SNP Links for Protein (Select 20128774) - SNP

Links from Protein

Items: 1 to 20 of 365

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Select item 14871682551.

rs1487168255 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 22:50265469 (GRCh38)
22:50703898 (GRCh37)
Canonical SPDI:: NC_000022.11:50265468:C:A
Gene:: MAPK11 (Varview)
Functional Consequence:: non_coding_transcript_variant,coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000022.11:g.50265469C>A, NC_000022.10:g.50703898C>A, NG_034042.1:g.9925G>T, NM_002751.7:c.867G>T, NM_002751.6:c.867G>T, NM_002751.5:c.867G>T, NR_110887.2:n.955G>T, NR_110887.1:n.968G>T, NM_138993.2:c.867G>T, XM_047441447.1:c.543G>T, NM_138993.1:c.867G>T

Select item 14862496852.

rs1486249685 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 22:50266304 (GRCh38)
22:50704733 (GRCh37)
Canonical SPDI:: NC_000022.11:50266303:G:A
Gene:: MAPK11 (Varview)
Functional Consequence:: non_coding_transcript_variant,coding_sequence_variant,synonymous_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_000022.11:g.50266304G>A, NC_000022.10:g.50704733G>A, NG_034042.1:g.9090C>T, NM_002751.7:c.684C>T, NM_002751.6:c.684C>T, NM_002751.5:c.684C>T, NR_110887.2:n.772C>T, NR_110887.1:n.785C>T, NM_138993.2:c.684C>T, XM_047441447.1:c.360C>T, NM_138993.1:c.684C>T

Select item 14859653773.

rs1485965377 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 22:50270197 (GRCh38)
22:50708626 (GRCh37)
Canonical SPDI:: NC_000022.11:50270196:G:A
Gene:: MAPK11 (Varview)
Functional Consequence:: non_coding_transcript_variant,coding_sequence_variant,genic_upstream_transcript_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000022.11:g.50270197G>A, NC_000022.10:g.50708626G>A, NG_034042.1:g.5197C>T, NM_002751.7:c.96C>T, NM_002751.6:c.96C>T, NM_002751.5:c.96C>T, NR_110887.2:n.184C>T, NR_110887.1:n.197C>T, NM_138993.2:c.96C>T, NM_138993.1:c.96C>T

Select item 14840719214.

rs1484071921 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 22:50267476 (GRCh38)
22:50705905 (GRCh37)
Canonical SPDI:: NC_000022.11:50267475:C:T
Gene:: MAPK11 (Varview)
Functional Consequence:: non_coding_transcript_variant,coding_sequence_variant,5_prime_UTR_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0./0 (GnomAD)
T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000022.11:g.50267476C>T, NC_000022.10:g.50705905C>T, NG_034042.1:g.7918G>A, NM_002751.7:c.312G>A, NM_002751.6:c.312G>A, NM_002751.5:c.312G>A, NR_110887.2:n.400G>A, NR_110887.1:n.413G>A, NM_138993.2:c.312G>A, XM_047441447.1:c.-13G>A, NM_138993.1:c.312G>A

Select item 14788124965.

rs1478812496 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 22:50267877 (GRCh38)
22:50706306 (GRCh37)
Canonical SPDI:: NC_000022.11:50267876:G:A,NC_000022.11:50267876:G:T
Gene:: MAPK11 (Varview)
Functional Consequence:: non_coding_transcript_variant,coding_sequence_variant,5_prime_UTR_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0./0 (GnomAD)
HGVS:: NC_000022.11:g.50267877G>A, NC_000022.11:g.50267877G>T, NC_000022.10:g.50706306G>A, NC_000022.10:g.50706306G>T, NG_034042.1:g.7517C>T, NG_034042.1:g.7517C>A, NM_002751.7:c.189C>T, NM_002751.7:c.189C>A, NM_002751.6:c.189C>T, NM_002751.6:c.189C>A, NM_002751.5:c.189C>T, NM_002751.5:c.189C>A, NR_110887.2:n.277C>T, NR_110887.2:n.277C>A, NR_110887.1:n.290C>T, NR_110887.1:n.290C>A, NM_138993.2:c.189C>T, NM_138993.2:c.189C>A, XM_047441447.1:c.-77C>T, XM_047441447.1:c.-77C>A, NM_138993.1:c.189C>T, NM_138993.1:c.189C>A

Select item 14741534646.

rs1474153464 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 22:50265345 (GRCh38)
22:50703774 (GRCh37)
Canonical SPDI:: NC_000022.11:50265344:C:T
Gene:: MAPK11 (Varview)
Functional Consequence:: non_coding_transcript_variant,coding_sequence_variant,missense_variant
Validated:: by frequency,by cluster
MAF:: T=0.000004/1 (GnomAD_exomes)
T=0.000007/1 (GnomAD)
HGVS:: NC_000022.11:g.50265345C>T, NC_000022.10:g.50703774C>T, NG_034042.1:g.10049G>A, NM_002751.7:c.991G>A, NM_002751.6:c.991G>A, NM_002751.5:c.991G>A, NR_110887.2:n.1079G>A, NR_110887.1:n.1092G>A, NM_138993.2:c.991G>A, XM_047441447.1:c.667G>A, NM_138993.1:c.991G>A, NP_002742.3:p.Glu331Lys, XP_047297403.1:p.Glu223Lys

Select item 14702805427.

rs1470280542 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 22:50267824 (GRCh38)
22:50706253 (GRCh37)
Canonical SPDI:: NC_000022.11:50267823:T:C
Gene:: MAPK11 (Varview)
Functional Consequence:: non_coding_transcript_variant,coding_sequence_variant,5_prime_UTR_variant,missense_variant
Validated:: by frequency
MAF:: C=0.000006/1 (GnomAD_exomes)
HGVS:: NC_000022.11:g.50267824T>C, NC_000022.10:g.50706253T>C, NG_034042.1:g.7570A>G, NM_002751.7:c.242A>G, NM_002751.6:c.242A>G, NM_002751.5:c.242A>G, NR_110887.2:n.330A>G, NR_110887.1:n.343A>G, NM_138993.2:c.242A>G, XM_047441447.1:c.-24A>G, NM_138993.1:c.242A>G, NP_002742.3:p.Glu81Gly

Select item 14694967098.

rs1469496709 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 22:50267944 (GRCh38)
22:50706373 (GRCh37)
Canonical SPDI:: NC_000022.11:50267943:G:A
Gene:: MAPK11 (Varview)
Functional Consequence:: upstream_transcript_variant,missense_variant,non_coding_transcript_variant,coding_sequence_variant,genic_upstream_transcript_variant
HGVS:: NC_000022.11:g.50267944G>A, NC_000022.10:g.50706373G>A, NG_034042.1:g.7450C>T, NM_002751.7:c.122C>T, NM_002751.6:c.122C>T, NM_002751.5:c.122C>T, NR_110887.2:n.210C>T, NR_110887.1:n.223C>T, NM_138993.2:c.122C>T, NM_138993.1:c.122C>T, NP_002742.3:p.Ala41Val

Select item 14642342599.

rs1464234259 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 22:50265643 (GRCh38)
22:50704072 (GRCh37)
Canonical SPDI:: NC_000022.11:50265642:C:T
Gene:: MAPK11 (Varview)
Functional Consequence:: non_coding_transcript_variant,synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000023/6 (TOPMED)
T=0.000029/4 (GnomAD)
HGVS:: NC_000022.11:g.50265643C>T, NC_000022.10:g.50704072C>T, NG_034042.1:g.9751G>A, NM_002751.7:c.780G>A, NM_002751.6:c.780G>A, NM_002751.5:c.780G>A, NR_110887.2:n.868G>A, NR_110887.1:n.881G>A, NM_138993.2:c.780G>A, XM_047441447.1:c.456G>A, NM_138993.1:c.780G>A

Select item 146270528410.

rs1462705284 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 22:50267595 (GRCh38)
22:50706024 (GRCh37)
Canonical SPDI:: NC_000022.11:50267594:G:A
Gene:: MAPK11 (Varview)
Functional Consequence:: non_coding_transcript_variant,intron_variant,synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000014/2 (GnomAD)
A=0.000015/4 (TOPMED)
HGVS:: NC_000022.11:g.50267595G>A, NC_000022.10:g.50706024G>A, NG_034042.1:g.7799C>T, NM_002751.7:c.279C>T, NM_002751.6:c.279C>T, NM_002751.5:c.279C>T, NR_110887.2:n.367C>T, NR_110887.1:n.380C>T, NM_138993.2:c.279C>T, NM_138993.1:c.279C>T

