SNP Links for Protein (Select 90193592) - SNP

Links from Protein

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Select item 14744468221.

rs1474446822 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 17:63929857 (GRCh38)
17:62007217 (GRCh37)
Canonical SPDI:: NC_000017.11:63929856:C:T
Gene:: CD79B (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_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_000017.11:g.63929857C>T, NC_000017.10:g.62007217C>T, NG_042788.1:g.12765C>T, NG_007368.1:g.7488G>A, NM_000626.4:c.462G>A, NM_000626.3:c.462G>A, NM_000626.2:c.462G>A, NM_021602.4:c.150G>A, NM_021602.3:c.150G>A, NM_021602.2:c.150G>A, NM_001039933.3:c.465G>A, NM_001039933.2:c.465G>A, NM_001039933.1:c.465G>A, NM_001329050.2:c.153G>A, NM_001329050.1:c.153G>A

Select item 14699436002.

rs1469943600 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 17:63929247 (GRCh38)
17:62006607 (GRCh37)
Canonical SPDI:: NC_000017.11:63929246:A:C
Gene:: CD79B (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000017.11:g.63929247A>C, NC_000017.10:g.62006607A>C, NG_042788.1:g.12155A>C, NG_007368.1:g.8098T>G, NM_000626.4:c.669T>G, NM_000626.3:c.669T>G, NM_000626.2:c.669T>G, NM_021602.4:c.357T>G, NM_021602.3:c.357T>G, NM_021602.2:c.357T>G, NM_001039933.3:c.672T>G, NM_001039933.2:c.672T>G, NM_001039933.1:c.672T>G, NM_001329050.2:c.360T>G, NM_001329050.1:c.360T>G

Select item 14671198853.

rs1467119885 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,G [Show Flanks]
Chromosome:: 17:63929277 (GRCh38)
17:62006637 (GRCh37)
Canonical SPDI:: NC_000017.11:63929276:C:A,NC_000017.11:63929276:C:G
Gene:: CD79B (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000017.11:g.63929277C>A, NC_000017.11:g.63929277C>G, NC_000017.10:g.62006637C>A, NC_000017.10:g.62006637C>G, NG_042788.1:g.12185C>A, NG_042788.1:g.12185C>G, NG_007368.1:g.8068G>T, NG_007368.1:g.8068G>C, NM_000626.4:c.639G>T, NM_000626.4:c.639G>C, NM_000626.3:c.639G>T, NM_000626.3:c.639G>C, NM_000626.2:c.639G>T, NM_000626.2:c.639G>C, NM_021602.4:c.327G>T, NM_021602.4:c.327G>C, NM_021602.3:c.327G>T, NM_021602.3:c.327G>C, NM_021602.2:c.327G>T, NM_021602.2:c.327G>C, NM_001039933.3:c.642G>T, NM_001039933.3:c.642G>C, NM_001039933.2:c.642G>T, NM_001039933.2:c.642G>C, NM_001039933.1:c.642G>T, NM_001039933.1:c.642G>C, NM_001329050.2:c.330G>T, NM_001329050.2:c.330G>C, NM_001329050.1:c.330G>T, NM_001329050.1:c.330G>C

Select item 14636323474.

rs1463632347 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 17:63929811 (GRCh38)
17:62007171 (GRCh37)
Canonical SPDI:: NC_000017.11:63929810:T:C
Gene:: CD79B (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000017.11:g.63929811T>C, NC_000017.10:g.62007171T>C, NG_042788.1:g.12719T>C, NG_007368.1:g.7534A>G, NM_000626.4:c.508A>G, NM_000626.3:c.508A>G, NM_000626.2:c.508A>G, NM_021602.4:c.196A>G, NM_021602.3:c.196A>G, NM_021602.2:c.196A>G, NM_001039933.3:c.511A>G, NM_001039933.2:c.511A>G, NM_001039933.1:c.511A>G, NM_001329050.2:c.199A>G, NM_001329050.1:c.199A>G, NP_000617.1:p.Ile170Val, NP_067613.1:p.Ile66Val, NP_001035022.1:p.Ile171Val, NP_001315979.1:p.Ile67Val

