SNP Links for Protein (Select 6912492) - SNP

Select item 14891819821.

rs1489181982 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 22:50610243 (GRCh38)
22:51048671 (GRCh37)
Canonical SPDI:: NC_000022.11:50610242:C:T
Gene:: MAPK8IP2 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000022.11:g.50610243C>T, NC_000022.10:g.51048671C>T, NG_032955.2:g.14559C>T, NM_012324.6:c.2335C>T, NM_012324.5:c.2335C>T, NM_012324.4:c.2335C>T, NM_012324.3:c.2335C>T, XM_011530679.3:c.2338C>T, XM_011530679.2:c.2338C>T, XM_011530679.1:c.2338C>T, XM_011530680.3:c.2224C>T, XM_011530680.2:c.2224C>T, XM_011530680.1:c.2224C>T, XM_011530681.3:c.2203C>T, XM_011530681.2:c.2203C>T, XM_011530681.1:c.2203C>T, NM_016431.3:c.2254C>T, NM_139124.1:c.1192C>T

Select item 14879284472.

rs1487928447 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 22:50604775 (GRCh38)
22:51043203 (GRCh37)
Canonical SPDI:: NC_000022.11:50604774:G:A
Gene:: MAPK8IP2 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: A=0.000007/1 (GnomAD_exomes)
HGVS:: NC_000022.11:g.50604775G>A, NC_000022.10:g.51043203G>A, NG_032955.2:g.9091G>A, NM_012324.6:c.1476G>A, NM_012324.5:c.1476G>A, NM_012324.4:c.1476G>A, NM_012324.3:c.1476G>A, XM_011530679.3:c.1479G>A, XM_011530679.2:c.1479G>A, XM_011530679.1:c.1479G>A, XM_011530680.3:c.1365G>A, XM_011530680.2:c.1365G>A, XM_011530680.1:c.1365G>A, XM_011530681.3:c.1344G>A, XM_011530681.2:c.1344G>A, XM_011530681.1:c.1344G>A, NM_016431.3:c.1395G>A, NM_139124.1:c.333G>A

Select item 14866530873.

rs1486653087 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 22:50610737 (GRCh38)
22:51049165 (GRCh37)
Canonical SPDI:: NC_000022.11:50610736:C:T
Gene:: MAPK8IP2 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
T=0.000014/2 (GnomAD)
HGVS:: NC_000022.11:g.50610737C>T, NC_000022.10:g.51049165C>T, NG_032955.2:g.15053C>T, NM_012324.6:c.2433C>T, NM_012324.5:c.2433C>T, NM_012324.4:c.2433C>T, NM_012324.3:c.2433C>T, XM_011530679.3:c.2436C>T, XM_011530679.2:c.2436C>T, XM_011530679.1:c.2436C>T, XM_011530680.3:c.2322C>T, XM_011530680.2:c.2322C>T, XM_011530680.1:c.2322C>T, XM_011530681.3:c.2301C>T, XM_011530681.2:c.2301C>T, XM_011530681.1:c.2301C>T, NM_016431.3:c.2352C>T, NM_139124.1:c.1290C>T

Select item 14862860574.

rs1486286057 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 22:50604648 (GRCh38)
22:51043076 (GRCh37)
Canonical SPDI:: NC_000022.11:50604647:G:C
Gene:: MAPK8IP2 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
HGVS:: NC_000022.11:g.50604648G>C, NC_000022.10:g.51043076G>C, NG_032955.2:g.8964G>C, NM_012324.6:c.1349G>C, NM_012324.5:c.1349G>C, NM_012324.4:c.1349G>C, NM_012324.3:c.1349G>C, XM_011530679.3:c.1352G>C, XM_011530679.2:c.1352G>C, XM_011530679.1:c.1352G>C, XM_011530680.3:c.1238G>C, XM_011530680.2:c.1238G>C, XM_011530680.1:c.1238G>C, XM_011530681.3:c.1217G>C, XM_011530681.2:c.1217G>C, XM_011530681.1:c.1217G>C, NM_016431.3:c.1268G>C, NP_036456.1:p.Trp450Ser, XP_011528981.1:p.Trp451Ser, XP_011528982.1:p.Trp413Ser, XP_011528983.1:p.Trp406Ser

Select item 14862565345.

rs1486256534 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 22:50604691 (GRCh38)
22:51043119 (GRCh37)
Canonical SPDI:: NC_000022.11:50604690:C:T
Gene:: MAPK8IP2 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000009/1 (GnomAD_exomes)
T=0.000011/3 (TOPMED)
HGVS:: NC_000022.11:g.50604691C>T, NC_000022.10:g.51043119C>T, NG_032955.2:g.9007C>T, NM_012324.6:c.1392C>T, NM_012324.5:c.1392C>T, NM_012324.4:c.1392C>T, NM_012324.3:c.1392C>T, XM_011530679.3:c.1395C>T, XM_011530679.2:c.1395C>T, XM_011530679.1:c.1395C>T, XM_011530680.3:c.1281C>T, XM_011530680.2:c.1281C>T, XM_011530680.1:c.1281C>T, XM_011530681.3:c.1260C>T, XM_011530681.2:c.1260C>T, XM_011530681.1:c.1260C>T, NM_016431.3:c.1311C>T

Select item 14862304896.

rs1486230489 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 22:50603982 (GRCh38)
22:51042411 (GRCh37)
Canonical SPDI:: NC_000022.11:50603981:T:C
Gene:: MAPK8IP2 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000022.11:g.50603982T>C, NC_000022.10:g.51042411T>C, NG_032955.2:g.8298T>C, NM_012324.6:c.683T>C, NM_012324.5:c.683T>C, NM_012324.4:c.683T>C, NM_012324.3:c.683T>C, XM_011530679.3:c.686T>C, XM_011530679.2:c.686T>C, XM_011530679.1:c.686T>C, XM_011530680.3:c.572T>C, XM_011530680.2:c.572T>C, XM_011530680.1:c.572T>C, XM_011530681.3:c.551T>C, XM_011530681.2:c.551T>C, XM_011530681.1:c.551T>C, NM_016431.3:c.602T>C, NP_036456.1:p.Ile228Thr, XP_011528981.1:p.Ile229Thr, XP_011528982.1:p.Ile191Thr, XP_011528983.1:p.Ile184Thr

Select item 14862025727.

rs1486202572 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 22:50605369 (GRCh38)
22:51043797 (GRCh37)
Canonical SPDI:: NC_000022.11:50605368:C:T
Gene:: MAPK8IP2 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (GnomAD_exomes)
T=0.000008/2 (TOPMED)
T=0.000014/2 (GnomAD)
HGVS:: NC_000022.11:g.50605369C>T, NC_000022.10:g.51043797C>T, NG_032955.2:g.9685C>T, NM_012324.6:c.1767C>T, NM_012324.5:c.1767C>T, NM_012324.4:c.1767C>T, NM_012324.3:c.1767C>T, XM_011530679.3:c.1770C>T, XM_011530679.2:c.1770C>T, XM_011530679.1:c.1770C>T, XM_011530680.3:c.1656C>T, XM_011530680.2:c.1656C>T, XM_011530680.1:c.1656C>T, XM_011530681.3:c.1635C>T, XM_011530681.2:c.1635C>T, XM_011530681.1:c.1635C>T, NM_016431.3:c.1686C>T, NM_139124.1:c.624C>T

Select item 14853100068.

rs1485310006 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 22:50600878 (GRCh38)
22:51039307 (GRCh37)
Canonical SPDI:: NC_000022.11:50600877:C:G
Gene:: MAPK8IP2 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
HGVS:: NC_000022.11:g.50600878C>G, NC_000022.10:g.51039307C>G, NG_032955.2:g.5194C>G, NM_012324.6:c.60C>G, NM_012324.5:c.60C>G, NM_012324.4:c.60C>G, NM_012324.3:c.60C>G, XM_011530679.3:c.60C>G, XM_011530679.2:c.60C>G, XM_011530679.1:c.60C>G, XM_011530680.3:c.60C>G, XM_011530680.2:c.60C>G, XM_011530680.1:c.60C>G, XM_011530681.3:c.60C>G, XM_011530681.2:c.60C>G, XM_011530681.1:c.60C>G, NM_139124.1:c.60C>G

Select item 14849752139.

rs1484975213 [Homo sapiens]

Variant type:: DELINS
Alleles:: GAC>- [Show Flanks]
Chromosome:: 22:50604275 (GRCh38)
22:51042703 (GRCh37)
Canonical SPDI:: NC_000022.11:50604270:CGACGAC:CGAC
Gene:: MAPK8IP2 (Varview)
Functional Consequence:: inframe_deletion,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: CGAC=0./0 (ALFA)
-=0.000008/2 (TOPMED)
-=0.000021/3 (GnomAD)
HGVS:: NC_000022.11:g.50604272GAC[1], NC_000022.10:g.51042700GAC[1], NG_032955.2:g.8588GAC[1], NM_012324.6:c.973GAC[1], NM_012324.5:c.973GAC[1], NM_012324.4:c.973GAC[1], NM_012324.3:c.973GAC[1], XM_011530679.3:c.976GAC[1], XM_011530679.2:c.976GAC[1], XM_011530679.1:c.976GAC[1], XM_011530680.3:c.862GAC[1], XM_011530680.2:c.862GAC[1], XM_011530680.1:c.862GAC[1], XM_011530681.3:c.841GAC[1], XM_011530681.2:c.841GAC[1], XM_011530681.1:c.841GAC[1], NM_016431.3:c.892GAC[1], NP_036456.1:p.Asp326del, XP_011528981.1:p.Asp327del, XP_011528982.1:p.Asp289del, XP_011528983.1:p.Asp282del

Select item 148489220310.

rs1484892203 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 22:50603226 (GRCh38)
22:51041655 (GRCh37)
Canonical SPDI:: NC_000022.11:50603225:A:G
Gene:: MAPK8IP2 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000022.11:g.50603226A>G, NC_000022.10:g.51041655A>G, NG_032955.2:g.7542A>G, NM_012324.6:c.175A>G, NM_012324.5:c.175A>G, NM_012324.4:c.175A>G, NM_012324.3:c.175A>G, XM_011530679.3:c.175A>G, XM_011530679.2:c.175A>G, XM_011530679.1:c.175A>G, XM_011530680.3:c.175A>G, XM_011530680.2:c.175A>G, XM_011530680.1:c.175A>G, XM_011530681.3:c.175A>G, XM_011530681.2:c.175A>G, XM_011530681.1:c.175A>G, NM_016431.3:c.94A>G, NM_139124.1:c.175A>G, NP_036456.1:p.Ser59Gly, XP_011528981.1:p.Ser59Gly, XP_011528982.1:p.Ser59Gly, XP_011528983.1:p.Ser59Gly

Select item 148465363311.

rs1484653633 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 22:50604900 (GRCh38)
22:51043328 (GRCh37)
Canonical SPDI:: NC_000022.11:50604899:A:G
Gene:: MAPK8IP2 (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=0.000021/3 (GnomAD)
G=0.000023/6 (TOPMED)
HGVS:: NC_000022.11:g.50604900A>G, NC_000022.10:g.51043328A>G, NG_032955.2:g.9216A>G, NM_012324.6:c.1601A>G, NM_012324.5:c.1601A>G, NM_012324.4:c.1601A>G, NM_012324.3:c.1601A>G, XM_011530679.3:c.1604A>G, XM_011530679.2:c.1604A>G, XM_011530679.1:c.1604A>G, XM_011530680.3:c.1490A>G, XM_011530680.2:c.1490A>G, XM_011530680.1:c.1490A>G, XM_011530681.3:c.1469A>G, XM_011530681.2:c.1469A>G, XM_011530681.1:c.1469A>G, NM_016431.3:c.1520A>G, NM_139124.1:c.458A>G, NP_036456.1:p.His534Arg, XP_011528981.1:p.His535Arg, XP_011528982.1:p.His497Arg, XP_011528983.1:p.His490Arg

Select item 148456494412.

rs1484564944 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 22:50605662 (GRCh38)
22:51044090 (GRCh37)
Canonical SPDI:: NC_000022.11:50605661:C:A,NC_000022.11:50605661:C:T
Gene:: MAPK8IP2 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
A=0.00004/1 (TOMMO)
HGVS:: NC_000022.11:g.50605662C>A, NC_000022.11:g.50605662C>T, NC_000022.10:g.51044090C>A, NC_000022.10:g.51044090C>T, NG_032955.2:g.9978C>A, NG_032955.2:g.9978C>T, NM_012324.6:c.1942C>A, NM_012324.6:c.1942C>T, NM_012324.5:c.1942C>A, NM_012324.5:c.1942C>T, NM_012324.4:c.1942C>A, NM_012324.4:c.1942C>T, NM_012324.3:c.1942C>A, NM_012324.3:c.1942C>T, XM_011530679.3:c.1945C>A, XM_011530679.3:c.1945C>T, XM_011530679.2:c.1945C>A, XM_011530679.2:c.1945C>T, XM_011530679.1:c.1945C>A, XM_011530679.1:c.1945C>T, XM_011530680.3:c.1831C>A, XM_011530680.3:c.1831C>T, XM_011530680.2:c.1831C>A, XM_011530680.2:c.1831C>T, XM_011530680.1:c.1831C>A, XM_011530680.1:c.1831C>T, XM_011530681.3:c.1810C>A, XM_011530681.3:c.1810C>T, XM_011530681.2:c.1810C>A, XM_011530681.2:c.1810C>T, XM_011530681.1:c.1810C>A, XM_011530681.1:c.1810C>T, NM_016431.3:c.1861C>A, NM_016431.3:c.1861C>T, NM_139124.1:c.799C>A, NM_139124.1:c.799C>T, NP_036456.1:p.Arg648Ser, NP_036456.1:p.Arg648Cys, XP_011528981.1:p.Arg649Ser, XP_011528981.1:p.Arg649Cys, XP_011528982.1:p.Arg611Ser, XP_011528982.1:p.Arg611Cys, XP_011528983.1:p.Arg604Ser, XP_011528983.1:p.Arg604Cys

Select item 148430052613.

rs1484300526 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 22:50604049 (GRCh38)
22:51042478 (GRCh37)
Canonical SPDI:: NC_000022.11:50604048:C:G,NC_000022.11:50604048:C:T
Gene:: MAPK8IP2 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
G=0.00003/8 (TOPMED)
G=0.000033/4 (GnomAD_exomes)
HGVS:: NC_000022.11:g.50604049C>G, NC_000022.11:g.50604049C>T, NC_000022.10:g.51042478C>G, NC_000022.10:g.51042478C>T, NG_032955.2:g.8365C>G, NG_032955.2:g.8365C>T, NM_012324.6:c.750C>G, NM_012324.6:c.750C>T, NM_012324.5:c.750C>G, NM_012324.5:c.750C>T, NM_012324.4:c.750C>G, NM_012324.4:c.750C>T, NM_012324.3:c.750C>G, NM_012324.3:c.750C>T, XM_011530679.3:c.753C>G, XM_011530679.3:c.753C>T, XM_011530679.2:c.753C>G, XM_011530679.2:c.753C>T, XM_011530679.1:c.753C>G, XM_011530679.1:c.753C>T, XM_011530680.3:c.639C>G, XM_011530680.3:c.639C>T, XM_011530680.2:c.639C>G, XM_011530680.2:c.639C>T, XM_011530680.1:c.639C>G, XM_011530680.1:c.639C>T, XM_011530681.3:c.618C>G, XM_011530681.3:c.618C>T, XM_011530681.2:c.618C>G, XM_011530681.2:c.618C>T, XM_011530681.1:c.618C>G, XM_011530681.1:c.618C>T, NM_016431.3:c.669C>G, NM_016431.3:c.669C>T

Select item 148414247214.

rs1484142472 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 22:50604399 (GRCh38)
22:51042827 (GRCh37)
Canonical SPDI:: NC_000022.11:50604398:G:A,NC_000022.11:50604398:G:T
Gene:: MAPK8IP2 (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)
A=0.000692/2 (KOREAN)
HGVS:: NC_000022.11:g.50604399G>A, NC_000022.11:g.50604399G>T, NC_000022.10:g.51042827G>A, NC_000022.10:g.51042827G>T, NG_032955.2:g.8715G>A, NG_032955.2:g.8715G>T, NM_012324.6:c.1100G>A, NM_012324.6:c.1100G>T, NM_012324.5:c.1100G>A, NM_012324.5:c.1100G>T, NM_012324.4:c.1100G>A, NM_012324.4:c.1100G>T, NM_012324.3:c.1100G>A, NM_012324.3:c.1100G>T, XM_011530679.3:c.1103G>A, XM_011530679.3:c.1103G>T, XM_011530679.2:c.1103G>A, XM_011530679.2:c.1103G>T, XM_011530679.1:c.1103G>A, XM_011530679.1:c.1103G>T, XM_011530680.3:c.989G>A, XM_011530680.3:c.989G>T, XM_011530680.2:c.989G>A, XM_011530680.2:c.989G>T, XM_011530680.1:c.989G>A, XM_011530680.1:c.989G>T, XM_011530681.3:c.968G>A, XM_011530681.3:c.968G>T, XM_011530681.2:c.968G>A, XM_011530681.2:c.968G>T, XM_011530681.1:c.968G>A, XM_011530681.1:c.968G>T, NM_016431.3:c.1019G>A, NM_016431.3:c.1019G>T, NP_036456.1:p.Arg367His, NP_036456.1:p.Arg367Leu, XP_011528981.1:p.Arg368His, XP_011528981.1:p.Arg368Leu, XP_011528982.1:p.Arg330His, XP_011528982.1:p.Arg330Leu, XP_011528983.1:p.Arg323His, XP_011528983.1:p.Arg323Leu

Select item 148387414615.

rs1483874146 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 22:50603225 (GRCh38)
22:51041654 (GRCh37)
Canonical SPDI:: NC_000022.11:50603224:C:G
Gene:: MAPK8IP2 (Varview)
Functional Consequence:: coding_sequence_variant,missense_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_000022.11:g.50603225C>G, NC_000022.10:g.51041654C>G, NG_032955.2:g.7541C>G, NM_012324.6:c.174C>G, NM_012324.5:c.174C>G, NM_012324.4:c.174C>G, NM_012324.3:c.174C>G, XM_011530679.3:c.174C>G, XM_011530679.2:c.174C>G, XM_011530679.1:c.174C>G, XM_011530680.3:c.174C>G, XM_011530680.2:c.174C>G, XM_011530680.1:c.174C>G, XM_011530681.3:c.174C>G, XM_011530681.2:c.174C>G, XM_011530681.1:c.174C>G, NM_016431.3:c.93C>G, NM_139124.1:c.174C>G, NP_036456.1:p.Asp58Glu, XP_011528981.1:p.Asp58Glu, XP_011528982.1:p.Asp58Glu, XP_011528983.1:p.Asp58Glu

Select item 148373251416.

rs1483732514 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 22:50603303 (GRCh38)
22:51041732 (GRCh37)
Canonical SPDI:: NC_000022.11:50603302:C:T
Gene:: MAPK8IP2 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000021/3 (GnomAD)
T=0.000023/6 (TOPMED)
HGVS:: NC_000022.11:g.50603303C>T, NC_000022.10:g.51041732C>T, NG_032955.2:g.7619C>T, NM_012324.6:c.252C>T, NM_012324.5:c.252C>T, NM_012324.4:c.252C>T, NM_012324.3:c.252C>T, XM_011530679.3:c.252C>T, XM_011530679.2:c.252C>T, XM_011530679.1:c.252C>T, XM_011530680.3:c.252C>T, XM_011530680.2:c.252C>T, XM_011530680.1:c.252C>T, XM_011530681.3:c.252C>T, XM_011530681.2:c.252C>T, XM_011530681.1:c.252C>T, NM_016431.3:c.171C>T, NM_139124.1:c.252C>T

Select item 148360139917.

rs1483601399 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 22:50603999 (GRCh38)
22:51042428 (GRCh37)
Canonical SPDI:: NC_000022.11:50603998:A:G
Gene:: MAPK8IP2 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by cluster
MAF:: G=0.000006/1 (GnomAD_exomes)
G=0.000007/1 (GnomAD)
HGVS:: NC_000022.11:g.50603999A>G, NC_000022.10:g.51042428A>G, NG_032955.2:g.8315A>G, NM_012324.6:c.700A>G, NM_012324.5:c.700A>G, NM_012324.4:c.700A>G, NM_012324.3:c.700A>G, XM_011530679.3:c.703A>G, XM_011530679.2:c.703A>G, XM_011530679.1:c.703A>G, XM_011530680.3:c.589A>G, XM_011530680.2:c.589A>G, XM_011530680.1:c.589A>G, XM_011530681.3:c.568A>G, XM_011530681.2:c.568A>G, XM_011530681.1:c.568A>G, NM_016431.3:c.619A>G, NP_036456.1:p.Ser234Gly, XP_011528981.1:p.Ser235Gly, XP_011528982.1:p.Ser197Gly, XP_011528983.1:p.Ser190Gly

Select item 148295179518.

rs1482951795 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 22:50604633 (GRCh38)
22:51043061 (GRCh37)
Canonical SPDI:: NC_000022.11:50604632:C:T
Gene:: MAPK8IP2 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
HGVS:: NC_000022.11:g.50604633C>T, NC_000022.10:g.51043061C>T, NG_032955.2:g.8949C>T, NM_012324.6:c.1334C>T, NM_012324.5:c.1334C>T, NM_012324.4:c.1334C>T, NM_012324.3:c.1334C>T, XM_011530679.3:c.1337C>T, XM_011530679.2:c.1337C>T, XM_011530679.1:c.1337C>T, XM_011530680.3:c.1223C>T, XM_011530680.2:c.1223C>T, XM_011530680.1:c.1223C>T, XM_011530681.3:c.1202C>T, XM_011530681.2:c.1202C>T, XM_011530681.1:c.1202C>T, NM_016431.3:c.1253C>T, NP_036456.1:p.Thr445Ile, XP_011528981.1:p.Thr446Ile, XP_011528982.1:p.Thr408Ile, XP_011528983.1:p.Thr401Ile

Select item 147913169319.

rs1479131693 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 22:50604276 (GRCh38)
22:51042704 (GRCh37)
Canonical SPDI:: NC_000022.11:50604275:A:G
Gene:: MAPK8IP2 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
HGVS:: NC_000022.11:g.50604276A>G, NC_000022.10:g.51042704A>G, NG_032955.2:g.8592A>G, NM_012324.6:c.977A>G, NM_012324.5:c.977A>G, NM_012324.4:c.977A>G, NM_012324.3:c.977A>G, XM_011530679.3:c.980A>G, XM_011530679.2:c.980A>G, XM_011530679.1:c.980A>G, XM_011530680.3:c.866A>G, XM_011530680.2:c.866A>G, XM_011530680.1:c.866A>G, XM_011530681.3:c.845A>G, XM_011530681.2:c.845A>G, XM_011530681.1:c.845A>G, NM_016431.3:c.896A>G, NP_036456.1:p.Asp326Gly, XP_011528981.1:p.Asp327Gly, XP_011528982.1:p.Asp289Gly, XP_011528983.1:p.Asp282Gly

Select item 147613497220.

rs1476134972 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 22:50604839 (GRCh38)
22:51043267 (GRCh37)
Canonical SPDI:: NC_000022.11:50604838:G:A
Gene:: MAPK8IP2 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
HGVS:: NC_000022.11:g.50604839G>A, NC_000022.10:g.51043267G>A, NG_032955.2:g.9155G>A, NM_012324.6:c.1540G>A, NM_012324.5:c.1540G>A, NM_012324.4:c.1540G>A, NM_012324.3:c.1540G>A, XM_011530679.3:c.1543G>A, XM_011530679.2:c.1543G>A, XM_011530679.1:c.1543G>A, XM_011530680.3:c.1429G>A, XM_011530680.2:c.1429G>A, XM_011530680.1:c.1429G>A, XM_011530681.3:c.1408G>A, XM_011530681.2:c.1408G>A, XM_011530681.1:c.1408G>A, NM_016431.3:c.1459G>A, NM_139124.1:c.397G>A, NP_036456.1:p.Val514Met, XP_011528981.1:p.Val515Met, XP_011528982.1:p.Val477Met, XP_011528983.1:p.Val470Met

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