Links from Protein
Items: 1 to 20 of 396
1.
rs1491358527 [Homo sapiens]- Variant type:
- DEL
- Alleles:
- CC>-
[Show Flanks]
- Chromosome:
- 11:55994260
(GRCh38)
11:55761736
(GRCh37)
- Canonical SPDI:
- NC_000011.10:55994259:CC:
- Gene:
- OR5F1 (Varview)
- Functional Consequence:
- frameshift_variant,coding_sequence_variant
- Validated:
- by frequency,by cluster
- MAF:
-=0.000004/1
(GnomAD_exomes)
-=0.000008/1
(ExAC)
- HGVS:
2.
rs1488815055 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- G>T
[Show Flanks]
- Chromosome:
- 11:55994621
(GRCh38)
11:55762097
(GRCh37)
- Canonical SPDI:
- NC_000011.10:55994620:G:T
- Gene:
- OR5F1 (Varview)
- Functional Consequence:
- missense_variant,coding_sequence_variant
- Validated:
- by frequency,by alfa
- MAF:
T=0./0
(
ALFA)
T=0.000007/1
(GnomAD)
- HGVS:
3.
rs1488276213 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- T>C
[Show Flanks]
- Chromosome:
- 11:55994371
(GRCh38)
11:55761847
(GRCh37)
- Canonical SPDI:
- NC_000011.10:55994370:T:C
- Gene:
- OR5F1 (Varview)
- Functional Consequence:
- coding_sequence_variant,synonymous_variant
- Validated:
- by frequency
- MAF:
C=0.000008/2
(GnomAD_exomes)
- HGVS:
4.
rs1487114682 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- T>C,G
[Show Flanks]
- Chromosome:
- 11:55994191
(GRCh38)
11:55761667
(GRCh37)
- Canonical SPDI:
- NC_000011.10:55994190:T:C,NC_000011.10:55994190:T:G
- Gene:
- OR5F1 (Varview)
- Functional Consequence:
- coding_sequence_variant,synonymous_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
C=0./0
(
ALFA)
C=0.000004/1
(TOPMED)
C=0.000008/2
(GnomAD_exomes)
G=0.000071/1
(TOMMO)
G=0.000546/1
(Korea1K)
- HGVS:
5.
rs1486789250 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- A>G,T
[Show Flanks]
- Chromosome:
- 11:55994089
(GRCh38)
11:55761565
(GRCh37)
- Canonical SPDI:
- NC_000011.10:55994088:A:G,NC_000011.10:55994088:A:T
- Gene:
- OR5F1 (Varview)
- Functional Consequence:
- coding_sequence_variant,synonymous_variant,stop_gained
- Validated:
- by frequency,by alfa
- MAF:
T=0./0
(
ALFA)
G=0.000004/1
(TOPMED)
- HGVS:
6.
rs1486280623 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- G>T
[Show Flanks]
- Chromosome:
- 11:55993878
(GRCh38)
11:55761354
(GRCh37)
- Canonical SPDI:
- NC_000011.10:55993877:G:T
- Gene:
- OR5F1 (Varview)
- Functional Consequence:
- missense_variant,coding_sequence_variant
- Validated:
- by frequency
- MAF:
T=0.000004/1
(GnomAD_exomes)
- HGVS:
7.
rs1485160241 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- G>A
[Show Flanks]
- Chromosome:
- 11:55993697
(GRCh38)
11:55761173
(GRCh37)
- Canonical SPDI:
- NC_000011.10:55993696:G:A
- Gene:
- OR5F1 (Varview)
- Functional Consequence:
- missense_variant,coding_sequence_variant
- Validated:
- by frequency,by cluster
- MAF:
A=0.000004/1
(GnomAD_exomes)
- HGVS:
8.
rs1482568887 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- GTGTATAA>-
[Show Flanks]
- Chromosome:
- 11:55994517
(GRCh38)
11:55761993
(GRCh37)
- Canonical SPDI:
- NC_000011.10:55994513:TAAGTGTATAA:TAA
- Gene:
- OR5F1 (Varview)
- Functional Consequence:
- frameshift_variant,coding_sequence_variant
- Validated:
- by frequency,by alfa
- MAF:
TAA=0.000111/1
(
ALFA)
-=0.000004/1
(GnomAD_exomes)
- HGVS:
9.
rs1481820605 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- G>A
[Show Flanks]
- Chromosome:
- 11:55993825
(GRCh38)
11:55761301
(GRCh37)
- Canonical SPDI:
- NC_000011.10:55993824:G:A
- Gene:
- OR5F1 (Varview)
- Functional Consequence:
- coding_sequence_variant,synonymous_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
A=0./0
(
ALFA)
A=0.000004/1
(TOPMED)
- HGVS:
10.
rs1480870454 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- T>C
[Show Flanks]
- Chromosome:
- 11:55994102
(GRCh38)
11:55761578
(GRCh37)
- Canonical SPDI:
- NC_000011.10:55994101:T:C
- Gene:
- OR5F1 (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:
11.