Select item 146050506711.

rs1460505067 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 22:50265479 (GRCh38)
22:50703908 (GRCh37)
Canonical SPDI:: NC_000022.11:50265478:C:T
Gene:: MAPK11 (Varview)
Functional Consequence:: non_coding_transcript_variant,missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000022.11:g.50265479C>T, NC_000022.10:g.50703908C>T, NG_034042.1:g.9915G>A, NM_002751.7:c.857G>A, NM_002751.6:c.857G>A, NM_002751.5:c.857G>A, NR_110887.2:n.945G>A, NR_110887.1:n.958G>A, NM_138993.2:c.857G>A, XM_047441447.1:c.533G>A, NM_138993.1:c.857G>A, NP_002742.3:p.Gly286Glu, XP_047297403.1:p.Gly178Glu

Select item 145047045012.

rs1450470450 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 22:50267042 (GRCh38)
22:50705471 (GRCh37)
Canonical SPDI:: NC_000022.11:50267041:C:T
Gene:: MAPK11 (Varview)
Functional Consequence:: non_coding_transcript_variant,missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: T=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000022.11:g.50267042C>T, NC_000022.10:g.50705471C>T, NG_034042.1:g.8352G>A, NM_002751.7:c.502G>A, NM_002751.6:c.502G>A, NM_002751.5:c.502G>A, NR_110887.2:n.590G>A, NR_110887.1:n.603G>A, NM_138993.2:c.502G>A, XM_047441447.1:c.178G>A, NM_138993.1:c.502G>A, NP_002742.3:p.Asp168Asn, XP_047297403.1:p.Asp60Asn

Select item 144934325613.

rs1449343256 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 22:50270288 (GRCh38)
22:50708717 (GRCh37)
Canonical SPDI:: NC_000022.11:50270287:G:A
Gene:: MAPK11 (Varview)
Functional Consequence:: non_coding_transcript_variant,genic_upstream_transcript_variant,missense_variant,coding_sequence_variant
HGVS:: NC_000022.11:g.50270288G>A, NC_000022.10:g.50708717G>A, NG_034042.1:g.5106C>T, NM_002751.7:c.5C>T, NM_002751.6:c.5C>T, NM_002751.5:c.5C>T, NR_110887.2:n.93C>T, NR_110887.1:n.106C>T, NM_138993.2:c.5C>T, NM_138993.1:c.5C>T, NP_002742.3:p.Ser2Leu

Select item 144761666914.

rs1447616669 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 22:50270188 (GRCh38)
22:50708617 (GRCh37)
Canonical SPDI:: NC_000022.11:50270187:G:A
Gene:: MAPK11 (Varview)
Functional Consequence:: non_coding_transcript_variant,genic_upstream_transcript_variant,synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000011/3 (TOPMED)
HGVS:: NC_000022.11:g.50270188G>A, NC_000022.10:g.50708617G>A, NG_034042.1:g.5206C>T, NM_002751.7:c.105C>T, NM_002751.6:c.105C>T, NM_002751.5:c.105C>T, NR_110887.2:n.193C>T, NR_110887.1:n.206C>T, NM_138993.2:c.105C>T, NM_138993.1:c.105C>T

Select item 144501868515.

rs1445018685 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 22:50265491 (GRCh38)
22:50703920 (GRCh37)
Canonical SPDI:: NC_000022.11:50265490:A:G
Gene:: MAPK11 (Varview)
Functional Consequence:: non_coding_transcript_variant,missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (GnomAD_exomes)
G=0.000007/1 (GnomAD)
G=0.000011/3 (TOPMED)
HGVS:: NC_000022.11:g.50265491A>G, NC_000022.10:g.50703920A>G, NG_034042.1:g.9903T>C, NM_002751.7:c.845T>C, NM_002751.6:c.845T>C, NM_002751.5:c.845T>C, NR_110887.2:n.933T>C, NR_110887.1:n.946T>C, NM_138993.2:c.845T>C, XM_047441447.1:c.521T>C, NM_138993.1:c.845T>C, NP_002742.3:p.Ile282Thr, XP_047297403.1:p.Ile174Thr

Select item 144192289616.

rs1441922896 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 22:50267926 (GRCh38)
22:50706355 (GRCh37)
Canonical SPDI:: NC_000022.11:50267925:C:A,NC_000022.11:50267925:C:T
Gene:: MAPK11 (Varview)
Functional Consequence:: non_coding_transcript_variant,upstream_transcript_variant,genic_upstream_transcript_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_000022.11:g.50267926C>A, NC_000022.11:g.50267926C>T, NC_000022.10:g.50706355C>A, NC_000022.10:g.50706355C>T, NG_034042.1:g.7468G>T, NG_034042.1:g.7468G>A, NM_002751.7:c.140G>T, NM_002751.7:c.140G>A, NM_002751.6:c.140G>T, NM_002751.6:c.140G>A, NM_002751.5:c.140G>T, NM_002751.5:c.140G>A, NR_110887.2:n.228G>T, NR_110887.2:n.228G>A, NR_110887.1:n.241G>T, NR_110887.1:n.241G>A, NM_138993.2:c.140G>T, NM_138993.2:c.140G>A, NM_138993.1:c.140G>T, NM_138993.1:c.140G>A, NP_002742.3:p.Arg47Leu, NP_002742.3:p.Arg47His

Select item 143923974017.

rs1439239740 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 22:50266997 (GRCh38)
22:50705426 (GRCh37)
Canonical SPDI:: NC_000022.11:50266996:C:G
Gene:: MAPK11 (Varview)
Functional Consequence:: non_coding_transcript_variant,missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000022.11:g.50266997C>G, NC_000022.10:g.50705426C>G, NG_034042.1:g.8397G>C, NM_002751.7:c.547G>C, NM_002751.6:c.547G>C, NM_002751.5:c.547G>C, NR_110887.2:n.635G>C, NR_110887.1:n.648G>C, NM_138993.2:c.547G>C, XM_047441447.1:c.223G>C, NM_138993.1:c.547G>C, NP_002742.3:p.Val183Leu, XP_047297403.1:p.Val75Leu

Select item 143817751218.

rs1438177512 [Homo sapiens]

Variant type:: DEL
Alleles:: GCTGCGGCA>- [Show Flanks]
Chromosome:: 22:50270226 (GRCh38)
22:50708655 (GRCh37)
Canonical SPDI:: NC_000022.11:50270225:GCTGCGGCA:
Gene:: MAPK11 (Varview)
Functional Consequence:: non_coding_transcript_variant,inframe_indel,genic_upstream_transcript_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
HGVS:: NC_000022.11:g.50270226_50270234del, NC_000022.10:g.50708655_50708663del, NG_034042.1:g.5160_5168del, NM_002751.7:c.59_67del, NM_002751.6:c.59_67del, NM_002751.5:c.59_67del, NR_110887.2:n.147_155del, NR_110887.1:n.160_168del, NM_138993.2:c.59_67del, NM_138993.1:c.59_67del, NP_002742.3:p.Val20_Arg23delinsGly

Select item 143794514319.

rs1437945143 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 22:50267874 (GRCh38)
22:50706303 (GRCh37)
Canonical SPDI:: NC_000022.11:50267873:G:A
Gene:: MAPK11 (Varview)
Functional Consequence:: 5_prime_UTR_variant,non_coding_transcript_variant,synonymous_variant,coding_sequence_variant
HGVS:: NC_000022.11:g.50267874G>A, NC_000022.10:g.50706303G>A, NG_034042.1:g.7520C>T, NM_002751.7:c.192C>T, NM_002751.6:c.192C>T, NM_002751.5:c.192C>T, NR_110887.2:n.280C>T, NR_110887.1:n.293C>T, NM_138993.2:c.192C>T, XM_047441447.1:c.-74C>T, NM_138993.1:c.192C>T

Select item 143600522420.

rs1436005224 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 22:50267852 (GRCh38)
22:50706281 (GRCh37)
Canonical SPDI:: NC_000022.11:50267851:G:T
Gene:: MAPK11 (Varview)
Functional Consequence:: 5_prime_UTR_variant,non_coding_transcript_variant,missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: T=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000022.11:g.50267852G>T, NC_000022.10:g.50706281G>T, NG_034042.1:g.7542C>A, NM_002751.7:c.214C>A, NM_002751.6:c.214C>A, NM_002751.5:c.214C>A, NR_110887.2:n.302C>A, NR_110887.1:n.315C>A, NM_138993.2:c.214C>A, XM_047441447.1:c.-52C>A, NM_138993.1:c.214C>A, NP_002742.3:p.Leu72Met

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