SNP Links for Protein (Select 4503417) - SNP

Warning: The NCBI web site requires JavaScript to function. more...

Links from Protein

Items: 1 to 20 of 410

<< First< Prev

Page of 21

Next >Last >>

Select item 14893486501.

rs1489348650 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 8:29337084 (GRCh38)
8:29194601 (GRCh37)
Canonical SPDI:: NC_000008.11:29337083:G:A
Gene:: DUSP4 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000008.11:g.29337084G>A, NC_000008.10:g.29194601G>A, NM_001394.7:c.1127C>T, NM_001394.6:c.1127C>T, NM_057158.4:c.854C>T, NM_057158.3:c.854C>T, NP_001385.1:p.Ser376Leu, NP_476499.1:p.Ser285Leu

Select item 14882367932.

rs1488236793 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 8:29340113 (GRCh38)
8:29197630 (GRCh37)
Canonical SPDI:: NC_000008.11:29340112:G:A
Gene:: DUSP4 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000008.11:g.29340113G>A, NC_000008.10:g.29197630G>A, NG_074321.1:g.2G>A, NM_001394.7:c.564C>T, NM_001394.6:c.564C>T, NM_057158.4:c.291C>T, NM_057158.3:c.291C>T

Select item 14866745643.

rs1486674564 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 8:29349909 (GRCh38)
8:29207426 (GRCh37)
Canonical SPDI:: NC_000008.11:29349908:C:G,NC_000008.11:29349908:C:T
Gene:: DUSP4 (Varview), LOC124901924 (Varview)
Functional Consequence:: missense_variant,genic_upstream_transcript_variant,2KB_upstream_variant,coding_sequence_variant,upstream_transcript_variant
Validated:: by frequency,by cluster
MAF:: G=0.000007/1 (GnomAD)
HGVS:: NC_000008.11:g.29349909C>G, NC_000008.11:g.29349909C>T, NC_000008.10:g.29207426C>G, NC_000008.10:g.29207426C>T, NM_001394.7:c.370G>C, NM_001394.7:c.370G>A, NM_001394.6:c.370G>C, NM_001394.6:c.370G>A, NP_001385.1:p.Val124Leu, NP_001385.1:p.Val124Met

Select item 14852507384.

rs1485250738 [Homo sapiens]

Variant type:: DEL
Alleles:: C>- [Show Flanks]
Chromosome:: 8:29350222 (GRCh38)
8:29207739 (GRCh37)
Canonical SPDI:: NC_000008.11:29350221:C:
Gene:: DUSP4 (Varview), LOC124901924 (Varview)
Functional Consequence:: upstream_transcript_variant,genic_upstream_transcript_variant,2KB_upstream_variant,frameshift_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
-=0.000004/1 (TOPMED)
HGVS:: NC_000008.11:g.29350222del, NC_000008.10:g.29207739del, NM_001394.7:c.57del, NM_001394.6:c.57del, NP_001385.1:p.Met19fs

Select item 14827922045.

rs1482792204 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 8:29338455 (GRCh38)
8:29195972 (GRCh37)
Canonical SPDI:: NC_000008.11:29338454:T:G
Gene:: DUSP4 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000056/2 (ALFA)
G=0.000004/1 (GnomAD_exomes)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000008.11:g.29338455T>G, NC_000008.10:g.29195972T>G, NM_001394.7:c.626A>C, NM_001394.6:c.626A>C, NM_057158.4:c.353A>C, NM_057158.3:c.353A>C, NP_001385.1:p.Tyr209Ser, NP_476499.1:p.Tyr118Ser

Select item 14744247616.

rs1474424761 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,T [Show Flanks]
Chromosome:: 8:29350094 (GRCh38)
8:29207611 (GRCh37)
Canonical SPDI:: NC_000008.11:29350093:A:C,NC_000008.11:29350093:A:T
Gene:: DUSP4 (Varview), LOC124901924 (Varview)
Functional Consequence:: missense_variant,upstream_transcript_variant,genic_upstream_transcript_variant,2KB_upstream_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000008.11:g.29350094A>C, NC_000008.11:g.29350094A>T, NC_000008.10:g.29207611A>C, NC_000008.10:g.29207611A>T, NM_001394.7:c.185T>G, NM_001394.7:c.185T>A, NM_001394.6:c.185T>G, NM_001394.6:c.185T>A, NP_001385.1:p.Leu62Arg, NP_001385.1:p.Leu62Gln

Select item 14669874237.

rs1466987423 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 8:29337278 (GRCh38)
8:29194795 (GRCh37)
Canonical SPDI:: NC_000008.11:29337277:C:T
Gene:: DUSP4 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000008.11:g.29337278C>T, NC_000008.10:g.29194795C>T, NM_001394.7:c.933G>A, NM_001394.6:c.933G>A, NM_057158.4:c.660G>A, NM_057158.3:c.660G>A

Select item 14662610448.

rs1466261044 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 8:29337047 (GRCh38)
8:29194564 (GRCh37)
Canonical SPDI:: NC_000008.11:29337046:G:A,NC_000008.11:29337046:G:T
Gene:: DUSP4 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000008.11:g.29337047G>A, NC_000008.11:g.29337047G>T, NC_000008.10:g.29194564G>A, NC_000008.10:g.29194564G>T, NM_001394.7:c.1164C>T, NM_001394.7:c.1164C>A, NM_001394.6:c.1164C>T, NM_001394.6:c.1164C>A, NM_057158.4:c.891C>T, NM_057158.4:c.891C>A, NM_057158.3:c.891C>T, NM_057158.3:c.891C>A

Select item 14642713219.

rs1464271321 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 8:29338421 (GRCh38)
8:29195938 (GRCh37)
Canonical SPDI:: NC_000008.11:29338420:C:A
Gene:: DUSP4 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: A=0.000047/1 (ALFA)
A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000008.11:g.29338421C>A, NC_000008.10:g.29195938C>A, NM_001394.7:c.660G>T, NM_001394.6:c.660G>T, NM_057158.4:c.387G>T, NM_057158.3:c.387G>T

Select item 145955024610.

rs1459550246 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 8:29350051 (GRCh38)
8:29207568 (GRCh37)
Canonical SPDI:: NC_000008.11:29350050:C:T
Gene:: DUSP4 (Varview), LOC124901924 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,synonymous_variant,coding_sequence_variant,2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency
MAF:: T=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000008.11:g.29350051C>T, NC_000008.10:g.29207568C>T, NM_001394.7:c.228G>A, NM_001394.6:c.228G>A

Select item 145745919211.

rs1457459192 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 8:29338311 (GRCh38)
8:29195828 (GRCh37)
Canonical SPDI:: NC_000008.11:29338310:G:T
Gene:: DUSP4 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: T=0.000111/1 (ALFA)
T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000008.11:g.29338311G>T, NC_000008.10:g.29195828G>T, NM_001394.7:c.770C>A, NM_001394.6:c.770C>A, NM_057158.4:c.497C>A, NM_057158.3:c.497C>A, NP_001385.1:p.Ser257Tyr, NP_476499.1:p.Ser166Tyr

Select item 145553423412.

rs1455534234 [Homo sapiens]

Variant type:: DELINS
Alleles:: C>- [Show Flanks]
Chromosome:: 8:29350275 (GRCh38)
8:29207792 (GRCh37)
Canonical SPDI:: NC_000008.11:29350274:CC:C
Gene:: DUSP4 (Varview), LOC124901924 (Varview)
Functional Consequence:: initiator_codon_variant,stop_gained,genic_upstream_transcript_variant,2KB_upstream_variant,upstream_transcript_variant
Validated:: by frequency
MAF:: -=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000008.11:g.29350276del, NC_000008.10:g.29207793del, NM_001394.7:c.4del, NM_001394.6:c.4del, NP_001385.1:p.Met1_Val2insTer

Select item 145502097113.

rs1455020971 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 8:29350036 (GRCh38)
8:29207553 (GRCh37)
Canonical SPDI:: NC_000008.11:29350035:C:T
Gene:: DUSP4 (Varview), LOC124901924 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,2KB_upstream_variant,coding_sequence_variant,synonymous_variant,upstream_transcript_variant
HGVS:: NC_000008.11:g.29350036C>T, NC_000008.10:g.29207553C>T, NM_001394.7:c.243G>A, NM_001394.6:c.243G>A

Select item 145493813014.

rs1454938130 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 8:29349998 (GRCh38)
8:29207515 (GRCh37)
Canonical SPDI:: NC_000008.11:29349997:C:T
Gene:: DUSP4 (Varview), LOC124901924 (Varview)
Functional Consequence:: missense_variant,genic_upstream_transcript_variant,2KB_upstream_variant,coding_sequence_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000014/2 (GnomAD)
T=0.000014/3 (GnomAD_exomes)
HGVS:: NC_000008.11:g.29349998C>T, NC_000008.10:g.29207515C>T, NM_001394.7:c.281G>A, NM_001394.6:c.281G>A, NP_001385.1:p.Arg94His

Select item 145407853615.

rs1454078536 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 8:29349982 (GRCh38)
8:29207499 (GRCh37)
Canonical SPDI:: NC_000008.11:29349981:G:A
Gene:: DUSP4 (Varview), LOC124901924 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,2KB_upstream_variant,coding_sequence_variant,synonymous_variant,upstream_transcript_variant
HGVS:: NC_000008.11:g.29349982G>A, NC_000008.10:g.29207499G>A, NM_001394.7:c.297C>T, NM_001394.6:c.297C>T

Select item 144803771916.

rs1448037719 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 8:29350078 (GRCh38)
8:29207595 (GRCh37)
Canonical SPDI:: NC_000008.11:29350077:C:T
Gene:: DUSP4 (Varview), LOC124901924 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,2KB_upstream_variant,coding_sequence_variant,synonymous_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000071/1 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000008.11:g.29350078C>T, NC_000008.10:g.29207595C>T, NM_001394.7:c.201G>A, NM_001394.6:c.201G>A

Select item 144662037417.

rs1446620374 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 8:29337173 (GRCh38)
8:29194690 (GRCh37)
Canonical SPDI:: NC_000008.11:29337172:G:A
Gene:: DUSP4 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: A=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000008.11:g.29337173G>A, NC_000008.10:g.29194690G>A, NM_001394.7:c.1038C>T, NM_001394.6:c.1038C>T, NM_057158.4:c.765C>T, NM_057158.3:c.765C>T

Select item 144497049018.

rs1444970490 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 8:29338334 (GRCh38)
8:29195851 (GRCh37)
Canonical SPDI:: NC_000008.11:29338333:A:G
Gene:: DUSP4 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000008/2 (GnomAD_exomes)
G=0.000008/2 (TOPMED)
HGVS:: NC_000008.11:g.29338334A>G, NC_000008.10:g.29195851A>G, NM_001394.7:c.747T>C, NM_001394.6:c.747T>C, NM_057158.4:c.474T>C, NM_057158.3:c.474T>C

Select item 144283429219.

rs1442834292 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C,T [Show Flanks]
Chromosome:: 8:29350124 (GRCh38)
8:29207641 (GRCh37)
Canonical SPDI:: NC_000008.11:29350123:G:C,NC_000008.11:29350123:G:T
Gene:: DUSP4 (Varview), LOC124901924 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,upstream_transcript_variant,2KB_upstream_variant,coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000008.11:g.29350124G>C, NC_000008.11:g.29350124G>T, NC_000008.10:g.29207641G>C, NC_000008.10:g.29207641G>T, NM_001394.7:c.155C>G, NM_001394.7:c.155C>A, NM_001394.6:c.155C>G, NM_001394.6:c.155C>A, NP_001385.1:p.Pro52Arg, NP_001385.1:p.Pro52Gln

Select item 144100051120.

rs1441000511 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 8:29337178 (GRCh38)
8:29194695 (GRCh37)
Canonical SPDI:: NC_000008.11:29337177:T:C
Gene:: DUSP4 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
HGVS:: NC_000008.11:g.29337178T>C, NC_000008.10:g.29194695T>C, NM_001394.7:c.1033A>G, NM_001394.6:c.1033A>G, NM_057158.4:c.760A>G, NM_057158.3:c.760A>G, NP_001385.1:p.Ser345Gly, NP_476499.1:p.Ser254Gly

<< First< Prev

Page of 21

Next >Last >>

Supplemental Content

Filters: Manage Filters

Find related data

Recent activity

Clear Turn Off Turn On

SNP Links for Protein (Select 4503417) (410)
SNP

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

dbSNP

Result Filters

Validation Status

Function Class

Variation Class

Annotation

Global MAF

Custom range

Additional filters

Display Settings:

Send to: