SNP Links for Protein (Select 347582593) - SNP

Links from Protein

Items: 1 to 20 of 802

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Select item 14905661201.

rs1490566120 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 10:62091703 (GRCh38)
10:63851462 (GRCh37)
Canonical SPDI:: NC_000010.11:62091702:G:A,NC_000010.11:62091702:G:C
Gene:: ARID5B (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0./0 (GnomAD)
HGVS:: NC_000010.11:g.62091703G>A, NC_000010.11:g.62091703G>C, NC_000010.10:g.63851462G>A, NC_000010.10:g.63851462G>C, NG_030027.1:g.195450G>A, NG_030027.1:g.195450G>C, NM_032199.3:c.2240G>A, NM_032199.3:c.2240G>C, NM_032199.2:c.2240G>A, NM_032199.2:c.2240G>C, NM_001244638.2:c.1511G>A, NM_001244638.2:c.1511G>C, NM_001244638.1:c.1511G>A, NM_001244638.1:c.1511G>C, NP_115575.1:p.Ser747Asn, NP_115575.1:p.Ser747Thr, NP_001231567.1:p.Ser504Asn, NP_001231567.1:p.Ser504Thr

Select item 14897363312.

rs1489736331 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 10:62059295 (GRCh38)
10:63819054 (GRCh37)
Canonical SPDI:: NC_000010.11:62059294:A:G
Gene:: ARID5B (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000010.11:g.62059295A>G, NC_000010.10:g.63819054A>G, NG_030027.1:g.163042A>G, NM_032199.3:c.1101A>G, NM_032199.2:c.1101A>G, NM_001244638.2:c.372A>G, NM_001244638.1:c.372A>G

Select item 14887690933.

rs1488769093 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 10:62092436 (GRCh38)
10:63852195 (GRCh37)
Canonical SPDI:: NC_000010.11:62092435:C:T
Gene:: ARID5B (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (GnomAD_exomes)
T=0.000007/1 (GnomAD)
HGVS:: NC_000010.11:g.62092436C>T, NC_000010.10:g.63852195C>T, NG_030027.1:g.196183C>T, NM_032199.3:c.2973C>T, NM_032199.2:c.2973C>T, NM_001244638.2:c.2244C>T, NM_001244638.1:c.2244C>T

Select item 14883489534.

rs1488348953 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 10:62091684 (GRCh38)
10:63851443 (GRCh37)
Canonical SPDI:: NC_000010.11:62091683:A:G
Gene:: ARID5B (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000010.11:g.62091684A>G, NC_000010.10:g.63851443A>G, NG_030027.1:g.195431A>G, NM_032199.3:c.2221A>G, NM_032199.2:c.2221A>G, NM_001244638.2:c.1492A>G, NM_001244638.1:c.1492A>G, NP_115575.1:p.Thr741Ala, NP_001231567.1:p.Thr498Ala

Select item 14878716755.

rs1487871675 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 10:62092356 (GRCh38)
10:63852115 (GRCh37)
Canonical SPDI:: NC_000010.11:62092355:C:G
Gene:: ARID5B (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000043/1 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
G=0.000012/3 (GnomAD_exomes)
HGVS:: NC_000010.11:g.62092356C>G, NC_000010.10:g.63852115C>G, NG_030027.1:g.196103C>G, NM_032199.3:c.2893C>G, NM_032199.2:c.2893C>G, NM_001244638.2:c.2164C>G, NM_001244638.1:c.2164C>G, NP_115575.1:p.Pro965Ala, NP_001231567.1:p.Pro722Ala

Select item 14875457286.

rs1487545728 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 10:62092001 (GRCh38)
10:63851760 (GRCh37)
Canonical SPDI:: NC_000010.11:62092000:C:G
Gene:: ARID5B (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000010.11:g.62092001C>G, NC_000010.10:g.63851760C>G, NG_030027.1:g.195748C>G, NM_032199.3:c.2538C>G, NM_032199.2:c.2538C>G, NM_001244638.2:c.1809C>G, NM_001244638.1:c.1809C>G, NP_115575.1:p.His846Gln, NP_001231567.1:p.His603Gln

Select item 14874316107.

rs1487431610 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 10:62092216 (GRCh38)
10:63851975 (GRCh37)
Canonical SPDI:: NC_000010.11:62092215:C:T
Gene:: ARID5B (Varview)
Functional Consequence:: coding_sequence_variant,missense_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_000010.11:g.62092216C>T, NC_000010.10:g.63851975C>T, NG_030027.1:g.195963C>T, NM_032199.3:c.2753C>T, NM_032199.2:c.2753C>T, NM_001244638.2:c.2024C>T, NM_001244638.1:c.2024C>T, NP_115575.1:p.Thr918Ile, NP_001231567.1:p.Thr675Ile

Select item 14856852678.

rs1485685267 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 10:62091603 (GRCh38)
10:63851362 (GRCh37)
Canonical SPDI:: NC_000010.11:62091602:C:T
Gene:: ARID5B (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000010.11:g.62091603C>T, NC_000010.10:g.63851362C>T, NG_030027.1:g.195350C>T, NM_032199.3:c.2140C>T, NM_032199.2:c.2140C>T, NM_001244638.2:c.1411C>T, NM_001244638.1:c.1411C>T, NP_115575.1:p.Pro714Ser, NP_001231567.1:p.Pro471Ser

Select item 14841242559.

rs1484124255 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 10:62092653 (GRCh38)
10:63852412 (GRCh37)
Canonical SPDI:: NC_000010.11:62092652:G:T
Gene:: ARID5B (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000010.11:g.62092653G>T, NC_000010.10:g.63852412G>T, NG_030027.1:g.196400G>T, NM_032199.3:c.3190G>T, NM_032199.2:c.3190G>T, NM_001244638.2:c.2461G>T, NM_001244638.1:c.2461G>T, NP_115575.1:p.Gly1064Cys, NP_001231567.1:p.Gly821Cys

Select item 148159336110.

rs1481593361 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 10:62091706 (GRCh38)
10:63851465 (GRCh37)
Canonical SPDI:: NC_000010.11:62091705:G:A
Gene:: ARID5B (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)
A=0.000007/1 (GnomAD)
A=0.000035/1 (TOMMO)
HGVS:: NC_000010.11:g.62091706G>A, NC_000010.10:g.63851465G>A, NG_030027.1:g.195453G>A, NM_032199.3:c.2243G>A, NM_032199.2:c.2243G>A, NM_001244638.2:c.1514G>A, NM_001244638.1:c.1514G>A, NP_115575.1:p.Arg748Gln, NP_001231567.1:p.Arg505Gln

Select item 148069694511.

rs1480696945 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 10:62092369 (GRCh38)
10:63852128 (GRCh37)
Canonical SPDI:: NC_000010.11:62092368:C:G
Gene:: ARID5B (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (GnomAD_exomes)
G=0.000004/1 (TOPMED)
HGVS:: NC_000010.11:g.62092369C>G, NC_000010.10:g.63852128C>G, NG_030027.1:g.196116C>G, NM_032199.3:c.2906C>G, NM_032199.2:c.2906C>G, NM_001244638.2:c.2177C>G, NM_001244638.1:c.2177C>G, NP_115575.1:p.Pro969Arg, NP_001231567.1:p.Pro726Arg

Select item 148067491312.

rs1480674913 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 10:62091609 (GRCh38)
10:63851368 (GRCh37)
Canonical SPDI:: NC_000010.11:62091608:T:C
Gene:: ARID5B (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
HGVS:: NC_000010.11:g.62091609T>C, NC_000010.10:g.63851368T>C, NG_030027.1:g.195356T>C, NM_032199.3:c.2146T>C, NM_032199.2:c.2146T>C, NM_001244638.2:c.1417T>C, NM_001244638.1:c.1417T>C

Select item 147878785613.

rs1478787856 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 10:62091062 (GRCh38)
10:63850821 (GRCh37)
Canonical SPDI:: NC_000010.11:62091061:G:A
Gene:: ARID5B (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000008/2 (GnomAD_exomes)
A=0.000008/2 (TOPMED)
A=0.00006/1 (TOMMO)
HGVS:: NC_000010.11:g.62091062G>A, NC_000010.10:g.63850821G>A, NG_030027.1:g.194809G>A, NM_032199.3:c.1599G>A, NM_032199.2:c.1599G>A, NM_001244638.2:c.870G>A, NM_001244638.1:c.870G>A

Select item 147826071814.

rs1478260718 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 10:62092721 (GRCh38)
10:63852480 (GRCh37)
Canonical SPDI:: NC_000010.11:62092720:G:C
Gene:: ARID5B (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
HGVS:: NC_000010.11:g.62092721G>C, NC_000010.10:g.63852480G>C, NG_030027.1:g.196468G>C, NM_032199.3:c.3258G>C, NM_032199.2:c.3258G>C, NM_001244638.2:c.2529G>C, NM_001244638.1:c.2529G>C

Select item 147797331515.

rs1477973315 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 10:62092021 (GRCh38)
10:63851780 (GRCh37)
Canonical SPDI:: NC_000010.11:62092020:C:T
Gene:: ARID5B (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: T=0.000111/1 (ALFA)
T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000010.11:g.62092021C>T, NC_000010.10:g.63851780C>T, NG_030027.1:g.195768C>T, NM_032199.3:c.2558C>T, NM_032199.2:c.2558C>T, NM_001244638.2:c.1829C>T, NM_001244638.1:c.1829C>T, NP_115575.1:p.Thr853Ile, NP_001231567.1:p.Thr610Ile

Select item 147777811416.

rs1477778114 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 10:62092722 (GRCh38)
10:63852481 (GRCh37)
Canonical SPDI:: NC_000010.11:62092721:T:C
Gene:: ARID5B (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000010.11:g.62092722T>C, NC_000010.10:g.63852481T>C, NG_030027.1:g.196469T>C, NM_032199.3:c.3259T>C, NM_032199.2:c.3259T>C, NM_001244638.2:c.2530T>C, NM_001244638.1:c.2530T>C, NP_115575.1:p.Cys1087Arg, NP_001231567.1:p.Cys844Arg

Select item 147713008517.

rs1477130085 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 10:62091911 (GRCh38)
10:63851670 (GRCh37)
Canonical SPDI:: NC_000010.11:62091910:A:G
Gene:: ARID5B (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000010.11:g.62091911A>G, NC_000010.10:g.63851670A>G, NG_030027.1:g.195658A>G, NM_032199.3:c.2448A>G, NM_032199.2:c.2448A>G, NM_001244638.2:c.1719A>G, NM_001244638.1:c.1719A>G

Select item 147417093918.

rs1474170939 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 10:62085898 (GRCh38)
10:63845657 (GRCh37)
Canonical SPDI:: NC_000010.11:62085897:G:A
Gene:: ARID5B (Varview)
Functional Consequence:: coding_sequence_variant,missense_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_000010.11:g.62085898G>A, NC_000010.10:g.63845657G>A, NG_030027.1:g.189645G>A, NM_032199.3:c.1396G>A, NM_032199.2:c.1396G>A, NM_001244638.2:c.667G>A, NM_001244638.1:c.667G>A, NP_115575.1:p.Glu466Lys, NP_001231567.1:p.Glu223Lys

Select item 147368132119.

rs1473681321 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 10:62092845 (GRCh38)
10:63852604 (GRCh37)
Canonical SPDI:: NC_000010.11:62092844:A:G
Gene:: ARID5B (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
G=0.000012/3 (GnomAD_exomes)
HGVS:: NC_000010.11:g.62092845A>G, NC_000010.10:g.63852604A>G, NG_030027.1:g.196592A>G, NM_032199.3:c.3382A>G, NM_032199.2:c.3382A>G, NM_001244638.2:c.2653A>G, NM_001244638.1:c.2653A>G, NP_115575.1:p.Arg1128Gly, NP_001231567.1:p.Arg885Gly

Select item 147153498820.

rs1471534988 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 10:62092338 (GRCh38)
10:63852097 (GRCh37)
Canonical SPDI:: NC_000010.11:62092337:C:G,NC_000010.11:62092337:C:T
Gene:: ARID5B (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000010.11:g.62092338C>G, NC_000010.11:g.62092338C>T, NC_000010.10:g.63852097C>G, NC_000010.10:g.63852097C>T, NG_030027.1:g.196085C>G, NG_030027.1:g.196085C>T, NM_032199.3:c.2875C>G, NM_032199.3:c.2875C>T, NM_032199.2:c.2875C>G, NM_032199.2:c.2875C>T, NM_001244638.2:c.2146C>G, NM_001244638.2:c.2146C>T, NM_001244638.1:c.2146C>G, NM_001244638.1:c.2146C>T, NP_115575.1:p.Pro959Ala, NP_115575.1:p.Pro959Ser, NP_001231567.1:p.Pro716Ala, NP_001231567.1:p.Pro716Ser

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