Links from Gene
Items: 1 to 20 of 966
1.
rs1490665087 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- C>G
[Show Flanks]
- Chromosome:
- 12:10808455
(GRCh38)
12:10961054
(GRCh37)
- Canonical SPDI:
- NC_000012.12:10808454:C:G
- Gene:
- TAS2R8 (Varview)
- Functional Consequence:
- 2KB_upstream_variant,upstream_transcript_variant
- Validated:
- by frequency,by alfa
- MAF:
G=0./0
(
ALFA)
G=0.000011/3
(TOPMED)
- HGVS:
2.
rs1490174350 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- A>C
[Show Flanks]
- Chromosome:
- 12:10808038
(GRCh38)
12:10960637
(GRCh37)
- Canonical SPDI:
- NC_000012.12:10808037:A:C
- Gene:
- TAS2R8 (Varview)
- Functional Consequence:
- 2KB_upstream_variant,upstream_transcript_variant
- Validated:
- by frequency,by alfa
- MAF:
C=0./0
(
ALFA)
C=0.000004/1
(TOPMED)
- HGVS:
3.
rs1490144098 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- T>C
[Show Flanks]
- Chromosome:
- 12:10807102
(GRCh38)
12:10959701
(GRCh37)
- Canonical SPDI:
- NC_000012.12:10807101:T:C
- Gene:
- TAS2R8 (Varview)
- Functional Consequence:
- 5_prime_UTR_variant
- Validated:
- by frequency,by alfa
- MAF:
C=0./0
(
ALFA)
C=0.000004/1
(TOPMED)
- HGVS:
4.
rs1489236468 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- G>A
[Show Flanks]
- Chromosome:
- 12:10808419
(GRCh38)
12:10961018
(GRCh37)
- Canonical SPDI:
- NC_000012.12:10808418:G:A
- Gene:
- TAS2R8 (Varview)
- Functional Consequence:
- 2KB_upstream_variant,upstream_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
A=0./0
(
ALFA)
A=0.000011/3
(TOPMED)
A=0.000021/3
(GnomAD)
- HGVS:
5.
rs1487604588 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- G>A,C
[Show Flanks]
- Chromosome:
- 12:10807374
(GRCh38)
12:10959973
(GRCh37)
- Canonical SPDI:
- NC_000012.12:10807373:G:A,NC_000012.12:10807373:G:C
- Gene:
- TAS2R8 (Varview)
- Functional Consequence:
- 2KB_upstream_variant,upstream_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
C=0./0
(
ALFA)
C=0.000004/1
(TOPMED)
A=0.001574/7
(Estonian)
- HGVS:
6.
rs1487287489 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- T>C
[Show Flanks]
- Chromosome:
- 12:10808871
(GRCh38)
12:10961470
(GRCh37)
- Canonical SPDI:
- NC_000012.12:10808870:T:C
- Gene:
- TAS2R9 (Varview), TAS2R8 (Varview)
- Functional Consequence:
- downstream_transcript_variant,2KB_upstream_variant,500B_downstream_variant,upstream_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
C=0./0
(
ALFA)
C=0.000007/1
(GnomAD)
C=0.000023/6
(TOPMED)
- HGVS:
7.
rs1487225844 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- G>A
[Show Flanks]
- Chromosome:
- 12:10808025
(GRCh38)
12:10960624
(GRCh37)
- Canonical SPDI:
- NC_000012.12:10808024:G:A
- Gene:
- TAS2R8 (Varview)
- Functional Consequence:
- 2KB_upstream_variant,upstream_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
A=0./0
(
ALFA)
A=0.000004/1
(TOPMED)
A=0.000007/1
(GnomAD)
- HGVS:
8.
rs1486749362 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- G>A
[Show Flanks]
- Chromosome:
- 12:10808866
(GRCh38)
12:10961465
(GRCh37)
- Canonical SPDI:
- NC_000012.12:10808865:G:A
- Gene:
- TAS2R9 (Varview), TAS2R8 (Varview)
- Functional Consequence:
- downstream_transcript_variant,2KB_upstream_variant,500B_downstream_variant,upstream_transcript_variant
- Validated:
- by frequency,by alfa
- MAF:
A=0./0
(
ALFA)
A=0.000004/1
(TOPMED)
- HGVS:
9.
rs1486116543 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- A>G
[Show Flanks]
- Chromosome:
- 12:10806214
(GRCh38)
12:10958813
(GRCh37)
- Canonical SPDI:
- NC_000012.12:10806213:A:G
- Gene:
- TAS2R8 (Varview)
- Functional Consequence:
- coding_sequence_variant,missense_variant
- Validated:
- by frequency
- MAF:
G=0.000004/1
(GnomAD_exomes)
- HGVS:
10.
