SNP Links for Protein (Select 9257222) - SNP

Links from Protein

Items: 1 to 20 of 593

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Select item 14897553691.

rs1489755369 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 13:40665754 (GRCh38)
13:41239891 (GRCh37)
Canonical SPDI:: NC_000013.11:40665753:G:T
Gene:: FOXO1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,genic_upstream_transcript_variant
HGVS:: NC_000013.11:g.40665754G>T, NC_000013.10:g.41239891G>T, NG_023244.1:g.5844C>A, NM_002015.4:c.459C>A, NM_002015.3:c.459C>A, NP_002006.2:p.Ser153Arg

Select item 14896219302.

rs1489621930 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 13:40560372 (GRCh38)
13:41134509 (GRCh37)
Canonical SPDI:: NC_000013.11:40560371:A:G
Gene:: FOXO1 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000013.11:g.40560372A>G, NC_000013.10:g.41134509A>G, NG_023244.1:g.111226T>C, NM_002015.4:c.1119T>C, NM_002015.3:c.1119T>C, XM_011535010.3:c.408T>C, XM_011535010.2:c.408T>C, XM_011535010.1:c.408T>C, XM_011535008.3:c.576T>C, XM_011535008.2:c.576T>C, XM_011535008.1:c.576T>C, XM_047430204.1:c.408T>C

Select item 14892583583.

rs1489258358 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 13:40666067 (GRCh38)
13:41240204 (GRCh37)
Canonical SPDI:: NC_000013.11:40666066:G:A
Gene:: FOXO1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000013.11:g.40666067G>A, NC_000013.10:g.41240204G>A, NG_023244.1:g.5531C>T, NM_002015.4:c.146C>T, NM_002015.3:c.146C>T, NP_002006.2:p.Ala49Val

Select item 14891534994.

rs1489153499 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 13:40665685 (GRCh38)
13:41239822 (GRCh37)
Canonical SPDI:: NC_000013.11:40665684:C:G,NC_000013.11:40665684:C:T
Gene:: FOXO1 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
T=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000013.11:g.40665685C>G, NC_000013.11:g.40665685C>T, NC_000013.10:g.41239822C>G, NC_000013.10:g.41239822C>T, NG_023244.1:g.5913G>C, NG_023244.1:g.5913G>A, NM_002015.4:c.528G>C, NM_002015.4:c.528G>A, NM_002015.3:c.528G>C, NM_002015.3:c.528G>A

Select item 14886426425.

rs1488642642 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 13:40560059 (GRCh38)
13:41134196 (GRCh37)
Canonical SPDI:: NC_000013.11:40560058:T:C
Gene:: FOXO1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by cluster
MAF:: C=0.000004/1 (GnomAD_exomes)
C=0.000007/1 (GnomAD)
HGVS:: NC_000013.11:g.40560059T>C, NC_000013.10:g.41134196T>C, NG_023244.1:g.111539A>G, NM_002015.4:c.1432A>G, NM_002015.3:c.1432A>G, XM_011535010.3:c.721A>G, XM_011535010.2:c.721A>G, XM_011535010.1:c.721A>G, XM_011535008.3:c.889A>G, XM_011535008.2:c.889A>G, XM_011535008.1:c.889A>G, XM_047430204.1:c.721A>G, NP_002006.2:p.Thr478Ala, XP_011533312.1:p.Thr241Ala, XP_011533310.1:p.Thr297Ala, XP_047286160.1:p.Thr241Ala

Select item 14877957906.

rs1487795790 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 13:40560467 (GRCh38)
13:41134604 (GRCh37)
Canonical SPDI:: NC_000013.11:40560466:C:T
Gene:: FOXO1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000013.11:g.40560467C>T, NC_000013.10:g.41134604C>T, NG_023244.1:g.111131G>A, NM_002015.4:c.1024G>A, NM_002015.3:c.1024G>A, XM_011535010.3:c.313G>A, XM_011535010.2:c.313G>A, XM_011535010.1:c.313G>A, XM_011535008.3:c.481G>A, XM_011535008.2:c.481G>A, XM_011535008.1:c.481G>A, XM_047430204.1:c.313G>A, NP_002006.2:p.Asp342Asn, XP_011533312.1:p.Asp105Asn, XP_011533310.1:p.Asp161Asn, XP_047286160.1:p.Asp105Asn

Select item 14877876267.

rs1487787626 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 13:40560726 (GRCh38)
13:41134863 (GRCh37)
Canonical SPDI:: NC_000013.11:40560725:T:C
Gene:: FOXO1 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000224/1 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000223/1 (Estonian)
HGVS:: NC_000013.11:g.40560726T>C, NC_000013.10:g.41134863T>C, NG_023244.1:g.110872A>G, NM_002015.4:c.765A>G, NM_002015.3:c.765A>G, XM_011535010.3:c.54A>G, XM_011535010.2:c.54A>G, XM_011535010.1:c.54A>G, XM_011535008.3:c.222A>G, XM_011535008.2:c.222A>G, XM_011535008.1:c.222A>G, XM_047430204.1:c.54A>G

Select item 14872313028.

rs1487231302 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 13:40559586 (GRCh38)
13:41133723 (GRCh37)
Canonical SPDI:: NC_000013.11:40559585:C:T
Gene:: FOXO1 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000013.11:g.40559586C>T, NC_000013.10:g.41133723C>T, NG_023244.1:g.112012G>A, NM_002015.4:c.1905G>A, NM_002015.3:c.1905G>A, XM_011535010.3:c.1194G>A, XM_011535010.2:c.1194G>A, XM_011535010.1:c.1194G>A, XM_011535008.3:c.1362G>A, XM_011535008.2:c.1362G>A, XM_011535008.1:c.1362G>A, XM_047430204.1:c.1194G>A

Select item 14827792939.

rs1482779293 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 13:40559678 (GRCh38)
13:41133815 (GRCh37)
Canonical SPDI:: NC_000013.11:40559677:T:C
Gene:: FOXO1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_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_000013.11:g.40559678T>C, NC_000013.10:g.41133815T>C, NG_023244.1:g.111920A>G, NM_002015.4:c.1813A>G, NM_002015.3:c.1813A>G, XM_011535010.3:c.1102A>G, XM_011535010.2:c.1102A>G, XM_011535010.1:c.1102A>G, XM_011535008.3:c.1270A>G, XM_011535008.2:c.1270A>G, XM_011535008.1:c.1270A>G, XM_047430204.1:c.1102A>G, NP_002006.2:p.Met605Val, XP_011533312.1:p.Met368Val, XP_011533310.1:p.Met424Val, XP_047286160.1:p.Met368Val

Select item 148274524510.

rs1482745245 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 13:40560355 (GRCh38)
13:41134492 (GRCh37)
Canonical SPDI:: NC_000013.11:40560354:T:C
Gene:: FOXO1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000008/2 (TOPMED)
HGVS:: NC_000013.11:g.40560355T>C, NC_000013.10:g.41134492T>C, NG_023244.1:g.111243A>G, NM_002015.4:c.1136A>G, NM_002015.3:c.1136A>G, XM_011535010.3:c.425A>G, XM_011535010.2:c.425A>G, XM_011535010.1:c.425A>G, XM_011535008.3:c.593A>G, XM_011535008.2:c.593A>G, XM_011535008.1:c.593A>G, XM_047430204.1:c.425A>G, NP_002006.2:p.Asn379Ser, XP_011533312.1:p.Asn142Ser, XP_011533310.1:p.Asn198Ser, XP_047286160.1:p.Asn142Ser

Select item 148249416911.

rs1482494169 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 13:40560218 (GRCh38)
13:41134355 (GRCh37)
Canonical SPDI:: NC_000013.11:40560217:T:C
Gene:: FOXO1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000013.11:g.40560218T>C, NC_000013.10:g.41134355T>C, NG_023244.1:g.111380A>G, NM_002015.4:c.1273A>G, NM_002015.3:c.1273A>G, XM_011535010.3:c.562A>G, XM_011535010.2:c.562A>G, XM_011535010.1:c.562A>G, XM_011535008.3:c.730A>G, XM_011535008.2:c.730A>G, XM_011535008.1:c.730A>G, XM_047430204.1:c.562A>G, NP_002006.2:p.Thr425Ala, XP_011533312.1:p.Thr188Ala, XP_011533310.1:p.Thr244Ala, XP_047286160.1:p.Thr188Ala

Select item 148244046612.

rs1482440466 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G [Show Flanks]
Chromosome:: 13:40665932 (GRCh38)
13:41240069 (GRCh37)
Canonical SPDI:: NC_000013.11:40665931:A:C,NC_000013.11:40665931:A:G
Gene:: FOXO1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000015/2 (GnomAD)
C=0.000719/20 (TOMMO)
HGVS:: NC_000013.11:g.40665932A>C, NC_000013.11:g.40665932A>G, NC_000013.10:g.41240069A>C, NC_000013.10:g.41240069A>G, NG_023244.1:g.5666T>G, NG_023244.1:g.5666T>C, NM_002015.4:c.281T>G, NM_002015.4:c.281T>C, NM_002015.3:c.281T>G, NM_002015.3:c.281T>C, NP_002006.2:p.Val94Gly, NP_002006.2:p.Val94Ala

Select item 148122047813.

