SNP Links for Protein (Select 41349482) - SNP

Links from Protein

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Select item 14879154211.

rs1487915421 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 12:11353848 (GRCh38)
12:11506782 (GRCh37)
Canonical SPDI:: NC_000012.12:11353847:G:A,NC_000012.12:11353847:G:C
Gene:: PRB1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
C=0.000004/1 (TOPMED)
HGVS:: NC_000012.12:g.11353848G>A, NC_000012.12:g.11353848G>C, NC_000012.11:g.11506782G>A, NC_000012.11:g.11506782G>C, NT_187658.1:g.548811G>A, NT_187658.1:g.548811G>C, NT_187588.1:g.23460C>T, NT_187588.1:g.23460C>G, NM_006248.4:c.504C>T, NM_006248.4:c.504C>G, NM_006248.3:c.504C>T, NM_006248.3:c.504C>G, NM_005039.3:c.255C>T, NM_005039.3:c.255C>G, NM_005039.4:c.255C>T, NM_005039.4:c.255C>G, NM_199353.2:c.255C>T, NM_199353.2:c.255C>G, NM_199354.2:c.255C>T, NM_199354.2:c.255C>G, NR_160307.2:n.293C>T, NR_160307.2:n.293C>G, NR_160307.1:n.292C>T, NR_160307.1:n.292C>G, NM_001367912.2:c.1059C>T, NM_001367912.2:c.1059C>G, NM_001367912.1:c.1059C>T, NM_001367912.1:c.1059C>G

Select item 14877005012.

rs1487700501 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 12:11353367 (GRCh38)
12:11506301 (GRCh37)
Canonical SPDI:: NC_000012.12:11353366:G:C
Gene:: PRB1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000012.12:g.11353367G>C, NC_000012.11:g.11506301G>C, NT_187658.1:g.548330G>C, NT_187588.1:g.23947C>G, NM_006248.4:c.991C>G, NM_006248.3:c.991C>G, NM_005039.3:c.736C>G, NM_005039.4:c.736C>G, NM_199353.2:c.337C>G, NR_160307.2:n.774C>G, NR_160307.1:n.773C>G, NM_001367912.2:c.1546C>G, NM_001367912.1:c.1546C>G

Select item 14864723463.

rs1486472346 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 12:11353461 (GRCh38)
12:11506395 (GRCh37)
Canonical SPDI:: NC_000012.12:11353460:A:T
Gene:: PRB1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: T=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000012.12:g.11353461A>T, NC_000012.11:g.11506395A>T, NT_187658.1:g.548424A>T, NT_187588.1:g.23853T>A, NM_006248.4:c.897T>A, NM_006248.3:c.897T>A, NM_005039.3:c.642T>A, NM_005039.4:c.642T>A, NR_160307.2:n.680T>A, NR_160307.1:n.679T>A, NM_001367912.2:c.1452T>A, NM_001367912.1:c.1452T>A

Select item 14862340584.

rs1486234058 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 12:11353318 (GRCh38)
12:11506252 (GRCh37)
Canonical SPDI:: NC_000012.12:11353317:C:T
Gene:: PRB1 (Varview)
Functional Consequence:: non_coding_transcript_variant
HGVS:: NC_000012.12:g.11353318C>T, NC_000012.11:g.11506252C>T, NT_187658.1:g.548281C>T, NT_187588.1:g.23996G>A, NM_006248.4:c.1040G>A, NM_006248.3:c.1040G>A, NM_005039.3:c.785G>A, NM_005039.4:c.785G>A, NM_199353.2:c.386G>A, NM_199354.2:c.326G>A, NR_160307.2:n.823G>A, NR_160307.1:n.822G>A, NM_001367912.2:c.1595G>A, NM_001367912.1:c.1595G>A

Select item 14845463665.

rs1484546366 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: 12:11353653 (GRCh38)
12:11506587 (GRCh37)
Canonical SPDI:: NC_000012.12:11353652:A:G,NC_000012.12:11353652:A:T
Gene:: PRB1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
G=0.00934/27 (KOREAN)
HGVS:: NC_000012.12:g.11353653A>G, NC_000012.12:g.11353653A>T, NC_000012.11:g.11506587A>G, NC_000012.11:g.11506587A>T, NT_187658.1:g.548616A>G, NT_187658.1:g.548616A>T, NT_187588.1:g.23658T>C, NT_187588.1:g.23658T>A, NM_006248.4:c.702T>C, NM_006248.4:c.702T>A, NM_006248.3:c.702T>C, NM_006248.3:c.702T>A, NM_005039.3:c.450T>C, NM_005039.3:c.450T>A, NM_005039.4:c.450T>C, NM_005039.4:c.450T>A, NR_160307.2:n.488T>C, NR_160307.2:n.488T>A, NR_160307.1:n.487T>C, NR_160307.1:n.487T>A, NM_001367912.2:c.1257T>C, NM_001367912.2:c.1257T>A, NM_001367912.1:c.1257T>C, NM_001367912.1:c.1257T>A

Select item 14831485286.

rs1483148528 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 12:11353408 (GRCh38)
12:11506342 (GRCh37)
Canonical SPDI:: NC_000012.12:11353407:C:A
Gene:: PRB1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
A=0.000004/1 (TOPMED)
HGVS:: NC_000012.12:g.11353408C>A, NC_000012.11:g.11506342C>A, NT_187658.1:g.548371C>A, NT_187588.1:g.23906G>T, NM_006248.4:c.950G>T, NM_006248.3:c.950G>T, NM_005039.3:c.695G>T, NM_005039.4:c.695G>T, NR_160307.2:n.733G>T, NR_160307.1:n.732G>T, NM_001367912.2:c.1505G>T, NM_001367912.1:c.1505G>T

Select item 14829600517.

rs1482960051 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 12:11353744 (GRCh38)
12:11506678 (GRCh37)
Canonical SPDI:: NC_000012.12:11353743:C:T
Gene:: PRB1 (Varview)
Functional Consequence:: non_coding_transcript_variant
HGVS:: NC_000012.12:g.11353744C>T, NC_000012.11:g.11506678C>T, NT_187658.1:g.548707C>T, NT_187588.1:g.23564G>A, NM_006248.4:c.608G>A, NM_006248.3:c.608G>A, NM_005039.3:c.359G>A, NM_005039.4:c.359G>A, NR_160307.2:n.397G>A, NR_160307.1:n.396G>A, NM_001367912.2:c.1163G>A, NM_001367912.1:c.1163G>A

Select item 14821613468.

rs1482161346 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 12:11353238 (GRCh38)
12:11506172 (GRCh37)
Canonical SPDI:: NC_000012.12:11353237:C:A
Gene:: PRB1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000012.12:g.11353238C>A, NC_000012.11:g.11506172C>A, NT_187658.1:g.548201C>A, NT_187588.1:g.24076G>T, NM_006248.4:c.1120G>T, NM_006248.3:c.1120G>T, NM_005039.3:c.865G>T, NM_005039.4:c.865G>T, NM_199353.2:c.466G>T, NM_199354.2:c.406G>T, NR_160307.2:n.903G>T, NR_160307.1:n.902G>T, NM_001367912.2:c.1675G>T, NM_001367912.1:c.1675G>T

Select item 14776670449.

rs1477667044 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 12:11354531 (GRCh38)
12:11507465 (GRCh37)
Canonical SPDI:: NC_000012.12:11354530:A:C
Gene:: PRB1 (Varview)
Functional Consequence:: non_coding_transcript_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_000012.12:g.11354531A>C, NC_000012.11:g.11507465A>C, NT_187658.1:g.549494A>C, NT_187588.1:g.21972T>G, NM_006248.4:c.88T>G, NM_006248.3:c.88T>G, NM_005039.3:c.88T>G, NM_005039.4:c.88T>G, NR_160307.2:n.126T>G, NR_160307.1:n.125T>G, NM_199353.2:c.88T>G, NM_199354.2:c.88T>G, NM_001367912.2:c.88T>G, NM_001367912.1:c.88T>G

Select item 147585176210.

rs1475851762 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 12:11353414 (GRCh38)
12:11506348 (GRCh37)
Canonical SPDI:: NC_000012.12:11353413:G:C
Gene:: PRB1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000012.12:g.11353414G>C, NC_000012.11:g.11506348G>C, NT_187658.1:g.548377G>C, NT_187588.1:g.23900C>G, NM_006248.4:c.944C>G, NM_006248.3:c.944C>G, NM_005039.3:c.689C>G, NM_005039.4:c.689C>G, NR_160307.2:n.727C>G, NR_160307.1:n.726C>G, NM_001367912.2:c.1499C>G, NM_001367912.1:c.1499C>G

Select item 147421762011.

rs1474217620 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 12:11353233 (GRCh38)
12:11506167 (GRCh37)
Canonical SPDI:: NC_000012.12:11353232:G:C
Gene:: PRB1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000008/1 (GnomAD)
C=0.000008/2 (TOPMED)
HGVS:: NC_000012.12:g.11353233G>C, NC_000012.11:g.11506167G>C, NT_187658.1:g.548196G>C, NT_187588.1:g.24081C>G, NM_006248.4:c.1125C>G, NM_006248.3:c.1125C>G, NM_005039.3:c.870C>G, NM_005039.4:c.870C>G, NM_199353.2:c.471C>G, NM_199354.2:c.411C>G, NR_160307.2:n.908C>G, NR_160307.1:n.907C>G, NM_001367912.2:c.1680C>G, NM_001367912.1:c.1680C>G

Select item 147262155412.

rs1472621554 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 12:11353853 (GRCh38)
12:11506787 (GRCh37)
Canonical SPDI:: NC_000012.12:11353852:C:T
Gene:: PRB1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000012.12:g.11353853C>T, NC_000012.11:g.11506787C>T, NT_187658.1:g.548816C>T, NT_187588.1:g.23452G>A, NM_006248.4:c.496G>A, NM_006248.3:c.496G>A, NM_005039.3:c.250G>A, NM_005039.4:c.250G>A, NM_199353.2:c.250G>A, NM_199354.2:c.250G>A, NR_160307.2:n.288G>A, NR_160307.1:n.287G>A, NM_001367912.2:c.1051G>A, NM_001367912.1:c.1051G>A

Select item 147173103013.

rs1471731030 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 12:11353467 (GRCh38)
12:11506401 (GRCh37)
Canonical SPDI:: NC_000012.12:11353466:G:A,NC_000012.12:11353466:G:T
Gene:: PRB1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0.00008/1 (ALFA)
HGVS:: NC_000012.12:g.11353467G>A, NC_000012.12:g.11353467G>T, NC_000012.11:g.11506401G>A, NC_000012.11:g.11506401G>T, NT_187658.1:g.548430G>A, NT_187658.1:g.548430G>T, NT_187588.1:g.23847T>C, NT_187588.1:g.23847T>A, NM_006248.4:c.891T>C, NM_006248.4:c.891T>A, NM_006248.3:c.891T>C, NM_006248.3:c.891T>A, NM_005039.3:c.636C>T, NM_005039.3:c.636C>A, NM_005039.4:c.636C>T, NM_005039.4:c.636C>A, NR_160307.2:n.674C>T, NR_160307.2:n.674C>A, NR_160307.1:n.673C>T, NR_160307.1:n.673C>A, NM_001367912.2:c.1446T>C, NM_001367912.2:c.1446T>A, NM_001367912.1:c.1446T>C, NM_001367912.1:c.1446T>A

Select item 146882098514.

rs1468820985 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 12:11353189 (GRCh38)
12:11506123 (GRCh37)
Canonical SPDI:: NC_000012.12:11353188:T:A
Gene:: PRB1 (Varview)
Functional Consequence:: non_coding_transcript_variant
HGVS:: NC_000012.12:g.11353189T>A, NC_000012.11:g.11506123T>A, NT_187658.1:g.548152T>A, NT_187588.1:g.24125A>T, NM_006248.4:c.1169A>T, NM_006248.3:c.1169A>T, NM_005039.3:c.914A>T, NM_005039.4:c.914A>T, NM_199353.2:c.515A>T, NM_199354.2:c.455A>T, NR_160307.2:n.952A>T, NR_160307.1:n.951A>T, NM_001367912.2:c.1724A>T, NM_001367912.1:c.1724A>T

Select item 146525405715.

rs1465254057 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C [Show Flanks]
Chromosome:: 12:11353302 (GRCh38)
12:11506236 (GRCh37)
Canonical SPDI:: NC_000012.12:11353301:T:A,NC_000012.12:11353301:T:C
Gene:: PRB1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
C=0.000004/1 (GnomAD_exomes)
A=0.000004/1 (TOPMED)
A=0.000008/1 (GnomAD)
HGVS:: NC_000012.12:g.11353302T>A, NC_000012.12:g.11353302T>C, NC_000012.11:g.11506236T>A, NC_000012.11:g.11506236T>C, NT_187658.1:g.548265T>A, NT_187658.1:g.548265T>C, NT_187588.1:g.24012A>T, NT_187588.1:g.24012A>G, NM_006248.4:c.1056A>T, NM_006248.4:c.1056A>G, NM_006248.3:c.1056A>T, NM_006248.3:c.1056A>G, NM_005039.3:c.801A>T, NM_005039.3:c.801A>G, NM_005039.4:c.801A>T, NM_005039.4:c.801A>G, NR_160307.2:n.839A>T, NR_160307.2:n.839A>G, NR_160307.1:n.838A>T, NR_160307.1:n.838A>G, NM_199353.2:c.402A>T, NM_199353.2:c.402A>G, NM_199354.2:c.342A>T, NM_199354.2:c.342A>G, NM_001367912.2:c.1611A>T, NM_001367912.2:c.1611A>G, NM_001367912.1:c.1611A>T, NM_001367912.1:c.1611A>G

Select item 146434446516.

rs1464344465 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C,T [Show Flanks]
Chromosome:: 12:11353602 (GRCh38)
12:11506536 (GRCh37)
Canonical SPDI:: NC_000012.12:11353601:G:C,NC_000012.12:11353601:G:T
Gene:: PRB1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000012/2 (GnomAD_exomes)
HGVS:: NC_000012.12:g.11353602G>C, NC_000012.12:g.11353602G>T, NC_000012.11:g.11506536G>C, NC_000012.11:g.11506536G>T, NT_187658.1:g.548565G>C, NT_187658.1:g.548565G>T, NT_187588.1:g.23709C>G, NT_187588.1:g.23709C>A, NM_006248.4:c.753C>G, NM_006248.4:c.753C>A, NM_006248.3:c.753C>G, NM_006248.3:c.753C>A, NM_005039.3:c.501C>G, NM_005039.3:c.501C>A, NM_005039.4:c.501C>G, NM_005039.4:c.501C>A, NR_160307.2:n.539C>G, NR_160307.2:n.539C>A, NR_160307.1:n.538C>G, NR_160307.1:n.538C>A, NM_001367912.2:c.1308C>G, NM_001367912.2:c.1308C>A, NM_001367912.1:c.1308C>G, NM_001367912.1:c.1308C>A

Select item 146139898317.

rs1461398983 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 12:11353800 (GRCh38)
12:11506734 (GRCh37)
Canonical SPDI:: NC_000012.12:11353799:G:A
Gene:: PRB1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000012.12:g.11353800G>A, NC_000012.11:g.11506734G>A, NT_187658.1:g.548763G>A, NT_187588.1:g.23508C>T, NM_006248.4:c.552C>T, NM_006248.3:c.552C>T, NM_005039.3:c.303C>T, NM_005039.4:c.303C>T, NM_199353.2:c.303C>T, NM_199354.2:c.303C>T, NR_160307.2:n.341C>T, NR_160307.1:n.340C>T, NM_001367912.2:c.1107C>T, NM_001367912.1:c.1107C>T

