SNP Links for Protein (Select 334191675) - SNP

Links from Protein

Items: 1 to 20 of 30

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Select item 14781096351.

rs1478109635 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 4:9329983 (GRCh38)
4:9331709 (GRCh37)
Canonical SPDI:: NC_000004.12:9329982:C:T
Gene:: USP17L25 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
HGVS:: NC_000004.12:g.9329983C>T, NC_000004.11:g.9331709C>T, NM_001242326.1:c.73C>T, NP_001229255.1:p.Pro25Ser

Select item 14638465832.

rs1463846583 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 4:9330116 (GRCh38)
4:9331842 (GRCh37)
Canonical SPDI:: NC_000004.12:9330115:C:T
Gene:: USP17L25 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by cluster
HGVS:: NC_000004.12:g.9330116C>T, NC_000004.11:g.9331842C>T, NM_001242326.1:c.206C>T, NP_001229255.1:p.Pro69Leu

Select item 14359424243.

rs1435942424 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 4:9330214 (GRCh38)
4:9331940 (GRCh37)
Canonical SPDI:: NC_000004.12:9330213:C:A
Gene:: USP17L25 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by cluster
MAF:: A=0.05/1 (GnomAD_exomes)
HGVS:: NC_000004.12:g.9330214C>A, NC_000004.11:g.9331940C>A, NM_001242326.1:c.304C>A, NP_001229255.1:p.Pro102Thr

Select item 14223729254.

rs1422372925 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 4:9330066 (GRCh38)
4:9331792 (GRCh37)
Canonical SPDI:: NC_000004.12:9330065:T:A
Gene:: USP17L25 (Varview)
Functional Consequence:: coding_sequence_variant,stop_gained
HGVS:: NC_000004.12:g.9330066T>A, NC_000004.11:g.9331792T>A, NM_001242326.1:c.156T>A, NP_001229255.1:p.Cys52Ter

Select item 14116096965.

rs1411609696 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 4:9330069 (GRCh38)
4:9331795 (GRCh37)
Canonical SPDI:: NC_000004.12:9330068:T:C
Gene:: USP17L25 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by cluster
MAF:: C=0.09/8 (KOREAN)
HGVS:: NC_000004.12:g.9330069T>C, NC_000004.11:g.9331795T>C, NM_001242326.1:c.159T>C

Select item 13993196166.

rs1399319616 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 4:9330102 (GRCh38)
4:9331828 (GRCh37)
Canonical SPDI:: NC_000004.12:9330101:C:G
Gene:: USP17L25 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by cluster
HGVS:: NC_000004.12:g.9330102C>G, NC_000004.11:g.9331828C>G, NM_001242326.1:c.192C>G

Select item 13719940077.

rs1371994007 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 4:9330145 (GRCh38)
4:9331871 (GRCh37)
Canonical SPDI:: NC_000004.12:9330144:G:T
Gene:: USP17L25 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
HGVS:: NC_000004.12:g.9330145G>T, NC_000004.11:g.9331871G>T, NM_001242326.1:c.235G>T, NP_001229255.1:p.Gly79Trp

Select item 13641240908.

rs1364124090 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 4:9330291 (GRCh38)
4:9332017 (GRCh37)
Canonical SPDI:: NC_000004.12:9330290:T:G
Gene:: USP17L25 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
HGVS:: NC_000004.12:g.9330291T>G, NC_000004.11:g.9332017T>G, NM_001242326.1:c.381T>G

Select item 13282427319.

rs1328242731 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 4:9330126 (GRCh38)
4:9331852 (GRCh37)
Canonical SPDI:: NC_000004.12:9330125:C:A
Gene:: USP17L25 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
HGVS:: NC_000004.12:g.9330126C>A, NC_000004.11:g.9331852C>A, NM_001242326.1:c.216C>A, NP_001229255.1:p.Ser72Arg

Select item 127317858010.

rs1273178580 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 4:9330258 (GRCh38)
4:9331984 (GRCh37)
Canonical SPDI:: NC_000004.12:9330257:G:A
Gene:: USP17L25 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by cluster
HGVS:: NC_000004.12:g.9330258G>A, NC_000004.11:g.9331984G>A, NM_001242326.1:c.348G>A

Select item 125795583411.

rs1257955834 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 4:9330459 (GRCh38)
4:9332185 (GRCh37)
Canonical SPDI:: NC_000004.12:9330458:A:G
Gene:: USP17L25 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by cluster
HGVS:: NC_000004.12:g.9330459A>G, NC_000004.11:g.9332185A>G, NM_001242326.1:c.549A>G

Select item 125448199912.

rs1254481999 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 4:9329977 (GRCh38)
4:9331703 (GRCh37)
Canonical SPDI:: NC_000004.12:9329976:T:C
Gene:: USP17L25 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by cluster
HGVS:: NC_000004.12:g.9329977T>C, NC_000004.11:g.9331703T>C, NM_001242326.1:c.67T>C, NP_001229255.1:p.Ser23Pro

Select item 121571218413.

rs1215712184 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 4:9330393 (GRCh38)
4:9332119 (GRCh37)
Canonical SPDI:: NC_000004.12:9330392:C:T
Gene:: USP17L25 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by cluster
HGVS:: NC_000004.12:g.9330393C>T, NC_000004.11:g.9332119C>T, NM_001242326.1:c.483C>T

Select item 119013013414.

rs1190130134 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 4:9329985 (GRCh38)
4:9331711 (GRCh37)
Canonical SPDI:: NC_000004.12:9329984:C:A
Gene:: USP17L25 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.03202/342 (ALFA)
HGVS:: NC_000004.12:g.9329985C>A, NC_000004.11:g.9331711C>A, NM_001242326.1:c.75C>A

Select item 117645185015.

rs1176451850 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 4:9329975 (GRCh38)
4:9331701 (GRCh37)
Canonical SPDI:: NC_000004.12:9329974:C:G
Gene:: USP17L25 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
HGVS:: NC_000004.12:g.9329975C>G, NC_000004.11:g.9331701C>G, NM_001242326.1:c.65C>G, NP_001229255.1:p.Ser22Cys

Select item 117100550216.

rs1171005502 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 4:9330076 (GRCh38)
4:9331802 (GRCh37)
Canonical SPDI:: NC_000004.12:9330075:G:C
Gene:: USP17L25 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by cluster
MAF:: C=0.1/1 (GnomAD_exomes)
HGVS:: NC_000004.12:g.9330076G>C, NC_000004.11:g.9331802G>C, NM_001242326.1:c.166G>C, NP_001229255.1:p.Ala56Pro

Select item 20184770317.

rs201847703 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 4:9330839 (GRCh38)
4:9332565 (GRCh37)
Canonical SPDI:: NC_000004.12:9330838:C:A,NC_000004.12:9330838:C:T
Gene:: USP17L25 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by cluster
HGVS:: NC_000004.12:g.9330839C>A, NC_000004.12:g.9330839C>T, NC_000004.11:g.9332565C>A, NC_000004.11:g.9332565C>T, NM_001242326.1:c.929C>A, NM_001242326.1:c.929C>T, NP_001229255.1:p.Pro310Gln, NP_001229255.1:p.Pro310Leu

Select item 20092939318.

rs200929393 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 4:9330723 (GRCh38)
4:9332449 (GRCh37)
Canonical SPDI:: NC_000004.12:9330722:C:T
Gene:: USP17L25 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
HGVS:: NC_000004.12:g.9330723C>T, NC_000004.11:g.9332449C>T, NM_001242326.1:c.813C>T

Select item 20005711819.

rs200057118 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 4:9331145 (GRCh38)
4:9332871 (GRCh37)
Canonical SPDI:: NC_000004.12:9331144:A:C
Gene:: USP17L25 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
HGVS:: NC_000004.12:g.9331145A>C, NC_000004.11:g.9332871A>C, NM_001242326.1:c.1235A>C, NP_001229255.1:p.His412Pro

Select item 19986025320.

rs199860253 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 4:9330979 (GRCh38)
4:9332705 (GRCh37)
Canonical SPDI:: NC_000004.12:9330978:T:G
Gene:: USP17L25 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by cluster
HGVS:: NC_000004.12:g.9330979T>G, NC_000004.11:g.9332705T>G, NM_001242326.1:c.1069T>G, NP_001229255.1:p.Ser357Ala

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