Links from Gene
Items: 1 to 20 of 950
1.
rs1490879022 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- G>A
[Show Flanks]
- Chromosome:
- 14:19976216
(GRCh38)
14:20444375
(GRCh37)
- Canonical SPDI:
- NC_000014.9:19976215:G:A
- Gene:
- OR4K15 (Varview)
- Functional Consequence:
- coding_sequence_variant,missense_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
A=0./0
(
ALFA)
A=0.000004/1
(TOPMED)
A=0.000007/1
(GnomAD)
- HGVS:
2.
rs1490026613 [Homo sapiens]- Variant type:
- DEL
- Alleles:
- G>-
[Show Flanks]
- Chromosome:
- 14:19976680
(GRCh38)
14:20444839
(GRCh37)
- Canonical SPDI:
- NC_000014.9:19976679:G:
- Gene:
- OR4K15 (Varview)
- Functional Consequence:
- 500B_downstream_variant,downstream_transcript_variant
- Validated:
- by frequency,by alfa
- MAF:
-=0./0
(
ALFA)
-=0.000004/1
(TOPMED)
- HGVS:
3.
rs1488559519 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- T>C
[Show Flanks]
- Chromosome:
- 14:19976543
(GRCh38)
14:20444702
(GRCh37)
- Canonical SPDI:
- NC_000014.9:19976542:T:C
- Gene:
- OR4K15 (Varview)
- Functional Consequence:
- coding_sequence_variant,missense_variant
- Validated:
- by frequency,by alfa
- MAF:
C=0./0
(
ALFA)
C=0.000004/1
(TOPMED)
- HGVS:
4.
rs1488267115 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- T>G
[Show Flanks]
- Chromosome:
- 14:19976097
(GRCh38)
14:20444256
(GRCh37)
- Canonical SPDI:
- NC_000014.9:19976096:T:G
- Gene:
- OR4K15 (Varview)
- Functional Consequence:
- coding_sequence_variant,missense_variant
- Validated:
- by frequency
- MAF:
G=0.000004/1
(GnomAD_exomes)
- HGVS:
5.
rs1487881973 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- C>T
[Show Flanks]
- Chromosome:
- 14:19975403
(GRCh38)
14:20443562
(GRCh37)
- Canonical SPDI:
- NC_000014.9:19975402:C:T
- Gene:
- OR4K15 (Varview)
- Functional Consequence:
- upstream_transcript_variant,2KB_upstream_variant
- Validated:
- by frequency,by alfa
- MAF:
T=0./0
(
ALFA)
T=0.000014/2
(GnomAD)
- HGVS:
6.
rs1485861093 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- T>A
[Show Flanks]
- Chromosome:
- 14:19976507
(GRCh38)
14:20444666
(GRCh37)
- Canonical SPDI:
- NC_000014.9:19976506:T:A
- Gene:
- OR4K15 (Varview)
- Functional Consequence:
- coding_sequence_variant,missense_variant
- Validated:
- by frequency
- MAF:
A=0.000004/1
(GnomAD_exomes)
- HGVS:
7.
rs1485849222 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- C>G
[Show Flanks]
- Chromosome:
- 14:19973724
(GRCh38)
14:20441883
(GRCh37)
- Canonical SPDI:
- NC_000014.9:19973723:C:G
- Gene:
- OR4K15 (Varview)
- Functional Consequence:
- upstream_transcript_variant,2KB_upstream_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
G=0.000071/1
(
ALFA)
G=0.000007/1
(GnomAD)
G=0.000011/3
(TOPMED)
- HGVS:
9.
rs1484637453 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- T>A,C
[Show Flanks]
- Chromosome:
- 14:19976308
(GRCh38)
14:20444467
(GRCh37)
- Canonical SPDI:
- NC_000014.9:19976307:T:A,NC_000014.9:19976307:T:C
- Gene:
- OR4K15 (Varview)
- Functional Consequence:
- coding_sequence_variant,missense_variant,synonymous_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
C=0.000051/1
(
ALFA)
C=0.000004/1
(GnomAD_exomes)
A=0.000004/1
(TOPMED)
- HGVS:
NC_000014.9:g.19976308T>A, NC_000014.9:g.19976308T>C, NW_025791796.1:g.178990T>A, NW_025791796.1:g.178990T>C, NC_000014.8:g.20444467T>A, NC_000014.8:g.20444467T>C, NM_001005486.2:c.718T>A, NM_001005486.2:c.718T>C, NM_001005486.1:c.790T>A, NM_001005486.1:c.790T>C, NP_001005486.2:p.Leu240Met
10.
rs1484362487 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- A>G
[Show Flanks]
- Chromosome:
- 14:19974983
(GRCh38)
14:20443142
(GRCh37)
- Canonical SPDI:
- NC_000014.9:19974982:A:G
- Gene:
- OR4K15 (Varview)
- Functional Consequence:
- upstream_transcript_variant,2KB_upstream_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
G=0.000142/2
(
ALFA)
G=0.000029/4
(GnomAD)
G=0.000064/17
(TOPMED)
- HGVS:
11.
rs1484191131 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- A>G,T
[Show Flanks]
- Chromosome:
- 14:19976605
(GRCh38)
14:20444764
(GRCh37)
- Canonical SPDI:
- NC_000014.9:19976604:A:G,NC_000014.9:19976604:A:T
- Gene:
- OR4K15 (Varview)
- Functional Consequence:
- 500B_downstream_variant,downstream_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
T=0./0
(
ALFA)
G=0.000008/1
(GnomAD_exomes)
T=0.000008/2
(TOPMED)
- HGVS:
12.
rs1483902665 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- T>C
[Show Flanks]
- Chromosome:
- 14:19975961
(GRCh38)
14:20444120
(GRCh37)
- Canonical SPDI:
- NC_000014.9:19975960:T:C
- Gene:
- OR4K15 (Varview)
- Functional Consequence:
- coding_sequence_variant,missense_variant
- Validated:
- by frequency
- MAF:
C=0.000004/1
(GnomAD_exomes)
- HGVS:
13.
rs1482805686 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- A>T
[Show Flanks]
- Chromosome:
- 14:19974535
(GRCh38)
14:20442694
(GRCh37)
- Canonical SPDI:
- NC_000014.9:19974534:A:T
- Gene:
- OR4K15 (Varview)
- Functional Consequence:
- upstream_transcript_variant,2KB_upstream_variant
- Validated:
- by frequency,by alfa
- MAF:
T=0./0
(
ALFA)
T=0.000021/3
(GnomAD)
- HGVS:
14.
rs1482335029 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- T>G
[Show Flanks]
- Chromosome:
- 14:19975236
(GRCh38)
14:20443395
(GRCh37)
- Canonical SPDI:
- NC_000014.9:19975235:T:G
- Gene:
- OR4K15 (Varview)
- Functional Consequence:
- upstream_transcript_variant,2KB_upstream_variant
- Validated:
- by frequency,by alfa
- MAF:
G=0.000071/1
(
ALFA)
G=0.000004/1
(TOPMED)
- HGVS:
15.
rs1481821812 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- A>G
[Show Flanks]
- Chromosome:
- 14:19974913
(GRCh38)
14:20443072
(GRCh37)
- Canonical SPDI:
- NC_000014.9:19974912:A:G
- Gene:
- OR4K15 (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:
16.
rs1481493367 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- G>A,T
[Show Flanks]
- Chromosome:
- 14:19973576
(GRCh38)
14:20441735
(GRCh37)
- Canonical SPDI:
- NC_000014.9:19973575:G:A,NC_000014.9:19973575:G:T
- Validated:
- by frequency,by alfa
- MAF:
T=0./0
(
ALFA)
A=0.000004/1
(TOPMED)
- HGVS:
17.
rs1480547203 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- C>A,T
[Show Flanks]
- Chromosome:
- 14:19976671
(GRCh38)
14:20444830
(GRCh37)
- Canonical SPDI:
- NC_000014.9:19976670:C:A,NC_000014.9:19976670:C:T
- Gene:
- OR4K15 (Varview)
- Functional Consequence:
- 500B_downstream_variant,downstream_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
T=0./0
(
ALFA)
T=0.000004/1
(TOPMED)
T=0.000007/1
(GnomAD)
- HGVS:
19.
rs1479061514 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- T>G
[Show Flanks]
- Chromosome:
- 14:19974043
(GRCh38)
14:20442202
(GRCh37)
- Canonical SPDI:
- NC_000014.9:19974042:T:G
- Gene:
- OR4K15 (Varview)
- Functional Consequence:
- upstream_transcript_variant,2KB_upstream_variant
- Validated:
- by frequency
- MAF:
G=0.000007/1
(GnomAD)
- HGVS:
20.
rs1478626003 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- G>A
[Show Flanks]
- Chromosome:
- 14:19974902
(GRCh38)
14:20443061
(GRCh37)
- Canonical SPDI:
- NC_000014.9:19974901:G:A
- Gene:
- OR4K15 (Varview)
- Functional Consequence:
- upstream_transcript_variant,2KB_upstream_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
A=0./0
(
ALFA)
A=0.000008/2
(TOPMED)
A=0.000014/2
(GnomAD)
- HGVS: