SNP Links for Protein (Select 11067749) - SNP

Select item 14908838631.

rs1490883863 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 9:134048084 (GRCh38)
9:136913206 (GRCh37)
Canonical SPDI:: NC_000009.12:134048083:T:C,NC_000009.12:134048083:T:G
Gene:: BRD3 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
C=0.000005/1 (GnomAD_exomes)
G=0.000007/1 (GnomAD)
HGVS:: NC_000009.12:g.134048084T>C, NC_000009.12:g.134048084T>G, NC_000009.11:g.136913206T>C, NC_000009.11:g.136913206T>G, XM_006717291.4:c.1085A>G, XM_006717291.4:c.1085A>C, XM_006717291.3:c.1085A>G, XM_006717291.3:c.1085A>C, XM_006717291.2:c.1085A>G, XM_006717291.2:c.1085A>C, XM_006717291.1:c.1085A>G, XM_006717291.1:c.1085A>C, NM_007371.4:c.1085A>G, NM_007371.4:c.1085A>C, NM_007371.3:c.1085A>G, NM_007371.3:c.1085A>C, XM_011519052.3:c.1085A>G, XM_011519052.3:c.1085A>C, XM_011519052.2:c.1085A>G, XM_011519052.2:c.1085A>C, XM_011519052.1:c.1085A>G, XM_011519052.1:c.1085A>C, XM_017015165.3:c.1085A>G, XM_017015165.3:c.1085A>C, XM_017015165.2:c.1085A>G, XM_017015165.2:c.1085A>C, XM_017015165.1:c.1085A>G, XM_017015165.1:c.1085A>C, XM_047423904.1:c.1085A>G, XM_047423904.1:c.1085A>C, XM_047423905.1:c.1085A>G, XM_047423905.1:c.1085A>C, XM_047423903.1:c.1085A>G, XM_047423903.1:c.1085A>C, XM_047423906.1:c.1085A>G, XM_047423906.1:c.1085A>C, XP_006717354.1:p.Lys362Arg, XP_006717354.1:p.Lys362Thr, NP_031397.1:p.Lys362Arg, NP_031397.1:p.Lys362Thr, XP_011517354.1:p.Lys362Arg, XP_011517354.1:p.Lys362Thr, XP_016870654.1:p.Lys362Arg, XP_016870654.1:p.Lys362Thr, XP_047279860.1:p.Lys362Arg, XP_047279860.1:p.Lys362Thr, XP_047279861.1:p.Lys362Arg, XP_047279861.1:p.Lys362Thr, XP_047279859.1:p.Lys362Arg, XP_047279859.1:p.Lys362Thr, XP_047279862.1:p.Lys362Arg, XP_047279862.1:p.Lys362Thr

Select item 14894819912.

rs1489481991 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 9:134036117 (GRCh38)
9:136901239 (GRCh37)
Canonical SPDI:: NC_000009.12:134036116:G:A
Gene:: BRD3 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000008/2 (TOPMED)
HGVS:: NC_000009.12:g.134036117G>A, NC_000009.11:g.136901239G>A, XM_006717291.4:c.1851C>T, XM_006717291.3:c.1851C>T, XM_006717291.2:c.1851C>T, XM_006717291.1:c.1851C>T, NM_007371.4:c.1851C>T, NM_007371.3:c.1851C>T, XM_011519052.3:c.1851C>T, XM_011519052.2:c.1851C>T, XM_011519052.1:c.1851C>T, XM_017015165.3:c.1851C>T, XM_017015165.2:c.1851C>T, XM_017015165.1:c.1851C>T, XM_047423904.1:c.1851C>T, XM_047423905.1:c.1851C>T, XM_047423903.1:c.1851C>T, XM_047423906.1:c.1851C>T

Select item 14890214093.

rs1489021409 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 9:134040104 (GRCh38)
9:136905226 (GRCh37)
Canonical SPDI:: NC_000009.12:134040103:G:A,NC_000009.12:134040103:G:C
Gene:: BRD3 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000015/4 (TOPMED)
HGVS:: NC_000009.12:g.134040104G>A, NC_000009.12:g.134040104G>C, NC_000009.11:g.136905226G>A, NC_000009.11:g.136905226G>C, XM_006717291.4:c.1573C>T, XM_006717291.4:c.1573C>G, XM_006717291.3:c.1573C>T, XM_006717291.3:c.1573C>G, XM_006717291.2:c.1573C>T, XM_006717291.2:c.1573C>G, XM_006717291.1:c.1573C>T, XM_006717291.1:c.1573C>G, NM_007371.4:c.1573C>T, NM_007371.4:c.1573C>G, NM_007371.3:c.1573C>T, NM_007371.3:c.1573C>G, XM_011519052.3:c.1573C>T, XM_011519052.3:c.1573C>G, XM_011519052.2:c.1573C>T, XM_011519052.2:c.1573C>G, XM_011519052.1:c.1573C>T, XM_011519052.1:c.1573C>G, XM_017015165.3:c.1573C>T, XM_017015165.3:c.1573C>G, XM_017015165.2:c.1573C>T, XM_017015165.2:c.1573C>G, XM_017015165.1:c.1573C>T, XM_017015165.1:c.1573C>G, XM_047423904.1:c.1573C>T, XM_047423904.1:c.1573C>G, XM_047423905.1:c.1573C>T, XM_047423905.1:c.1573C>G, XM_047423903.1:c.1573C>T, XM_047423903.1:c.1573C>G, XM_047423906.1:c.1573C>T, XM_047423906.1:c.1573C>G, XP_006717354.1:p.Pro525Ser, XP_006717354.1:p.Pro525Ala, NP_031397.1:p.Pro525Ser, NP_031397.1:p.Pro525Ala, XP_011517354.1:p.Pro525Ser, XP_011517354.1:p.Pro525Ala, XP_016870654.1:p.Pro525Ser, XP_016870654.1:p.Pro525Ala, XP_047279860.1:p.Pro525Ser, XP_047279860.1:p.Pro525Ala, XP_047279861.1:p.Pro525Ser, XP_047279861.1:p.Pro525Ala, XP_047279859.1:p.Pro525Ser, XP_047279859.1:p.Pro525Ala, XP_047279862.1:p.Pro525Ser, XP_047279862.1:p.Pro525Ala

Select item 14876230424.

rs1487623042 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 9:134050441 (GRCh38)
9:136915563 (GRCh37)
Canonical SPDI:: NC_000009.12:134050440:G:A
Gene:: BRD3 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by cluster
HGVS:: NC_000009.12:g.134050441G>A, NC_000009.11:g.136915563G>A, XM_006717291.4:c.647C>T, XM_006717291.3:c.647C>T, XM_006717291.2:c.647C>T, XM_006717291.1:c.647C>T, NM_007371.4:c.647C>T, NM_007371.3:c.647C>T, XM_011519052.3:c.647C>T, XM_011519052.2:c.647C>T, XM_011519052.1:c.647C>T, XM_017015165.3:c.647C>T, XM_017015165.2:c.647C>T, XM_017015165.1:c.647C>T, XM_047423904.1:c.647C>T, XM_047423905.1:c.647C>T, XM_047423903.1:c.647C>T, XM_047423906.1:c.647C>T, XP_006717354.1:p.Ala216Val, NP_031397.1:p.Ala216Val, XP_011517354.1:p.Ala216Val, XP_016870654.1:p.Ala216Val, XP_047279860.1:p.Ala216Val, XP_047279861.1:p.Ala216Val, XP_047279859.1:p.Ala216Val, XP_047279862.1:p.Ala216Val

Select item 14870049205.

rs1487004920 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 9:134041890 (GRCh38)
9:136907012 (GRCh37)
Canonical SPDI:: NC_000009.12:134041889:G:C
Gene:: BRD3 (Varview)
Functional Consequence:: coding_sequence_variant,missense_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_000009.12:g.134041890G>C, NC_000009.11:g.136907012G>C, XM_006717291.4:c.1277C>G, XM_006717291.3:c.1277C>G, XM_006717291.2:c.1277C>G, XM_006717291.1:c.1277C>G, NM_007371.4:c.1277C>G, NM_007371.3:c.1277C>G, XM_011519052.3:c.1277C>G, XM_011519052.2:c.1277C>G, XM_011519052.1:c.1277C>G, XM_017015165.3:c.1277C>G, XM_017015165.2:c.1277C>G, XM_017015165.1:c.1277C>G, XM_047423904.1:c.1277C>G, XM_047423905.1:c.1277C>G, XM_047423903.1:c.1277C>G, XM_047423906.1:c.1277C>G, XP_006717354.1:p.Pro426Arg, NP_031397.1:p.Pro426Arg, XP_011517354.1:p.Pro426Arg, XP_016870654.1:p.Pro426Arg, XP_047279860.1:p.Pro426Arg, XP_047279861.1:p.Pro426Arg, XP_047279859.1:p.Pro426Arg, XP_047279862.1:p.Pro426Arg

Select item 14866583636.

rs1486658363 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 9:134045305 (GRCh38)
9:136910427 (GRCh37)
Canonical SPDI:: NC_000009.12:134045304:G:A
Gene:: BRD3 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000009.12:g.134045305G>A, NC_000009.11:g.136910427G>A, XM_006717291.4:c.1203C>T, XM_006717291.3:c.1203C>T, XM_006717291.2:c.1203C>T, XM_006717291.1:c.1203C>T, NM_007371.4:c.1203C>T, NM_007371.3:c.1203C>T, XM_011519052.3:c.1203C>T, XM_011519052.2:c.1203C>T, XM_011519052.1:c.1203C>T, XM_017015165.3:c.1203C>T, XM_017015165.2:c.1203C>T, XM_017015165.1:c.1203C>T, XM_047423904.1:c.1203C>T, XM_047423905.1:c.1203C>T, XM_047423903.1:c.1203C>T, XM_047423906.1:c.1203C>T

Select item 14864348367.

rs1486434836 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 9:134040235 (GRCh38)
9:136905357 (GRCh37)
Canonical SPDI:: NC_000009.12:134040234:G:C
Gene:: BRD3 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000011/3 (TOPMED)
HGVS:: NC_000009.12:g.134040235G>C, NC_000009.11:g.136905357G>C, XM_006717291.4:c.1442C>G, XM_006717291.3:c.1442C>G, XM_006717291.2:c.1442C>G, XM_006717291.1:c.1442C>G, NM_007371.4:c.1442C>G, NM_007371.3:c.1442C>G, XM_011519052.3:c.1442C>G, XM_011519052.2:c.1442C>G, XM_011519052.1:c.1442C>G, XM_017015165.3:c.1442C>G, XM_017015165.2:c.1442C>G, XM_017015165.1:c.1442C>G, XM_047423904.1:c.1442C>G, XM_047423905.1:c.1442C>G, XM_047423903.1:c.1442C>G, XM_047423906.1:c.1442C>G, XP_006717354.1:p.Ser481Cys, NP_031397.1:p.Ser481Cys, XP_011517354.1:p.Ser481Cys, XP_016870654.1:p.Ser481Cys, XP_047279860.1:p.Ser481Cys, XP_047279861.1:p.Ser481Cys, XP_047279859.1:p.Ser481Cys, XP_047279862.1:p.Ser481Cys

Select item 14848273918.

rs1484827391 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 9:134034735 (GRCh38)
9:136899857 (GRCh37)
Canonical SPDI:: NC_000009.12:134034734:C:T
Gene:: BRD3 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
HGVS:: NC_000009.12:g.134034735C>T, NC_000009.11:g.136899857C>T, XM_006717291.4:c.2031G>A, XM_006717291.3:c.2031G>A, XM_006717291.2:c.2031G>A, XM_006717291.1:c.2031G>A, NM_007371.4:c.2031G>A, NM_007371.3:c.2031G>A, XM_011519052.3:c.2031G>A, XM_011519052.2:c.2031G>A, XM_011519052.1:c.2031G>A, XM_017015165.3:c.2028G>A, XM_017015165.2:c.2028G>A, XM_017015165.1:c.2028G>A, XM_047423904.1:c.2031G>A, XM_047423905.1:c.2028G>A, XM_047423903.1:c.2031G>A, XM_047423906.1:c.2028G>A

Select item 14837644229.

rs1483764422 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 9:134040116 (GRCh38)
9:136905238 (GRCh37)
Canonical SPDI:: NC_000009.12:134040115:C:A,NC_000009.12:134040115:C:T
Gene:: BRD3 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by cluster
HGVS:: NC_000009.12:g.134040116C>A, NC_000009.12:g.134040116C>T, NC_000009.11:g.136905238C>A, NC_000009.11:g.136905238C>T, XM_006717291.4:c.1561G>T, XM_006717291.4:c.1561G>A, XM_006717291.3:c.1561G>T, XM_006717291.3:c.1561G>A, XM_006717291.2:c.1561G>T, XM_006717291.2:c.1561G>A, XM_006717291.1:c.1561G>T, XM_006717291.1:c.1561G>A, NM_007371.4:c.1561G>T, NM_007371.4:c.1561G>A, NM_007371.3:c.1561G>T, NM_007371.3:c.1561G>A, XM_011519052.3:c.1561G>T, XM_011519052.3:c.1561G>A, XM_011519052.2:c.1561G>T, XM_011519052.2:c.1561G>A, XM_011519052.1:c.1561G>T, XM_011519052.1:c.1561G>A, XM_017015165.3:c.1561G>T, XM_017015165.3:c.1561G>A, XM_017015165.2:c.1561G>T, XM_017015165.2:c.1561G>A, XM_017015165.1:c.1561G>T, XM_017015165.1:c.1561G>A, XM_047423904.1:c.1561G>T, XM_047423904.1:c.1561G>A, XM_047423905.1:c.1561G>T, XM_047423905.1:c.1561G>A, XM_047423903.1:c.1561G>T, XM_047423903.1:c.1561G>A, XM_047423906.1:c.1561G>T, XM_047423906.1:c.1561G>A, XP_006717354.1:p.Ala521Ser, XP_006717354.1:p.Ala521Thr, NP_031397.1:p.Ala521Ser, NP_031397.1:p.Ala521Thr, XP_011517354.1:p.Ala521Ser, XP_011517354.1:p.Ala521Thr, XP_016870654.1:p.Ala521Ser, XP_016870654.1:p.Ala521Thr, XP_047279860.1:p.Ala521Ser, XP_047279860.1:p.Ala521Thr, XP_047279861.1:p.Ala521Ser, XP_047279861.1:p.Ala521Thr, XP_047279859.1:p.Ala521Ser, XP_047279859.1:p.Ala521Thr, XP_047279862.1:p.Ala521Ser, XP_047279862.1:p.Ala521Thr

Select item 147991925210.

rs1479919252 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 9:134048328 (GRCh38)
9:136913450 (GRCh37)
Canonical SPDI:: NC_000009.12:134048327:T:C
Gene:: BRD3 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000009.12:g.134048328T>C, NC_000009.11:g.136913450T>C, XM_006717291.4:c.841A>G, XM_006717291.3:c.841A>G, XM_006717291.2:c.841A>G, XM_006717291.1:c.841A>G, NM_007371.4:c.841A>G, NM_007371.3:c.841A>G, XM_011519052.3:c.841A>G, XM_011519052.2:c.841A>G, XM_011519052.1:c.841A>G, XM_017015165.3:c.841A>G, XM_017015165.2:c.841A>G, XM_017015165.1:c.841A>G, XM_047423904.1:c.841A>G, XM_047423905.1:c.841A>G, XM_047423903.1:c.841A>G, XM_047423906.1:c.841A>G, XP_006717354.1:p.Ser281Gly, NP_031397.1:p.Ser281Gly, XP_011517354.1:p.Ser281Gly, XP_016870654.1:p.Ser281Gly, XP_047279860.1:p.Ser281Gly, XP_047279861.1:p.Ser281Gly, XP_047279859.1:p.Ser281Gly, XP_047279862.1:p.Ser281Gly

Select item 147944728011.

rs1479447280 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 9:134045314 (GRCh38)
9:136910436 (GRCh37)
Canonical SPDI:: NC_000009.12:134045313:C:A
Gene:: BRD3 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000142/2 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000023/6 (TOPMED)
HGVS:: NC_000009.12:g.134045314C>A, NC_000009.11:g.136910436C>A, XM_006717291.4:c.1194G>T, XM_006717291.3:c.1194G>T, XM_006717291.2:c.1194G>T, XM_006717291.1:c.1194G>T, NM_007371.4:c.1194G>T, NM_007371.3:c.1194G>T, XM_011519052.3:c.1194G>T, XM_011519052.2:c.1194G>T, XM_011519052.1:c.1194G>T, XM_017015165.3:c.1194G>T, XM_017015165.2:c.1194G>T, XM_017015165.1:c.1194G>T, XM_047423904.1:c.1194G>T, XM_047423905.1:c.1194G>T, XM_047423903.1:c.1194G>T, XM_047423906.1:c.1194G>T

