SNP Links for Protein (Select 402478628) - SNP

Links from Protein

Items: 1 to 20 of 155

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Select item 14870707721.

rs1487070772 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:161629886 (GRCh38)
1:161599676 (GRCh37)
Canonical SPDI:: NC_000001.11:161629885:C:T
Gene:: FCGR3B (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000001.11:g.161629886C>T, NC_000001.10:g.161599676C>T, NG_032926.2:g.7078G>A, NM_000570.5:c.211G>A, NM_000570.4:c.211G>A, NM_001271036.2:c.160G>A, NM_001271036.1:c.160G>A, NM_001244753.2:c.211G>A, NM_001244753.1:c.319G>A, NM_001271035.2:c.208G>A, NM_001271035.1:c.316G>A, NM_001271037.2:c.160G>A, NM_001271037.1:c.160G>A, NP_000561.3:p.Ala71Thr, NP_001257965.1:p.Ala54Thr, NP_001231682.2:p.Ala71Thr, NP_001257964.2:p.Ala70Thr, NP_001257966.1:p.Ala54Thr

Select item 14851466042.

rs1485146604 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 1:161629834 (GRCh38)
1:161599624 (GRCh37)
Canonical SPDI:: NC_000001.11:161629833:C:G
Gene:: FCGR3B (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000009/2 (GnomAD_exomes)
HGVS:: NC_000001.11:g.161629834C>G, NC_000001.10:g.161599624C>G, NG_032926.2:g.7130G>C, NM_000570.5:c.263G>C, NM_000570.4:c.263G>C, NM_001271036.2:c.212G>C, NM_001271036.1:c.212G>C, NM_001244753.2:c.263G>C, NM_001244753.1:c.371G>C, NM_001271035.2:c.260G>C, NM_001271035.1:c.368G>C, NM_001271037.2:c.212G>C, NM_001271037.1:c.212G>C, NP_000561.3:p.Arg88Thr, NP_001257965.1:p.Arg71Thr, NP_001231682.2:p.Arg88Thr, NP_001257964.2:p.Arg87Thr, NP_001257966.1:p.Arg71Thr

Select item 14829020333.

rs1482902033 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 1:161624522 (GRCh38)
1:161594312 (GRCh37)
Canonical SPDI:: NC_000001.11:161624521:T:C
Gene:: FCGR3B (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000071/1 (ALFA)
C=0.000015/2 (GnomAD)
HGVS:: NC_000001.11:g.161624522T>C, NC_000001.10:g.161594312T>C, NG_032926.2:g.12442A>G, NM_000570.5:c.695A>G, NM_000570.4:c.695A>G, NM_001271036.2:c.644A>G, NM_001271036.1:c.644A>G, NM_001244753.2:c.695A>G, NM_001244753.1:c.803A>G, NM_001271035.2:c.692A>G, NM_001271035.1:c.800A>G, NM_001271037.2:c.386A>G, NM_001271037.1:c.386A>G, NP_000561.3:p.Asn232Ser, NP_001257965.1:p.Asn215Ser, NP_001231682.2:p.Asn232Ser, NP_001257964.2:p.Asn231Ser, NP_001257966.1:p.Asn129Ser

Select item 14756892574.

rs1475689257 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 1:161629890 (GRCh38)
1:161599680 (GRCh37)
Canonical SPDI:: NC_000001.11:161629889:G:C
Gene:: FCGR3B (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.161629890G>C, NC_000001.10:g.161599680G>C, NG_032926.2:g.7074C>G, NM_000570.5:c.207C>G, NM_000570.4:c.207C>G, NM_001271036.2:c.156C>G, NM_001271036.1:c.156C>G, NM_001244753.2:c.207C>G, NM_001244753.1:c.315C>G, NM_001271035.2:c.204C>G, NM_001271035.1:c.312C>G, NM_001271037.2:c.156C>G, NM_001271037.1:c.156C>G, NP_000561.3:p.Ser69Arg, NP_001257965.1:p.Ser52Arg, NP_001231682.2:p.Ser69Arg, NP_001257964.2:p.Ser68Arg, NP_001257966.1:p.Ser52Arg

Select item 14736058075.

rs1473605807 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:161624577 (GRCh38)
1:161594367 (GRCh37)
Canonical SPDI:: NC_000001.11:161624576:C:T
Gene:: FCGR3B (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.161624577C>T, NC_000001.10:g.161594367C>T, NG_032926.2:g.12387G>A, NM_000570.5:c.640G>A, NM_000570.4:c.640G>A, NM_001271036.2:c.589G>A, NM_001271036.1:c.589G>A, NM_001244753.2:c.640G>A, NM_001244753.1:c.748G>A, NM_001271035.2:c.637G>A, NM_001271035.1:c.745G>A, NM_001271037.2:c.331G>A, NM_001271037.1:c.331G>A, NG_075530.1:g.39C>T, NP_000561.3:p.Val214Met, NP_001257965.1:p.Val197Met, NP_001231682.2:p.Val214Met, NP_001257964.2:p.Val213Met, NP_001257966.1:p.Val111Met

Select item 14735213216.

rs1473521321 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:161629970 (GRCh38)
1:161599760 (GRCh37)
Canonical SPDI:: NC_000001.11:161629969:C:T
Gene:: FCGR3B (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000028/3 (GnomAD)
HGVS:: NC_000001.11:g.161629970C>T, NC_000001.10:g.161599760C>T, NG_032926.2:g.6994G>A, NM_000570.5:c.127G>A, NM_000570.4:c.127G>A, NM_001271036.2:c.76G>A, NM_001271036.1:c.76G>A, NM_001244753.2:c.127G>A, NM_001244753.1:c.235G>A, NM_001271035.2:c.124G>A, NM_001271035.1:c.232G>A, NM_001271037.2:c.76G>A, NM_001271037.1:c.76G>A, NP_000561.3:p.Val43Met, NP_001257965.1:p.Val26Met, NP_001231682.2:p.Val43Met, NP_001257964.2:p.Val42Met, NP_001257966.1:p.Val26Met

Select item 14734816557.

rs1473481655 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 1:161630370 (GRCh38)
1:161600160 (GRCh37)
Canonical SPDI:: NC_000001.11:161630369:G:T
Gene:: FCGR3B (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.161630370G>T, NC_000001.10:g.161600160G>T, NG_032926.2:g.6594C>A, NM_000570.5:c.59C>A, NM_000570.4:c.59C>A, NM_001271036.2:c.8C>A, NM_001271036.1:c.8C>A, NM_001244753.2:c.59C>A, NM_001244753.1:c.167C>A, NM_001271035.2:c.59C>A, NM_001271035.1:c.167C>A, NM_001271037.2:c.8C>A, NM_001271037.1:c.8C>A, NP_000561.3:p.Thr20Asn, NP_001257965.1:p.Thr3Asn, NP_001231682.2:p.Thr20Asn, NP_001257964.2:p.Thr20Asn, NP_001257966.1:p.Thr3Asn

Select item 14637809888.

rs1463780988 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:161629792 (GRCh38)
1:161599582 (GRCh37)
Canonical SPDI:: NC_000001.11:161629791:A:G
Gene:: FCGR3B (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.161629792A>G, NC_000001.10:g.161599582A>G, NG_032926.2:g.7172T>C, NM_000570.5:c.305T>C, NM_000570.4:c.305T>C, NM_001271036.2:c.254T>C, NM_001271036.1:c.254T>C, NM_001244753.2:c.305T>C, NM_001244753.1:c.413T>C, NM_001271035.2:c.302T>C, NM_001271035.1:c.410T>C, NM_001271037.2:c.254T>C, NM_001271037.1:c.254T>C, NP_000561.3:p.Leu102Pro, NP_001257965.1:p.Leu85Pro, NP_001231682.2:p.Leu102Pro, NP_001257964.2:p.Leu101Pro, NP_001257966.1:p.Leu85Pro

Select item 14545522479.

rs1454552247 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 1:161629996 (GRCh38)
1:161599786 (GRCh37)
Canonical SPDI:: NC_000001.11:161629995:C:A,NC_000001.11:161629995:C:T
Gene:: FCGR3B (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,stop_gained
Validated:: by frequency
MAF:: A=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.161629996C>A, NC_000001.11:g.161629996C>T, NC_000001.10:g.161599786C>A, NC_000001.10:g.161599786C>T, NG_032926.2:g.6968G>T, NG_032926.2:g.6968G>A, NM_000570.5:c.101G>T, NM_000570.5:c.101G>A, NM_000570.4:c.101G>T, NM_000570.4:c.101G>A, NM_001271036.2:c.50G>T, NM_001271036.2:c.50G>A, NM_001271036.1:c.50G>T, NM_001271036.1:c.50G>A, NM_001244753.2:c.101G>T, NM_001244753.2:c.101G>A, NM_001244753.1:c.209G>T, NM_001244753.1:c.209G>A, NM_001271035.2:c.98G>T, NM_001271035.2:c.98G>A, NM_001271035.1:c.206G>T, NM_001271035.1:c.206G>A, NM_001271037.2:c.50G>T, NM_001271037.2:c.50G>A, NM_001271037.1:c.50G>T, NM_001271037.1:c.50G>A, NP_000561.3:p.Trp34Leu, NP_000561.3:p.Trp34Ter, NP_001257965.1:p.Trp17Leu, NP_001257965.1:p.Trp17Ter, NP_001231682.2:p.Trp34Leu, NP_001231682.2:p.Trp34Ter, NP_001257964.2:p.Trp33Leu, NP_001257964.2:p.Trp33Ter, NP_001257966.1:p.Trp17Leu, NP_001257966.1:p.Trp17Ter

Select item 143802097510.

rs1438020975 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 1:161630026 (GRCh38)
1:161599816 (GRCh37)
Canonical SPDI:: NC_000001.11:161630025:G:C
Gene:: FCGR3B (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: C=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.161630026G>C, NC_000001.10:g.161599816G>C, NG_032926.2:g.6938C>G, NM_000570.5:c.71C>G, NM_000570.4:c.71C>G, NM_001271036.2:c.20C>G, NM_001271036.1:c.20C>G, NM_001244753.2:c.71C>G, NM_001244753.1:c.179C>G, NM_001271035.2:c.68C>G, NM_001271035.1:c.176C>G, NM_001271037.2:c.20C>G, NM_001271037.1:c.20C>G, NP_000561.3:p.Pro24Arg, NP_001257965.1:p.Pro7Arg, NP_001231682.2:p.Pro24Arg, NP_001257964.2:p.Pro23Arg, NP_001257966.1:p.Pro7Arg

Select item 143740448011.

rs1437404480 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 1:161629982 (GRCh38)
1:161599772 (GRCh37)
Canonical SPDI:: NC_000001.11:161629981:C:G,NC_000001.11:161629981:C:T
Gene:: FCGR3B (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: G=0.00001/2 (GnomAD_exomes)
HGVS:: NC_000001.11:g.161629982C>G, NC_000001.11:g.161629982C>T, NC_000001.10:g.161599772C>G, NC_000001.10:g.161599772C>T, NG_032926.2:g.6982G>C, NG_032926.2:g.6982G>A, NM_000570.5:c.115G>C, NM_000570.5:c.115G>A, NM_000570.4:c.115G>C, NM_000570.4:c.115G>A, NM_001271036.2:c.64G>C, NM_001271036.2:c.64G>A, NM_001271036.1:c.64G>C, NM_001271036.1:c.64G>A, NM_001244753.2:c.115G>C, NM_001244753.2:c.115G>A, NM_001244753.1:c.223G>C, NM_001244753.1:c.223G>A, NM_001271035.2:c.112G>C, NM_001271035.2:c.112G>A, NM_001271035.1:c.220G>C, NM_001271035.1:c.220G>A, NM_001271037.2:c.64G>C, NM_001271037.2:c.64G>A, NM_001271037.1:c.64G>C, NM_001271037.1:c.64G>A, NP_000561.3:p.Glu39Gln, NP_000561.3:p.Glu39Lys, NP_001257965.1:p.Glu22Gln, NP_001257965.1:p.Glu22Lys, NP_001231682.2:p.Glu39Gln, NP_001231682.2:p.Glu39Lys, NP_001257964.2:p.Glu38Gln, NP_001257964.2:p.Glu38Lys, NP_001257966.1:p.Glu22Gln, NP_001257966.1:p.Glu22Lys

Select item 143211283112.

