SNP Links for Protein (Select 530407651) - SNP

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Links from Protein

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Select item 14900148261.

rs1490014826 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 16:1968831 (GRCh38)
16:2018832 (GRCh37)
Canonical SPDI:: NC_000016.10:1968830:A:G
Gene:: RNF151 (Varview)
Functional Consequence:: coding_sequence_variant,3_prime_UTR_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
HGVS:: NC_000016.10:g.1968831A>G, NC_000016.9:g.2018832A>G, NW_025791799.1:g.34979A>G, NM_174903.6:c.644A>G, NM_174903.5:c.644A>G, NM_174903.4:c.644A>G, XM_005255129.5:c.671A>G, XM_005255129.4:c.671A>G, XM_005255129.3:c.671A>G, XM_005255129.2:c.671A>G, XM_005255129.1:c.671A>G, NM_001348711.2:c.*404A>G, NM_001348711.1:c.*404A>G, NP_777563.2:p.Glu215Gly, XP_005255186.1:p.Glu224Gly

Select item 14891504432.

rs1489150443 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 16:1967818 (GRCh38)
16:2017819 (GRCh37)
Canonical SPDI:: NC_000016.10:1967817:C:G
Gene:: RNF151 (Varview)
Functional Consequence:: coding_sequence_variant,intron_variant,synonymous_variant
HGVS:: NC_000016.10:g.1967818C>G, NC_000016.9:g.2017819C>G, NW_025791799.1:g.33966C>G, NM_174903.6:c.243C>G, NM_174903.5:c.243C>G, NM_174903.4:c.243C>G, XM_005255129.5:c.270C>G, XM_005255129.4:c.270C>G, XM_005255129.3:c.270C>G, XM_005255129.2:c.270C>G, XM_005255129.1:c.270C>G

Select item 14885684743.

rs1488568474 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 16:1967764 (GRCh38)
16:2017765 (GRCh37)
Canonical SPDI:: NC_000016.10:1967763:G:A
Gene:: RNF151 (Varview)
Functional Consequence:: coding_sequence_variant,intron_variant,synonymous_variant
HGVS:: NC_000016.10:g.1967764G>A, NC_000016.9:g.2017765G>A, NW_025791799.1:g.33912G>A, NM_174903.6:c.189G>A, NM_174903.5:c.189G>A, NM_174903.4:c.189G>A, XM_005255129.5:c.216G>A, XM_005255129.4:c.216G>A, XM_005255129.3:c.216G>A, XM_005255129.2:c.216G>A, XM_005255129.1:c.216G>A

Select item 14879160694.

rs1487916069 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 16:1968635 (GRCh38)
16:2018636 (GRCh37)
Canonical SPDI:: NC_000016.10:1968634:C:G,NC_000016.10:1968634:C:T
Gene:: RNF151 (Varview)
Functional Consequence:: coding_sequence_variant,3_prime_UTR_variant,missense_variant,synonymous_variant
Validated:: by frequency,by cluster
MAF:: T=0.000006/1 (GnomAD_exomes)
HGVS:: NC_000016.10:g.1968635C>G, NC_000016.10:g.1968635C>T, NC_000016.9:g.2018636C>G, NC_000016.9:g.2018636C>T, NW_025791799.1:g.34783C>G, NW_025791799.1:g.34783C>T, NM_174903.6:c.448C>G, NM_174903.6:c.448C>T, NM_174903.5:c.448C>G, NM_174903.5:c.448C>T, NM_174903.4:c.448C>G, NM_174903.4:c.448C>T, XM_005255129.5:c.475C>G, XM_005255129.5:c.475C>T, XM_005255129.4:c.475C>G, XM_005255129.4:c.475C>T, XM_005255129.3:c.475C>G, XM_005255129.3:c.475C>T, XM_005255129.2:c.475C>G, XM_005255129.2:c.475C>T, XM_005255129.1:c.475C>G, XM_005255129.1:c.475C>T, NM_001348711.2:c.*208C>G, NM_001348711.2:c.*208C>T, NM_001348711.1:c.*208C>G, NM_001348711.1:c.*208C>T, NP_777563.2:p.Leu150Val, XP_005255186.1:p.Leu159Val

Select item 14869372575.

rs1486937257 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 16:1968814 (GRCh38)
16:2018815 (GRCh37)
Canonical SPDI:: NC_000016.10:1968813:A:G
Gene:: RNF151 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000005/1 (GnomAD_exomes)
G=0.000007/1 (GnomAD)
HGVS:: NC_000016.10:g.1968814A>G, NC_000016.9:g.2018815A>G, NW_025791799.1:g.34962A>G, NM_174903.6:c.627A>G, NM_174903.5:c.627A>G, NM_174903.4:c.627A>G, XM_005255129.5:c.654A>G, XM_005255129.4:c.654A>G, XM_005255129.3:c.654A>G, XM_005255129.2:c.654A>G, XM_005255129.1:c.654A>G, NM_001348711.2:c.*387A>G, NM_001348711.1:c.*387A>G

Select item 14858694756.

rs1485869475 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 16:1968670 (GRCh38)
16:2018671 (GRCh37)
Canonical SPDI:: NC_000016.10:1968669:C:T
Gene:: RNF151 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant,3_prime_UTR_variant
HGVS:: NC_000016.10:g.1968670C>T, NC_000016.9:g.2018671C>T, NW_025791799.1:g.34818C>T, NM_174903.6:c.483C>T, NM_174903.5:c.483C>T, NM_174903.4:c.483C>T, XM_005255129.5:c.510C>T, XM_005255129.4:c.510C>T, XM_005255129.3:c.510C>T, XM_005255129.2:c.510C>T, XM_005255129.1:c.510C>T, NM_001348711.2:c.*243C>T, NM_001348711.1:c.*243C>T

Select item 14811931927.

rs1481193192 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 16:1968766 (GRCh38)
16:2018767 (GRCh37)
Canonical SPDI:: NC_000016.10:1968765:C:T
Gene:: RNF151 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: T=0.000111/1 (ALFA)
T=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000016.10:g.1968766C>T, NC_000016.9:g.2018767C>T, NW_025791799.1:g.34914C>T, NM_174903.6:c.579C>T, NM_174903.5:c.579C>T, NM_174903.4:c.579C>T, XM_005255129.5:c.606C>T, XM_005255129.4:c.606C>T, XM_005255129.3:c.606C>T, XM_005255129.2:c.606C>T, XM_005255129.1:c.606C>T, NM_001348711.2:c.*339C>T, NM_001348711.1:c.*339C>T

Select item 14784196788.

rs1478419678 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 16:1967281 (GRCh38)
16:2017282 (GRCh37)
Canonical SPDI:: NC_000016.10:1967280:G:A
Gene:: RNF151 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000016.10:g.1967281G>A, NC_000016.9:g.2017282G>A, NW_025791799.1:g.33429G>A, NM_174903.6:c.11G>A, NM_174903.5:c.11G>A, NM_174903.4:c.11G>A, XM_005255129.5:c.38G>A, XM_005255129.4:c.38G>A, XM_005255129.3:c.38G>A, XM_005255129.2:c.38G>A, XM_005255129.1:c.38G>A, NM_001348711.2:c.11G>A, NM_001348711.1:c.11G>A, NP_777563.2:p.Gly4Glu, XP_005255186.1:p.Gly13Glu, NP_001335640.1:p.Gly4Glu

Select item 14771727859.

rs1477172785 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 16:1968596 (GRCh38)
16:2018597 (GRCh37)
Canonical SPDI:: NC_000016.10:1968595:G:A
Gene:: RNF151 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0./0 (GnomAD)
HGVS:: NC_000016.10:g.1968596G>A, NC_000016.9:g.2018597G>A, NW_025791799.1:g.34744G>A, NM_174903.6:c.409G>A, NM_174903.5:c.409G>A, NM_174903.4:c.409G>A, XM_005255129.5:c.436G>A, XM_005255129.4:c.436G>A, XM_005255129.3:c.436G>A, XM_005255129.2:c.436G>A, XM_005255129.1:c.436G>A, NM_001348711.2:c.*169G>A, NM_001348711.1:c.*169G>A, NP_777563.2:p.Gly137Arg, XP_005255186.1:p.Gly146Arg

Select item 147502207610.

rs1475022076 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 16:1968624 (GRCh38)
16:2018625 (GRCh37)
Canonical SPDI:: NC_000016.10:1968623:G:A
Gene:: RNF151 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000016.10:g.1968624G>A, NC_000016.9:g.2018625G>A, NW_025791799.1:g.34772G>A, NM_174903.6:c.437G>A, NM_174903.5:c.437G>A, NM_174903.4:c.437G>A, XM_005255129.5:c.464G>A, XM_005255129.4:c.464G>A, XM_005255129.3:c.464G>A, XM_005255129.2:c.464G>A, XM_005255129.1:c.464G>A, NM_001348711.2:c.*197G>A, NM_001348711.1:c.*197G>A, NP_777563.2:p.Cys146Tyr, XP_005255186.1:p.Cys155Tyr

Select item 147043690911.

rs1470436909 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 16:1967796 (GRCh38)
16:2017797 (GRCh37)
Canonical SPDI:: NC_000016.10:1967795:A:G
Gene:: RNF151 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000016.10:g.1967796A>G, NC_000016.9:g.2017797A>G, NW_025791799.1:g.33944A>G, NM_174903.6:c.221A>G, NM_174903.5:c.221A>G, NM_174903.4:c.221A>G, XM_005255129.5:c.248A>G, XM_005255129.4:c.248A>G, XM_005255129.3:c.248A>G, XM_005255129.2:c.248A>G, XM_005255129.1:c.248A>G, NP_777563.2:p.Lys74Arg, XP_005255186.1:p.Lys83Arg

Select item 146725636912.

rs1467256369 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 16:1967733 (GRCh38)
16:2017734 (GRCh37)
Canonical SPDI:: NC_000016.10:1967732:C:T
Gene:: RNF151 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,intron_variant
HGVS:: NC_000016.10:g.1967733C>T, NC_000016.9:g.2017734C>T, NW_025791799.1:g.33881C>T, NM_174903.6:c.158C>T, NM_174903.5:c.158C>T, NM_174903.4:c.158C>T, XM_005255129.5:c.185C>T, XM_005255129.4:c.185C>T, XM_005255129.3:c.185C>T, XM_005255129.2:c.185C>T, XM_005255129.1:c.185C>T, NP_777563.2:p.Thr53Ile, XP_005255186.1:p.Thr62Ile

Select item 146423474713.

rs1464234747 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C [Show Flanks]
Chromosome:: 16:1968778 (GRCh38)
16:2018779 (GRCh37)
Canonical SPDI:: NC_000016.10:1968777:T:A,NC_000016.10:1968777:T:C
Gene:: RNF151 (Varview)
Functional Consequence:: synonymous_variant,3_prime_UTR_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000016.10:g.1968778T>A, NC_000016.10:g.1968778T>C, NC_000016.9:g.2018779T>A, NC_000016.9:g.2018779T>C, NW_025791799.1:g.34926T>A, NW_025791799.1:g.34926T>C, NM_174903.6:c.591T>A, NM_174903.6:c.591T>C, NM_174903.5:c.591T>A, NM_174903.5:c.591T>C, NM_174903.4:c.591T>A, NM_174903.4:c.591T>C, XM_005255129.5:c.618T>A, XM_005255129.5:c.618T>C, XM_005255129.4:c.618T>A, XM_005255129.4:c.618T>C, XM_005255129.3:c.618T>A, XM_005255129.3:c.618T>C, XM_005255129.2:c.618T>A, XM_005255129.2:c.618T>C, XM_005255129.1:c.618T>A, XM_005255129.1:c.618T>C, NM_001348711.2:c.*351T>A, NM_001348711.2:c.*351T>C, NM_001348711.1:c.*351T>A, NM_001348711.1:c.*351T>C

Select item 146310225014.

rs1463102250 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 16:1968736 (GRCh38)
16:2018737 (GRCh37)
Canonical SPDI:: NC_000016.10:1968735:G:A
Gene:: RNF151 (Varview)
Functional Consequence:: synonymous_variant,3_prime_UTR_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000028/1 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000006/1 (GnomAD_exomes)
A=0.000014/2 (GnomAD)
HGVS:: NC_000016.10:g.1968736G>A, NC_000016.9:g.2018737G>A, NW_025791799.1:g.34884G>A, NM_174903.6:c.549G>A, NM_174903.5:c.549G>A, NM_174903.4:c.549G>A, XM_005255129.5:c.576G>A, XM_005255129.4:c.576G>A, XM_005255129.3:c.576G>A, XM_005255129.2:c.576G>A, XM_005255129.1:c.576G>A, NM_001348711.2:c.*309G>A, NM_001348711.1:c.*309G>A

Select item 146217629915.

rs1462176299 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 16:1968606 (GRCh38)
16:2018607 (GRCh37)
Canonical SPDI:: NC_000016.10:1968605:A:T
Gene:: RNF151 (Varview)
Functional Consequence:: missense_variant,3_prime_UTR_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000005/1 (GnomAD_exomes)
T=0.000021/3 (GnomAD)
HGVS:: NC_000016.10:g.1968606A>T, NC_000016.9:g.2018607A>T, NW_025791799.1:g.34754A>T, NM_174903.6:c.419A>T, NM_174903.5:c.419A>T, NM_174903.4:c.419A>T, XM_005255129.5:c.446A>T, XM_005255129.4:c.446A>T, XM_005255129.3:c.446A>T, XM_005255129.2:c.446A>T, XM_005255129.1:c.446A>T, NM_001348711.2:c.*179A>T, NM_001348711.1:c.*179A>T, NP_777563.2:p.Gln140Leu, XP_005255186.1:p.Gln149Leu

Select item 145754770216.

rs1457547702 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 16:1968722 (GRCh38)
16:2018723 (GRCh37)
Canonical SPDI:: NC_000016.10:1968721:C:G
Gene:: RNF151 (Varview)
Functional Consequence:: missense_variant,3_prime_UTR_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: G=0.000047/1 (ALFA)
G=0.000006/1 (GnomAD_exomes)
HGVS:: NC_000016.10:g.1968722C>G, NC_000016.9:g.2018723C>G, NW_025791799.1:g.34870C>G, NM_174903.6:c.535C>G, NM_174903.5:c.535C>G, NM_174903.4:c.535C>G, XM_005255129.5:c.562C>G, XM_005255129.4:c.562C>G, XM_005255129.3:c.562C>G, XM_005255129.2:c.562C>G, XM_005255129.1:c.562C>G, NM_001348711.2:c.*295C>G, NM_001348711.1:c.*295C>G, NP_777563.2:p.Leu179Val, XP_005255186.1:p.Leu188Val

Select item 145273155117.

rs1452731551 [Homo sapiens]

Variant type:: INS
Alleles:: ->TAT [Show Flanks]
Chromosome:: 16:1968448 (GRCh38)
16:2018450 (GRCh37)
Canonical SPDI:: NC_000016.10:1968448::TAT
Gene:: RNF151 (Varview)
Functional Consequence:: inframe_insertion,3_prime_UTR_variant,coding_sequence_variant
Validated:: by frequency,by cluster
MAF:: TAT=0.00001/2 (GnomAD_exomes)
TAT=0.000035/1 (TOMMO)
TAT=0.001092/2 (Korea1K)
HGVS:: NC_000016.10:g.1968448_1968449insTAT, NC_000016.9:g.2018449_2018450insTAT, NW_025791799.1:g.34596_34597insTAT, NM_174903.6:c.261_262insTAT, NM_174903.5:c.261_262insTAT, NM_174903.4:c.261_262insTAT, XM_005255129.5:c.288_289insTAT, XM_005255129.4:c.288_289insTAT, XM_005255129.3:c.288_289insTAT, XM_005255129.2:c.288_289insTAT, XM_005255129.1:c.288_289insTAT, NM_001348711.2:c.*21_*22insTAT, NM_001348711.1:c.*21_*22insTAT, NP_777563.2:p.Ala88_Gly89insTyr, XP_005255186.1:p.Ala97_Gly98insTyr

Select item 144246508318.

rs1442465083 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 16:1968718 (GRCh38)
16:2018719 (GRCh37)
Canonical SPDI:: NC_000016.10:1968717:C:A
Gene:: RNF151 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000016.10:g.1968718C>A, NC_000016.9:g.2018719C>A, NW_025791799.1:g.34866C>A, NM_174903.6:c.531C>A, NM_174903.5:c.531C>A, NM_174903.4:c.531C>A, XM_005255129.5:c.558C>A, XM_005255129.4:c.558C>A, XM_005255129.3:c.558C>A, XM_005255129.2:c.558C>A, XM_005255129.1:c.558C>A, NM_001348711.2:c.*291C>A, NM_001348711.1:c.*291C>A

Select item 144227413619.

rs1442274136 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 16:1968597 (GRCh38)
16:2018598 (GRCh37)
Canonical SPDI:: NC_000016.10:1968596:G:A
Gene:: RNF151 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000016.10:g.1968597G>A, NC_000016.9:g.2018598G>A, NW_025791799.1:g.34745G>A, NM_174903.6:c.410G>A, NM_174903.5:c.410G>A, NM_174903.4:c.410G>A, XM_005255129.5:c.437G>A, XM_005255129.4:c.437G>A, XM_005255129.3:c.437G>A, XM_005255129.2:c.437G>A, XM_005255129.1:c.437G>A, NM_001348711.2:c.*170G>A, NM_001348711.1:c.*170G>A, NP_777563.2:p.Gly137Glu, XP_005255186.1:p.Gly146Glu

Select item 144225330220.

rs1442253302 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAC>- [Show Flanks]
Chromosome:: 16:1968683 (GRCh38)
16:2018684 (GRCh37)
Canonical SPDI:: NC_000016.10:1968680:ACAAC:AC
Gene:: RNF151 (Varview)
Functional Consequence:: inframe_deletion,coding_sequence_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AC=0./0 (ALFA)
-=0.000014/2 (GnomAD)
-=0.000015/4 (TOPMED)
-=0.000035/1 (TOMMO)
HGVS:: NC_000016.10:g.1968683_1968685del, NC_000016.9:g.2018684_2018686del, NW_025791799.1:g.34831_34833del, NM_174903.6:c.496_498del, NM_174903.5:c.496_498del, NM_174903.4:c.496_498del, XM_005255129.5:c.523_525del, XM_005255129.4:c.523_525del, XM_005255129.3:c.523_525del, XM_005255129.2:c.523_525del, XM_005255129.1:c.523_525del, NM_001348711.2:c.*256_*258del, NM_001348711.1:c.*256_*258del, NP_777563.2:p.Asn166del, XP_005255186.1:p.Asn175del

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