SNP Links for Protein (Select 12965176) - SNP

Links from Protein

Items: 1 to 20 of 365

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Select item 14883422551.

rs1488342255 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 12:10801990 (GRCh38)
12:10954589 (GRCh37)
Canonical SPDI:: NC_000012.12:10801989:A:G
Gene:: TAS2R7 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000012.12:g.10801990A>G, NC_000012.11:g.10954589A>G, NT_187658.1:g.696A>G, NW_003571050.1:g.696A>G, NM_023919.2:c.581T>C, NP_076408.1:p.Phe194Ser

Select item 14877280422.

rs1487728042 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 12:10802125 (GRCh38)
12:10954724 (GRCh37)
Canonical SPDI:: NC_000012.12:10802124:G:C
Gene:: TAS2R7 (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_000012.12:g.10802125G>C, NC_000012.11:g.10954724G>C, NT_187658.1:g.831G>C, NW_003571050.1:g.831G>C, NM_023919.2:c.446C>G, NP_076408.1:p.Thr149Ser

Select item 14813387573.

rs1481338757 [Homo sapiens]

Variant type:: DEL
Alleles:: A>- [Show Flanks]
Chromosome:: 12:10802400 (GRCh38)
12:10954999 (GRCh37)
Canonical SPDI:: NC_000012.12:10802399:A:
Gene:: TAS2R7 (Varview)
Functional Consequence:: coding_sequence_variant,frameshift_variant
Validated:: by frequency
MAF:: -=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000012.12:g.10802400del, NC_000012.11:g.10954999del, NT_187658.1:g.1106del, NW_003571050.1:g.1106del, NM_023919.2:c.171del, NP_076408.1:p.Leu58fs

Select item 14790560764.

rs1479056076 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 12:10802561 (GRCh38)
12:10955160 (GRCh37)
Canonical SPDI:: NC_000012.12:10802560:T:C
Gene:: TAS2R7 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000012.12:g.10802561T>C, NC_000012.11:g.10955160T>C, NT_187658.1:g.1267T>C, NW_003571050.1:g.1267T>C, NM_023919.2:c.10A>G, NP_076408.1:p.Lys4Glu

Select item 14789935555.

rs1478993555 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 12:10801966 (GRCh38)
12:10954565 (GRCh37)
Canonical SPDI:: NC_000012.12:10801965:A:T
Gene:: TAS2R7 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000012.12:g.10801966A>T, NC_000012.11:g.10954565A>T, NT_187658.1:g.672A>T, NW_003571050.1:g.672A>T, NM_023919.2:c.605T>A, NP_076408.1:p.Phe202Tyr

Select item 14753300686.

rs1475330068 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 12:10802056 (GRCh38)
12:10954655 (GRCh37)
Canonical SPDI:: NC_000012.12:10802055:C:G
Gene:: TAS2R7 (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_000012.12:g.10802056C>G, NC_000012.11:g.10954655C>G, NT_187658.1:g.762C>G, NW_003571050.1:g.762C>G, NM_023919.2:c.515G>C, NP_076408.1:p.Cys172Ser

Select item 14746399007.

rs1474639900 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 12:10801838 (GRCh38)
12:10954437 (GRCh37)
Canonical SPDI:: NC_000012.12:10801837:T:C
Gene:: TAS2R7 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000012.12:g.10801838T>C, NC_000012.11:g.10954437T>C, NT_187658.1:g.544T>C, NW_003571050.1:g.544T>C, NM_023919.2:c.733A>G, NP_076408.1:p.Ile245Val

Select item 14714024148.

rs1471402414 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 12:10802423 (GRCh38)
12:10955022 (GRCh37)
Canonical SPDI:: NC_000012.12:10802422:T:C
Gene:: TAS2R7 (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=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000012.12:g.10802423T>C, NC_000012.11:g.10955022T>C, NT_187658.1:g.1129T>C, NW_003571050.1:g.1129T>C, NM_023919.2:c.148A>G, NP_076408.1:p.Ser50Gly

Select item 14683424049.

rs1468342404 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G [Show Flanks]
Chromosome:: 12:10801753 (GRCh38)
12:10954352 (GRCh37)
Canonical SPDI:: NC_000012.12:10801752:A:C,NC_000012.12:10801752:A:G
Gene:: TAS2R7 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
HGVS:: NC_000012.12:g.10801753A>C, NC_000012.12:g.10801753A>G, NC_000012.11:g.10954352A>C, NC_000012.11:g.10954352A>G, NT_187658.1:g.459A>C, NT_187658.1:g.459A>G, NW_003571050.1:g.459A>C, NW_003571050.1:g.459A>G, NM_023919.2:c.818T>G, NM_023919.2:c.818T>C, NP_076408.1:p.Ile273Arg, NP_076408.1:p.Ile273Thr

Select item 146832099810.