Select item 146000169618.

rs1460001696 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C [Show Flanks]
Chromosome:: 12:11354526 (GRCh38)
12:11507460 (GRCh37)
Canonical SPDI:: NC_000012.12:11354525:T:A,NC_000012.12:11354525:T:C
Gene:: PRB1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by cluster
HGVS:: NC_000012.12:g.11354526T>A, NC_000012.12:g.11354526T>C, NC_000012.11:g.11507460T>A, NC_000012.11:g.11507460T>C, NT_187658.1:g.549489T>A, NT_187658.1:g.549489T>C, NT_187588.1:g.21977A>T, NT_187588.1:g.21977A>G, NM_006248.4:c.93A>T, NM_006248.4:c.93A>G, NM_006248.3:c.93A>T, NM_006248.3:c.93A>G, NM_005039.3:c.93A>T, NM_005039.3:c.93A>G, NM_005039.4:c.93A>T, NM_005039.4:c.93A>G, NR_160307.2:n.131A>T, NR_160307.2:n.131A>G, NR_160307.1:n.130A>T, NR_160307.1:n.130A>G, NM_199353.2:c.93A>T, NM_199353.2:c.93A>G, NM_199354.2:c.93A>T, NM_199354.2:c.93A>G, NM_001367912.2:c.93A>T, NM_001367912.2:c.93A>G, NM_001367912.1:c.93A>T, NM_001367912.1:c.93A>G

Select item 145967946319.

rs1459679463 [Homo sapiens]

Variant type:: DELINS
Alleles:: G>- [Show Flanks]
Chromosome:: 12:11353270 (GRCh38)
12:11506204 (GRCh37)
Canonical SPDI:: NC_000012.12:11353269:GG:G
Gene:: PRB1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: GG=0./0 (ALFA)
-=0.000008/2 (TOPMED)
HGVS:: NC_000012.12:g.11353271del, NC_000012.11:g.11506205del, NT_187658.1:g.548234del, NT_187588.1:g.24044del, NM_006248.4:c.1088del, NM_006248.3:c.1088del, NM_005039.3:c.833del, NM_005039.4:c.833del, NM_199353.2:c.434del, NM_199354.2:c.374del, NR_160307.2:n.871del, NR_160307.1:n.870del, NM_001367912.2:c.1643del, NM_001367912.1:c.1643del

Select item 145895282220.

rs1458952822 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 12:11353973 (GRCh38)
12:11506907 (GRCh37)
Canonical SPDI:: NC_000012.12:11353972:C:G,NC_000012.12:11353972:C:T
Gene:: PRB1 (Varview)
Functional Consequence:: non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0.000031/1 (ALFA)
T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000012.12:g.11353973C>G, NC_000012.12:g.11353973C>T, NC_000012.11:g.11506907C>G, NC_000012.11:g.11506907C>T, NT_187658.1:g.548936C>G, NT_187658.1:g.548936C>T, NT_187588.1:g.23332G>C, NT_187588.1:g.23332G>A, NM_006248.4:c.376G>C, NM_006248.4:c.376G>A, NM_006248.3:c.376G>C, NM_006248.3:c.376G>A, NM_005039.3:c.130G>C, NM_005039.3:c.130G>A, NM_005039.4:c.130G>C, NM_005039.4:c.130G>A, NM_199353.2:c.130G>C, NM_199353.2:c.130G>A, NM_199354.2:c.130G>C, NM_199354.2:c.130G>A, NR_160307.2:n.168G>C, NR_160307.2:n.168G>A, NR_160307.1:n.167G>C, NR_160307.1:n.167G>A, NM_001367912.2:c.931G>C, NM_001367912.2:c.931G>A, NM_001367912.1:c.931G>C, NM_001367912.1:c.931G>A

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