Canonical SPDI:: NC_000001.11:1334403:CCC:CC
Gene:: TAS1R3 (Varview)
Functional Consequence:: frameshift_variant,coding_sequence_variant
Validated:: by frequency
MAF:: -=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.1334406del, NC_000001.10:g.1269786del, NG_008048.2:g.19709del, NM_152228.3:c.2501del, NM_152228.2:c.2501del, NM_152228.1:c.2501del, XM_017002435.2:c.2627del, XM_017002435.1:c.2627del, XM_017002436.2:c.2624del, XM_017002436.1:c.2624del, XM_047431571.1:c.2498del, NP_689414.2:p.Pro834fs, XP_016857924.1:p.Pro876fs, XP_016857925.1:p.Pro875fs, XP_047287527.1:p.Pro833fs

Select item 14854894339.

rs1485489433 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 1:1331847 (GRCh38)
1:1267227 (GRCh37)
Canonical SPDI:: NC_000001.11:1331846:A:T
Gene:: TAS1R3 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.1331847A>T, NC_000001.10:g.1267227A>T, NM_152228.3:c.401A>T, NM_152228.2:c.401A>T, NM_152228.1:c.401A>T, XM_017002435.2:c.401A>T, XM_017002435.1:c.401A>T, XM_017002436.2:c.401A>T, XM_017002436.1:c.401A>T, XM_047431571.1:c.401A>T, NP_689414.2:p.Tyr134Phe, XP_016857924.1:p.Tyr134Phe, XP_016857925.1:p.Tyr134Phe, XP_047287527.1:p.Tyr134Phe

Select item 148498617610.

rs1484986176 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:1333837 (GRCh38)
1:1269217 (GRCh37)
Canonical SPDI:: NC_000001.11:1333836:C:T
Gene:: TAS1R3 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000019/5 (TOPMED)
T=0.000021/3 (GnomAD)
HGVS:: NC_000001.11:g.1333837C>T, NC_000001.10:g.1269217C>T, NG_008048.2:g.20276G>A, NM_152228.3:c.1932C>T, NM_152228.2:c.1932C>T, NM_152228.1:c.1932C>T, XM_017002435.2:c.2058C>T, XM_017002435.1:c.2058C>T, XM_017002436.2:c.2055C>T, XM_017002436.1:c.2055C>T, XM_047431571.1:c.1929C>T

Select item 148402046011.

rs1484020460 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C [Show Flanks]
Chromosome:: 1:1334028 (GRCh38)
1:1269408 (GRCh37)
Canonical SPDI:: NC_000001.11:1334027:T:A,NC_000001.11:1334027:T:C
Gene:: TAS1R3 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by cluster
MAF:: A=0.000004/1 (GnomAD_exomes)
C=0.000035/1 (TOMMO)
HGVS:: NC_000001.11:g.1334028T>A, NC_000001.11:g.1334028T>C, NC_000001.10:g.1269408T>A, NC_000001.10:g.1269408T>C, NG_008048.2:g.20085A>T, NG_008048.2:g.20085A>G, NM_152228.3:c.2123T>A, NM_152228.3:c.2123T>C, NM_152228.2:c.2123T>A, NM_152228.2:c.2123T>C, NM_152228.1:c.2123T>A, NM_152228.1:c.2123T>C, XM_017002435.2:c.2249T>A, XM_017002435.2:c.2249T>C, XM_017002435.1:c.2249T>A, XM_017002435.1:c.2249T>C, XM_017002436.2:c.2246T>A, XM_017002436.2:c.2246T>C, XM_017002436.1:c.2246T>A, XM_017002436.1:c.2246T>C, XM_047431571.1:c.2120T>A, XM_047431571.1:c.2120T>C, NP_689414.2:p.Val708Glu, NP_689414.2:p.Val708Ala, XP_016857924.1:p.Val750Glu, XP_016857924.1:p.Val750Ala, XP_016857925.1:p.Val749Glu, XP_016857925.1:p.Val749Ala, XP_047287527.1:p.Val707Glu, XP_047287527.1:p.Val707Ala

Select item 148379301712.

rs1483793017 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:1332304 (GRCh38)
1:1267684 (GRCh37)
Canonical SPDI:: NC_000001.11:1332303:A:G
Gene:: TAS1R3 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
HGVS:: NC_000001.11:g.1332304A>G, NC_000001.10:g.1267684A>G, NM_152228.3:c.773A>G, NM_152228.2:c.773A>G, NM_152228.1:c.773A>G, XM_017002435.2:c.773A>G, XM_017002435.1:c.773A>G, XM_017002436.2:c.773A>G, XM_017002436.1:c.773A>G, XM_047431571.1:c.773A>G, NP_689414.2:p.Asp258Gly, XP_016857924.1:p.Asp258Gly, XP_016857925.1:p.Asp258Gly, XP_047287527.1:p.Asp258Gly

Select item 148250400713.

rs1482504007 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:1334165 (GRCh38)
1:1269545 (GRCh37)
Canonical SPDI:: NC_000001.11:1334164:C:T
Gene:: TAS1R3 (Varview)
Functional Consequence:: stop_gained,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: T=0.000111/1 (ALFA)
T=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.1334165C>T, NC_000001.10:g.1269545C>T, NG_008048.2:g.19948G>A, NM_152228.3:c.2260C>T, NM_152228.2:c.2260C>T, NM_152228.1:c.2260C>T, XM_017002435.2:c.2386C>T, XM_017002435.1:c.2386C>T, XM_017002436.2:c.2383C>T, XM_017002436.1:c.2383C>T, XM_047431571.1:c.2257C>T, NP_689414.2:p.Gln754Ter, XP_016857924.1:p.Gln796Ter, XP_016857925.1:p.Gln795Ter, XP_047287527.1:p.Gln753Ter

Select item 148163425914.

rs1481634259 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 1:1332994 (GRCh38)
1:1268374 (GRCh37)
Canonical SPDI:: NC_000001.11:1332993:T:C,NC_000001.11:1332993:T:G
Gene:: TAS1R3 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: G=0.0001/1 (ALFA)
HGVS:: NC_000001.11:g.1332994T>C, NC_000001.11:g.1332994T>G, NC_000001.10:g.1268374T>C, NC_000001.10:g.1268374T>G, NM_152228.3:c.1349T>C, NM_152228.3:c.1349T>G, NM_152228.2:c.1349T>C, NM_152228.2:c.1349T>G, NM_152228.1:c.1349T>C, NM_152228.1:c.1349T>G, XM_017002435.2:c.1349T>C, XM_017002435.2:c.1349T>G, XM_017002435.1:c.1349T>C, XM_017002435.1:c.1349T>G, XM_017002436.2:c.1349T>C, XM_017002436.2:c.1349T>G, XM_017002436.1:c.1349T>C, XM_017002436.1:c.1349T>G, XM_047431571.1:c.1349T>C, XM_047431571.1:c.1349T>G, NP_689414.2:p.Val450Ala, NP_689414.2:p.Val450Gly, XP_016857924.1:p.Val450Ala, XP_016857924.1:p.Val450Gly, XP_016857925.1:p.Val450Ala, XP_016857925.1:p.Val450Gly, XP_047287527.1:p.Val450Ala, XP_047287527.1:p.Val450Gly

Select item 148121936515.

rs1481219365 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:1333667 (GRCh38)
1:1269047 (GRCh37)
Canonical SPDI:: NC_000001.11:1333666:G:A
Gene:: TAS1R3 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.1333667G>A, NC_000001.10:g.1269047G>A, NG_008048.2:g.20446C>T, NM_152228.3:c.1762G>A, NM_152228.2:c.1762G>A, NM_152228.1:c.1762G>A, XM_017002435.2:c.1888G>A, XM_017002435.1:c.1888G>A, XM_017002436.2:c.1885G>A, XM_017002436.1:c.1885G>A, XM_047431571.1:c.1759G>A, NP_689414.2:p.Gly588Arg, XP_016857924.1:p.Gly630Arg, XP_016857925.1:p.Gly629Arg, XP_047287527.1:p.Gly587Arg

Select item 148054647916.

rs1480546479 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 1:1332361 (GRCh38)
1:1267741 (GRCh37)
Canonical SPDI:: NC_000001.11:1332360:T:C
Gene:: TAS1R3 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000001.11:g.1332361T>C, NC_000001.10:g.1267741T>C, NM_152228.3:c.830T>C, NM_152228.2:c.830T>C, NM_152228.1:c.830T>C, XM_017002435.2:c.830T>C, XM_017002435.1:c.830T>C, XM_017002436.2:c.830T>C, XM_017002436.1:c.830T>C, XM_047431571.1:c.830T>C, NP_689414.2:p.Val277Ala, XP_016857924.1:p.Val277Ala, XP_016857925.1:p.Val277Ala, XP_047287527.1:p.Val277Ala

Select item 147967620717.

rs1479676207 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:1332127 (GRCh38)
1:1267507 (GRCh37)
Canonical SPDI:: NC_000001.11:1332126:A:G
Gene:: TAS1R3 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.1332127A>G, NC_000001.10:g.1267507A>G, NM_152228.3:c.596A>G, NM_152228.2:c.596A>G, NM_152228.1:c.596A>G, XM_017002435.2:c.596A>G, XM_017002435.1:c.596A>G, XM_017002436.2:c.596A>G, XM_017002436.1:c.596A>G, XM_047431571.1:c.596A>G, NP_689414.2:p.Glu199Gly, XP_016857924.1:p.Glu199Gly, XP_016857925.1:p.Glu199Gly, XP_047287527.1:p.Glu199Gly

Select item 147964311918.

rs1479643119 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:1331418 (GRCh38)
1:1266798 (GRCh37)
Canonical SPDI:: NC_000001.11:1331417:C:T
Gene:: TAS1R3 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.1331418C>T, NC_000001.10:g.1266798C>T, NM_152228.3:c.73C>T, NM_152228.2:c.73C>T, NM_152228.1:c.73C>T, XM_017002435.2:c.73C>T, XM_017002435.1:c.73C>T, XM_017002436.2:c.73C>T, XM_017002436.1:c.73C>T, XM_047431571.1:c.73C>T

Select item 147837253019.

rs1478372530 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 1:1333380 (GRCh38)
1:1268760 (GRCh37)
Canonical SPDI:: NC_000001.11:1333379:G:A,NC_000001.11:1333379:G:T
Gene:: TAS1R3 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,splice_donor_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000001.11:g.1333380G>A, NC_000001.11:g.1333380G>T, NC_000001.10:g.1268760G>A, NC_000001.10:g.1268760G>T, NG_008048.2:g.20733C>T, NG_008048.2:g.20733C>A, XM_017002435.2:c.1601G>A, XM_017002435.2:c.1601G>T, XM_017002435.1:c.1601G>A, XM_017002435.1:c.1601G>T, XM_017002436.2:c.1598G>A, XM_017002436.2:c.1598G>T, XM_017002436.1:c.1598G>A, XM_017002436.1:c.1598G>T, XP_016857924.1:p.Gly534Asp, XP_016857924.1:p.Gly534Val, XP_016857925.1:p.Gly533Asp, XP_016857925.1:p.Gly533Val

Select item 147768444220.

rs1477684442 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 1:1331859 (GRCh38)
1:1267239 (GRCh37)
Canonical SPDI:: NC_000001.11:1331858:T:A
Gene:: TAS1R3 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.1331859T>A, NC_000001.10:g.1267239T>A, NM_152228.3:c.413T>A, NM_152228.2:c.413T>A, NM_152228.1:c.413T>A, XM_017002435.2:c.413T>A, XM_017002435.1:c.413T>A, XM_017002436.2:c.413T>A, XM_017002436.1:c.413T>A, XM_047431571.1:c.413T>A, NP_689414.2:p.Val138Glu, XP_016857924.1:p.Val138Glu, XP_016857925.1:p.Val138Glu, XP_047287527.1:p.Val138Glu

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