SNP Links for Gene (Select 2214) - SNP

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Select item 14909289641.

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:: NC_000001.11:g.161551505G>A, NC_000001.10:g.161521295G>A, NG_009066.1:g.4119C>T

Select item 14905128542.

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:: NC_000001.11:g.161552241AGA[1], NC_000001.10:g.161522031AGA[1], NG_009066.1:g.3379CTT[1]

Select item 14904118843.

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:: NC_000001.11:g.161550461C>T, NC_000001.10:g.161520251C>T, NG_009066.1:g.5163G>A, XM_047449443.1:c.-579G>A, XM_047449444.1:c.-579G>A

Select item 14903436934.

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:: NC_000001.11:g.161546335G>C, NC_000001.11:g.161546335G>T, NC_000001.10:g.161516125G>C, NC_000001.10:g.161516125G>T, NG_009066.1:g.9289C>G, NG_009066.1:g.9289C>A

Select item 14900865615.

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:: NC_000001.11:g.161551063C>A, NC_000001.11:g.161551063C>G, NC_000001.11:g.161551063C>T, NC_000001.10:g.161520853C>A, NC_000001.10:g.161520853C>G, NC_000001.10:g.161520853C>T, NG_009066.1:g.4561G>T, NG_009066.1:g.4561G>C, NG_009066.1:g.4561G>A

Select item 14898653126.

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:: NC_000001.11:g.161547380A>G, NC_000001.10:g.161517170A>G, NG_009066.1:g.8244T>C

Select item 14898540997.

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:: NC_000001.11:g.161545935G>A, NC_000001.10:g.161515725G>A, NG_009066.1:g.9689C>T

Select item 14898042298.

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:: NC_000001.11:g.161545024C>T, NC_000001.10:g.161514814C>T, NG_009066.1:g.10600G>A

Select item 14894927819.

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:: NC_000001.11:g.161543761T>C, NC_000001.10:g.161513551T>C, NG_009066.1:g.11863A>G

Select item 148944108810.

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

Select item 148898105211.

rs1488981052 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 1:161543944 (GRCh38)
1:161513734 (GRCh37)
Canonical SPDI:: NC_000001.11:161543943:A:T
Gene:: FCGR3A (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000001.11:g.161543944A>T, NC_000001.10:g.161513734A>T, NG_009066.1:g.11680T>A

Select item 148872825712.

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:: NC_000001.11:g.161550699G>C, NC_000001.10:g.161520489G>C, NG_009066.1:g.4925C>G, NM_001329120.2:c.-108C>G, NM_001329120.1:c.-108C>G, NM_001386450.1:c.-108C>G

Select item 148855923513.

rs1488559235 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:161543400 (GRCh38)
1:161513190 (GRCh37)
Canonical SPDI:: NC_000001.11:161543399:C:T
Gene:: FCGR3A (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000019/5 (TOPMED)
T=0.000546/1 (Korea1K)
HGVS:: NC_000001.11:g.161543400C>T, NC_000001.10:g.161513190C>T, NG_009066.1:g.12224G>A

Select item 148854410914.

rs1488544109 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 1:161549718 (GRCh38)
1:161519508 (GRCh37)
Canonical SPDI:: NC_000001.11:161549717:G:A,NC_000001.11:161549717:G:C
Gene:: FCGR3A (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.161549718G>A, NC_000001.11:g.161549718G>C, NC_000001.10:g.161519508G>A, NC_000001.10:g.161519508G>C, NG_009066.1:g.5906C>T, NG_009066.1:g.5906C>G, NM_000569.8:c.19C>T, NM_000569.8:c.19C>G, NM_000569.7:c.334C>T, NM_000569.7:c.334C>G, NM_000569.6:c.127C>T, NM_000569.6:c.127C>G, NM_001127592.2:c.334C>T, NM_001127592.2:c.334C>G, NM_001127592.1:c.127C>T, NM_001127592.1:c.127C>G, NM_001329120.2:c.19C>T, NM_001329120.2:c.19C>G, NM_001329120.1:c.19C>T, NM_001329120.1:c.19C>G, NM_001127595.2:c.19C>T, NM_001127595.2:c.19C>G, NM_001127595.1:c.19C>T, NM_001127595.1:c.19C>G, NM_001127596.2:c.19C>T, NM_001127596.2:c.19C>G, NM_001127596.1:c.19C>T, NM_001127596.1:c.19C>G, NM_001127593.1:c.19C>T, NM_001127593.1:c.19C>G, NM_001386450.1:c.19C>T, NM_001386450.1:c.19C>G, NM_001329122.1:c.334C>T, NM_001329122.1:c.334C>G, XM_047449443.1:c.106C>T, XM_047449443.1:c.106C>G, XM_047449444.1:c.88C>T, XM_047449444.1:c.88C>G, NP_000560.7:p.Pro7Ser, NP_000560.7:p.Pro7Ala, NP_001121064.2:p.Pro112Ser, NP_001121064.2:p.Pro112Ala, NP_001316049.1:p.Pro7Ser, NP_001316049.1:p.Pro7Ala, NP_001121067.1:p.Pro7Ser, NP_001121067.1:p.Pro7Ala, NP_001121068.1:p.Pro7Ser, NP_001121068.1:p.Pro7Ala, NP_001121065.1:p.Pro7Ser, NP_001121065.1:p.Pro7Ala, NP_001373379.1:p.Pro7Ser, NP_001373379.1:p.Pro7Ala, NP_001316051.1:p.Pro112Ser, NP_001316051.1:p.Pro112Ala, XP_047305399.1:p.Pro36Ser, XP_047305399.1:p.Pro36Ala, XP_047305400.1:p.Pro30Ser, XP_047305400.1:p.Pro30Ala

Select item 148843986415.

rs1488439864 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C,T [Show Flanks]
Chromosome:: 1:161543762 (GRCh38)
1:161513552 (GRCh37)
Canonical SPDI:: NC_000001.11:161543761:G:A,NC_000001.11:161543761:G:C,NC_000001.11:161543761:G:T
Gene:: FCGR3A (Varview)
Functional Consequence:: intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
A=0.000007/1 (GnomAD)
T=0.000011/3 (TOPMED)
HGVS:: NC_000001.11:g.161543762G>A, NC_000001.11:g.161543762G>C, NC_000001.11:g.161543762G>T, NC_000001.10:g.161513552G>A, NC_000001.10:g.161513552G>C, NC_000001.10:g.161513552G>T, NG_009066.1:g.11862C>T, NG_009066.1:g.11862C>G, NG_009066.1:g.11862C>A

Select item 148829541816.

rs1488295418 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:161549019 (GRCh38)
1:161518809 (GRCh37)
Canonical SPDI:: NC_000001.11:161549018:A:G
Gene:: FCGR3A (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
HGVS:: NC_000001.11:g.161549019A>G, NC_000001.10:g.161518809A>G, NG_009066.1:g.6605T>C, NM_000569.8:c.53T>C, NM_000569.7:c.368T>C, NM_000569.6:c.161T>C, NM_001127592.2:c.368T>C, NM_001127592.1:c.161T>C, NM_001329120.2:c.53T>C, NM_001329120.1:c.53T>C, NM_001127595.2:c.53T>C, NM_001127595.1:c.53T>C, NM_001127596.2:c.53T>C, NM_001127596.1:c.53T>C, NM_001127593.1:c.53T>C, NM_001386450.1:c.53T>C, NM_001329122.1:c.368T>C, XM_047449443.1:c.140T>C, XM_047449444.1:c.122T>C, NP_000560.7:p.Met18Thr, NP_001121064.2:p.Met123Thr, NP_001316049.1:p.Met18Thr, NP_001121067.1:p.Met18Thr, NP_001121068.1:p.Met18Thr, NP_001121065.1:p.Met18Thr, NP_001373379.1:p.Met18Thr, NP_001316051.1:p.Met123Thr, XP_047305399.1:p.Met47Thr, XP_047305400.1:p.Met41Thr

Select item 148829058317.

rs1488290583 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:161551547 (GRCh38)
1:161521337 (GRCh37)
Canonical SPDI:: NC_000001.11:161551546: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=0.000008/2 (TOPMED)
A=0.000014/2 (GnomAD)
A=0.000342/1 (KOREAN)
HGVS:: NC_000001.11:g.161551547G>A, NC_000001.10:g.161521337G>A, NG_009066.1:g.4077C>T

Select item 148809058118.

rs1488090581 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:161552055 (GRCh38)
1:161521845 (GRCh37)
Canonical SPDI:: NC_000001.11:161552054:C:T
Gene:: FCGR3A (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa
MAF:: T=0.0007/3 (ALFA)
HGVS:: NC_000001.11:g.161552055C>T, NC_000001.10:g.161521845C>T, NG_009066.1:g.3569G>A

Select item 148804090819.

rs1488040908 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 1:161549840 (GRCh38)
1:161519630 (GRCh37)
Canonical SPDI:: NC_000001.11:161549839:C:A,NC_000001.11:161549839:C:T
Gene:: FCGR3A (Varview)
Functional Consequence:: intron_variant,upstream_transcript_variant,coding_sequence_variant,missense_variant,genic_upstream_transcript_variant
HGVS:: NC_000001.11:g.161549840C>A, NC_000001.11:g.161549840C>T, NC_000001.10:g.161519630C>A, NC_000001.10:g.161519630C>T, NG_009066.1:g.5784G>T, NG_009066.1:g.5784G>A, NM_001127592.2:c.212G>T, NM_001127592.2:c.212G>A, NM_001127592.1:c.5G>T, NM_001127592.1:c.5G>A, NM_001329122.1:c.212G>T, NM_001329122.1:c.212G>A, NM_000569.7:c.212G>T, NM_000569.7:c.212G>A, NM_000569.6:c.5G>T, NM_000569.6:c.5G>A, NP_001121064.2:p.Gly71Val, NP_001121064.2:p.Gly71Asp, NP_001316051.1:p.Gly71Val, NP_001316051.1:p.Gly71Asp

Select item 148789818420.

rs1487898184 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 1:161550441 (GRCh38)
1:161520231 (GRCh37)
Canonical SPDI:: NC_000001.11:161550440:T:C,NC_000001.11:161550440:T:G
Gene:: FCGR3A (Varview)
Functional Consequence:: intron_variant,upstream_transcript_variant,5_prime_UTR_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.161550441T>C, NC_000001.11:g.161550441T>G, NC_000001.10:g.161520231T>C, NC_000001.10:g.161520231T>G, NG_009066.1:g.5183A>G, NG_009066.1:g.5183A>C, XM_047449443.1:c.-559A>G, XM_047449443.1:c.-559A>C, XM_047449444.1:c.-559A>G, XM_047449444.1:c.-559A>C

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