SNP Links for Protein (Select 91718899) - SNP

Links from Protein

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Select item 14870936521.

rs1487093652 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C,T [Show Flanks]
Chromosome:: 16:30123202 (GRCh38)
16:30134523 (GRCh37)
Canonical SPDI:: NC_000016.10:30123201:G:A,NC_000016.10:30123201:G:C,NC_000016.10:30123201:G:T
Gene:: MAPK3 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
HGVS:: NC_000016.10:g.30123202G>A, NC_000016.10:g.30123202G>C, NC_000016.10:g.30123202G>T, NC_000016.9:g.30134523G>A, NC_000016.9:g.30134523G>C, NC_000016.9:g.30134523G>T, NG_029936.1:g.5108C>T, NG_029936.1:g.5108C>G, NG_029936.1:g.5108C>A, NM_002746.3:c.8C>T, NM_002746.3:c.8C>G, NM_002746.3:c.8C>A, NM_002746.2:c.8C>T, NM_002746.2:c.8C>G, NM_002746.2:c.8C>A, NM_001040056.3:c.8C>T, NM_001040056.3:c.8C>G, NM_001040056.3:c.8C>A, NM_001040056.2:c.8C>T, NM_001040056.2:c.8C>G, NM_001040056.2:c.8C>A, NM_001109891.2:c.8C>T, NM_001109891.2:c.8C>G, NM_001109891.2:c.8C>A, NM_001109891.1:c.8C>T, NM_001109891.1:c.8C>G, NM_001109891.1:c.8C>A, XR_243293.2:n.19C>T, XR_243293.2:n.19C>G, XR_243293.2:n.19C>A, XR_243293.1:n.108C>T, XR_243293.1:n.108C>G, XR_243293.1:n.108C>A, NP_002737.2:p.Ala3Val, NP_002737.2:p.Ala3Gly, NP_002737.2:p.Ala3Glu, NP_001035145.1:p.Ala3Val, NP_001035145.1:p.Ala3Gly, NP_001035145.1:p.Ala3Glu, NP_001103361.1:p.Ala3Val, NP_001103361.1:p.Ala3Gly, NP_001103361.1:p.Ala3Glu

Select item 14851365972.

rs1485136597 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 16:30121829 (GRCh38)
16:30133150 (GRCh37)
Canonical SPDI:: NC_000016.10:30121828:T:C
Gene:: MAPK3 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (GnomAD_exomes)
C=0.000007/1 (GnomAD)
HGVS:: NC_000016.10:g.30121829T>C, NC_000016.9:g.30133150T>C, NG_029936.1:g.6481A>G, NM_002746.3:c.348A>G, NM_002746.2:c.348A>G, NM_001040056.3:c.348A>G, NM_001040056.2:c.348A>G, NM_001109891.2:c.348A>G, NM_001109891.1:c.348A>G, XR_243293.2:n.359A>G, XR_243293.1:n.448A>G

Select item 14838436813.

rs1483843681 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 16:30121956 (GRCh38)
16:30133277 (GRCh37)
Canonical SPDI:: NC_000016.10:30121955:C:G,NC_000016.10:30121955:C:T
Gene:: MAPK3 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,non_coding_transcript_variant
Validated:: by cluster
HGVS:: NC_000016.10:g.30121956C>G, NC_000016.10:g.30121956C>T, NC_000016.9:g.30133277C>G, NC_000016.9:g.30133277C>T, NG_029936.1:g.6354G>C, NG_029936.1:g.6354G>A, NM_002746.3:c.221G>C, NM_002746.3:c.221G>A, NM_002746.2:c.221G>C, NM_002746.2:c.221G>A, NM_001040056.3:c.221G>C, NM_001040056.3:c.221G>A, NM_001040056.2:c.221G>C, NM_001040056.2:c.221G>A, NM_001109891.2:c.221G>C, NM_001109891.2:c.221G>A, NM_001109891.1:c.221G>C, NM_001109891.1:c.221G>A, XR_243293.2:n.232G>C, XR_243293.2:n.232G>A, XR_243293.1:n.321G>C, XR_243293.1:n.321G>A, NP_002737.2:p.Ser74Thr, NP_002737.2:p.Ser74Asn, NP_001035145.1:p.Ser74Thr, NP_001035145.1:p.Ser74Asn, NP_001103361.1:p.Ser74Thr, NP_001103361.1:p.Ser74Asn

Select item 14822784884.

rs1482278488 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 16:30118050 (GRCh38)
16:30129371 (GRCh37)
Canonical SPDI:: NC_000016.10:30118049:G:A
Gene:: MAPK3 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant,non_coding_transcript_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_000016.10:g.30118050G>A, NC_000016.9:g.30129371G>A, NG_029936.1:g.10260C>T, NM_002746.3:c.657C>T, NM_002746.2:c.657C>T, NM_001040056.3:c.657C>T, NM_001040056.2:c.657C>T, NM_001109891.2:c.657C>T, NM_001109891.1:c.657C>T, XR_243293.2:n.668C>T, XR_243293.1:n.757C>T

Select item 14786592545.

rs1478659254 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 16:30118403 (GRCh38)
16:30129724 (GRCh37)
Canonical SPDI:: NC_000016.10:30118402:G:A
Gene:: MAPK3 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000224/1 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000223/1 (Estonian)
HGVS:: NC_000016.10:g.30118403G>A, NC_000016.9:g.30129724G>A, NG_029936.1:g.9907C>T, NM_002746.3:c.489C>T, NM_002746.2:c.489C>T, NM_001040056.3:c.489C>T, NM_001040056.2:c.489C>T, NM_001109891.2:c.489C>T, NM_001109891.1:c.489C>T, XR_243293.2:n.500C>T, XR_243293.1:n.589C>T

Select item 14762552696.

rs1476255269 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 16:30117694 (GRCh38)
16:30129015 (GRCh37)
Canonical SPDI:: NC_000016.10:30117693:G:A
Gene:: MAPK3 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000019/5 (TOPMED)
HGVS:: NC_000016.10:g.30117694G>A, NC_000016.9:g.30129015G>A, NG_029936.1:g.10616C>T, NM_002746.3:c.751C>T, NM_002746.2:c.751C>T, NM_001040056.3:c.751C>T, NM_001040056.2:c.751C>T, NM_001109891.2:c.751C>T, NM_001109891.1:c.751C>T, XR_243293.2:n.762C>T, XR_243293.1:n.851C>T

Select item 14738632247.

rs1473863224 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 16:30118078 (GRCh38)
16:30129399 (GRCh37)
Canonical SPDI:: NC_000016.10:30118077:T:G
Gene:: MAPK3 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000071/1 (ALFA)
G=0.000004/1 (GnomAD_exomes)
G=0.000008/2 (TOPMED)
HGVS:: NC_000016.10:g.30118078T>G, NC_000016.9:g.30129399T>G, NG_029936.1:g.10232A>C, NM_002746.3:c.629A>C, NM_002746.2:c.629A>C, NM_001040056.3:c.629A>C, NM_001040056.2:c.629A>C, NM_001109891.2:c.629A>C, NM_001109891.1:c.629A>C, XR_243293.2:n.640A>C, XR_243293.1:n.729A>C, NP_002737.2:p.Tyr210Ser, NP_001035145.1:p.Tyr210Ser, NP_001103361.1:p.Tyr210Ser

Select item 14723455308.

rs1472345530 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 16:30118375 (GRCh38)
16:30129696 (GRCh37)
Canonical SPDI:: NC_000016.10:30118374:G:C
Gene:: MAPK3 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,non_coding_transcript_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000016.10:g.30118375G>C, NC_000016.9:g.30129696G>C, NG_029936.1:g.9935C>G, NM_002746.3:c.517C>G, NM_002746.2:c.517C>G, NM_001040056.3:c.517C>G, NM_001040056.2:c.517C>G, NM_001109891.2:c.517C>G, NM_001109891.1:c.517C>G, XR_243293.2:n.528C>G, XR_243293.1:n.617C>G, NP_002737.2:p.Leu173Val, NP_001035145.1:p.Leu173Val, NP_001103361.1:p.Leu173Val

Select item 14722949519.

rs1472294951 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 16:30116992 (GRCh38)
16:30128313 (GRCh37)
Canonical SPDI:: NC_000016.10:30116991:G:T
Gene:: MAPK3 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,non_coding_transcript_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000016.10:g.30116992G>T, NC_000016.9:g.30128313G>T, NG_029936.1:g.11318C>A, NM_002746.3:c.919C>A, NM_002746.2:c.919C>A, NM_001040056.3:c.919C>A, NM_001040056.2:c.919C>A, NM_001109891.2:c.787C>A, NM_001109891.1:c.787C>A, XR_243293.2:n.930C>A, XR_243293.1:n.1019C>A, NP_002737.2:p.Leu307Met, NP_001035145.1:p.Leu307Met, NP_001103361.1:p.Leu263Met

Select item 146841465310.

rs1468414653 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,G,T [Show Flanks]
Chromosome:: 16:30123154 (GRCh38)
16:30134475 (GRCh37)
Canonical SPDI:: NC_000016.10:30123153:C:A,NC_000016.10:30123153:C:G,NC_000016.10:30123153:C:T
Gene:: MAPK3 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
HGVS:: NC_000016.10:g.30123154C>A, NC_000016.10:g.30123154C>G, NC_000016.10:g.30123154C>T, NC_000016.9:g.30134475C>A, NC_000016.9:g.30134475C>G, NC_000016.9:g.30134475C>T, NG_029936.1:g.5156G>T, NG_029936.1:g.5156G>C, NG_029936.1:g.5156G>A, NM_002746.3:c.56G>T, NM_002746.3:c.56G>C, NM_002746.3:c.56G>A, NM_002746.2:c.56G>T, NM_002746.2:c.56G>C, NM_002746.2:c.56G>A, NM_001040056.3:c.56G>T, NM_001040056.3:c.56G>C, NM_001040056.3:c.56G>A, NM_001040056.2:c.56G>T, NM_001040056.2:c.56G>C, NM_001040056.2:c.56G>A, NM_001109891.2:c.56G>T, NM_001109891.2:c.56G>C, NM_001109891.2:c.56G>A, NM_001109891.1:c.56G>T, NM_001109891.1:c.56G>C, NM_001109891.1:c.56G>A, XR_243293.2:n.67G>T, XR_243293.2:n.67G>C, XR_243293.2:n.67G>A, XR_243293.1:n.156G>T, XR_243293.1:n.156G>C, XR_243293.1:n.156G>A, NP_002737.2:p.Gly19Val, NP_002737.2:p.Gly19Ala, NP_002737.2:p.Gly19Glu, NP_001035145.1:p.Gly19Val, NP_001035145.1:p.Gly19Ala, NP_001035145.1:p.Gly19Glu, NP_001103361.1:p.Gly19Val, NP_001103361.1:p.Gly19Ala, NP_001103361.1:p.Gly19Glu

Select item 146544495011.

rs1465444950 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->G [Show Flanks]
Chromosome:: 16:30121951 (GRCh38)
16:30133273 (GRCh37)
Canonical SPDI:: NC_000016.10:30121951:GGGG:GGGGG
Gene:: MAPK3 (Varview)
Functional Consequence:: non_coding_transcript_variant,frameshift_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: GGGGG=0./0 (ALFA)
HGVS:: NC_000016.10:g.30121955dup, NC_000016.9:g.30133276dup, NG_029936.1:g.6358dup, NM_002746.3:c.225dup, NM_002746.2:c.225dup, NM_001040056.3:c.225dup, NM_001040056.2:c.225dup, NM_001109891.2:c.225dup, NM_001109891.1:c.225dup, XR_243293.2:n.236dup, XR_243293.1:n.325dup, NP_002737.2:p.Phe76fs, NP_001035145.1:p.Phe76fs, NP_001103361.1:p.Phe76fs

Select item 146539626312.

rs1465396263 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 16:30117673 (GRCh38)
16:30128994 (GRCh37)
Canonical SPDI:: NC_000016.10:30117672:G:T
Gene:: MAPK3 (Varview)
Functional Consequence:: non_coding_transcript_variant,missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000016.10:g.30117673G>T, NC_000016.9:g.30128994G>T, NG_029936.1:g.10637C>A, NM_002746.3:c.772C>A, NM_002746.2:c.772C>A, NM_001040056.3:c.772C>A, NM_001040056.2:c.772C>A, NM_001109891.2:c.772C>A, NM_001109891.1:c.772C>A, XR_243293.2:n.783C>A, XR_243293.1:n.872C>A, NP_002737.2:p.Leu258Met, NP_001035145.1:p.Leu258Met, NP_001103361.1:p.Leu258Met

Select item 146470451513.

rs1464704515 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 16:30123191 (GRCh38)
16:30134512 (GRCh37)
Canonical SPDI:: NC_000016.10:30123190:G:C
Gene:: MAPK3 (Varview)
Functional Consequence:: non_coding_transcript_variant,missense_variant,coding_sequence_variant
Validated:: by frequency,by cluster
MAF:: C=0.00015/4 (TOMMO)
HGVS:: NC_000016.10:g.30123191G>C, NC_000016.9:g.30134512G>C, NG_029936.1:g.5119C>G, NM_002746.3:c.19C>G, NM_002746.2:c.19C>G, NM_001040056.3:c.19C>G, NM_001040056.2:c.19C>G, NM_001109891.2:c.19C>G, NM_001109891.1:c.19C>G, XR_243293.2:n.30C>G, XR_243293.1:n.119C>G, NP_002737.2:p.Gln7Glu, NP_001035145.1:p.Gln7Glu, NP_001103361.1:p.Gln7Glu

Select item 146192104414.

rs1461921044 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,G,T [Show Flanks]
Chromosome:: 16:30123173 (GRCh38)
16:30134494 (GRCh37)
Canonical SPDI:: NC_000016.10:30123172:C:A,NC_000016.10:30123172:C:G,NC_000016.10:30123172:C:T
Gene:: MAPK3 (Varview)
Functional Consequence:: non_coding_transcript_variant,stop_gained,missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
T=0.000034/2 (GnomAD_exomes)
G=0.001079/18 (TOMMO)
HGVS:: NC_000016.10:g.30123173C>A, NC_000016.10:g.30123173C>G, NC_000016.10:g.30123173C>T, NC_000016.9:g.30134494C>A, NC_000016.9:g.30134494C>G, NC_000016.9:g.30134494C>T, NG_029936.1:g.5137G>T, NG_029936.1:g.5137G>C, NG_029936.1:g.5137G>A, NM_002746.3:c.37G>T, NM_002746.3:c.37G>C, NM_002746.3:c.37G>A, NM_002746.2:c.37G>T, NM_002746.2:c.37G>C, NM_002746.2:c.37G>A, NM_001040056.3:c.37G>T, NM_001040056.3:c.37G>C, NM_001040056.3:c.37G>A, NM_001040056.2:c.37G>T, NM_001040056.2:c.37G>C, NM_001040056.2:c.37G>A, NM_001109891.2:c.37G>T, NM_001109891.2:c.37G>C, NM_001109891.2:c.37G>A, NM_001109891.1:c.37G>T, NM_001109891.1:c.37G>C, NM_001109891.1:c.37G>A, XR_243293.2:n.48G>T, XR_243293.2:n.48G>C, XR_243293.2:n.48G>A, XR_243293.1:n.137G>T, XR_243293.1:n.137G>C, XR_243293.1:n.137G>A, NP_002737.2:p.Glu13Ter, NP_002737.2:p.Glu13Gln, NP_002737.2:p.Glu13Lys, NP_001035145.1:p.Glu13Ter, NP_001035145.1:p.Glu13Gln, NP_001035145.1:p.Glu13Lys, NP_001103361.1:p.Glu13Ter, NP_001103361.1:p.Glu13Gln, NP_001103361.1:p.Glu13Lys

Select item 145811985215.

rs1458119852 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 16:30117186 (GRCh38)
16:30128507 (GRCh37)
Canonical SPDI:: NC_000016.10:30117185:C:T
Gene:: MAPK3 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant,stop_gained,coding_sequence_variant
Validated:: by cluster
HGVS:: NC_000016.10:g.30117186C>T, NC_000016.9:g.30128507C>T, NG_029936.1:g.11124G>A, NM_002746.3:c.875G>A, NM_002746.2:c.875G>A, NM_001040056.3:c.875G>A, NM_001040056.2:c.875G>A, XR_243293.2:n.886G>A, XR_243293.1:n.975G>A, NP_002737.2:p.Trp292Ter, NP_001035145.1:p.Trp292Ter

Select item 145638321316.

rs1456383213 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 16:30117278 (GRCh38)
16:30128599 (GRCh37)
Canonical SPDI:: NC_000016.10:30117277:C:T
Gene:: MAPK3 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant,synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
HGVS:: NC_000016.10:g.30117278C>T, NC_000016.9:g.30128599C>T, NG_029936.1:g.11032G>A, NM_002746.3:c.783G>A, NM_002746.2:c.783G>A, NM_001040056.3:c.783G>A, NM_001040056.2:c.783G>A, XR_243293.2:n.794G>A, XR_243293.1:n.883G>A