rs1432112831 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 1:161624534 (GRCh38)
1:161594324 (GRCh37)
Canonical SPDI:: NC_000001.11:161624533:G:C
Gene:: FCGR3B (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.161624534G>C, NC_000001.10:g.161594324G>C, NG_032926.2:g.12430C>G, NM_000570.5:c.683C>G, NM_000570.4:c.683C>G, NM_001271036.2:c.632C>G, NM_001271036.1:c.632C>G, NM_001244753.2:c.683C>G, NM_001244753.1:c.791C>G, NM_001271035.2:c.680C>G, NM_001271035.1:c.788C>G, NM_001271037.2:c.374C>G, NM_001271037.1:c.374C>G, NP_000561.3:p.Ser228Cys, NP_001257965.1:p.Ser211Cys, NP_001231682.2:p.Ser228Cys, NP_001257964.2:p.Ser227Cys, NP_001257966.1:p.Ser125Cys

Select item 143063963513.

rs1430639635 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 1:161629840 (GRCh38)
1:161599630 (GRCh37)
Canonical SPDI:: NC_000001.11:161629839:T:G
Gene:: FCGR3B (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.161629840T>G, NC_000001.10:g.161599630T>G, NG_032926.2:g.7124A>C, NM_000570.5:c.257A>C, NM_000570.4:c.257A>C, NM_001271036.2:c.206A>C, NM_001271036.1:c.206A>C, NM_001244753.2:c.257A>C, NM_001244753.1:c.365A>C, NM_001271035.2:c.254A>C, NM_001271035.1:c.362A>C, NM_001271037.2:c.206A>C, NM_001271037.1:c.206A>C, NP_000561.3:p.Glu86Ala, NP_001257965.1:p.Glu69Ala, NP_001231682.2:p.Glu86Ala, NP_001257964.2:p.Glu85Ala, NP_001257966.1:p.Glu69Ala

Select item 141710706914.

rs1417107069 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:161630010 (GRCh38)
1:161599800 (GRCh37)
Canonical SPDI:: NC_000001.11:161630009:G:A
Gene:: FCGR3B (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: A=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.161630010G>A, NC_000001.10:g.161599800G>A, NG_032926.2:g.6954C>T, NM_000570.5:c.87C>T, NM_000570.4:c.87C>T, NM_001271036.2:c.36C>T, NM_001271036.1:c.36C>T, NM_001244753.2:c.87C>T, NM_001244753.1:c.195C>T, NM_001271035.2:c.84C>T, NM_001271035.1:c.192C>T, NM_001271037.2:c.36C>T, NM_001271037.1:c.36C>T

Select item 140990668915.

rs1409906689 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 1:161629892 (GRCh38)
1:161599682 (GRCh37)
Canonical SPDI:: NC_000001.11:161629891:T:C
Gene:: FCGR3B (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.161629892T>C, NC_000001.10:g.161599682T>C, NG_032926.2:g.7072A>G, NM_000570.5:c.205A>G, NM_000570.4:c.205A>G, NM_001271036.2:c.154A>G, NM_001271036.1:c.154A>G, NM_001244753.2:c.205A>G, NM_001244753.1:c.313A>G, NM_001271035.2:c.202A>G, NM_001271035.1:c.310A>G, NM_001271037.2:c.154A>G, NM_001271037.1:c.154A>G, NP_000561.3:p.Ser69Gly, NP_001257965.1:p.Ser52Gly, NP_001231682.2:p.Ser69Gly, NP_001257964.2:p.Ser68Gly, NP_001257966.1:p.Ser52Gly

Select item 140549178616.

rs1405491786 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:161624541 (GRCh38)
1:161594331 (GRCh37)
Canonical SPDI:: NC_000001.11:161624540:A:G
Gene:: FCGR3B (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000011/3 (TOPMED)
G=0.000015/2 (GnomAD)
HGVS:: NC_000001.11:g.161624541A>G, NC_000001.10:g.161594331A>G, NG_032926.2:g.12423T>C, NM_000570.5:c.676T>C, NM_000570.4:c.676T>C, NM_001271036.2:c.625T>C, NM_001271036.1:c.625T>C, NM_001244753.2:c.676T>C, NM_001244753.1:c.784T>C, NM_001271035.2:c.673T>C, NM_001271035.1:c.781T>C, NM_001271037.2:c.367T>C, NM_001271037.1:c.367T>C, NG_075530.1:g.3A>G, NP_000561.3:p.Tyr226His, NP_001257965.1:p.Tyr209His, NP_001231682.2:p.Tyr226His, NP_001257964.2:p.Tyr225His, NP_001257966.1:p.Tyr123His

Select item 139743395617.

rs1397433956 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:161624539 (GRCh38)
1:161594329 (GRCh37)
Canonical SPDI:: NC_000001.11:161624538:A:G
Gene:: FCGR3B (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.161624539A>G, NC_000001.10:g.161594329A>G, NG_032926.2:g.12425T>C, NM_000570.5:c.678T>C, NM_000570.4:c.678T>C, NM_001271036.2:c.627T>C, NM_001271036.1:c.627T>C, NM_001244753.2:c.678T>C, NM_001244753.1:c.786T>C, NM_001271035.2:c.675T>C, NM_001271035.1:c.783T>C, NM_001271037.2:c.369T>C, NM_001271037.1:c.369T>C, NG_075530.1:g.1A>G

Select item 139024030618.

rs1390240306 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C,T [Show Flanks]
Chromosome:: 1:161624566 (GRCh38)
1:161594356 (GRCh37)
Canonical SPDI:: NC_000001.11:161624565:G:C,NC_000001.11:161624565:G:T
Gene:: FCGR3B (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
T=0.000004/1 (GnomAD_exomes)
C=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.161624566G>C, NC_000001.11:g.161624566G>T, NC_000001.10:g.161594356G>C, NC_000001.10:g.161594356G>T, NG_032926.2:g.12398C>G, NG_032926.2:g.12398C>A, NM_000570.5:c.651C>G, NM_000570.5:c.651C>A, NM_000570.4:c.651C>G, NM_000570.4:c.651C>A, NM_001271036.2:c.600C>G, NM_001271036.2:c.600C>A, NM_001271036.1:c.600C>G, NM_001271036.1:c.600C>A, NM_001244753.2:c.651C>G, NM_001244753.2:c.651C>A, NM_001244753.1:c.759C>G, NM_001244753.1:c.759C>A, NM_001271035.2:c.648C>G, NM_001271035.2:c.648C>A, NM_001271035.1:c.756C>G, NM_001271035.1:c.756C>A, NM_001271037.2:c.342C>G, NM_001271037.2:c.342C>A, NM_001271037.1:c.342C>G, NM_001271037.1:c.342C>A, NG_075530.1:g.28G>C, NG_075530.1:g.28G>T

Select item 137883132819.

rs1378831328 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:161630016 (GRCh38)
1:161599806 (GRCh37)
Canonical SPDI:: NC_000001.11:161630015:C:T
Gene:: FCGR3B (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000001.11:g.161630016C>T, NC_000001.10:g.161599806C>T, NG_032926.2:g.6948G>A, NM_000570.5:c.81G>A, NM_000570.4:c.81G>A, NM_001271036.2:c.30G>A, NM_001271036.1:c.30G>A, NM_001244753.2:c.81G>A, NM_001244753.1:c.189G>A, NM_001271035.2:c.78G>A, NM_001271035.1:c.186G>A, NM_001271037.2:c.30G>A, NM_001271037.1:c.30G>A

Select item 137387206220.

rs1373872062 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 1:161629789 (GRCh38)
1:161599579 (GRCh37)
Canonical SPDI:: NC_000001.11:161629788:T:A
Gene:: FCGR3B (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.161629789T>A, NC_000001.10:g.161599579T>A, NG_032926.2:g.7175A>T, NM_000570.5:c.308A>T, NM_000570.4:c.308A>T, NM_001271036.2:c.257A>T, NM_001271036.1:c.257A>T, NM_001244753.2:c.308A>T, NM_001244753.1:c.416A>T, NM_001271035.2:c.305A>T, NM_001271035.1:c.413A>T, NM_001271037.2:c.257A>T, NM_001271037.1:c.257A>T, NP_000561.3:p.Glu103Val, NP_001257965.1:p.Glu86Val, NP_001231682.2:p.Glu103Val, NP_001257964.2:p.Glu102Val, NP_001257966.1:p.Glu86Val

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