Links from Nucleotide
Items: 1 to 20 of 4104
1.
rs1490928964 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- G>A
[Show Flanks]
- Chromosome:
- 1:161551505
(GRCh38)
1:161521295
(GRCh37)
- Canonical SPDI:
- NC_000001.11:161551504:G:A
- Gene:
- FCGR3A (Varview)
- Functional Consequence:
- upstream_transcript_variant,2KB_upstream_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.
rs1490890703 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- T>G
[Show Flanks]
- Chromosome:
- 1:161554397
(GRCh38)
1:161524187
(GRCh37)
- Canonical SPDI:
- NC_000001.11:161554396:T:G
- Validated:
- by frequency,by alfa
- MAF:
G=0.000071/1
(
ALFA)
G=0.000007/1
(GnomAD)
- HGVS:
4.
rs1490515081 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- A>T
[Show Flanks]
- Chromosome:
- 1:161540332
(GRCh38)
1:161510122
(GRCh37)
- Canonical SPDI:
- NC_000001.11:161540331:A:T
- Validated:
- by frequency,by alfa
- MAF:
T=0./0
(
ALFA)
T=0.000007/1
(GnomAD)
- HGVS:
5.
rs1490512854 [Homo sapiens]- Variant type:
- DELINS
- Alleles:
- AGA>-
[Show Flanks]
- Chromosome:
- 1:161552244
(GRCh38)
1:161522034
(GRCh37)
- Canonical SPDI:
- NC_000001.11:161552239:AAGAAGA:AAGA
- Gene:
- FCGR3A (Varview)
- Functional Consequence:
- upstream_transcript_variant,2KB_upstream_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
AAGA=0.00034/4
(
ALFA)
-=0.00874/56
(1000Genomes)
- HGVS:
6.
rs1490411884 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- C>T
[Show Flanks]
- Chromosome:
- 1:161550461
(GRCh38)
1:161520251
(GRCh37)
- Canonical SPDI:
- NC_000001.11:161550460:C:T
- Gene:
- FCGR3A (Varview)
- Functional Consequence:
- intron_variant,upstream_transcript_variant,5_prime_UTR_variant,genic_upstream_transcript_variant
- Validated:
- by frequency,by alfa
- MAF:
T=0.000071/1
(
ALFA)
T=0.000008/2
(TOPMED)
- HGVS:
7.
rs1490343693 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- G>C,T
[Show Flanks]
- Chromosome:
- 1:161546335
(GRCh38)
1:161516125
(GRCh37)
- Canonical SPDI:
- NC_000001.11:161546334:G:C,NC_000001.11:161546334:G:T
- Gene:
- FCGR3A (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
T=0./0
(
ALFA)
C=0.000007/1
(GnomAD)
- HGVS:
8.
rs1490242019 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- G>A,T
[Show Flanks]
- Chromosome:
- 1:161540298
(GRCh38)
1:161510088
(GRCh37)
- Canonical SPDI:
- NC_000001.11:161540297:G:A,NC_000001.11:161540297:G:T
- Validated:
- by frequency,by alfa,by cluster
- MAF:
T=0./0
(
ALFA)
T=0.000008/2
(TOPMED)
T=0.000014/2
(GnomAD)
A=0.000035/1
(TOMMO)
- HGVS:
9.
rs1490086561 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- C>A,G,T
[Show Flanks]
- Chromosome:
- 1:161551063
(GRCh38)
1:161520853
(GRCh37)
- Canonical SPDI:
- NC_000001.11:161551062:C:A,NC_000001.11:161551062:C:G,NC_000001.11:161551062:C:T
- Gene:
- FCGR3A (Varview)
- Functional Consequence:
- upstream_transcript_variant,2KB_upstream_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
G=0./0
(
ALFA)
A=0.00016/1
(1000Genomes)
- HGVS:
10.
rs1490064421 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- C>G
[Show Flanks]
- Chromosome:
- 1:161540044
(GRCh38)
1:161509834
(GRCh37)
- Canonical SPDI:
- NC_000001.11:161540043:C:G
- Validated:
- by frequency,by alfa,by cluster
- MAF:
G=0./0
(
ALFA)
G=0.000086/12
(GnomAD)
G=0.000106/28
(TOPMED)
- HGVS:
11.
rs1489865312 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- A>G
[Show Flanks]
- Chromosome:
- 1:161547380
(GRCh38)
1:161517170
(GRCh37)
- Canonical SPDI:
- NC_000001.11:161547379:A:G
- Gene:
- FCGR3A (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
G=0./0
(
ALFA)
G=0.00085/14
(TOMMO)
G=0.0024/7
(KOREAN)
- HGVS:
12.