Select item 14629910865.

rs1462991086 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 17:63929785 (GRCh38)
17:62007145 (GRCh37)
Canonical SPDI:: NC_000017.11:63929784:G:A
Gene:: CD79B (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000017.11:g.63929785G>A, NC_000017.10:g.62007145G>A, NG_042788.1:g.12693G>A, NG_007368.1:g.7560C>T, NM_000626.4:c.534C>T, NM_000626.3:c.534C>T, NM_000626.2:c.534C>T, NM_021602.4:c.222C>T, NM_021602.3:c.222C>T, NM_021602.2:c.222C>T, NM_001039933.3:c.537C>T, NM_001039933.2:c.537C>T, NM_001039933.1:c.537C>T, NM_001329050.2:c.225C>T, NM_001329050.1:c.225C>T

Select item 14616500986.

rs1461650098 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 17:63932257 (GRCh38)
17:62009617 (GRCh37)
Canonical SPDI:: NC_000017.11:63932256:G:C
Gene:: CD79B (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000017.11:g.63932257G>C, NC_000017.10:g.62009617G>C, NG_042788.1:g.15165G>C, NG_007368.1:g.5088C>G, NM_000626.4:c.5C>G, NM_000626.3:c.5C>G, NM_000626.2:c.5C>G, NM_021602.4:c.5C>G, NM_021602.3:c.5C>G, NM_021602.2:c.5C>G, NM_001039933.3:c.5C>G, NM_001039933.2:c.5C>G, NM_001039933.1:c.5C>G, NM_001329050.2:c.5C>G, NM_001329050.1:c.5C>G, NP_000617.1:p.Ala2Gly, NP_067613.1:p.Ala2Gly, NP_001035022.1:p.Ala2Gly, NP_001315979.1:p.Ala2Gly

Select item 14606469397.

rs1460646939 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 17:63930105 (GRCh38)
17:62007465 (GRCh37)
Canonical SPDI:: NC_000017.11:63930104:G:A
Gene:: CD79B (Varview)
Functional Consequence:: synonymous_variant,intron_variant,coding_sequence_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000017.11:g.63930105G>A, NC_000017.10:g.62007465G>A, NG_042788.1:g.13013G>A, NG_007368.1:g.7240C>T, NM_000626.4:c.399C>T, NM_000626.3:c.399C>T, NM_000626.2:c.399C>T, NM_001039933.3:c.402C>T, NM_001039933.2:c.402C>T, NM_001039933.1:c.402C>T

Select item 14511077928.

rs1451107792 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 17:63929770 (GRCh38)
17:62007130 (GRCh37)
Canonical SPDI:: NC_000017.11:63929769:C:T
Gene:: CD79B (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_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_000017.11:g.63929770C>T, NC_000017.10:g.62007130C>T, NG_042788.1:g.12678C>T, NG_007368.1:g.7575G>A, NM_000626.4:c.549G>A, NM_000626.3:c.549G>A, NM_000626.2:c.549G>A, NM_021602.4:c.237G>A, NM_021602.3:c.237G>A, NM_021602.2:c.237G>A, NM_001039933.3:c.552G>A, NM_001039933.2:c.552G>A, NM_001039933.1:c.552G>A, NM_001329050.2:c.240G>A, NM_001329050.1:c.240G>A

Select item 14496015909.

rs1449601590 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 17:63930381 (GRCh38)
17:62007741 (GRCh37)
Canonical SPDI:: NC_000017.11:63930380:A:G
Gene:: CD79B (Varview)
Functional Consequence:: synonymous_variant,intron_variant,coding_sequence_variant
HGVS:: NC_000017.11:g.63930381A>G, NC_000017.10:g.62007741A>G, NG_042788.1:g.13289A>G, NG_007368.1:g.6964T>C, NM_000626.4:c.123T>C, NM_000626.3:c.123T>C, NM_000626.2:c.123T>C, NM_001039933.3:c.126T>C, NM_001039933.2:c.126T>C, NM_001039933.1:c.126T>C