rs1468320998 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 12:10801995 (GRCh38)
12:10954594 (GRCh37)
Canonical SPDI:: NC_000012.12:10801994:G:A
Gene:: TAS2R7 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000071/1 (ALFA)
A=0.000008/2 (TOPMED)
A=0.000014/2 (GnomAD)
HGVS:: NC_000012.12:g.10801995G>A, NC_000012.11:g.10954594G>A, NT_187658.1:g.701G>A, NW_003571050.1:g.701G>A, NM_023919.2:c.576C>T

Select item 146712852411.

rs1467128524 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 12:10802080 (GRCh38)
12:10954679 (GRCh37)
Canonical SPDI:: NC_000012.12:10802079:C:T
Gene:: TAS2R7 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000012.12:g.10802080C>T, NC_000012.11:g.10954679C>T, NT_187658.1:g.786C>T, NW_003571050.1:g.786C>T, NM_023919.2:c.491G>A, NP_076408.1:p.Arg164Lys

Select item 146592184612.

rs1465921846 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 12:10801627 (GRCh38)
12:10954226 (GRCh37)
Canonical SPDI:: NC_000012.12:10801626:T:C
Gene:: TAS2R7 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000111/1 (ALFA)
C=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000012.12:g.10801627T>C, NC_000012.11:g.10954226T>C, NT_187658.1:g.333T>C, NW_003571050.1:g.333T>C, NM_023919.2:c.944A>G, NP_076408.1:p.His315Arg

Select item 146457113513.

rs1464571135 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 12:10801728 (GRCh38)
12:10954327 (GRCh37)
Canonical SPDI:: NC_000012.12:10801727:A:G
Gene:: TAS2R7 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000012.12:g.10801728A>G, NC_000012.11:g.10954327A>G, NT_187658.1:g.434A>G, NW_003571050.1:g.434A>G, NM_023919.2:c.843T>C

Select item 145834167314.

rs1458341673 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 12:10801757 (GRCh38)
12:10954356 (GRCh37)
Canonical SPDI:: NC_000012.12:10801756:A:G
Gene:: TAS2R7 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: G=0.000084/1 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000012.12:g.10801757A>G, NC_000012.11:g.10954356A>G, NT_187658.1:g.463A>G, NW_003571050.1:g.463A>G, NM_023919.2:c.814T>C, NP_076408.1:p.Ser272Pro

Select item 145719584615.

rs1457195846 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 12:10802050 (GRCh38)
12:10954649 (GRCh37)
Canonical SPDI:: NC_000012.12:10802049:A:G
Gene:: TAS2R7 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000012.12:g.10802050A>G, NC_000012.11:g.10954649A>G, NT_187658.1:g.756A>G, NW_003571050.1:g.756A>G, NM_023919.2:c.521T>C, NP_076408.1:p.Val174Ala

Select item 145314085516.

rs1453140855 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 12:10802008 (GRCh38)
12:10954607 (GRCh37)
Canonical SPDI:: NC_000012.12:10802007:A:G
Gene:: TAS2R7 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000012.12:g.10802008A>G, NC_000012.11:g.10954607A>G, NT_187658.1:g.714A>G, NW_003571050.1:g.714A>G, NM_023919.2:c.563T>C, NP_076408.1:p.Leu188Pro

Select item 144963340417.

rs1449633404 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 12:10802041 (GRCh38)
12:10954640 (GRCh37)
Canonical SPDI:: NC_000012.12:10802040:G:T
Gene:: TAS2R7 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000012.12:g.10802041G>T, NC_000012.11:g.10954640G>T, NT_187658.1:g.747G>T, NW_003571050.1:g.747G>T, NM_023919.2:c.530C>A, NP_076408.1:p.Thr177Asn

Select item 144304284118.

rs1443042841 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 12:10802435 (GRCh38)
12:10955034 (GRCh37)
Canonical SPDI:: NC_000012.12:10802434:A:T
Gene:: TAS2R7 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: T=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000012.12:g.10802435A>T, NC_000012.11:g.10955034A>T, NT_187658.1:g.1141A>T, NW_003571050.1:g.1141A>T, NM_023919.2:c.136T>A, NP_076408.1:p.Leu46Ile

Select item 143735263919.

rs1437352639 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 12:10802090 (GRCh38)
12:10954689 (GRCh37)
Canonical SPDI:: NC_000012.12:10802089:T:G
Gene:: TAS2R7 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000012.12:g.10802090T>G, NC_000012.11:g.10954689T>G, NT_187658.1:g.796T>G, NW_003571050.1:g.796T>G, NM_023919.2:c.481A>C, NP_076408.1:p.Lys161Gln

Select item 143264409420.

rs1432644094 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 12:10801738 (GRCh38)
12:10954337 (GRCh37)
Canonical SPDI:: NC_000012.12:10801737:G:A
Gene:: TAS2R7 (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_000012.12:g.10801738G>A, NC_000012.11:g.10954337G>A, NT_187658.1:g.444G>A, NW_003571050.1:g.444G>A, NM_023919.2:c.833C>T, NP_076408.1:p.Pro278Leu

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