Select item 145502571717.

rs1455025717 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 16:30123093 (GRCh38)
16:30134414 (GRCh37)
Canonical SPDI:: NC_000016.10:30123092:G:C
Gene:: MAPK3 (Varview)
Functional Consequence:: non_coding_transcript_variant,synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: C=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000016.10:g.30123093G>C, NC_000016.9:g.30134414G>C, NG_029936.1:g.5217C>G, NM_002746.3:c.117C>G, NM_002746.2:c.117C>G, NM_001040056.3:c.117C>G, NM_001040056.2:c.117C>G, NM_001109891.2:c.117C>G, NM_001109891.1:c.117C>G, XR_243293.2:n.128C>G, XR_243293.1:n.217C>G

Select item 145216433518.

rs1452164335 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 16:30123156 (GRCh38)
16:30134477 (GRCh37)
Canonical SPDI:: NC_000016.10:30123155:C:G,NC_000016.10:30123155:C:T
Gene:: MAPK3 (Varview)
Functional Consequence:: non_coding_transcript_variant,synonymous_variant,missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000016.10:g.30123156C>G, NC_000016.10:g.30123156C>T, NC_000016.9:g.30134477C>G, NC_000016.9:g.30134477C>T, NG_029936.1:g.5154G>C, NG_029936.1:g.5154G>A, NM_002746.3:c.54G>C, NM_002746.3:c.54G>A, NM_002746.2:c.54G>C, NM_002746.2:c.54G>A, NM_001040056.3:c.54G>C, NM_001040056.3:c.54G>A, NM_001040056.2:c.54G>C, NM_001040056.2:c.54G>A, NM_001109891.2:c.54G>C, NM_001109891.2:c.54G>A, NM_001109891.1:c.54G>C, NM_001109891.1:c.54G>A, XR_243293.2:n.65G>C, XR_243293.2:n.65G>A, XR_243293.1:n.154G>C, XR_243293.1:n.154G>A, NP_002737.2:p.Glu18Asp, NP_001035145.1:p.Glu18Asp, NP_001103361.1:p.Glu18Asp

Select item 144975676219.

rs1449756762 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 16:30118132 (GRCh38)
16:30129453 (GRCh37)
Canonical SPDI:: NC_000016.10:30118131:T:A
Gene:: MAPK3 (Varview)
Functional Consequence:: non_coding_transcript_variant,missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000016.10:g.30118132T>A, NC_000016.9:g.30129453T>A, NG_029936.1:g.10178A>T, NM_002746.3:c.575A>T, NM_002746.2:c.575A>T, NM_001040056.3:c.575A>T, NM_001040056.2:c.575A>T, NM_001109891.2:c.575A>T, NM_001109891.1:c.575A>T, XR_243293.2:n.586A>T, XR_243293.1:n.675A>T, NP_002737.2:p.Asp192Val, NP_001035145.1:p.Asp192Val, NP_001103361.1:p.Asp192Val

Select item 144812253120.

rs1448122531 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 16:30117170 (GRCh38)
16:30128491 (GRCh37)
Canonical SPDI:: NC_000016.10:30117169:G:A,NC_000016.10:30117169:G:C
Gene:: MAPK3 (Varview)
Functional Consequence:: intron_variant,non_coding_transcript_variant,synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000071/1 (ALFA)
C=0.000004/1 (GnomAD_exomes)
C=0.000004/1 (TOPMED)
HGVS:: NC_000016.10:g.30117170G>A, NC_000016.10:g.30117170G>C, NC_000016.9:g.30128491G>A, NC_000016.9:g.30128491G>C, NG_029936.1:g.11140C>T, NG_029936.1:g.11140C>G, NM_002746.3:c.891C>T, NM_002746.3:c.891C>G, NM_002746.2:c.891C>T, NM_002746.2:c.891C>G, NM_001040056.3:c.891C>T, NM_001040056.3:c.891C>G, NM_001040056.2:c.891C>T, NM_001040056.2:c.891C>G, XR_243293.2:n.902C>T, XR_243293.2:n.902C>G, XR_243293.1:n.991C>T, XR_243293.1:n.991C>G

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