Select item 144329279010.

rs1443292790 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 17:63929438 (GRCh38)
17:62006798 (GRCh37)
Canonical SPDI:: NC_000017.11:63929437:T:C
Gene:: CD79B (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: C=0.00007/2 (ALFA)
HGVS:: NC_000017.11:g.63929438T>C, NC_000017.10:g.62006798T>C, NG_042788.1:g.12346T>C, NG_007368.1:g.7907A>G, NM_000626.4:c.587A>G, NM_000626.3:c.587A>G, NM_000626.2:c.587A>G, NM_021602.4:c.275A>G, NM_021602.3:c.275A>G, NM_021602.2:c.275A>G, NM_001039933.3:c.590A>G, NM_001039933.2:c.590A>G, NM_001039933.1:c.590A>G, NM_001329050.2:c.278A>G, NM_001329050.1:c.278A>G, NP_000617.1:p.Tyr196Cys, NP_067613.1:p.Tyr92Cys, NP_001035022.1:p.Tyr197Cys, NP_001315979.1:p.Tyr93Cys

Select item 144319498711.

rs1443194987 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 17:63930371 (GRCh38)
17:62007731 (GRCh37)
Canonical SPDI:: NC_000017.11:63930370:G:A,NC_000017.11:63930370:G:T
Gene:: CD79B (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,intron_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
A=0.00472/1 (Vietnamese)
HGVS:: NC_000017.11:g.63930371G>A, NC_000017.11:g.63930371G>T, NC_000017.10:g.62007731G>A, NC_000017.10:g.62007731G>T, NG_042788.1:g.13279G>A, NG_042788.1:g.13279G>T, NG_007368.1:g.6974C>T, NG_007368.1:g.6974C>A, NM_000626.4:c.133C>T, NM_000626.4:c.133C>A, NM_000626.3:c.133C>T, NM_000626.3:c.133C>A, NM_000626.2:c.133C>T, NM_000626.2:c.133C>A, NM_001039933.3:c.136C>T, NM_001039933.3:c.136C>A, NM_001039933.2:c.136C>T, NM_001039933.2:c.136C>A, NM_001039933.1:c.136C>T, NM_001039933.1:c.136C>A, NP_000617.1:p.Arg45Trp, NP_001035022.1:p.Arg46Trp

Select item 143646259712.

rs1436462597 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 17:63930265 (GRCh38)
17:62007625 (GRCh37)
Canonical SPDI:: NC_000017.11:63930264:T:C
Gene:: CD79B (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,intron_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000017.11:g.63930265T>C, NC_000017.10:g.62007625T>C, NG_042788.1:g.13173T>C, NG_007368.1:g.7080A>G, NM_000626.4:c.239A>G, NM_000626.3:c.239A>G, NM_000626.2:c.239A>G, NM_001039933.3:c.242A>G, NM_001039933.2:c.242A>G, NM_001039933.1:c.242A>G, NP_000617.1:p.Gln80Arg, NP_001035022.1:p.Gln81Arg

Select item 143190826113.

rs1431908261 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 17:63932240 (GRCh38)
17:62009600 (GRCh37)
Canonical SPDI:: NC_000017.11:63932239:G:A
Gene:: CD79B (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000017.11:g.63932240G>A, NC_000017.10:g.62009600G>A, NG_042788.1:g.15148G>A, NG_007368.1:g.5105C>T, NM_000626.4:c.22C>T, NM_000626.3:c.22C>T, NM_000626.2:c.22C>T, NM_021602.4:c.22C>T, NM_021602.3:c.22C>T, NM_021602.2:c.22C>T, NM_001039933.3:c.22C>T, NM_001039933.2:c.22C>T, NM_001039933.1:c.22C>T, NM_001329050.2:c.22C>T, NM_001329050.1:c.22C>T, NP_000617.1:p.Pro8Ser, NP_067613.1:p.Pro8Ser, NP_001035022.1:p.Pro8Ser, NP_001315979.1:p.Pro8Ser

Select item 141556117014.

rs1415561170 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 17:63929789 (GRCh38)
17:62007149 (GRCh37)
Canonical SPDI:: NC_000017.11:63929788:A:G
Gene:: CD79B (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
HGVS:: NC_000017.11:g.63929789A>G, NC_000017.10:g.62007149A>G, NG_042788.1:g.12697A>G, NG_007368.1:g.7556T>C, NM_000626.4:c.530T>C, NM_000626.3:c.530T>C, NM_000626.2:c.530T>C, NM_021602.4:c.218T>C, NM_021602.3:c.218T>C, NM_021602.2:c.218T>C, NM_001039933.3:c.533T>C, NM_001039933.2:c.533T>C, NM_001039933.1:c.533T>C, NM_001329050.2:c.221T>C, NM_001329050.1:c.221T>C, NP_000617.1:p.Ile177Thr, NP_067613.1:p.Ile73Thr, NP_001035022.1:p.Ile178Thr, NP_001315979.1:p.Ile74Thr

Select item 140127287715.

rs1401272877 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 17:63930352 (GRCh38)
17:62007712 (GRCh37)
Canonical SPDI:: NC_000017.11:63930351:C:T
Gene:: CD79B (Varview)
Functional Consequence:: coding_sequence_variant,intron_variant,missense_variant
Clinical significance:: uncertain-significance
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000031/1 (ALFA)
T=0.000004/1 (GnomAD_exomes)
T=0.000004/1 (TOPMED)
HGVS:: NC_000017.11:g.63930352C>T, NC_000017.10:g.62007712C>T, NG_042788.1:g.13260C>T, NG_007368.1:g.6993G>A, NM_000626.4:c.152G>A, NM_000626.3:c.152G>A, NM_000626.2:c.152G>A, NM_001039933.3:c.155G>A, NM_001039933.2:c.155G>A, NM_001039933.1:c.155G>A, NP_000617.1:p.Arg51His, NP_001035022.1:p.Arg52His

Select item 139830010016.

rs1398300100 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 17:63932199 (GRCh38)
17:62009559 (GRCh37)
Canonical SPDI:: NC_000017.11:63932198:G:A,NC_000017.11:63932198:G:C
Gene:: CD79B (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000342/1 (KOREAN)
HGVS:: NC_000017.11:g.63932199G>A, NC_000017.11:g.63932199G>C, NC_000017.10:g.62009559G>A, NC_000017.10:g.62009559G>C, NG_042788.1:g.15107G>A, NG_042788.1:g.15107G>C, NG_007368.1:g.5146C>T, NG_007368.1:g.5146C>G, NM_000626.4:c.63C>T, NM_000626.4:c.63C>G, NM_000626.3:c.63C>T, NM_000626.3:c.63C>G, NM_000626.2:c.63C>T, NM_000626.2:c.63C>G, NM_021602.4:c.63C>T, NM_021602.4:c.63C>G, NM_021602.3:c.63C>T, NM_021602.3:c.63C>G, NM_021602.2:c.63C>T, NM_021602.2:c.63C>G, NM_001039933.3:c.63C>T, NM_001039933.3:c.63C>G, NM_001039933.2:c.63C>T, NM_001039933.2:c.63C>G, NM_001039933.1:c.63C>T, NM_001039933.1:c.63C>G, NM_001329050.2:c.63C>T, NM_001329050.2:c.63C>G, NM_001329050.1:c.63C>T, NM_001329050.1:c.63C>G

Select item 139035293617.

rs1390352936 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 17:63931338 (GRCh38)
17:62008698 (GRCh37)
Canonical SPDI:: NC_000017.11:63931337:T:C
Gene:: CD79B (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=0.000004/1 (TOPMED)
HGVS:: NC_000017.11:g.63931338T>C, NC_000017.10:g.62008698T>C, NG_042788.1:g.14246T>C, NG_007368.1:g.6007A>G, NM_000626.4:c.115A>G, NM_000626.3:c.115A>G, NM_000626.2:c.115A>G, NM_021602.4:c.115A>G, NM_021602.3:c.115A>G, NM_021602.2:c.115A>G, NM_001039933.3:c.118A>G, NM_001039933.2:c.118A>G, NM_001039933.1:c.118A>G, NM_001329050.2:c.118A>G, NM_001329050.1:c.118A>G, NP_000617.1:p.Lys39Glu, NP_067613.1:p.Lys39Glu, NP_001035022.1:p.Lys40Glu, NP_001315979.1:p.Lys40Glu

Select item 138955936318.

rs1389559363 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 17:63930115 (GRCh38)
17:62007475 (GRCh37)
Canonical SPDI:: NC_000017.11:63930114:G:A
Gene:: CD79B (Varview)
Functional Consequence:: coding_sequence_variant,intron_variant,missense_variant
Clinical significance:: uncertain-significance
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000054/1 (ALFA)
A=0.000004/1 (GnomAD_exomes)
A=0.000019/5 (TOPMED)
A=0.000021/3 (GnomAD)
A=0.000223/1 (Estonian)
HGVS:: NC_000017.11:g.63930115G>A, NC_000017.10:g.62007475G>A, NG_042788.1:g.13023G>A, NG_007368.1:g.7230C>T, NM_000626.4:c.389C>T, NM_000626.3:c.389C>T, NM_000626.2:c.389C>T, NM_001039933.3:c.392C>T, NM_001039933.2:c.392C>T, NM_001039933.1:c.392C>T, NP_000617.1:p.Ser130Leu, NP_001035022.1:p.Ser131Leu

Select item 138766887019.

rs1387668870 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 17:63929776 (GRCh38)
17:62007136 (GRCh37)
Canonical SPDI:: NC_000017.11:63929775:C:T
Gene:: CD79B (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000017.11:g.63929776C>T, NC_000017.10:g.62007136C>T, NG_042788.1:g.12684C>T, NG_007368.1:g.7569G>A, NM_000626.4:c.543G>A, NM_000626.3:c.543G>A, NM_000626.2:c.543G>A, NM_021602.4:c.231G>A, NM_021602.3:c.231G>A, NM_021602.2:c.231G>A, NM_001039933.3:c.546G>A, NM_001039933.2:c.546G>A, NM_001039933.1:c.546G>A, NM_001329050.2:c.234G>A, NM_001329050.1:c.234G>A

Select item 138744019420.

rs1387440194 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 17:63932254 (GRCh38)
17:62009614 (GRCh37)
Canonical SPDI:: NC_000017.11:63932253:C:T
Gene:: CD79B (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)
HGVS:: NC_000017.11:g.63932254C>T, NC_000017.10:g.62009614C>T, NG_042788.1:g.15162C>T, NG_007368.1:g.5091G>A, NM_000626.4:c.8G>A, NM_000626.3:c.8G>A, NM_000626.2:c.8G>A, NM_021602.4:c.8G>A, NM_021602.3:c.8G>A, NM_021602.2:c.8G>A, NM_001039933.3:c.8G>A, NM_001039933.2:c.8G>A, NM_001039933.1:c.8G>A, NM_001329050.2:c.8G>A, NM_001329050.1:c.8G>A, NP_000617.1:p.Arg3Lys, NP_067613.1:p.Arg3Lys, NP_001035022.1:p.Arg3Lys, NP_001315979.1:p.Arg3Lys

dbSNP

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