rs1478754873 [Homo sapiens]- Variant type:
- DEL
- Alleles:
- C>-
[Show Flanks]
- Chromosome:
- 11:55994618
(GRCh38)
11:55762094
(GRCh37)
- Canonical SPDI:
- NC_000011.10:55994617:C:
- Gene:
- OR5F1 (Varview)
- Functional Consequence:
- frameshift_variant,coding_sequence_variant
- Validated:
- by frequency
- MAF:
-=0.000011/2
(GnomAD_exomes)
- HGVS:
12.
rs1478426840 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- G>A
[Show Flanks]
- Chromosome:
- 11:55994328
(GRCh38)
11:55761804
(GRCh37)
- Canonical SPDI:
- NC_000011.10:55994327:G:A
- Gene:
- OR5F1 (Varview)
- Functional Consequence:
- coding_sequence_variant,stop_gained
- Validated:
- by frequency,by alfa,by cluster
- MAF:
A=0./0
(
ALFA)
A=0.000004/1
(TOPMED)
A=0.000014/2
(GnomAD)
- HGVS:
13.
rs1476255891 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- C>T
[Show Flanks]
- Chromosome:
- 11:55994187
(GRCh38)
11:55761663
(GRCh37)
- Canonical SPDI:
- NC_000011.10:55994186:C:T
- Gene:
- OR5F1 (Varview)
- Functional Consequence:
- coding_sequence_variant,missense_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
T=0.000028/1
(
ALFA)
T=0.000008/2
(GnomAD_exomes)
T=0.000014/2
(GnomAD)
T=0.000015/4
(TOPMED)
- HGVS:
14.
rs1475249177 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- C>T
[Show Flanks]
- Chromosome:
- 11:55993722
(GRCh38)
11:55761198
(GRCh37)
- Canonical SPDI:
- NC_000011.10:55993721:C:T
- Gene:
- OR5F1 (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)
- HGVS:
15.
rs1471978185 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- G>A
[Show Flanks]
- Chromosome:
- 11:55994508
(GRCh38)
11:55761984
(GRCh37)
- Canonical SPDI:
- NC_000011.10:55994507:G:A
- Gene:
- OR5F1 (Varview)
- Functional Consequence:
- coding_sequence_variant,synonymous_variant
- Validated:
- by frequency,by alfa
- MAF:
A=0.000043/1
(
ALFA)
A=0.000004/1
(GnomAD_exomes)
A=0.000004/1
(TOPMED)
- HGVS:
16.
rs1471223430 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- C>T
[Show Flanks]
- Chromosome:
- 11:55994218
(GRCh38)
11:55761694
(GRCh37)
- Canonical SPDI:
- NC_000011.10:55994217:C:T
- Gene:
- OR5F1 (Varview)
- Functional Consequence:
- coding_sequence_variant,missense_variant
- Validated:
- by frequency
- MAF:
T=0.000004/1
(GnomAD_exomes)
- HGVS:
17.
rs1469330606 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- G>A,C
[Show Flanks]
- Chromosome:
- 11:55993841
(GRCh38)
11:55761317
(GRCh37)
- Canonical SPDI:
- NC_000011.10:55993840:G:A,NC_000011.10:55993840:G:C
- Gene:
- OR5F1 (Varview)
- Functional Consequence:
- coding_sequence_variant,missense_variant
- Validated:
- by frequency,by alfa
- MAF:
C=0./0
(
ALFA)
A=0.000004/1
(TOPMED)
- HGVS:
18.
rs1464533146 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- A>C
[Show Flanks]
- Chromosome:
- 11:55994160
(GRCh38)
11:55761636
(GRCh37)
- Canonical SPDI:
- NC_000011.10:55994159:A:C
- Gene:
- OR5F1 (Varview)
- Functional Consequence:
- coding_sequence_variant,missense_variant
- Validated:
- by frequency,by alfa
- MAF:
C=0./0
(
ALFA)
C=0.000004/1
(TOPMED)
- HGVS:
19.
rs1464012501 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- A>G
[Show Flanks]
- Chromosome:
- 11:55994021
(GRCh38)
11:55761497
(GRCh37)
- Canonical SPDI:
- NC_000011.10:55994020:A:G
- Gene:
- OR5F1 (Varview)
- Functional Consequence:
- coding_sequence_variant,missense_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
G=0.000028/1
(
ALFA)
G=0.000007/1
(GnomAD)
G=0.000011/3
(TOPMED)
- HGVS:
20.
rs1463986600 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- G>T
[Show Flanks]
- Chromosome:
- 11:55994082
(GRCh38)
11:55761558
(GRCh37)
- Canonical SPDI:
- NC_000011.10:55994081:G:T
- Gene:
- OR5F1 (Varview)
- Functional Consequence:
- coding_sequence_variant,missense_variant
- Validated:
- by frequency
- MAF:
T=0.000004/1
(GnomAD_exomes)
- HGVS: