SNP Links for Protein (Select 4502211) - SNP

Links from Protein

Items: 1 to 20 of 133

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Select item 14908235311.

rs1490823531 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 14:49893938 (GRCh38)
14:50360656 (GRCh37)
Canonical SPDI:: NC_000014.9:49893937:G:C
Gene:: ARF6 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000014.9:g.49893938G>C, NC_000014.8:g.50360656G>C, NM_001663.4:c.202G>C, NM_001663.3:c.202G>C, NP_001654.1:p.Asp68His

Select item 14811088942.

rs1481108894 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 14:49893849 (GRCh38)
14:50360567 (GRCh37)
Canonical SPDI:: NC_000014.9:49893848:C:T
Gene:: ARF6 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: T=0.000047/1 (ALFA)
T=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000014.9:g.49893849C>T, NC_000014.8:g.50360567C>T, NM_001663.4:c.113C>T, NM_001663.3:c.113C>T, NP_001654.1:p.Ser38Leu

Select item 14550773173.

rs1455077317 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 14:49893940 (GRCh38)
14:50360658 (GRCh37)
Canonical SPDI:: NC_000014.9:49893939:C:T
Gene:: ARF6 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000014.9:g.49893940C>T, NC_000014.8:g.50360658C>T, NM_001663.4:c.204C>T, NM_001663.3:c.204C>T

Select item 14489369094.

rs1448936909 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 14:49893847 (GRCh38)
14:50360565 (GRCh37)
Canonical SPDI:: NC_000014.9:49893846:G:A
Gene:: ARF6 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000014.9:g.49893847G>A, NC_000014.8:g.50360565G>A, NM_001663.4:c.111G>A, NM_001663.3:c.111G>A

Select item 14480059745.

rs1448005974 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 14:49893999 (GRCh38)
14:50360717 (GRCh37)
Canonical SPDI:: NC_000014.9:49893998:T:C
Gene:: ARF6 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000014.9:g.49893999T>C, NC_000014.8:g.50360717T>C, NM_001663.4:c.263T>C, NM_001663.3:c.263T>C, NP_001654.1:p.Val88Ala

Select item 14468700806.

rs1446870080 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 14:49894153 (GRCh38)
14:50360871 (GRCh37)
Canonical SPDI:: NC_000014.9:49894152:G:T
Gene:: ARF6 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000014.9:g.49894153G>T, NC_000014.8:g.50360871G>T, NM_001663.4:c.417G>T, NM_001663.3:c.417G>T

Select item 14440706067.

rs1444070606 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 14:49893839 (GRCh38)
14:50360557 (GRCh37)
Canonical SPDI:: NC_000014.9:49893838:C:T
Gene:: ARF6 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_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_000014.9:g.49893839C>T, NC_000014.8:g.50360557C>T, NM_001663.4:c.103C>T, NM_001663.3:c.103C>T

Select item 14415877388.

rs1441587738 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 14:49893746 (GRCh38)
14:50360464 (GRCh37)
Canonical SPDI:: NC_000014.9:49893745:G:A
Gene:: ARF6 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
A=0.000004/1 (TOPMED)
HGVS:: NC_000014.9:g.49893746G>A, NC_000014.8:g.50360464G>A, NM_001663.4:c.10G>A, NM_001663.3:c.10G>A, NP_001654.1:p.Val4Met

Select item 14359044399.

rs1435904439 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 14:49893833 (GRCh38)
14:50360551 (GRCh37)
Canonical SPDI:: NC_000014.9:49893832:T:G
Gene:: ARF6 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000014.9:g.49893833T>G, NC_000014.8:g.50360551T>G, NM_001663.4:c.97T>G, NM_001663.3:c.97T>G, NP_001654.1:p.Leu33Val

Select item 142710068810.

rs1427100688 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 14:49894020 (GRCh38)
14:50360738 (GRCh37)
Canonical SPDI:: NC_000014.9:49894019:G:T
Gene:: ARF6 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000014.9:g.49894020G>T, NC_000014.8:g.50360738G>T, NM_001663.4:c.284G>T, NM_001663.3:c.284G>T, NP_001654.1:p.Arg95Leu

Select item 140677897711.

rs1406778977 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 14:49893901 (GRCh38)
14:50360619 (GRCh37)
Canonical SPDI:: NC_000014.9:49893900:A:G
Gene:: ARF6 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000014.9:g.49893901A>G, NC_000014.8:g.50360619A>G, NM_001663.4:c.165A>G, NM_001663.3:c.165A>G

Select item 140493956012.

rs1404939560 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 14:49893786 (GRCh38)
14:50360504 (GRCh37)
Canonical SPDI:: NC_000014.9:49893785:T:A
Gene:: ARF6 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000014.9:g.49893786T>A, NC_000014.8:g.50360504T>A, NM_001663.4:c.50T>A, NM_001663.3:c.50T>A, NP_001654.1:p.Leu17His

Select item 139666655713.

rs1396666557 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 14:49894112 (GRCh38)
14:50360830 (GRCh37)
Canonical SPDI:: NC_000014.9:49894111:C:T
Gene:: ARF6 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
HGVS:: NC_000014.9:g.49894112C>T, NC_000014.8:g.50360830C>T, NM_001663.4:c.376C>T, NM_001663.3:c.376C>T

Select item 138661773214.

rs1386617732 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 14:49894213 (GRCh38)
14:50360931 (GRCh37)
Canonical SPDI:: NC_000014.9:49894212:G:A,NC_000014.9:49894212:G:T
Gene:: ARF6 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000051/1 (ALFA)
A=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000014.9:g.49894213G>A, NC_000014.9:g.49894213G>T, NC_000014.8:g.50360931G>A, NC_000014.8:g.50360931G>T, NM_001663.4:c.477G>A, NM_001663.4:c.477G>T, NM_001663.3:c.477G>A, NM_001663.3:c.477G>T

Select item 138624821415.

rs1386248214 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 14:49894135 (GRCh38)
14:50360853 (GRCh37)
Canonical SPDI:: NC_000014.9:49894134:C:T
Gene:: ARF6 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by cluster
MAF:: T=0.000004/1 (GnomAD_exomes)
T=0.000546/1 (Korea1K)
HGVS:: NC_000014.9:g.49894135C>T, NC_000014.8:g.50360853C>T, NM_001663.4:c.399C>T, NM_001663.3:c.399C>T

Select item 138600778916.

rs1386007789 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 14:49893832 (GRCh38)
14:50360550 (GRCh37)
Canonical SPDI:: NC_000014.9:49893831:G:A
Gene:: ARF6 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000071/1 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000011/3 (TOPMED)
HGVS:: NC_000014.9:g.49893832G>A, NC_000014.8:g.50360550G>A, NM_001663.4:c.96G>A, NM_001663.3:c.96G>A

Select item 138591355617.

rs1385913556 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 14:49893976 (GRCh38)
14:50360694 (GRCh37)
Canonical SPDI:: NC_000014.9:49893975:G:C
Gene:: ARF6 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000014.9:g.49893976G>C, NC_000014.8:g.50360694G>C, NM_001663.4:c.240G>C, NM_001663.3:c.240G>C

Select item 138286719818.

rs1382867198 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 14:49894026 (GRCh38)
14:50360744 (GRCh37)
Canonical SPDI:: NC_000014.9:49894025:A:G
Gene:: ARF6 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000014.9:g.49894026A>G, NC_000014.8:g.50360744A>G, NM_001663.4:c.290A>G, NM_001663.3:c.290A>G, NP_001654.1:p.Asp97Gly

Select item 137918439419.

rs1379184394 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 14:49893841 (GRCh38)
14:50360559 (GRCh37)
Canonical SPDI:: NC_000014.9:49893840:G:A
Gene:: ARF6 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
HGVS:: NC_000014.9:g.49893841G>A, NC_000014.8:g.50360559G>A, NM_001663.4:c.105G>A, NM_001663.3:c.105G>A

Select item 136667553820.

rs1366675538 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 14:49894015 (GRCh38)
14:50360733 (GRCh37)
Canonical SPDI:: NC_000014.9:49894014:C:T
Gene:: ARF6 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000014.9:g.49894015C>T, NC_000014.8:g.50360733C>T, NM_001663.4:c.279C>T, NM_001663.3:c.279C>T

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