Links from Gene
Items: 1 to 20 of 929
3.
rs1489447531 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- C>T
[Show Flanks]
- Chromosome:
- 14:21571223
(GRCh38)
14:22039354
(GRCh37)
- Canonical SPDI:
- NC_000014.9:21571222:C:T
- Gene:
- OR10G3 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa
- MAF:
T=0./0
(
ALFA)
T=0.000004/1
(TOPMED)
- HGVS:
4.
rs1489292447 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- T>C
[Show Flanks]
- Chromosome:
- 14:21571925
(GRCh38)
14:22040057
(GRCh37)
- Canonical SPDI:
- NC_000014.9:21571924:T:C
- Gene:
- OR10G3 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa
- MAF:
C=0./0
(
ALFA)
C=0.000004/1
(TOPMED)
- HGVS:
5.
rs1487890705 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- G>T
[Show Flanks]
- Chromosome:
- 14:21572263
(GRCh38)
14:22040395
(GRCh37)
- Canonical SPDI:
- NC_000014.9:21572262:G:T
- Gene:
- OR10G3 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
T=0./0
(
ALFA)
T=0.00001/1
(GnomAD)
- HGVS:
6.
rs1487845610 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- A>C
[Show Flanks]
- Chromosome:
- 14:21572547
(GRCh38)
14:22040688
(GRCh37)
- Canonical SPDI:
- NC_000014.9:21572546:A:C
- Gene:
- OR10G3 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa
- MAF:
C=0./0
(
ALFA)
C=0.000007/1
(GnomAD)
- HGVS:
7.
rs1487617084 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- G>A
[Show Flanks]
- Chromosome:
- 14:21570841
(GRCh38)
14:22038972
(GRCh37)
- Canonical SPDI:
- NC_000014.9:21570840:G:A
- Gene:
- OR10G3 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
A=0./0
(
ALFA)
A=0.000011/3
(TOPMED)
A=0.000014/2
(GnomAD)
- HGVS:
8.
rs1487455219 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- A>G
[Show Flanks]
- Chromosome:
- 14:21569687
(GRCh38)
14:22037818
(GRCh37)
- Canonical SPDI:
- NC_000014.9:21569686:A:G
- Gene:
- OR10G3 (Varview)
- Functional Consequence:
- 3_prime_UTR_variant
- Validated:
- by frequency,by alfa
- MAF:
G=0./0
(
ALFA)
G=0.000004/1
(TOPMED)
- HGVS:
10.
rs1487341587 has merged into rs397852312 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- AAAAAAAAAAAAAA>-,A,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
[Show Flanks]
- Chromosome:
- 14:21572618
(GRCh38)
14:22040759
(GRCh37)
- Canonical SPDI:
- NC_000014.9:21572608:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAA,NC_000014.9:21572608:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAA,NC_000014.9:21572608:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000014.9:21572608:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000014.9:21572608:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000014.9:21572608:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000014.9:21572608:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000014.9:21572608:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000014.9:21572608:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000014.9:21572608:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:21572608:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:21572608:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:21572608:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:21572608:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:21572608:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:21572608:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:21572608:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:21572608:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:21572608:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:21572608:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:21572608:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:21572608:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:21572608:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:21572608:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:21572608:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:21572608:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:21572608:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:21572608:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:21572608:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:21572608:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:21572608:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:21572608:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000014.9:21572608:AAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
- Gene:
- OR10G3 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
- HGVS:
NC_000014.9:g.21572618_21572631del, NC_000014.9:g.21572619_21572631del, NC_000014.9:g.21572624_21572631del, NC_000014.9:g.21572625_21572631del, NC_000014.9:g.21572626_21572631del, NC_000014.9:g.21572627_21572631del, NC_000014.9:g.21572628_21572631del, NC_000014.9:g.21572629_21572631del, NC_000014.9:g.21572630_21572631del, NC_000014.9:g.21572631del, NC_000014.9:g.21572631dup, NC_000014.9:g.21572630_21572631dup, NC_000014.9:g.21572629_21572631dup, NC_000014.9:g.21572628_21572631dup, NC_000014.9:g.21572627_21572631dup, NC_000014.9:g.21572626_21572631dup, NC_000014.9:g.21572625_21572631dup, NC_000014.9:g.21572624_21572631dup, NC_000014.9:g.21572623_21572631dup, NC_000014.9:g.21572622_21572631dup, NC_000014.9:g.21572621_21572631dup, NC_000014.9:g.21572620_21572631dup, NC_000014.9:g.21572619_21572631dup, NC_000014.9:g.21572618_21572631dup, NC_000014.9:g.21572617_21572631dup, NC_000014.9:g.21572616_21572631dup, NC_000014.9:g.21572615_21572631dup, NC_000014.9:g.21572614_21572631dup, NC_000014.9:g.21572611_21572631dup, NC_000014.9:g.21572610_21572631dup, NC_000014.9:g.21572631_21572632insAAAAAAAAAAAAAAAAAAAAAAAA, NC_000014.9:g.21572631_21572632insAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000014.9:g.21572631_21572632insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000014.8:g.22040767_22040769dup, NC_000014.8:g.22040759_22040769del, NC_000014.8:g.22040760_22040769del, NC_000014.8:g.22040765_22040769del, NC_000014.8:g.22040766_22040769del, NC_000014.8:g.22040767_22040769del, NC_000014.8:g.22040768_22040769del, NC_000014.8:g.22040769del, NC_000014.8:g.22040769dup, NC_000014.8:g.22040768_22040769dup, NC_000014.8:g.22040766_22040769dup, NC_000014.8:g.22040765_22040769dup, NC_000014.8:g.22040764_22040769dup, NC_000014.8:g.22040763_22040769dup, NC_000014.8:g.22040762_22040769dup, NC_000014.8:g.22040761_22040769dup, NC_000014.8:g.22040760_22040769dup, NC_000014.8:g.22040759_22040769dup, NC_000014.8:g.22040758_22040769dup, NC_000014.8:g.22040757_22040769dup, NC_000014.8:g.22040756_22040769dup, NC_000014.8:g.22040755_22040769dup, NC_000014.8:g.22040754_22040769dup, NC_000014.8:g.22040753_22040769dup, NC_000014.8:g.22040752_22040769dup, NC_000014.8:g.22040751_22040769dup, NC_000014.8:g.22040750_22040769dup, NC_000014.8:g.22040769_22040770insAAAAAAAAAAAAAAAAAAAAA, NC_000014.8:g.22040769_22040770insAAAAAAAAAAAAAAAAAAAAAAAA, NC_000014.8:g.22040769_22040770insAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000014.8:g.22040769_22040770insAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000014.8:g.22040769_22040770insAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000014.8:g.22040769_22040770insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
11.
rs1486198876 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- G>T
[Show Flanks]
- Chromosome:
- 14:21569498
(GRCh38)
14:22037629
(GRCh37)
- Canonical SPDI:
- NC_000014.9:21569497:G:T
- Gene:
- OR10G3 (Varview)
- Functional Consequence:
- 3_prime_UTR_variant
- Validated:
- by frequency,by alfa
- MAF:
T=0./0
(
ALFA)
T=0.000004/1
(TOPMED)
- HGVS:
12.
rs1485081185 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- C>T
[Show Flanks]
- Chromosome:
- 14:21572166
(GRCh38)
14:22040298
(GRCh37)
- Canonical SPDI:
- NC_000014.9:21572165:C:T
- Gene:
- OR10G3 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa
- MAF:
T=0./0
(
ALFA)
T=0.000004/1
(TOPMED)
- HGVS:
14.
rs1483808559 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- T>C
[Show Flanks]
- Chromosome:
- 14:21570135
(GRCh38)
14:22038266
(GRCh37)
- Canonical SPDI:
- NC_000014.9:21570134:T:C
- Gene:
- OR10G3 (Varview)
- Functional Consequence:
- coding_sequence_variant,missense_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
C=0./0
(
ALFA)
C=0.000004/1
(GnomAD_exomes)
C=0.000007/1
(GnomAD)
- HGVS:
15.
rs1483228918 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- A>G
[Show Flanks]
- Chromosome:
- 14:21569939
(GRCh38)
14:22038070
(GRCh37)
- Canonical SPDI:
- NC_000014.9:21569938:A:G
- Gene:
- OR10G3 (Varview)
- Functional Consequence:
- coding_sequence_variant,missense_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
G=0./0
(
ALFA)
G=0.000004/1
(GnomAD_exomes)
G=0.000004/1
(TOPMED)
- HGVS:
16.
rs1483108334 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- G>A
[Show Flanks]
- Chromosome:
- 14:21572744
(GRCh38)
14:22040882
(GRCh37)
- Canonical SPDI:
- NC_000014.9:21572743:G:A
- Gene:
- OR10G3 (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
A=0./0
(
ALFA)
A=0.000004/1
(TOPMED)
A=0.000007/1
(GnomAD)
- HGVS:
17.
rs1482441171 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- G>C
[Show Flanks]
- Chromosome:
- 14:21569319
(GRCh38)
14:22037450
(GRCh37)
- Canonical SPDI:
- NC_000014.9:21569318:G:C
- Gene:
- OR10G3 (Varview)
- Functional Consequence:
- 3_prime_UTR_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
C=0./0
(
ALFA)
C=0.000004/1
(TOPMED)
C=0.000007/1
(GnomAD)
- HGVS:
18.
rs1481375849 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- C>A
[Show Flanks]
- Chromosome:
- 14:21569933
(GRCh38)
14:22038064
(GRCh37)
- Canonical SPDI:
- NC_000014.9:21569932:C:A
- Gene:
- OR10G3 (Varview)
- Functional Consequence:
- coding_sequence_variant,missense_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
A=0.000071/1
(
ALFA)
A=0.000007/1
(GnomAD)
A=0.000019/5
(TOPMED)
- HGVS:
20.
rs1480281694 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- A>G
[Show Flanks]
- Chromosome:
- 14:21570010
(GRCh38)
14:22038141
(GRCh37)
- Canonical SPDI:
- NC_000014.9:21570009:A:G
- Gene:
- OR10G3 (Varview)
- Functional Consequence:
- coding_sequence_variant,synonymous_variant
- Validated:
- by frequency
- MAF:
G=0.000004/1
(GnomAD_exomes)
- HGVS: