SNP Links for Protein (Select 156416012) - SNP

Links from Protein

Items: 1 to 20 of 295

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Select item 14840620911.

rs1484062091 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 1:163074549 (GRCh38)
1:163044339 (GRCh37)
Canonical SPDI:: NC_000001.11:163074548:C:G
Gene:: RGS4 (Varview), LOC124904446 (Varview)
Functional Consequence:: 2KB_upstream_variant,missense_variant,upstream_transcript_variant,3_prime_UTR_variant,coding_sequence_variant
Validated:: by frequency,by cluster
MAF:: G=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.163074549C>G, NC_000001.10:g.163044339C>G, NG_023312.1:g.10944C>G, NM_005613.6:c.607C>G, NM_005613.5:c.607C>G, NM_001102445.3:c.898C>G, NM_001102445.2:c.898C>G, NM_001113380.1:c.553C>G, NM_001113381.1:c.*158C>G, NP_005604.1:p.Gln203Glu, NP_001095915.1:p.Gln300Glu, NP_001106851.1:p.Gln185Glu

Select item 14822872082.

rs1482287208 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:163074523 (GRCh38)
1:163044313 (GRCh37)
Canonical SPDI:: NC_000001.11:163074522:C:T
Gene:: RGS4 (Varview), LOC124904446 (Varview)
Functional Consequence:: 2KB_upstream_variant,missense_variant,upstream_transcript_variant,3_prime_UTR_variant,coding_sequence_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.163074523C>T, NC_000001.10:g.163044313C>T, NG_023312.1:g.10918C>T, NM_005613.6:c.581C>T, NM_005613.5:c.581C>T, NM_001102445.3:c.872C>T, NM_001102445.2:c.872C>T, NM_001113380.1:c.527C>T, NM_001113381.1:c.*132C>T, NP_005604.1:p.Ser194Leu, NP_001095915.1:p.Ser291Leu, NP_001106851.1:p.Ser176Leu

Select item 14721458793.

rs1472145879 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 1:163069302 (GRCh38)
1:163039092 (GRCh37)
Canonical SPDI:: NC_000001.11:163069301:T:A
Gene:: RGS4 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,coding_sequence_variant,5_prime_UTR_variant,upstream_transcript_variant,missense_variant
Validated:: by frequency
MAF:: A=0.000006/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.163069302T>A, NC_000001.10:g.163039092T>A, NG_023312.1:g.5697T>A, NM_001102445.3:c.109T>A, NM_001102445.2:c.109T>A, NM_001113381.1:c.-183T>A, NM_005613.5:c.-183T>A, NP_001095915.1:p.Ser37Thr

Select item 14664198484.

rs1466419848 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 1:163069357 (GRCh38)
1:163039147 (GRCh37)
Canonical SPDI:: NC_000001.11:163069356:C:A,NC_000001.11:163069356:C:T
Gene:: RGS4 (Varview)
Functional Consequence:: upstream_transcript_variant,missense_variant,genic_upstream_transcript_variant,coding_sequence_variant,5_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.163069357C>A, NC_000001.11:g.163069357C>T, NC_000001.10:g.163039147C>A, NC_000001.10:g.163039147C>T, NG_023312.1:g.5752C>A, NG_023312.1:g.5752C>T, NM_001102445.3:c.164C>A, NM_001102445.3:c.164C>T, NM_001102445.2:c.164C>A, NM_001102445.2:c.164C>T, NM_001113381.1:c.-128C>A, NM_001113381.1:c.-128C>T, NM_005613.5:c.-128C>A, NM_005613.5:c.-128C>T, NP_001095915.1:p.Ala55Glu, NP_001095915.1:p.Ala55Val

Select item 14661533865.

rs1466153386 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,G,T [Show Flanks]
Chromosome:: 1:163072470 (GRCh38)
1:163042260 (GRCh37)
Canonical SPDI:: NC_000001.11:163072469:C:A,NC_000001.11:163072469:C:G,NC_000001.11:163072469:C:T
Gene:: RGS4 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
A=0.000008/1 (ExAC)
G=0.000008/2 (TOPMED)
HGVS:: NC_000001.11:g.163072470C>A, NC_000001.11:g.163072470C>G, NC_000001.11:g.163072470C>T, NC_000001.10:g.163042260C>A, NC_000001.10:g.163042260C>G, NC_000001.10:g.163042260C>T, NG_023312.1:g.8865C>A, NG_023312.1:g.8865C>G, NG_023312.1:g.8865C>T, NM_005613.6:c.120C>A, NM_005613.6:c.120C>G, NM_005613.6:c.120C>T, NM_005613.5:c.120C>A, NM_005613.5:c.120C>G, NM_005613.5:c.120C>T, NM_001102445.3:c.411C>A, NM_001102445.3:c.411C>G, NM_001102445.3:c.411C>T, NM_001102445.2:c.411C>A, NM_001102445.2:c.411C>G, NM_001102445.2:c.411C>T, NM_001113380.1:c.66C>A, NM_001113380.1:c.66C>G, NM_001113380.1:c.66C>T, NM_001113381.1:c.120C>A, NM_001113381.1:c.120C>G, NM_001113381.1:c.120C>T, NP_005604.1:p.Asn40Lys, NP_005604.1:p.Asn40Lys, NP_001095915.1:p.Asn137Lys, NP_001095915.1:p.Asn137Lys, NP_001106851.1:p.Asn22Lys, NP_001106851.1:p.Asn22Lys, NP_001106852.1:p.Asn40Lys, NP_001106852.1:p.Asn40Lys

Select item 14651266336.

rs1465126633 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:163069471 (GRCh38)
1:163039261 (GRCh37)
Canonical SPDI:: NC_000001.11:163069470:A:G
Gene:: RGS4 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,missense_variant,coding_sequence_variant,5_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
G=0.000008/2 (GnomAD_exomes)
G=0.000035/1 (TOMMO)
HGVS:: NC_000001.11:g.163069471A>G, NC_000001.10:g.163039261A>G, NG_023312.1:g.5866A>G, NM_005613.6:c.-14A>G, NM_005613.5:c.-14A>G, NM_001102445.3:c.278A>G, NM_001102445.2:c.278A>G, NM_001113381.1:c.-14A>G, NP_001095915.1:p.Lys93Arg

Select item 14634867987.

rs1463486798 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G [Show Flanks]
Chromosome:: 1:163068965 (GRCh38)
1:163038755 (GRCh37)
Canonical SPDI:: NC_000001.11:163068964:A:C,NC_000001.11:163068964:A:G
Gene:: RGS4 (Varview)
Functional Consequence:: upstream_transcript_variant,synonymous_variant,missense_variant,genic_upstream_transcript_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000224/1 (ALFA)
C=0.000007/1 (GnomAD)
G=0.000035/1 (TOMMO)
C=0.000223/1 (Estonian)
HGVS:: NC_000001.11:g.163068965A>C, NC_000001.11:g.163068965A>G, NC_000001.10:g.163038755A>C, NC_000001.10:g.163038755A>G, NG_023312.1:g.5360A>C, NG_023312.1:g.5360A>G, NM_001102445.3:c.31A>C, NM_001102445.3:c.31A>G, NM_001102445.2:c.31A>C, NM_001102445.2:c.31A>G, NP_001095915.1:p.Arg11Gly

Select item 14594649658.

rs1459464965 [Homo sapiens]

Variant type:: DELINS
Alleles:: AGG>- [Show Flanks]
Chromosome:: 1:163069527 (GRCh38)
1:163039317 (GRCh37)
Canonical SPDI:: NC_000001.11:163069522:GAGGAGG:GAGG
Gene:: RGS4 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,coding_sequence_variant,splice_donor_variant
Validated:: by frequency,by alfa
MAF:: GAGG=0.000111/1 (ALFA)
-=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.163069524AGG[1], NC_000001.10:g.163039314AGG[1], NG_023312.1:g.5919AGG[1]

Select item 14582180419.

rs1458218041 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:163068970 (GRCh38)
1:163038760 (GRCh37)
Canonical SPDI:: NC_000001.11:163068969:A:G
Gene:: RGS4 (Varview)
Functional Consequence:: coding_sequence_variant,genic_upstream_transcript_variant,upstream_transcript_variant,synonymous_variant
Validated:: by frequency,by cluster
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.163068970A>G, NC_000001.10:g.163038760A>G, NG_023312.1:g.5365A>G, NM_001102445.3:c.36A>G, NM_001102445.2:c.36A>G

Select item 145597377710.

rs1455973777 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 1:163073592 (GRCh38)
1:163043382 (GRCh37)
Canonical SPDI:: NC_000001.11:163073591:T:C,NC_000001.11:163073591:T:G
Gene:: RGS4 (Varview), LOC124904446 (Varview)
Functional Consequence:: coding_sequence_variant,upstream_transcript_variant,intron_variant,synonymous_variant,missense_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000071/1 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.163073592T>C, NC_000001.11:g.163073592T>G, NC_000001.10:g.163043382T>C, NC_000001.10:g.163043382T>G, NG_023312.1:g.9987T>C, NG_023312.1:g.9987T>G, NM_005613.6:c.348T>C, NM_005613.6:c.348T>G, NM_005613.5:c.348T>C, NM_005613.5:c.348T>G, NM_001102445.3:c.639T>C, NM_001102445.3:c.639T>G, NM_001102445.2:c.639T>C, NM_001102445.2:c.639T>G, NM_001113380.1:c.294T>C, NM_001113380.1:c.294T>G, NP_005604.1:p.Asn116Lys, NP_001095915.1:p.Asn213Lys, NP_001106851.1:p.Asn98Lys

Select item 144878694411.

rs1448786944 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:163069490 (GRCh38)
1:163039280 (GRCh37)
Canonical SPDI:: NC_000001.11:163069489:C:T
Gene:: RGS4 (Varview)
Functional Consequence:: coding_sequence_variant,genic_upstream_transcript_variant,synonymous_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=0.000021/3 (GnomAD)
HGVS:: NC_000001.11:g.163069490C>T, NC_000001.10:g.163039280C>T, NG_023312.1:g.5885C>T, NM_005613.6:c.6C>T, NM_005613.5:c.6C>T, NM_001102445.3:c.297C>T, NM_001102445.2:c.297C>T, NM_001113381.1:c.6C>T

Select item 144437476712.

rs1444374767 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 1:163073577 (GRCh38)
1:163043367 (GRCh37)
Canonical SPDI:: NC_000001.11:163073576:C:G,NC_000001.11:163073576:C:T
Gene:: RGS4 (Varview), LOC124904446 (Varview)
Functional Consequence:: coding_sequence_variant,intron_variant,synonymous_variant,upstream_transcript_variant,2KB_upstream_variant
HGVS:: NC_000001.11:g.163073577C>G, NC_000001.11:g.163073577C>T, NC_000001.10:g.163043367C>G, NC_000001.10:g.163043367C>T, NG_023312.1:g.9972C>G, NG_023312.1:g.9972C>T, NM_005613.6:c.333C>G, NM_005613.6:c.333C>T, NM_005613.5:c.333C>G, NM_005613.5:c.333C>T, NM_001102445.3:c.624C>G, NM_001102445.3:c.624C>T, NM_001102445.2:c.624C>G, NM_001102445.2:c.624C>T, NM_001113380.1:c.279C>G, NM_001113380.1:c.279C>T

Select item 144196239613.

rs1441962396 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:163069443 (GRCh38)
1:163039233 (GRCh37)
Canonical SPDI:: NC_000001.11:163069442:C:T
Gene:: RGS4 (Varview)
Functional Consequence:: coding_sequence_variant,5_prime_UTR_variant,genic_upstream_transcript_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: T=0.000047/1 (ALFA)
T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.163069443C>T, NC_000001.10:g.163039233C>T, NG_023312.1:g.5838C>T, NM_005613.6:c.-42C>T, NM_005613.5:c.-42C>T, NM_001102445.3:c.250C>T, NM_001102445.2:c.250C>T, NM_001113381.1:c.-42C>T, NP_001095915.1:p.Arg84Cys

Select item 144136950714.

rs1441369507 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:163069367 (GRCh38)
1:163039157 (GRCh37)
Canonical SPDI:: NC_000001.11:163069366:C:T
Gene:: RGS4 (Varview)
Functional Consequence:: coding_sequence_variant,5_prime_UTR_variant,genic_upstream_transcript_variant,synonymous_variant
HGVS:: NC_000001.11:g.163069367C>T, NC_000001.10:g.163039157C>T, NG_023312.1:g.5762C>T, NM_005613.6:c.-118C>T, NM_005613.5:c.-118C>T, NM_001102445.3:c.174C>T, NM_001102445.2:c.174C>T, NM_001113381.1:c.-118C>T

Select item 144096933215.

rs1440969332 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 1:163073466 (GRCh38)
1:163043256 (GRCh37)
Canonical SPDI:: NC_000001.11:163073465:A:T
Gene:: RGS4 (Varview), LOC124904446 (Varview)
Functional Consequence:: synonymous_variant,2KB_upstream_variant,intron_variant,coding_sequence_variant,upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000001.11:g.163073466A>T, NC_000001.10:g.163043256A>T, NG_023312.1:g.9861A>T, NM_005613.6:c.222A>T, NM_005613.5:c.222A>T, NM_001102445.3:c.513A>T, NM_001102445.2:c.513A>T, NM_001113380.1:c.168A>T

Select item 143614669116.

rs1436146691 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 1:163072862 (GRCh38)
1:163042652 (GRCh37)
Canonical SPDI:: NC_000001.11:163072861:T:C
Gene:: RGS4 (Varview), LOC124904446 (Varview)
Functional Consequence:: 500B_downstream_variant,coding_sequence_variant,synonymous_variant,downstream_transcript_variant
Validated:: by frequency
MAF:: C=0.000012/3 (GnomAD_exomes)
HGVS:: NC_000001.11:g.163072862T>C, NC_000001.10:g.163042652T>C, NG_023312.1:g.9257T>C, NM_005613.6:c.207T>C, NM_005613.5:c.207T>C, NM_001102445.3:c.498T>C, NM_001102445.2:c.498T>C, NM_001113380.1:c.153T>C, NM_001113381.1:c.207T>C

Select item 142641665917.

rs1426416659 [Homo sapiens]

Variant type:: DELINS
Alleles:: GA>- [Show Flanks]
Chromosome:: 1:163069340 (GRCh38)
1:163039130 (GRCh37)
Canonical SPDI:: NC_000001.11:163069336:AGAGA:AGA
Gene:: RGS4 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,5_prime_UTR_variant,frameshift_variant,coding_sequence_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AGA=0./0 (ALFA)
-=0.000007/1 (GnomAD)
-=0.000008/2 (TOPMED)
HGVS:: NC_000001.11:g.163069338GA[1], NC_000001.10:g.163039128GA[1], NG_023312.1:g.5733GA[1], NM_001102445.3:c.147_148del, NM_001102445.2:c.147_148del, NM_001113381.1:c.-147GA[1], NM_005613.5:c.-147GA[1], NP_001095915.1:p.Glu49fs

Select item 142431543818.

rs1424315438 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 1:163072440 (GRCh38)
1:163042230 (GRCh37)
Canonical SPDI:: NC_000001.11:163072439:T:C
Gene:: RGS4 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (GnomAD_exomes)
C=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.163072440T>C, NC_000001.10:g.163042230T>C, NG_023312.1:g.8835T>C, NM_005613.6:c.90T>C, NM_005613.5:c.90T>C, NM_001102445.3:c.381T>C, NM_001102445.2:c.381T>C, NM_001113380.1:c.36T>C, NM_001113381.1:c.90T>C

Select item 142184032119.

rs1421840321 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 1:163069393 (GRCh38)
1:163039183 (GRCh37)
Canonical SPDI:: NC_000001.11:163069392:C:G,NC_000001.11:163069392:C:T
Gene:: RGS4 (Varview)
Functional Consequence:: coding_sequence_variant,5_prime_UTR_variant,genic_upstream_transcript_variant,missense_variant
Validated:: by frequency
MAF:: G=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.163069393C>G, NC_000001.11:g.163069393C>T, NC_000001.10:g.163039183C>G, NC_000001.10:g.163039183C>T, NG_023312.1:g.5788C>G, NG_023312.1:g.5788C>T, NM_005613.6:c.-92C>G, NM_005613.6:c.-92C>T, NM_005613.5:c.-92C>G, NM_005613.5:c.-92C>T, NM_001102445.3:c.200C>G, NM_001102445.3:c.200C>T, NM_001102445.2:c.200C>G, NM_001102445.2:c.200C>T, NM_001113381.1:c.-92C>G, NM_001113381.1:c.-92C>T, NP_001095915.1:p.Thr67Ser, NP_001095915.1:p.Thr67Ile

Select item 141611486620.

rs1416114866 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 1:163072402 (GRCh38)
1:163042192 (GRCh37)
Canonical SPDI:: NC_000001.11:163072401:G:T
Gene:: RGS4 (Varview)
Functional Consequence:: missense_variant,5_prime_UTR_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000066/1 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000446/2 (Estonian)
HGVS:: NC_000001.11:g.163072402G>T, NC_000001.10:g.163042192G>T, NG_023312.1:g.8797G>T, NM_005613.6:c.52G>T, NM_005613.5:c.52G>T, NM_001102445.3:c.343G>T, NM_001102445.2:c.343G>T, NM_001113380.1:c.-3G>T, NM_001113381.1:c.52G>T, NP_005604.1:p.Asp18Tyr, NP_001095915.1:p.Asp115Tyr, NP_001106852.1:p.Asp18Tyr

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