SNP Links for Protein (Select 13027612) - SNP

Links from Protein

Items: 1 to 20 of 248

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Select item 14891802211.

rs1489180221 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 4:52865516 (GRCh38)
4:53731683 (GRCh37)
Canonical SPDI:: NC_000004.12:52865515:A:G
Gene:: RASL11B (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (GnomAD_exomes)
G=0.000008/2 (TOPMED)
HGVS:: NC_000004.12:g.52865516A>G, NC_000004.11:g.53731683A>G, NM_023940.3:c.458A>G, NM_023940.2:c.458A>G, NP_076429.1:p.Lys153Arg

Select item 14888546972.

rs1488854697 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 4:52864527 (GRCh38)
4:53730694 (GRCh37)
Canonical SPDI:: NC_000004.12:52864526:T:G
Gene:: RASL11B (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000004.12:g.52864527T>G, NC_000004.11:g.53730694T>G, NM_023940.3:c.249T>G, NM_023940.2:c.249T>G

Select item 14822604673.

rs1482260467 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 4:52865365 (GRCh38)
4:53731532 (GRCh37)
Canonical SPDI:: NC_000004.12:52865364:C:T
Gene:: RASL11B (Varview)
Functional Consequence:: coding_sequence_variant,stop_gained
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000004.12:g.52865365C>T, NC_000004.11:g.53731532C>T, NM_023940.3:c.307C>T, NM_023940.2:c.307C>T, NP_076429.1:p.Gln103Ter

Select item 14806541074.

rs1480654107 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 4:52863302 (GRCh38)
4:53729469 (GRCh37)
Canonical SPDI:: NC_000004.12:52863301:C:T
Gene:: RASL11B (Varview), LOC124900700 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000004.12:g.52863302C>T, NC_000004.11:g.53729469C>T, NM_023940.3:c.177C>T, NM_023940.2:c.177C>T

Select item 14776746825.

rs1477674682 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 4:52862623 (GRCh38)
4:53728790 (GRCh37)
Canonical SPDI:: NC_000004.12:52862622:T:C,NC_000004.12:52862622:T:G
Gene:: RASL11B (Varview), LOC124900700 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,upstream_transcript_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000004.12:g.52862623T>C, NC_000004.12:g.52862623T>G, NC_000004.11:g.53728790T>C, NC_000004.11:g.53728790T>G, NG_063806.1:g.382T>C, NG_063806.1:g.382T>G, NM_023940.3:c.116T>C, NM_023940.3:c.116T>G, NM_023940.2:c.116T>C, NM_023940.2:c.116T>G, NP_076429.1:p.Val39Ala, NP_076429.1:p.Val39Gly

Select item 14765345586.

rs1476534558 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 4:52865524 (GRCh38)
4:53731691 (GRCh37)
Canonical SPDI:: NC_000004.12:52865523:C:G
Gene:: RASL11B (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000004.12:g.52865524C>G, NC_000004.11:g.53731691C>G, NM_023940.3:c.466C>G, NM_023940.2:c.466C>G, NP_076429.1:p.Leu156Val

Select item 14763518657.

rs1476351865 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 4:52865428 (GRCh38)
4:53731595 (GRCh37)
Canonical SPDI:: NC_000004.12:52865427:A:G
Gene:: RASL11B (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000004.12:g.52865428A>G, NC_000004.11:g.53731595A>G, NM_023940.3:c.370A>G, NM_023940.2:c.370A>G, NP_076429.1:p.Lys124Glu

Select item 14758960648.

rs1475896064 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 4:52864529 (GRCh38)
4:53730696 (GRCh37)
Canonical SPDI:: NC_000004.12:52864528:A:G
Gene:: RASL11B (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000004.12:g.52864529A>G, NC_000004.11:g.53730696A>G, NM_023940.3:c.251A>G, NM_023940.2:c.251A>G, NP_076429.1:p.Gln84Arg

Select item 14742095109.

rs1474209510 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 4:52865460 (GRCh38)
4:53731627 (GRCh37)
Canonical SPDI:: NC_000004.12:52865459:G:T
Gene:: RASL11B (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)
T=0.000008/2 (TOPMED)
HGVS:: NC_000004.12:g.52865460G>T, NC_000004.11:g.53731627G>T, NM_023940.3:c.402G>T, NM_023940.2:c.402G>T, NP_076429.1:p.Gln134His

Select item 146633477910.

rs1466334779 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 4:52865704 (GRCh38)
4:53731871 (GRCh37)
Canonical SPDI:: NC_000004.12:52865703:A:T
Gene:: RASL11B (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0./0 (GnomAD)
T=0.000016/4 (GnomAD_exomes)
HGVS:: NC_000004.12:g.52865704A>T, NC_000004.11:g.53731871A>T, NM_023940.3:c.646A>T, NM_023940.2:c.646A>T, NP_076429.1:p.Thr216Ser

Select item 146357416811.

rs1463574168 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 4:52862556 (GRCh38)
4:53728723 (GRCh37)
Canonical SPDI:: NC_000004.12:52862555:G:A,NC_000004.12:52862555:G:C
Gene:: RASL11B (Varview), LOC124900700 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant,coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000004.12:g.52862556G>A, NC_000004.12:g.52862556G>C, NC_000004.11:g.53728723G>A, NC_000004.11:g.53728723G>C, NG_063806.1:g.315G>A, NG_063806.1:g.315G>C, NM_023940.3:c.49G>A, NM_023940.3:c.49G>C, NM_023940.2:c.49G>A, NM_023940.2:c.49G>C, NP_076429.1:p.Gly17Ser, NP_076429.1:p.Gly17Arg

Select item 146051909512.

rs1460519095 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C [Show Flanks]
Chromosome:: 4:52862605 (GRCh38)
4:53728772 (GRCh37)
Canonical SPDI:: NC_000004.12:52862604:T:A,NC_000004.12:52862604:T:C
Gene:: RASL11B (Varview), LOC124900700 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant,coding_sequence_variant,missense_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_000004.12:g.52862605T>A, NC_000004.12:g.52862605T>C, NC_000004.11:g.53728772T>A, NC_000004.11:g.53728772T>C, NG_063806.1:g.364T>A, NG_063806.1:g.364T>C, NM_023940.3:c.98T>A, NM_023940.3:c.98T>C, NM_023940.2:c.98T>A, NM_023940.2:c.98T>C, NP_076429.1:p.Leu33Gln, NP_076429.1:p.Leu33Pro

Select item 145793713713.

rs1457937137 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 4:52865675 (GRCh38)
4:53731842 (GRCh37)
Canonical SPDI:: NC_000004.12:52865674:A:T
Gene:: RASL11B (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000004.12:g.52865675A>T, NC_000004.11:g.53731842A>T, NM_023940.3:c.617A>T, NM_023940.2:c.617A>T, NP_076429.1:p.Gln206Leu

Select item 145749694814.

rs1457496948 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 4:52865349 (GRCh38)
4:53731516 (GRCh37)
Canonical SPDI:: NC_000004.12:52865348:C:T
Gene:: RASL11B (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (GnomAD_exomes)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000004.12:g.52865349C>T, NC_000004.11:g.53731516C>T, NM_023940.3:c.291C>T, NM_023940.2:c.291C>T

Select item 145388716115.

rs1453887161 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 4:52865724 (GRCh38)
4:53731891 (GRCh37)
Canonical SPDI:: NC_000004.12:52865723:C:G
Gene:: RASL11B (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000004.12:g.52865724C>G, NC_000004.11:g.53731891C>G, NM_023940.3:c.666C>G, NM_023940.2:c.666C>G

Select item 145307989516.

rs1453079895 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 4:52864537 (GRCh38)
4:53730704 (GRCh37)
Canonical SPDI:: NC_000004.12:52864536:G:A
Gene:: RASL11B (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000004.12:g.52864537G>A, NC_000004.11:g.53730704G>A, NM_023940.3:c.259G>A, NM_023940.2:c.259G>A, NP_076429.1:p.Asp87Asn

Select item 144848381817.

rs1448483818 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 4:52862595 (GRCh38)
4:53728762 (GRCh37)
Canonical SPDI:: NC_000004.12:52862594:G:A
Gene:: RASL11B (Varview), LOC124900700 (Varview)
Functional Consequence:: upstream_transcript_variant,2KB_upstream_variant,missense_variant,coding_sequence_variant
HGVS:: NC_000004.12:g.52862595G>A, NC_000004.11:g.53728762G>A, NG_063806.1:g.354G>A, NM_023940.3:c.88G>A, NM_023940.2:c.88G>A, NP_076429.1:p.Gly30Ser

Select item 144187639318.

rs1441876393 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 4:52865619 (GRCh38)
4:53731786 (GRCh37)
Canonical SPDI:: NC_000004.12:52865618:T:C
Gene:: RASL11B (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000004.12:g.52865619T>C, NC_000004.11:g.53731786T>C, NM_023940.3:c.561T>C, NM_023940.2:c.561T>C

Select item 144139915819.

rs1441399158 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 4:52865607 (GRCh38)
4:53731774 (GRCh37)
Canonical SPDI:: NC_000004.12:52865606:C:T
Gene:: RASL11B (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (GnomAD_exomes)
T=0.000007/1 (GnomAD)
T=0.000008/2 (TOPMED)
HGVS:: NC_000004.12:g.52865607C>T, NC_000004.11:g.53731774C>T, NM_023940.3:c.549C>T, NM_023940.2:c.549C>T

Select item 143339002120.

rs1433390021 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 4:52862570 (GRCh38)
4:53728737 (GRCh37)
Canonical SPDI:: NC_000004.12:52862569:C:T
Gene:: RASL11B (Varview), LOC124900700 (Varview)
Functional Consequence:: 2KB_upstream_variant,synonymous_variant,upstream_transcript_variant,coding_sequence_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000004.12:g.52862570C>T, NC_000004.11:g.53728737C>T, NG_063806.1:g.329C>T, NM_023940.3:c.63C>T, NM_023940.2:c.63C>T

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Items: 1 to 20 of 248

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