rs1489854099 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- G>A
[Show Flanks]
- Chromosome:
- 1:161545935
(GRCh38)
1:161515725
(GRCh37)
- Canonical SPDI:
- NC_000001.11:161545934:G:A
- Gene:
- FCGR3A (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
A=0./0
(
ALFA)
A=0.000004/1
(TOPMED)
A=0.000014/2
(GnomAD)
- HGVS:
13.
rs1489804229 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- C>T
[Show Flanks]
- Chromosome:
- 1:161545024
(GRCh38)
1:161514814
(GRCh37)
- Canonical SPDI:
- NC_000001.11:161545023:C:T
- Gene:
- FCGR3A (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
T=0./0
(
ALFA)
T=0.000007/1
(GnomAD)
T=0.000019/5
(TOPMED)
- HGVS:
14.
rs1489589186 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- A>G,T
[Show Flanks]
- Chromosome:
- 1:161555585
(GRCh38)
1:161525375
(GRCh37)
- Canonical SPDI:
- NC_000001.11:161555584:A:G,NC_000001.11:161555584:A:T
- Validated:
- by frequency,by alfa,by cluster
- MAF:
T=0./0
(
ALFA)
G=0.000004/1
(TOPMED)
G=0.000007/1
(GnomAD)
- HGVS:
15.
rs1489492781 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- T>C
[Show Flanks]
- Chromosome:
- 1:161543761
(GRCh38)
1:161513551
(GRCh37)
- Canonical SPDI:
- NC_000001.11:161543760:T:C
- Gene:
- FCGR3A (Varview)
- Functional Consequence:
- intron_variant
- Validated:
- by frequency,by alfa
- MAF:
C=0./0
(
ALFA)
C=0.000004/1
(TOPMED)
- HGVS:
16.
rs1489441088 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- C>T
[Show Flanks]
- Chromosome:
- 1:161542838
(GRCh38)
1:161512628
(GRCh37)
- Canonical SPDI:
- NC_000001.11:161542837:C:T
- Gene:
- FCGR3A (Varview)
- Functional Consequence:
- 3_prime_UTR_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
T=0./0
(
ALFA)
T=0.000004/1
(TOPMED)
T=0.000007/1
(GnomAD)
- HGVS:
NC_000001.11:g.161542838C>T, NC_000001.10:g.161512628C>T, NG_009066.1:g.12786G>A, NM_000569.8:c.*174G>A, NM_000569.7:c.*174G>A, NM_000569.6:c.*174G>A, NM_001127592.2:c.*174G>A, NM_001127592.1:c.*174G>A, NM_001329120.2:c.*174G>A, NM_001329120.1:c.*174G>A, NM_001127595.2:c.*174G>A, NM_001127595.1:c.*174G>A, NM_001127596.2:c.*174G>A, NM_001127596.1:c.*174G>A, NM_001127593.1:c.*174G>A, NM_001386450.1:c.*174G>A, NM_001329122.1:c.*174G>A, XM_047449443.1:c.*174G>A, XM_047449444.1:c.*174G>A
18.
rs1488728257 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- G>C
[Show Flanks]
- Chromosome:
- 1:161550699
(GRCh38)
1:161520489
(GRCh37)
- Canonical SPDI:
- NC_000001.11:161550698:G:C
- Gene:
- FCGR3A (Varview)
- Functional Consequence:
- upstream_transcript_variant,5_prime_UTR_variant,genic_upstream_transcript_variant
- Validated:
- by frequency,by alfa,by cluster
- MAF:
C=0./0
(
ALFA)
C=0.000078/11
(GnomAD)
- HGVS:
19.
rs1488618581 [Homo sapiens]- Variant type:
- SNV
- Alleles:
- C>A,T
[Show Flanks]
- Chromosome:
- 1:161540128
(GRCh38)
1:161509918
(GRCh37)
- Canonical SPDI:
- NC_000001.11:161540127:C:A,NC_000001.11:161540127:C:T
- Validated:
- by frequency,by alfa
- MAF:
T=0./0
(
ALFA)
T=0.000011/3
(TOPMED)
- HGVS:
20.
rs1488614001 [Homo sapiens]- Variant type:
- DEL
- Alleles:
- A>-
[Show Flanks]
- Chromosome:
- 1:161555165
(GRCh38)
1:161524955
(GRCh37)
- Canonical SPDI:
- NC_000001.11:161555164:A:
- Validated:
- by frequency,by alfa
- MAF:
-=0./0
(
ALFA)
-=0.000004/1
(TOPMED)
- HGVS: