SNP Links for Protein (Select 20986510) - SNP

Links from Protein

Items: 1 to 20 of 295

<< First< Prev

Page of 15

Next >Last >>

Select item 14889916571.

rs1488991657 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C,T [Show Flanks]
Chromosome:: 4:86017296 (GRCh38)
4:86938449 (GRCh37)
Canonical SPDI:: NC_000004.12:86017295:G:C,NC_000004.12:86017295:G:T
Gene:: MAPK10 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,3_prime_UTR_variant,missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000004.12:g.86017296G>C, NC_000004.12:g.86017296G>T, NC_000004.11:g.86938449G>C, NC_000004.11:g.86938449G>T, NG_013325.2:g.440835C>G, NG_013325.2:g.440835C>A, NM_002753.6:c.*63C>G, NM_002753.6:c.*63C>A, NM_002753.5:c.*63C>G, NM_002753.5:c.*63C>A, NM_002753.4:c.*63C>G, NM_002753.4:c.*63C>A, NM_002753.3:c.*63C>G, NM_002753.3:c.*63C>A, NM_138980.4:c.1213C>G, NM_138980.4:c.1213C>A, NM_138980.3:c.1213C>G, NM_138980.3:c.1213C>A, NM_138980.2:c.1213C>G, NM_138980.2:c.1213C>A, NM_138982.4:c.1327C>G, NM_138982.4:c.1327C>A, NM_138982.3:c.1327C>G, NM_138982.3:c.1327C>A, NM_138982.2:c.1327C>G, NM_138982.2:c.1327C>A, NM_001363657.3:c.*63C>G, NM_001363657.3:c.*63C>A, NM_001363657.2:c.*63C>G, NM_001363657.2:c.*63C>A, NM_001363657.1:c.*63C>G, NM_001363657.1:c.*63C>A, NM_001351625.3:c.*63C>G, NM_001351625.3:c.*63C>A, NM_001351625.2:c.*63C>G, NM_001351625.2:c.*63C>A, NM_001351625.1:c.*63C>G, NM_001351625.1:c.*63C>A, NM_001351624.2:c.1213C>G, NM_001351624.2:c.1213C>A, NM_001351624.1:c.1213C>G, NM_001351624.1:c.1213C>A, NM_001318069.2:c.1327C>G, NM_001318069.2:c.1327C>A, NM_001318069.1:c.1327C>G, NM_001318069.1:c.1327C>A, NM_001318068.1:c.892C>G, NM_001318068.1:c.892C>A, NM_001318067.1:c.1327C>G, NM_001318067.1:c.1327C>A, NM_138981.2:c.*63C>G, NM_138981.2:c.*63C>A, XM_047415964.1:c.1369C>G, XM_047415964.1:c.1369C>A, NP_620446.1:p.Gln405Glu, NP_620446.1:p.Gln405Lys, NP_620448.1:p.Gln443Glu, NP_620448.1:p.Gln443Lys, NP_001338553.1:p.Gln405Glu, NP_001338553.1:p.Gln405Lys, NP_001304998.1:p.Gln443Glu, NP_001304998.1:p.Gln443Lys, NP_001304997.1:p.Gln298Glu, NP_001304997.1:p.Gln298Lys, NP_001304996.1:p.Gln443Glu, NP_001304996.1:p.Gln443Lys, XP_047271920.1:p.Gln457Glu, XP_047271920.1:p.Gln457Lys

Select item 14866967862.

rs1486696786 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 4:86107283 (GRCh38)
4:87028436 (GRCh37)
Canonical SPDI:: NC_000004.12:86107282:T:C
Gene:: MAPK10 (Varview)
Functional Consequence:: 5_prime_UTR_variant,coding_sequence_variant,synonymous_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_000004.12:g.86107283T>C, NC_000004.11:g.87028436T>C, NG_013325.2:g.350848A>G, NM_002753.6:c.306A>G, NM_002753.5:c.306A>G, NM_002753.4:c.306A>G, NM_002753.3:c.306A>G, NM_138980.4:c.192A>G, NM_138980.3:c.192A>G, NM_138980.2:c.192A>G, NM_138982.4:c.306A>G, NM_138982.3:c.306A>G, NM_138982.2:c.306A>G, NM_001363657.3:c.192A>G, NM_001363657.2:c.192A>G, NM_001363657.1:c.192A>G, NM_001351625.3:c.192A>G, NM_001351625.2:c.192A>G, NM_001351625.1:c.192A>G, NM_001351624.2:c.192A>G, NM_001351624.1:c.192A>G, NM_001318069.2:c.306A>G, NM_001318069.1:c.306A>G, NM_001318068.1:c.-71A>G, NM_001318067.1:c.306A>G, NM_138981.2:c.-71A>G, XM_047415964.1:c.348A>G, XM_047415967.1:c.348A>G, XM_047415966.1:c.348A>G, XM_047415968.1:c.348A>G, XM_047415965.1:c.348A>G

Select item 14812353923.

rs1481235392 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 4:86098555 (GRCh38)
4:87019708 (GRCh37)
Canonical SPDI:: NC_000004.12:86098554:A:T
Gene:: MAPK10 (Varview)
Functional Consequence:: coding_sequence_variant,intron_variant,genic_downstream_transcript_variant,synonymous_variant,downstream_transcript_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000004.12:g.86098555A>T, NC_000004.11:g.87019708A>T, NG_013325.2:g.359576T>A, NM_002753.6:c.771T>A, NM_002753.5:c.771T>A, NM_002753.4:c.771T>A, NM_002753.3:c.771T>A, NM_138980.4:c.657T>A, NM_138980.3:c.657T>A, NM_138980.2:c.657T>A, NM_138982.4:c.771T>A, NM_138982.3:c.771T>A, NM_138982.2:c.771T>A, NM_001351625.3:c.657T>A, NM_001351625.2:c.657T>A, NM_001351625.1:c.657T>A, NM_001351624.2:c.657T>A, NM_001351624.1:c.657T>A, NM_001318069.2:c.771T>A, NM_001318069.1:c.771T>A, NM_138981.2:c.336T>A, XM_047415964.1:c.813T>A

Select item 14719863494.

rs1471986349 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 4:86064305 (GRCh38)
4:86985458 (GRCh37)
Canonical SPDI:: NC_000004.12:86064304:G:A
Gene:: MAPK10 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000008/2 (GnomAD_exomes)
A=0.000008/2 (TOPMED)
HGVS:: NC_000004.12:g.86064305G>A, NC_000004.11:g.86985458G>A, NG_013325.2:g.393826C>T, NM_002753.6:c.1071C>T, NM_002753.5:c.1071C>T, NM_002753.4:c.1071C>T, NM_002753.3:c.1071C>T, NM_138980.4:c.957C>T, NM_138980.3:c.957C>T, NM_138980.2:c.957C>T, NM_138982.4:c.1071C>T, NM_138982.3:c.1071C>T, NM_138982.2:c.1071C>T, NM_001363657.3:c.957C>T, NM_001363657.2:c.957C>T, NM_001363657.1:c.957C>T, NM_001351625.3:c.957C>T, NM_001351625.2:c.957C>T, NM_001351625.1:c.957C>T, NM_001351624.2:c.957C>T, NM_001351624.1:c.957C>T, NM_001318069.2:c.1071C>T, NM_001318069.1:c.1071C>T, NM_001318068.1:c.636C>T, NM_001318067.1:c.1071C>T, NM_138981.2:c.636C>T, XM_047415964.1:c.1113C>T

Select item 14669950565.

rs1466995056 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 4:86017235 (GRCh38)
4:86938388 (GRCh37)
Canonical SPDI:: NC_000004.12:86017234:C:T
Gene:: MAPK10 (Varview)
Functional Consequence:: 3_prime_UTR_variant,missense_variant,coding_sequence_variant,genic_downstream_transcript_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=0.000007/1 (GnomAD)
HGVS:: NC_000004.12:g.86017235C>T, NC_000004.11:g.86938388C>T, NG_013325.2:g.440896G>A, NM_002753.6:c.*124G>A, NM_002753.5:c.*124G>A, NM_002753.4:c.*124G>A, NM_002753.3:c.*124G>A, NM_138980.4:c.1274G>A, NM_138980.3:c.1274G>A, NM_138980.2:c.1274G>A, NM_138982.4:c.1388G>A, NM_138982.3:c.1388G>A, NM_138982.2:c.1388G>A, NM_001363657.3:c.*124G>A, NM_001363657.2:c.*124G>A, NM_001363657.1:c.*124G>A, NM_001351625.3:c.*124G>A, NM_001351625.2:c.*124G>A, NM_001351625.1:c.*124G>A, NM_001351624.2:c.1274G>A, NM_001351624.1:c.1274G>A, NM_001318069.2:c.1388G>A, NM_001318069.1:c.1388G>A, NM_001318068.1:c.953G>A, NM_001318067.1:c.1388G>A, NM_138981.2:c.*124G>A, XM_047415964.1:c.1430G>A, NP_620446.1:p.Cys425Tyr, NP_620448.1:p.Cys463Tyr, NP_001338553.1:p.Cys425Tyr, NP_001304998.1:p.Cys463Tyr, NP_001304997.1:p.Cys318Tyr, NP_001304996.1:p.Cys463Tyr, XP_047271920.1:p.Cys477Tyr

Select item 14664288596.

rs1466428859 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 4:86098586 (GRCh38)
4:87019739 (GRCh37)
Canonical SPDI:: NC_000004.12:86098585:C:T
Gene:: MAPK10 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,downstream_transcript_variant,intron_variant,stop_gained,coding_sequence_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000004.12:g.86098586C>T, NC_000004.11:g.87019739C>T, NG_013325.2:g.359545G>A, NM_002753.6:c.740G>A, NM_002753.5:c.740G>A, NM_002753.4:c.740G>A, NM_002753.3:c.740G>A, NM_138980.4:c.626G>A, NM_138980.3:c.626G>A, NM_138980.2:c.626G>A, NM_138982.4:c.740G>A, NM_138982.3:c.740G>A, NM_138982.2:c.740G>A, NM_001351625.3:c.626G>A, NM_001351625.2:c.626G>A, NM_001351625.1:c.626G>A, NM_001351624.2:c.626G>A, NM_001351624.1:c.626G>A, NM_001318069.2:c.740G>A, NM_001318069.1:c.740G>A, NM_138981.2:c.305G>A, XM_047415964.1:c.782G>A, NP_002744.1:p.Trp247Ter, NP_620446.1:p.Trp209Ter, NP_620448.1:p.Trp247Ter, NP_001338554.1:p.Trp209Ter, NP_001338553.1:p.Trp209Ter, NP_001304998.1:p.Trp247Ter, XP_047271920.1:p.Trp261Ter

Select item 14626655617.

rs1462665561 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 4:86017321 (GRCh38)
4:86938474 (GRCh37)
Canonical SPDI:: NC_000004.12:86017320:A:G
Gene:: MAPK10 (Varview)
Functional Consequence:: 3_prime_UTR_variant,genic_downstream_transcript_variant,synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
HGVS:: NC_000004.12:g.86017321A>G, NC_000004.11:g.86938474A>G, NG_013325.2:g.440810T>C, NM_002753.6:c.*38T>C, NM_002753.5:c.*38T>C, NM_002753.4:c.*38T>C, NM_002753.3:c.*38T>C, NM_138980.4:c.1188T>C, NM_138980.3:c.1188T>C, NM_138980.2:c.1188T>C, NM_138982.4:c.1302T>C, NM_138982.3:c.1302T>C, NM_138982.2:c.1302T>C, NM_001363657.3:c.*38T>C, NM_001363657.2:c.*38T>C, NM_001363657.1:c.*38T>C, NM_001351625.3:c.*38T>C, NM_001351625.2:c.*38T>C, NM_001351625.1:c.*38T>C, NM_001351624.2:c.1188T>C, NM_001351624.1:c.1188T>C, NM_001318069.2:c.1302T>C, NM_001318069.1:c.1302T>C, NM_001318068.1:c.867T>C, NM_001318067.1:c.1302T>C, NM_138981.2:c.*38T>C, XM_047415964.1:c.1344T>C

Select item 14602632188.

rs1460263218 [Homo sapiens]

Variant type:: DELINS
Alleles:: CAA>- [Show Flanks]
Chromosome:: 4:86064371 (GRCh38)
4:86985524 (GRCh37)
Canonical SPDI:: NC_000004.12:86064366:ACAACAA:ACAA
Gene:: MAPK10 (Varview)
Functional Consequence:: inframe_deletion,genic_downstream_transcript_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: ACAA=0./0 (ALFA)
-=0.000004/1 (GnomAD_exomes)
-=0.000007/1 (GnomAD)
-=0.000008/2 (TOPMED)
HGVS:: NC_000004.12:g.86064368CAA[1], NC_000004.11:g.86985521CAA[1], NG_013325.2:g.393759TGT[1], NM_002753.6:c.1004TGT[1], NM_002753.5:c.1004TGT[1], NM_002753.4:c.1004TGT[1], NM_002753.3:c.1004TGT[1], NM_138980.4:c.890TGT[1], NM_138980.3:c.890TGT[1], NM_138980.2:c.890TGT[1], NM_138982.4:c.1004TGT[1], NM_138982.3:c.1004TGT[1], NM_138982.2:c.1004TGT[1], NM_001363657.3:c.890TGT[1], NM_001363657.2:c.890TGT[1], NM_001363657.1:c.890TGT[1], NM_001351625.3:c.890TGT[1], NM_001351625.2:c.890TGT[1], NM_001351625.1:c.890TGT[1], NM_001351624.2:c.890TGT[1], NM_001351624.1:c.890TGT[1], NM_001318069.2:c.1004TGT[1], NM_001318069.1:c.1004TGT[1], NM_001318068.1:c.569TGT[1], NM_001318067.1:c.1004TGT[1], NM_138981.2:c.569TGT[1], XM_047415964.1:c.1046TGT[1], NP_002744.1:p.Leu336del, NP_620446.1:p.Leu298del, NP_620448.1:p.Leu336del, NP_001350586.1:p.Leu298del, NP_001338554.1:p.Leu298del, NP_001338553.1:p.Leu298del, NP_001304998.1:p.Leu336del, NP_001304997.1:p.Leu191del, NP_001304996.1:p.Leu336del, XP_047271920.1:p.Leu350del

Select item 14583814729.

rs1458381472 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 4:86067907 (GRCh38)
4:86989060 (GRCh37)
Canonical SPDI:: NC_000004.12:86067906:G:C
Gene:: MAPK10 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000004.12:g.86067907G>C, NC_000004.11:g.86989060G>C, NG_013325.2:g.390224C>G, NM_002753.6:c.851C>G, NM_002753.5:c.851C>G, NM_002753.4:c.851C>G, NM_002753.3:c.851C>G, NM_138980.4:c.737C>G, NM_138980.3:c.737C>G, NM_138980.2:c.737C>G, NM_138982.4:c.851C>G, NM_138982.3:c.851C>G, NM_138982.2:c.851C>G, NM_001363657.3:c.737C>G, NM_001363657.2:c.737C>G, NM_001363657.1:c.737C>G, NM_001351625.3:c.737C>G, NM_001351625.2:c.737C>G, NM_001351625.1:c.737C>G, NM_001351624.2:c.737C>G, NM_001351624.1:c.737C>G, NM_001318069.2:c.851C>G, NM_001318069.1:c.851C>G, NM_001318068.1:c.416C>G, NM_001318067.1:c.851C>G, NM_138981.2:c.416C>G, XM_047415964.1:c.893C>G, NP_002744.1:p.Pro284Arg, NP_620446.1:p.Pro246Arg, NP_620448.1:p.Pro284Arg, NP_001350586.1:p.Pro246Arg, NP_001338554.1:p.Pro246Arg, NP_001338553.1:p.Pro246Arg, NP_001304998.1:p.Pro284Arg, NP_001304997.1:p.Pro139Arg, NP_001304996.1:p.Pro284Arg, XP_047271920.1:p.Pro298Arg

Select item 144929193310.

rs1449291933 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 4:86031378 (GRCh38)
4:86952531 (GRCh37)
Canonical SPDI:: NC_000004.12:86031377:T:A
Gene:: MAPK10 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000004.12:g.86031378T>A, NC_000004.11:g.86952531T>A, NG_013325.2:g.426753A>T, NM_002753.6:c.1164A>T, NM_002753.5:c.1164A>T, NM_002753.4:c.1164A>T, NM_002753.3:c.1164A>T, NM_138980.4:c.1050A>T, NM_138980.3:c.1050A>T, NM_138980.2:c.1050A>T, NM_138982.4:c.1164A>T, NM_138982.3:c.1164A>T, NM_138982.2:c.1164A>T, NM_001363657.3:c.1050A>T, NM_001363657.2:c.1050A>T, NM_001363657.1:c.1050A>T, NM_001351625.3:c.1050A>T, NM_001351625.2:c.1050A>T, NM_001351625.1:c.1050A>T, NM_001351624.2:c.1050A>T, NM_001351624.1:c.1050A>T, NM_001318069.2:c.1164A>T, NM_001318069.1:c.1164A>T, NM_001318068.1:c.729A>T, NM_001318067.1:c.1164A>T, NM_138981.2:c.729A>T, XM_047415964.1:c.1206A>T, NP_002744.1:p.Glu388Asp, NP_620446.1:p.Glu350Asp, NP_620448.1:p.Glu388Asp, NP_001350586.1:p.Glu350Asp, NP_001338554.1:p.Glu350Asp, NP_001338553.1:p.Glu350Asp, NP_001304998.1:p.Glu388Asp, NP_001304997.1:p.Glu243Asp, NP_001304996.1:p.Glu388Asp, XP_047271920.1:p.Glu402Asp

Select item 143964079311.

rs1439640793 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 4:86101965 (GRCh38)
4:87023118 (GRCh37)
Canonical SPDI:: NC_000004.12:86101964:G:A
Gene:: MAPK10 (Varview)
Functional Consequence:: stop_gained,coding_sequence_variant
HGVS:: NC_000004.12:g.86101965G>A, NC_000004.11:g.87023118G>A, NG_013325.2:g.356166C>T, NM_002753.6:c.493C>T, NM_002753.5:c.493C>T, NM_002753.4:c.493C>T, NM_002753.3:c.493C>T, NM_138980.4:c.379C>T, NM_138980.3:c.379C>T, NM_138980.2:c.379C>T, NM_138982.4:c.493C>T, NM_138982.3:c.493C>T, NM_138982.2:c.493C>T, NM_001363657.3:c.379C>T, NM_001363657.2:c.379C>T, NM_001363657.1:c.379C>T, NM_001351625.3:c.379C>T, NM_001351625.2:c.379C>T, NM_001351625.1:c.379C>T, NM_001351624.2:c.379C>T, NM_001351624.1:c.379C>T, NM_001318069.2:c.493C>T, NM_001318069.1:c.493C>T, NM_001318068.1:c.58C>T, NM_001318067.1:c.493C>T, NM_138981.2:c.58C>T, XM_047415964.1:c.535C>T, XM_047415967.1:c.535C>T, XM_047415966.1:c.535C>T, XM_047415968.1:c.535C>T, XM_047415965.1:c.535C>T, NP_002744.1:p.Arg165Ter, NP_620446.1:p.Arg127Ter, NP_620448.1:p.Arg165Ter, NP_001350586.1:p.Arg127Ter, NP_001338554.1:p.Arg127Ter, NP_001338553.1:p.Arg127Ter, NP_001304998.1:p.Arg165Ter, NP_001304997.1:p.Arg20Ter, NP_001304996.1:p.Arg165Ter, XP_047271920.1:p.Arg179Ter, XP_047271923.1:p.Arg179Ter, XP_047271922.1:p.Arg179Ter, XP_047271924.1:p.Arg179Ter, XP_047271921.1:p.Arg179Ter

Select item 143620687212.

rs1436206872 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 4:86101987 (GRCh38)
4:87023140 (GRCh37)
Canonical SPDI:: NC_000004.12:86101986:A:T
Gene:: MAPK10 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000004.12:g.86101987A>T, NC_000004.11:g.87023140A>T, NG_013325.2:g.356144T>A, NM_002753.6:c.471T>A, NM_002753.5:c.471T>A, NM_002753.4:c.471T>A, NM_002753.3:c.471T>A, NM_138980.4:c.357T>A, NM_138980.3:c.357T>A, NM_138980.2:c.357T>A, NM_138982.4:c.471T>A, NM_138982.3:c.471T>A, NM_138982.2:c.471T>A, NM_001363657.3:c.357T>A, NM_001363657.2:c.357T>A, NM_001363657.1:c.357T>A, NM_001351625.3:c.357T>A, NM_001351625.2:c.357T>A, NM_001351625.1:c.357T>A, NM_001351624.2:c.357T>A, NM_001351624.1:c.357T>A, NM_001318069.2:c.471T>A, NM_001318069.1:c.471T>A, NM_001318068.1:c.36T>A, NM_001318067.1:c.471T>A, NM_138981.2:c.36T>A, XM_047415964.1:c.513T>A, XM_047415967.1:c.513T>A, XM_047415966.1:c.513T>A, XM_047415968.1:c.513T>A, XM_047415965.1:c.513T>A

Select item 143247629213.

rs1432476292 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 4:86067894 (GRCh38)
4:86989047 (GRCh37)
Canonical SPDI:: NC_000004.12:86067893:C:T
Gene:: MAPK10 (Varview)
Functional Consequence:: synonymous_variant,genic_downstream_transcript_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000004.12:g.86067894C>T, NC_000004.11:g.86989047C>T, NG_013325.2:g.390237G>A, NM_002753.6:c.864G>A, NM_002753.5:c.864G>A, NM_002753.4:c.864G>A, NM_002753.3:c.864G>A, NM_138980.4:c.750G>A, NM_138980.3:c.750G>A, NM_138980.2:c.750G>A, NM_138982.4:c.864G>A, NM_138982.3:c.864G>A, NM_138982.2:c.864G>A, NM_001363657.3:c.750G>A, NM_001363657.2:c.750G>A, NM_001363657.1:c.750G>A, NM_001351625.3:c.750G>A, NM_001351625.2:c.750G>A, NM_001351625.1:c.750G>A, NM_001351624.2:c.750G>A, NM_001351624.1:c.750G>A, NM_001318069.2:c.864G>A, NM_001318069.1:c.864G>A, NM_001318068.1:c.429G>A, NM_001318067.1:c.864G>A, NM_138981.2:c.429G>A, XM_047415964.1:c.906G>A

Select item 143119389414.

