SNP Links for Protein (Select 334191681) - SNP

Select item 2021412561.

rs202141256 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 4:9344960 (GRCh38)
4:9346686 (GRCh37)
Canonical SPDI:: NC_000004.12:9344959:C:T
Gene:: USP17L27 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
HGVS:: NC_000004.12:g.9344960C>T, NC_000004.11:g.9346686C>T, NM_001242330.1:c.813C>T

Select item 2019940762.

rs201994076 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 4:9345607 (GRCh38)
4:9347333 (GRCh37)
Canonical SPDI:: NC_000004.12:9345606:T:A
Gene:: USP17L27 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by cluster
HGVS:: NC_000004.12:g.9345607T>A, NC_000004.11:g.9347333T>A, NM_001242330.1:c.1460T>A, NP_001229259.1:p.Leu487Gln

Select item 2013399983.

rs201339998 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 4:9345216 (GRCh38)
4:9346942 (GRCh37)
Canonical SPDI:: NC_000004.12:9345215:T:G
Gene:: USP17L27 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by cluster
HGVS:: NC_000004.12:g.9345216T>G, NC_000004.11:g.9346942T>G, NM_001242330.1:c.1069T>G, NP_001229259.1:p.Ser357Ala

Select item 2012964524.

rs201296452 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 4:9345382 (GRCh38)
4:9347108 (GRCh37)
Canonical SPDI:: NC_000004.12:9345381:A:C
Gene:: USP17L27 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
HGVS:: NC_000004.12:g.9345382A>C, NC_000004.11:g.9347108A>C, NM_001242330.1:c.1235A>C, NP_001229259.1:p.His412Pro

Select item 2012363675.

rs201236367 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 4:9344908 (GRCh38)
4:9346634 (GRCh37)
Canonical SPDI:: NC_000004.12:9344907:G:C
Gene:: USP17L27 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by cluster
HGVS:: NC_000004.12:g.9344908G>C, NC_000004.11:g.9346634G>C, NM_001242330.1:c.761G>C, NP_001229259.1:p.Cys254Ser

Select item 2006618836.

rs200661883 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 4:9345590 (GRCh38)
4:9347316 (GRCh37)
Canonical SPDI:: NC_000004.12:9345589:A:G
Gene:: USP17L27 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by cluster
HGVS:: NC_000004.12:g.9345590A>G, NC_000004.11:g.9347316A>G, NM_001242330.1:c.1443A>G

Select item 2003311507.

rs200331150 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 4:9345381 (GRCh38)
4:9347107 (GRCh37)
Canonical SPDI:: NC_000004.12:9345380:C:T
Gene:: USP17L27 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by cluster
HGVS:: NC_000004.12:g.9345381C>T, NC_000004.11:g.9347107C>T, NM_001242330.1:c.1234C>T, NP_001229259.1:p.His412Tyr

Select item 2003129868.

rs200312986 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 4:9345076 (GRCh38)
4:9346802 (GRCh37)
Canonical SPDI:: NC_000004.12:9345075:C:A,NC_000004.12:9345075:C:T
Gene:: USP17L27 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by cluster
HGVS:: NC_000004.12:g.9345076C>A, NC_000004.12:g.9345076C>T, NC_000004.11:g.9346802C>A, NC_000004.11:g.9346802C>T, NM_001242330.1:c.929C>A, NM_001242330.1:c.929C>T, NP_001229259.1:p.Pro310Gln, NP_001229259.1:p.Pro310Leu

Select item 1997515539.

rs199751553 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 4:9345621 (GRCh38)
4:9347347 (GRCh37)
Canonical SPDI:: NC_000004.12:9345620:T:A
Gene:: USP17L27 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by cluster
HGVS:: NC_000004.12:g.9345621T>A, NC_000004.11:g.9347347T>A, NM_001242330.1:c.1474T>A, NP_001229259.1:p.Ser492Thr

Select item 19968863810.

rs199688638 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 4:9345238 (GRCh38)
4:9346964 (GRCh37)
Canonical SPDI:: NC_000004.12:9345237:G:A,NC_000004.12:9345237:G:C
Gene:: USP17L27 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by cluster
HGVS:: NC_000004.12:g.9345238G>A, NC_000004.12:g.9345238G>C, NC_000004.11:g.9346964G>A, NC_000004.11:g.9346964G>C, NM_001242330.1:c.1091G>A, NM_001242330.1:c.1091G>C, NP_001229259.1:p.Ser364Asn, NP_001229259.1:p.Ser364Thr

Select item 19950361911.

rs199503619 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 4:9345437 (GRCh38)
4:9347163 (GRCh37)
Canonical SPDI:: NC_000004.12:9345436:G:C
Gene:: USP17L27 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by cluster
HGVS:: NC_000004.12:g.9345437G>C, NC_000004.11:g.9347163G>C, NM_001242330.1:c.1290G>C, NP_001229259.1:p.Gln430His

dbSNP

Result Filters

Validation Status

Function Class

Annotation

Global MAF

Custom range

Additional filters

Display Settings:

Send to:

Links from Protein

Items: 11

Display Settings:

Send to:

Supplemental Content

Find related data

Recent activity