rs1485132301 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- T>A
[Show Flanks]
- Chromosome:
- 12:10806050
(GRCh38)
12:10958649
(GRCh37)
- Canonical SPDI:
- NC_000012.12:10806049:T:A
- Gene:
- TAS2R8 (Varview)
- Functional Consequence:
- downstream_transcript_variant,500B_downstream_variant
- Validated:
- by frequency,by cluster
- MAF:
A=0.000007/1
(GnomAD)
- HGVS:
11.
rs1483477554 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- T>C
[Show Flanks]
- Chromosome:
- 12:10808446
(GRCh38)
12:10961045
(GRCh37)
- Canonical SPDI:
- NC_000012.12:10808445:T:C
- Gene:
- TAS2R8 (Varview)
- Functional Consequence:
- 2KB_upstream_variant,upstream_transcript_variant
- Validated:
- by frequency,by alfa
- MAF:
C=0./0
(
ALFA)
C=0.000007/1
(GnomAD)
- HGVS:
12.
rs1482311754 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- T>C
[Show Flanks]
- Chromosome:
- 12:10805736
(GRCh38)
12:10958335
(GRCh37)
- Canonical SPDI:
- NC_000012.12:10805735:T:C
- Gene:
- TAS2R8 (Varview)
- Functional Consequence:
- downstream_transcript_variant,500B_downstream_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
C=0./0
(
ALFA)
C=0.000008/2
(TOPMED)
C=0.000014/2
(GnomAD)
- HGVS:
13.
rs1480935360 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- T>C
[Show Flanks]
- Chromosome:
- 12:10808533
(GRCh38)
12:10961132
(GRCh37)
- Canonical SPDI:
- NC_000012.12:10808532:T:C
- Gene:
- TAS2R8 (Varview)
- Functional Consequence:
- upstream_transcript_variant,2KB_upstream_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
C=0./0
(
ALFA)
C=0.000004/1
(TOPMED)
C=0.000007/1
(GnomAD)
- HGVS:
14.
rs1480911210 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- T>A
[Show Flanks]
- Chromosome:
- 12:10806902
(GRCh38)
12:10959501
(GRCh37)
- Canonical SPDI:
- NC_000012.12:10806901:T:A
- Gene:
- TAS2R8 (Varview)
- Functional Consequence:
- coding_sequence_variant,missense_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
A=0.000031/1
(
ALFA)
A=0.000004/1
(TOPMED)
A=0.000014/2
(GnomAD)
- HGVS:
15.
rs1479953138 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- C>T
[Show Flanks]
- Chromosome:
- 12:10808097
(GRCh38)
12:10960696
(GRCh37)
- Canonical SPDI:
- NC_000012.12:10808096:C:T
- Gene:
- TAS2R8 (Varview)
- Functional Consequence:
- upstream_transcript_variant,2KB_upstream_variant
- Validated:
- by frequency,by alfa
- MAF:
T=0./0
(
ALFA)
T=0.000004/1
(TOPMED)
- HGVS:
16.
rs1478771030 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- T>C
[Show Flanks]
- Chromosome:
- 12:10805780
(GRCh38)
12:10958379
(GRCh37)
- Canonical SPDI:
- NC_000012.12:10805779:T:C
- Gene:
- TAS2R8 (Varview)
- Functional Consequence:
- downstream_transcript_variant,500B_downstream_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
C=0.000142/2
(
ALFA)
C=0.00003/8
(TOPMED)
C=0.000043/6
(GnomAD)
- HGVS:
17.
rs1478740811 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- A>G
[Show Flanks]
- Chromosome:
- 12:10808233
(GRCh38)
12:10960832
(GRCh37)
- Canonical SPDI:
- NC_000012.12:10808232:A:G
- Gene:
- TAS2R8 (Varview)
- Functional Consequence:
- upstream_transcript_variant,2KB_upstream_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
G=0./0
(
ALFA)
G=0.000004/1
(TOPMED)
G=0.000007/1
(GnomAD)
- HGVS:
18.
rs1478078728 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- T>C
[Show Flanks]
- Chromosome:
- 12:10805630
(GRCh38)
12:10958229
(GRCh37)
- Canonical SPDI:
- NC_000012.12:10805629:T:C
- Gene:
- TAS2R8 (Varview)
- Functional Consequence:
- downstream_transcript_variant,500B_downstream_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
C=0./0
(
ALFA)
C=0.000004/1
(TOPMED)
- HGVS:
19.
rs1478049214 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- A>G
[Show Flanks]
- Chromosome:
- 12:10806620
(GRCh38)
12:10959219
(GRCh37)
- Canonical SPDI:
- NC_000012.12:10806619:A:G
- Gene:
- TAS2R8 (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:
20.
rs1477175801 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- A>C,G
[Show Flanks]
- Chromosome:
- 12:10805560
(GRCh38)
12:10958159
(GRCh37)
- Canonical SPDI:
- NC_000012.12:10805559:A:C,NC_000012.12:10805559:A:G
- Gene:
- TAS2R8 (Varview)
- Functional Consequence:
- downstream_transcript_variant,500B_downstream_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
G=0./0
(
ALFA)
G=0.000007/1
(GnomAD)
- HGVS: