SNP Links for Protein (Select 22027630) - SNP

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Links from Protein

Items: 1 to 20 of 345

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Select item 14879413881.

rs1487941388 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 11:36501258 (GRCh38)
11:36522808 (GRCh37)
Canonical SPDI:: NC_000011.10:36501257:G:T
Gene:: TRAF6 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.36501258G>T, NC_000011.9:g.36522808G>T, NM_004620.4:c.258C>A, NM_004620.3:c.258C>A, NM_145803.3:c.258C>A, NM_145803.2:c.258C>A

Select item 14815312252.

rs1481531225 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G [Show Flanks]
Chromosome:: 11:36494994 (GRCh38)
11:36516544 (GRCh37)
Canonical SPDI:: NC_000011.10:36494993:A:C,NC_000011.10:36494993:A:G
Gene:: TRAF6 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
G=0.000004/1 (GnomAD_exomes)
C=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.36494994A>C, NC_000011.10:g.36494994A>G, NC_000011.9:g.36516544A>C, NC_000011.9:g.36516544A>G, NM_004620.4:c.660T>G, NM_004620.4:c.660T>C, NM_004620.3:c.660T>G, NM_004620.3:c.660T>C, NM_145803.3:c.660T>G, NM_145803.3:c.660T>C, NM_145803.2:c.660T>G, NM_145803.2:c.660T>C

Select item 14796800913.

rs1479680091 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:36497254 (GRCh38)
11:36518804 (GRCh37)
Canonical SPDI:: NC_000011.10:36497253:G:A
Gene:: TRAF6 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: A=0.000071/1 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.36497254G>A, NC_000011.9:g.36518804G>A, NM_004620.4:c.460C>T, NM_004620.3:c.460C>T, NM_145803.3:c.460C>T, NM_145803.2:c.460C>T, NP_004611.1:p.His154Tyr, NP_665802.1:p.His154Tyr

Select item 14795767024.

rs1479576702 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 11:36490014 (GRCh38)
11:36511564 (GRCh37)
Canonical SPDI:: NC_000011.10:36490013:G:C
Gene:: TRAF6 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.36490014G>C, NC_000011.9:g.36511564G>C, NM_004620.4:c.1393C>G, NM_004620.3:c.1393C>G, NM_145803.3:c.1393C>G, NM_145803.2:c.1393C>G, NP_004611.1:p.Pro465Ala, NP_665802.1:p.Pro465Ala

Select item 14774274445.

rs1477427444 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:36492564 (GRCh38)
11:36514114 (GRCh37)
Canonical SPDI:: NC_000011.10:36492563:C:T
Gene:: TRAF6 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
HGVS:: NC_000011.10:g.36492564C>T, NC_000011.9:g.36514114C>T, NM_004620.4:c.743G>A, NM_004620.3:c.743G>A, NM_145803.3:c.743G>A, NM_145803.2:c.743G>A, NP_004611.1:p.Gly248Asp, NP_665802.1:p.Gly248Asp

Select item 14758209716.

rs1475820971 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 11:36490158 (GRCh38)
11:36511708 (GRCh37)
Canonical SPDI:: NC_000011.10:36490157:C:G,NC_000011.10:36490157:C:T
Gene:: TRAF6 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (GnomAD_exomes)
G=0.000007/1 (GnomAD)
G=0.000008/2 (TOPMED)
HGVS:: NC_000011.10:g.36490158C>G, NC_000011.10:g.36490158C>T, NC_000011.9:g.36511708C>G, NC_000011.9:g.36511708C>T, NM_004620.4:c.1249G>C, NM_004620.4:c.1249G>A, NM_004620.3:c.1249G>C, NM_004620.3:c.1249G>A, NM_145803.3:c.1249G>C, NM_145803.3:c.1249G>A, NM_145803.2:c.1249G>C, NM_145803.2:c.1249G>A, NP_004611.1:p.Glu417Gln, NP_004611.1:p.Glu417Lys, NP_665802.1:p.Glu417Gln, NP_665802.1:p.Glu417Lys

Select item 14736661477.

rs1473666147 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:36490393 (GRCh38)
11:36511943 (GRCh37)
Canonical SPDI:: NC_000011.10:36490392:C:T
Gene:: TRAF6 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
HGVS:: NC_000011.10:g.36490393C>T, NC_000011.9:g.36511943C>T, NM_004620.4:c.1014G>A, NM_004620.3:c.1014G>A, NM_145803.3:c.1014G>A, NM_145803.2:c.1014G>A

Select item 14702968678.

rs1470296867 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:36490434 (GRCh38)
11:36511984 (GRCh37)
Canonical SPDI:: NC_000011.10:36490433:T:C
Gene:: TRAF6 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (GnomAD_exomes)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.36490434T>C, NC_000011.9:g.36511984T>C, NM_004620.4:c.973A>G, NM_004620.3:c.973A>G, NM_145803.3:c.973A>G, NM_145803.2:c.973A>G, NP_004611.1:p.Met325Val, NP_665802.1:p.Met325Val

Select item 14664956069.

rs1466495606 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 11:36497124 (GRCh38)
11:36518674 (GRCh37)
Canonical SPDI:: NC_000011.10:36497123:G:T
Gene:: TRAF6 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.36497124G>T, NC_000011.9:g.36518674G>T, NM_004620.4:c.590C>A, NM_004620.3:c.590C>A, NM_145803.3:c.590C>A, NM_145803.2:c.590C>A, NP_004611.1:p.Ala197Glu, NP_665802.1:p.Ala197Glu

Select item 146581538410.

rs1465815384 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:36490099 (GRCh38)
11:36511649 (GRCh37)
Canonical SPDI:: NC_000011.10:36490098:A:G
Gene:: TRAF6 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000014/2 (GnomAD)
G=0.000015/4 (TOPMED)
HGVS:: NC_000011.10:g.36490099A>G, NC_000011.9:g.36511649A>G, NM_004620.4:c.1308T>C, NM_004620.3:c.1308T>C, NM_145803.3:c.1308T>C, NM_145803.2:c.1308T>C

Select item 146001625511.

rs1460016255 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:36497204 (GRCh38)
11:36518754 (GRCh37)
Canonical SPDI:: NC_000011.10:36497203:T:C
Gene:: TRAF6 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.36497204T>C, NC_000011.9:g.36518754T>C, NM_004620.4:c.510A>G, NM_004620.3:c.510A>G, NM_145803.3:c.510A>G, NM_145803.2:c.510A>G

Select item 145766075312.

rs1457660753 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:36498541 (GRCh38)
11:36520091 (GRCh37)
Canonical SPDI:: NC_000011.10:36498540:C:T
Gene:: TRAF6 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.36498541C>T, NC_000011.9:g.36520091C>T, NM_004620.4:c.396G>A, NM_004620.3:c.396G>A, NM_145803.3:c.396G>A, NM_145803.2:c.396G>A

Select item 145556471813.

rs1455564718 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:36492556 (GRCh38)
11:36514106 (GRCh37)
Canonical SPDI:: NC_000011.10:36492555:C:T
Gene:: TRAF6 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: T=0.000051/1 (ALFA)
T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.36492556C>T, NC_000011.9:g.36514106C>T, NM_004620.4:c.751G>A, NM_004620.3:c.751G>A, NM_145803.3:c.751G>A, NM_145803.2:c.751G>A, NP_004611.1:p.Glu251Lys, NP_665802.1:p.Glu251Lys

Select item 145535692414.

rs1455356924 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 11:36501305 (GRCh38)
11:36522855 (GRCh37)
Canonical SPDI:: NC_000011.10:36501304:G:C
Gene:: TRAF6 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.36501305G>C, NC_000011.9:g.36522855G>C, NM_004620.4:c.211C>G, NM_004620.3:c.211C>G, NM_145803.3:c.211C>G, NM_145803.2:c.211C>G, NP_004611.1:p.Pro71Ala, NP_665802.1:p.Pro71Ala

Select item 145308876815.

rs1453088768 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 11:36501462 (GRCh38)
11:36523012 (GRCh37)
Canonical SPDI:: NC_000011.10:36501461:G:C
Gene:: TRAF6 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.36501462G>C, NC_000011.9:g.36523012G>C, NM_004620.4:c.54C>G, NM_004620.3:c.54C>G, NM_145803.3:c.54C>G, NM_145803.2:c.54C>G, NP_004611.1:p.Asp18Glu, NP_665802.1:p.Asp18Glu

Select item 145174546116.

rs1451745461 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:36501381 (GRCh38)
11:36522931 (GRCh37)
Canonical SPDI:: NC_000011.10:36501380:G:A
Gene:: TRAF6 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.36501381G>A, NC_000011.9:g.36522931G>A, NM_004620.4:c.135C>T, NM_004620.3:c.135C>T, NM_145803.3:c.135C>T, NM_145803.2:c.135C>T

Select item 144805081517.

rs1448050815 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 11:36498514 (GRCh38)
11:36520064 (GRCh37)
Canonical SPDI:: NC_000011.10:36498513:G:C
Gene:: TRAF6 (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_000011.10:g.36498514G>C, NC_000011.9:g.36520064G>C, NM_004620.4:c.423C>G, NM_004620.3:c.423C>G, NM_145803.3:c.423C>G, NM_145803.2:c.423C>G, NP_004611.1:p.His141Gln, NP_665802.1:p.His141Gln

Select item 144781307218.

rs1447813072 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:36490320 (GRCh38)
11:36511870 (GRCh37)
Canonical SPDI:: NC_000011.10:36490319:G:A
Gene:: TRAF6 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.36490320G>A, NC_000011.9:g.36511870G>A, NM_004620.4:c.1087C>T, NM_004620.3:c.1087C>T, NM_145803.3:c.1087C>T, NM_145803.2:c.1087C>T, NP_004611.1:p.His363Tyr, NP_665802.1:p.His363Tyr

Select item 144197556819.

rs1441975568 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C,T [Show Flanks]
Chromosome:: 11:36490575 (GRCh38)
11:36512125 (GRCh37)
Canonical SPDI:: NC_000011.10:36490574:G:C,NC_000011.10:36490574:G:T
Gene:: TRAF6 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
HGVS:: NC_000011.10:g.36490575G>C, NC_000011.10:g.36490575G>T, NC_000011.9:g.36512125G>C, NC_000011.9:g.36512125G>T, NM_004620.4:c.832C>G, NM_004620.4:c.832C>A, NM_004620.3:c.832C>G, NM_004620.3:c.832C>A, NM_145803.3:c.832C>G, NM_145803.3:c.832C>A, NM_145803.2:c.832C>G, NM_145803.2:c.832C>A, NP_004611.1:p.His278Asp, NP_004611.1:p.His278Asn, NP_665802.1:p.His278Asp, NP_665802.1:p.His278Asn

Select item 144058041120.

rs1440580411 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 11:36490376 (GRCh38)
11:36511926 (GRCh37)
Canonical SPDI:: NC_000011.10:36490375:A:T
Gene:: TRAF6 (Varview)
Functional Consequence:: missense_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_000011.10:g.36490376A>T, NC_000011.9:g.36511926A>T, NM_004620.4:c.1031T>A, NM_004620.3:c.1031T>A, NM_145803.3:c.1031T>A, NM_145803.2:c.1031T>A, NP_004611.1:p.Ile344Asn, NP_665802.1:p.Ile344Asn

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