rs1431193894 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 4:86102014 (GRCh38)
4:87023167 (GRCh37)
Canonical SPDI:: NC_000004.12:86102013:C:T
Gene:: MAPK10 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000004.12:g.86102014C>T, NC_000004.11:g.87023167C>T, NG_013325.2:g.356117G>A, NM_002753.6:c.444G>A, NM_002753.5:c.444G>A, NM_002753.4:c.444G>A, NM_002753.3:c.444G>A, NM_138980.4:c.330G>A, NM_138980.3:c.330G>A, NM_138980.2:c.330G>A, NM_138982.4:c.444G>A, NM_138982.3:c.444G>A, NM_138982.2:c.444G>A, NM_001363657.3:c.330G>A, NM_001363657.2:c.330G>A, NM_001363657.1:c.330G>A, NM_001351625.3:c.330G>A, NM_001351625.2:c.330G>A, NM_001351625.1:c.330G>A, NM_001351624.2:c.330G>A, NM_001351624.1:c.330G>A, NM_001318069.2:c.444G>A, NM_001318069.1:c.444G>A, NM_001318068.1:c.9G>A, NM_001318067.1:c.444G>A, NM_138981.2:c.9G>A, XM_047415964.1:c.486G>A, XM_047415967.1:c.486G>A, XM_047415966.1:c.486G>A, XM_047415968.1:c.486G>A, XM_047415965.1:c.486G>A

Select item 142966188315.

rs1429661883 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 4:86159412 (GRCh38)
4:87080565 (GRCh37)
Canonical SPDI:: NC_000004.12:86159411:T:C,NC_000004.12:86159411:T:G
Gene:: MAPK10 (Varview), MAPK10-AS1 (Varview)
Functional Consequence:: 5_prime_UTR_variant,coding_sequence_variant,missense_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
HGVS:: NC_000004.12:g.86159412T>C, NC_000004.12:g.86159412T>G, NC_000004.11:g.87080565T>C, NC_000004.11:g.87080565T>G, NG_013325.2:g.298719A>G, NG_013325.2:g.298719A>C, NM_002753.6:c.122A>G, NM_002753.6:c.122A>C, NM_002753.5:c.122A>G, NM_002753.5:c.122A>C, NM_002753.4:c.122A>G, NM_002753.4:c.122A>C, NM_002753.3:c.122A>G, NM_002753.3:c.122A>C, NM_138980.4:c.8A>G, NM_138980.4:c.8A>C, NM_138980.3:c.8A>G, NM_138980.3:c.8A>C, NM_138980.2:c.8A>G, NM_138980.2:c.8A>C, NM_138982.4:c.122A>G, NM_138982.4:c.122A>C, NM_138982.3:c.122A>G, NM_138982.3:c.122A>C, NM_138982.2:c.122A>G, NM_138982.2:c.122A>C, NM_001363657.3:c.8A>G, NM_001363657.3:c.8A>C, NM_001363657.2:c.8A>G, NM_001363657.2:c.8A>C, NM_001363657.1:c.8A>G, NM_001363657.1:c.8A>C, NM_001351625.3:c.8A>G, NM_001351625.3:c.8A>C, NM_001351625.2:c.8A>G, NM_001351625.2:c.8A>C, NM_001351625.1:c.8A>G, NM_001351625.1:c.8A>C, NM_001351624.2:c.8A>G, NM_001351624.2:c.8A>C, NM_001351624.1:c.8A>G, NM_001351624.1:c.8A>C, NM_001318069.2:c.122A>G, NM_001318069.2:c.122A>C, NM_001318069.1:c.122A>G, NM_001318069.1:c.122A>C, NM_001318068.1:c.-255A>G, NM_001318068.1:c.-255A>C, NM_001318067.1:c.122A>G, NM_001318067.1:c.122A>C, XM_047415964.1:c.164A>G, XM_047415964.1:c.164A>C, XM_047415967.1:c.164A>G, XM_047415967.1:c.164A>C, XM_047415966.1:c.164A>G, XM_047415966.1:c.164A>C, XM_047415968.1:c.164A>G, XM_047415968.1:c.164A>C, XM_047415965.1:c.164A>G, XM_047415965.1:c.164A>C, NP_002744.1:p.Lys41Arg, NP_002744.1:p.Lys41Thr, NP_620446.1:p.Lys3Arg, NP_620446.1:p.Lys3Thr, NP_620448.1:p.Lys41Arg, NP_620448.1:p.Lys41Thr, NP_001350586.1:p.Lys3Arg, NP_001350586.1:p.Lys3Thr, NP_001338554.1:p.Lys3Arg, NP_001338554.1:p.Lys3Thr, NP_001338553.1:p.Lys3Arg, NP_001338553.1:p.Lys3Thr, NP_001304998.1:p.Lys41Arg, NP_001304998.1:p.Lys41Thr, NP_001304996.1:p.Lys41Arg, NP_001304996.1:p.Lys41Thr, XP_047271920.1:p.Lys55Arg, XP_047271920.1:p.Lys55Thr, XP_047271923.1:p.Lys55Arg, XP_047271923.1:p.Lys55Thr, XP_047271922.1:p.Lys55Arg, XP_047271922.1:p.Lys55Thr, XP_047271924.1:p.Lys55Arg, XP_047271924.1:p.Lys55Thr, XP_047271921.1:p.Lys55Arg, XP_047271921.1:p.Lys55Thr

Select item 142912213716.

rs1429122137 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 4:86017360 (GRCh38)
4:86938513 (GRCh37)
Canonical SPDI:: NC_000004.12:86017359:C:T
Gene:: MAPK10 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,coding_sequence_variant,synonymous_variant,terminator_codon_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000011/3 (TOPMED)
HGVS:: NC_000004.12:g.86017360C>T, NC_000004.11:g.86938513C>T, NG_013325.2:g.440771G>A, NM_002753.6:c.1268G>A, NM_002753.5:c.1268G>A, NM_002753.4:c.1268G>A, NM_002753.3:c.1268G>A, NM_138980.4:c.1149G>A, NM_138980.3:c.1149G>A, NM_138980.2:c.1149G>A, NM_138982.4:c.1263G>A, NM_138982.3:c.1263G>A, NM_138982.2:c.1263G>A, NM_001363657.3:c.1154G>A, NM_001363657.2:c.1154G>A, NM_001363657.1:c.1154G>A, NM_001351625.3:c.1154G>A, NM_001351625.2:c.1154G>A, NM_001351625.1:c.1154G>A, NM_001351624.2:c.1149G>A, NM_001351624.1:c.1149G>A, NM_001318069.2:c.1263G>A, NM_001318069.1:c.1263G>A, NM_001318068.1:c.828G>A, NM_001318067.1:c.1263G>A, NM_138981.2:c.833G>A, XM_047415964.1:c.1305G>A

Select item 142596689417.

rs1425966894 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 4:86067867 (GRCh38)
4:86989020 (GRCh37)
Canonical SPDI:: NC_000004.12:86067866:A:G
Gene:: MAPK10 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000008/2 (GnomAD_exomes)
G=0.000008/2 (TOPMED)
HGVS:: NC_000004.12:g.86067867A>G, NC_000004.11:g.86989020A>G, NG_013325.2:g.390264T>C, NM_002753.6:c.891T>C, NM_002753.5:c.891T>C, NM_002753.4:c.891T>C, NM_002753.3:c.891T>C, NM_138980.4:c.777T>C, NM_138980.3:c.777T>C, NM_138980.2:c.777T>C, NM_138982.4:c.891T>C, NM_138982.3:c.891T>C, NM_138982.2:c.891T>C, NM_001363657.3:c.777T>C, NM_001363657.2:c.777T>C, NM_001363657.1:c.777T>C, NM_001351625.3:c.777T>C, NM_001351625.2:c.777T>C, NM_001351625.1:c.777T>C, NM_001351624.2:c.777T>C, NM_001351624.1:c.777T>C, NM_001318069.2:c.891T>C, NM_001318069.1:c.891T>C, NM_001318068.1:c.456T>C, NM_001318067.1:c.891T>C, NM_138981.2:c.456T>C, XM_047415964.1:c.933T>C

Select item 142302870618.

rs1423028706 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 4:86159424 (GRCh38)
4:87080577 (GRCh37)
Canonical SPDI:: NC_000004.12:86159423:T:A
Gene:: MAPK10 (Varview), MAPK10-AS1 (Varview)
Functional Consequence:: 5_prime_UTR_variant,coding_sequence_variant,missense_variant,intron_variant
HGVS:: NC_000004.12:g.86159424T>A, NC_000004.11:g.87080577T>A, NG_013325.2:g.298707A>T, NM_002753.6:c.110A>T, NM_002753.5:c.110A>T, NM_002753.4:c.110A>T, NM_002753.3:c.110A>T, NM_138980.4:c.-5A>T, NM_138980.3:c.-5A>T, NM_138980.2:c.-5A>T, NM_138982.4:c.110A>T, NM_138982.3:c.110A>T, NM_138982.2:c.110A>T, NM_001363657.3:c.-5A>T, NM_001363657.2:c.-5A>T, NM_001363657.1:c.-5A>T, NM_001351625.3:c.-5A>T, NM_001351625.2:c.-5A>T, NM_001351625.1:c.-5A>T, NM_001351624.2:c.-5A>T, NM_001351624.1:c.-5A>T, NM_001318069.2:c.110A>T, NM_001318069.1:c.110A>T, NM_001318068.1:c.-267A>T, NM_001318067.1:c.110A>T, XM_047415964.1:c.152A>T, XM_047415967.1:c.152A>T, XM_047415966.1:c.152A>T, XM_047415968.1:c.152A>T, XM_047415965.1:c.152A>T, NP_002744.1:p.Tyr37Phe, NP_620448.1:p.Tyr37Phe, NP_001304998.1:p.Tyr37Phe, NP_001304996.1:p.Tyr37Phe, XP_047271920.1:p.Tyr51Phe, XP_047271923.1:p.Tyr51Phe, XP_047271922.1:p.Tyr51Phe, XP_047271924.1:p.Tyr51Phe, XP_047271921.1:p.Tyr51Phe

Select item 141698178419.

rs1416981784 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 4:86107348 (GRCh38)
4:87028501 (GRCh37)
Canonical SPDI:: NC_000004.12:86107347:C:T
Gene:: MAPK10 (Varview)
Functional Consequence:: 5_prime_UTR_variant,missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000071/1 (ALFA)
T=0.000004/1 (GnomAD_exomes)
T=0.000014/2 (GnomAD)
T=0.000023/6 (TOPMED)
HGVS:: NC_000004.12:g.86107348C>T, NC_000004.11:g.87028501C>T, NG_013325.2:g.350783G>A, NM_002753.6:c.241G>A, NM_002753.5:c.241G>A, NM_002753.4:c.241G>A, NM_002753.3:c.241G>A, NM_138980.4:c.127G>A, NM_138980.3:c.127G>A, NM_138980.2:c.127G>A, NM_138982.4:c.241G>A, NM_138982.3:c.241G>A, NM_138982.2:c.241G>A, NM_001363657.3:c.127G>A, NM_001363657.2:c.127G>A, NM_001363657.1:c.127G>A, NM_001351625.3:c.127G>A, NM_001351625.2:c.127G>A, NM_001351625.1:c.127G>A, NM_001351624.2:c.127G>A, NM_001351624.1:c.127G>A, NM_001318069.2:c.241G>A, NM_001318069.1:c.241G>A, NM_001318068.1:c.-136G>A, NM_001318067.1:c.241G>A, NM_138981.2:c.-136G>A, XM_047415964.1:c.283G>A, XM_047415967.1:c.283G>A, XM_047415966.1:c.283G>A, XM_047415968.1:c.283G>A, XM_047415965.1:c.283G>A, NP_002744.1:p.Ala81Thr, NP_620446.1:p.Ala43Thr, NP_620448.1:p.Ala81Thr, NP_001350586.1:p.Ala43Thr, NP_001338554.1:p.Ala43Thr, NP_001338553.1:p.Ala43Thr, NP_001304998.1:p.Ala81Thr, NP_001304996.1:p.Ala81Thr, XP_047271920.1:p.Ala95Thr, XP_047271923.1:p.Ala95Thr, XP_047271922.1:p.Ala95Thr, XP_047271924.1:p.Ala95Thr, XP_047271921.1:p.Ala95Thr

Select item 140921650920.

rs1409216509 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 4:86159303 (GRCh38)
4:87080456 (GRCh37)
Canonical SPDI:: NC_000004.12:86159302:T:G
Gene:: MAPK10 (Varview), MAPK10-AS1 (Varview)
Functional Consequence:: synonymous_variant,5_prime_UTR_variant,intron_variant,coding_sequence_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000004.12:g.86159303T>G, NC_000004.11:g.87080456T>G, NG_013325.2:g.298828A>C, NM_002753.6:c.231A>C, NM_002753.5:c.231A>C, NM_002753.4:c.231A>C, NM_002753.3:c.231A>C, NM_138980.4:c.117A>C, NM_138980.3:c.117A>C, NM_138980.2:c.117A>C, NM_138982.4:c.231A>C, NM_138982.3:c.231A>C, NM_138982.2:c.231A>C, NM_001363657.3:c.117A>C, NM_001363657.2:c.117A>C, NM_001363657.1:c.117A>C, NM_001351625.3:c.117A>C, NM_001351625.2:c.117A>C, NM_001351625.1:c.117A>C, NM_001351624.2:c.117A>C, NM_001351624.1:c.117A>C, NM_001318069.2:c.231A>C, NM_001318069.1:c.231A>C, NM_001318068.1:c.-146A>C, NM_001318067.1:c.231A>C, XM_047415964.1:c.273A>C, XM_047415967.1:c.273A>C, XM_047415966.1:c.273A>C, XM_047415968.1:c.273A>C, XM_047415965.1:c.273A>C

<< First< Prev

Page of 15

Next >Last >>

dbSNP

Result Filters

Clinical Significance

Validation Status

Publication

Function Class

Variation Class

Annotation

Global MAF

Custom range

Additional filters

Display Settings:

Send to:

Links from Protein

Items: 1 to 20 of 295

Display Settings:

Send to:

Supplemental Content

Find related data

Recent activity