Select item 147902966412.

rs1479029664 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 9:134036087 (GRCh38)
9:136901209 (GRCh37)
Canonical SPDI:: NC_000009.12:134036086:C:G,NC_000009.12:134036086:C:T
Gene:: BRD3 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by cluster
MAF:: T=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000009.12:g.134036087C>G, NC_000009.12:g.134036087C>T, NC_000009.11:g.136901209C>G, NC_000009.11:g.136901209C>T, XM_006717291.4:c.1881G>C, XM_006717291.4:c.1881G>A, XM_006717291.3:c.1881G>C, XM_006717291.3:c.1881G>A, XM_006717291.2:c.1881G>C, XM_006717291.2:c.1881G>A, XM_006717291.1:c.1881G>C, XM_006717291.1:c.1881G>A, NM_007371.4:c.1881G>C, NM_007371.4:c.1881G>A, NM_007371.3:c.1881G>C, NM_007371.3:c.1881G>A, XM_011519052.3:c.1881G>C, XM_011519052.3:c.1881G>A, XM_011519052.2:c.1881G>C, XM_011519052.2:c.1881G>A, XM_011519052.1:c.1881G>C, XM_011519052.1:c.1881G>A, XM_017015165.3:c.1881G>C, XM_017015165.3:c.1881G>A, XM_017015165.2:c.1881G>C, XM_017015165.2:c.1881G>A, XM_017015165.1:c.1881G>C, XM_017015165.1:c.1881G>A, XM_047423904.1:c.1881G>C, XM_047423904.1:c.1881G>A, XM_047423905.1:c.1881G>C, XM_047423905.1:c.1881G>A, XM_047423903.1:c.1881G>C, XM_047423903.1:c.1881G>A, XM_047423906.1:c.1881G>C, XM_047423906.1:c.1881G>A

Select item 147855335213.

rs1478553352 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 9:134034749 (GRCh38)
9:136899871 (GRCh37)
Canonical SPDI:: NC_000009.12:134034748:G:A
Gene:: BRD3 (Varview)
Functional Consequence:: coding_sequence_variant,stop_gained
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000009.12:g.134034749G>A, NC_000009.11:g.136899871G>A, XM_006717291.4:c.2017C>T, XM_006717291.3:c.2017C>T, XM_006717291.2:c.2017C>T, XM_006717291.1:c.2017C>T, NM_007371.4:c.2017C>T, NM_007371.3:c.2017C>T, XM_011519052.3:c.2017C>T, XM_011519052.2:c.2017C>T, XM_011519052.1:c.2017C>T, XM_017015165.3:c.2014C>T, XM_017015165.2:c.2014C>T, XM_017015165.1:c.2014C>T, XM_047423904.1:c.2017C>T, XM_047423905.1:c.2014C>T, XM_047423903.1:c.2017C>T, XM_047423906.1:c.2014C>T, XP_006717354.1:p.Gln673Ter, NP_031397.1:p.Gln673Ter, XP_011517354.1:p.Gln673Ter, XP_016870654.1:p.Gln672Ter, XP_047279860.1:p.Gln673Ter, XP_047279861.1:p.Gln672Ter, XP_047279859.1:p.Gln673Ter, XP_047279862.1:p.Gln672Ter

Select item 147814481514.

rs1478144815 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 9:134048212 (GRCh38)
9:136913334 (GRCh37)
Canonical SPDI:: NC_000009.12:134048211:G:A,NC_000009.12:134048211:G:C
Gene:: BRD3 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_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_000009.12:g.134048212G>A, NC_000009.12:g.134048212G>C, NC_000009.11:g.136913334G>A, NC_000009.11:g.136913334G>C, XM_006717291.4:c.957C>T, XM_006717291.4:c.957C>G, XM_006717291.3:c.957C>T, XM_006717291.3:c.957C>G, XM_006717291.2:c.957C>T, XM_006717291.2:c.957C>G, XM_006717291.1:c.957C>T, XM_006717291.1:c.957C>G, NM_007371.4:c.957C>T, NM_007371.4:c.957C>G, NM_007371.3:c.957C>T, NM_007371.3:c.957C>G, XM_011519052.3:c.957C>T, XM_011519052.3:c.957C>G, XM_011519052.2:c.957C>T, XM_011519052.2:c.957C>G, XM_011519052.1:c.957C>T, XM_011519052.1:c.957C>G, XM_017015165.3:c.957C>T, XM_017015165.3:c.957C>G, XM_017015165.2:c.957C>T, XM_017015165.2:c.957C>G, XM_017015165.1:c.957C>T, XM_017015165.1:c.957C>G, XM_047423904.1:c.957C>T, XM_047423904.1:c.957C>G, XM_047423905.1:c.957C>T, XM_047423905.1:c.957C>G, XM_047423903.1:c.957C>T, XM_047423903.1:c.957C>G, XM_047423906.1:c.957C>T, XM_047423906.1:c.957C>G

Select item 147505182015.

rs1475051820 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 9:134053316 (GRCh38)
9:136918438 (GRCh37)
Canonical SPDI:: NC_000009.12:134053315:C:A
Gene:: BRD3 (Varview), LOC100130548 (Varview)
Functional Consequence:: coding_sequence_variant,2KB_upstream_variant,upstream_transcript_variant,missense_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000009.12:g.134053316C>A, NC_000009.11:g.136918438C>A, XM_006717291.4:c.162G>T, XM_006717291.3:c.162G>T, XM_006717291.2:c.162G>T, XM_006717291.1:c.162G>T, NM_007371.4:c.162G>T, NM_007371.3:c.162G>T, XM_011519052.3:c.162G>T, XM_011519052.2:c.162G>T, XM_011519052.1:c.162G>T, XM_017015165.3:c.162G>T, XM_017015165.2:c.162G>T, XM_017015165.1:c.162G>T, XM_047423904.1:c.162G>T, XM_047423905.1:c.162G>T, XM_047423903.1:c.162G>T, XM_047423906.1:c.162G>T, XP_006717354.1:p.Gln54His, NP_031397.1:p.Gln54His, XP_011517354.1:p.Gln54His, XP_016870654.1:p.Gln54His, XP_047279860.1:p.Gln54His, XP_047279861.1:p.Gln54His, XP_047279859.1:p.Gln54His, XP_047279862.1:p.Gln54His

Select item 147497114316.

rs1474971143 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 9:134036306 (GRCh38)
9:136901428 (GRCh37)
Canonical SPDI:: NC_000009.12:134036305:G:A
Gene:: BRD3 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: A=0.000048/1 (ALFA)
A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000009.12:g.134036306G>A, NC_000009.11:g.136901428G>A, XM_006717291.4:c.1662C>T, XM_006717291.3:c.1662C>T, XM_006717291.2:c.1662C>T, XM_006717291.1:c.1662C>T, NM_007371.4:c.1662C>T, NM_007371.3:c.1662C>T, XM_011519052.3:c.1662C>T, XM_011519052.2:c.1662C>T, XM_011519052.1:c.1662C>T, XM_017015165.3:c.1662C>T, XM_017015165.2:c.1662C>T, XM_017015165.1:c.1662C>T, XM_047423904.1:c.1662C>T, XM_047423905.1:c.1662C>T, XM_047423903.1:c.1662C>T, XM_047423906.1:c.1662C>T

Select item 147369720717.

rs1473697207 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 9:134041802 (GRCh38)
9:136906924 (GRCh37)
Canonical SPDI:: NC_000009.12:134041801:C:T
Gene:: BRD3 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
T=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000009.12:g.134041802C>T, NC_000009.11:g.136906924C>T, XM_006717291.4:c.1365G>A, XM_006717291.3:c.1365G>A, XM_006717291.2:c.1365G>A, XM_006717291.1:c.1365G>A, NM_007371.4:c.1365G>A, NM_007371.3:c.1365G>A, XM_011519052.3:c.1365G>A, XM_011519052.2:c.1365G>A, XM_011519052.1:c.1365G>A, XM_017015165.3:c.1365G>A, XM_017015165.2:c.1365G>A, XM_017015165.1:c.1365G>A, XM_047423904.1:c.1365G>A, XM_047423905.1:c.1365G>A, XM_047423903.1:c.1365G>A, XM_047423906.1:c.1365G>A

Select item 147236753618.

rs1472367536 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 9:134048388 (GRCh38)
9:136913510 (GRCh37)
Canonical SPDI:: NC_000009.12:134048387:T:C
Gene:: BRD3 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000009.12:g.134048388T>C, NC_000009.11:g.136913510T>C, XM_006717291.4:c.781A>G, XM_006717291.3:c.781A>G, XM_006717291.2:c.781A>G, XM_006717291.1:c.781A>G, NM_007371.4:c.781A>G, NM_007371.3:c.781A>G, XM_011519052.3:c.781A>G, XM_011519052.2:c.781A>G, XM_011519052.1:c.781A>G, XM_017015165.3:c.781A>G, XM_017015165.2:c.781A>G, XM_017015165.1:c.781A>G, XM_047423904.1:c.781A>G, XM_047423905.1:c.781A>G, XM_047423903.1:c.781A>G, XM_047423906.1:c.781A>G, XP_006717354.1:p.Ser261Gly, NP_031397.1:p.Ser261Gly, XP_011517354.1:p.Ser261Gly, XP_016870654.1:p.Ser261Gly, XP_047279860.1:p.Ser261Gly, XP_047279861.1:p.Ser261Gly, XP_047279859.1:p.Ser261Gly, XP_047279862.1:p.Ser261Gly

Select item 146980903719.

rs1469809037 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 9:134036064 (GRCh38)
9:136901186 (GRCh37)
Canonical SPDI:: NC_000009.12:134036063:G:A
Gene:: BRD3 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000009.12:g.134036064G>A, NC_000009.11:g.136901186G>A, XM_006717291.4:c.1904C>T, XM_006717291.3:c.1904C>T, XM_006717291.2:c.1904C>T, XM_006717291.1:c.1904C>T, NM_007371.4:c.1904C>T, NM_007371.3:c.1904C>T, XM_011519052.3:c.1904C>T, XM_011519052.2:c.1904C>T, XM_011519052.1:c.1904C>T, XM_017015165.3:c.1904C>T, XM_017015165.2:c.1904C>T, XM_017015165.1:c.1904C>T, XM_047423904.1:c.1904C>T, XM_047423905.1:c.1904C>T, XM_047423903.1:c.1904C>T, XM_047423906.1:c.1904C>T, XP_006717354.1:p.Ser635Phe, NP_031397.1:p.Ser635Phe, XP_011517354.1:p.Ser635Phe, XP_016870654.1:p.Ser635Phe, XP_047279860.1:p.Ser635Phe, XP_047279861.1:p.Ser635Phe, XP_047279859.1:p.Ser635Phe, XP_047279862.1:p.Ser635Phe

Select item 146636064720.

rs1466360647 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 9:134048378 (GRCh38)
9:136913500 (GRCh37)
Canonical SPDI:: NC_000009.12:134048377:G:A
Gene:: BRD3 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000009.12:g.134048378G>A, NC_000009.11:g.136913500G>A, XM_006717291.4:c.791C>T, XM_006717291.3:c.791C>T, XM_006717291.2:c.791C>T, XM_006717291.1:c.791C>T, NM_007371.4:c.791C>T, NM_007371.3:c.791C>T, XM_011519052.3:c.791C>T, XM_011519052.2:c.791C>T, XM_011519052.1:c.791C>T, XM_017015165.3:c.791C>T, XM_017015165.2:c.791C>T, XM_017015165.1:c.791C>T, XM_047423904.1:c.791C>T, XM_047423905.1:c.791C>T, XM_047423903.1:c.791C>T, XM_047423906.1:c.791C>T, XP_006717354.1:p.Pro264Leu, NP_031397.1:p.Pro264Leu, XP_011517354.1:p.Pro264Leu, XP_016870654.1:p.Pro264Leu, XP_047279860.1:p.Pro264Leu, XP_047279861.1:p.Pro264Leu, XP_047279859.1:p.Pro264Leu, XP_047279862.1:p.Pro264Leu

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Result Filters

Clinical Significance

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Global MAF

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Items: 1 to 20 of 751

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