rs1481220478 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 13:40559949 (GRCh38)
13:41134086 (GRCh37)
Canonical SPDI:: NC_000013.11:40559948:G:A
Gene:: FOXO1 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000014/2 (GnomAD)
A=0.000034/9 (TOPMED)
HGVS:: NC_000013.11:g.40559949G>A, NC_000013.10:g.41134086G>A, NG_023244.1:g.111649C>T, NM_002015.4:c.1542C>T, NM_002015.3:c.1542C>T, XM_011535010.3:c.831C>T, XM_011535010.2:c.831C>T, XM_011535010.1:c.831C>T, XM_011535008.3:c.999C>T, XM_011535008.2:c.999C>T, XM_011535008.1:c.999C>T, XM_047430204.1:c.831C>T

Select item 148072857714.

rs1480728577 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 13:40665976 (GRCh38)
13:41240113 (GRCh37)
Canonical SPDI:: NC_000013.11:40665975:C:G,NC_000013.11:40665975:C:T
Gene:: FOXO1 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant,missense_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000011/3 (TOPMED)
HGVS:: NC_000013.11:g.40665976C>G, NC_000013.11:g.40665976C>T, NC_000013.10:g.41240113C>G, NC_000013.10:g.41240113C>T, NG_023244.1:g.5622G>C, NG_023244.1:g.5622G>A, NM_002015.4:c.237G>C, NM_002015.4:c.237G>A, NM_002015.3:c.237G>C, NM_002015.3:c.237G>A, NP_002006.2:p.Glu79Asp

Select item 147870223215.

rs1478702232 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 13:40665812 (GRCh38)
13:41239949 (GRCh37)
Canonical SPDI:: NC_000013.11:40665811:T:G
Gene:: FOXO1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.00016/1 (1000Genomes)
G=0.00057/1 (Korea1K)
G=0.00935/2 (Vietnamese)
T=0.5/1 (SGDP_PRJ)
HGVS:: NC_000013.11:g.40665812T>G, NC_000013.10:g.41239949T>G, NG_023244.1:g.5786A>C, NM_002015.4:c.401A>C, NM_002015.3:c.401A>C, NP_002006.2:p.His134Pro

Select item 147771986816.

rs1477719868 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 13:40559924 (GRCh38)
13:41134061 (GRCh37)
Canonical SPDI:: NC_000013.11:40559923:T:C
Gene:: FOXO1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000013.11:g.40559924T>C, NC_000013.10:g.41134061T>C, NG_023244.1:g.111674A>G, NM_002015.4:c.1567A>G, NM_002015.3:c.1567A>G, XM_011535010.3:c.856A>G, XM_011535010.2:c.856A>G, XM_011535010.1:c.856A>G, XM_011535008.3:c.1024A>G, XM_011535008.2:c.1024A>G, XM_011535008.1:c.1024A>G, XM_047430204.1:c.856A>G, NP_002006.2:p.Thr523Ala, XP_011533312.1:p.Thr286Ala, XP_011533310.1:p.Thr342Ala, XP_047286160.1:p.Thr286Ala

Select item 147705377917.

rs1477053779 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C [Show Flanks]
Chromosome:: 13:40560666 (GRCh38)
13:41134803 (GRCh37)
Canonical SPDI:: NC_000013.11:40560665:T:A,NC_000013.11:40560665:T:C
Gene:: FOXO1 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000013.11:g.40560666T>A, NC_000013.11:g.40560666T>C, NC_000013.10:g.41134803T>A, NC_000013.10:g.41134803T>C, NG_023244.1:g.110932A>T, NG_023244.1:g.110932A>G, NM_002015.4:c.825A>T, NM_002015.4:c.825A>G, NM_002015.3:c.825A>T, NM_002015.3:c.825A>G, XM_011535010.3:c.114A>T, XM_011535010.3:c.114A>G, XM_011535010.2:c.114A>T, XM_011535010.2:c.114A>G, XM_011535010.1:c.114A>T, XM_011535010.1:c.114A>G, XM_011535008.3:c.282A>T, XM_011535008.3:c.282A>G, XM_011535008.2:c.282A>T, XM_011535008.2:c.282A>G, XM_011535008.1:c.282A>T, XM_011535008.1:c.282A>G, XM_047430204.1:c.114A>T, XM_047430204.1:c.114A>G

Select item 147639958618.

rs1476399586 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 13:40560076 (GRCh38)
13:41134213 (GRCh37)
Canonical SPDI:: NC_000013.11:40560075:G:C
Gene:: FOXO1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: C=0.000066/2 (ALFA)
C=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000013.11:g.40560076G>C, NC_000013.10:g.41134213G>C, NG_023244.1:g.111522C>G, NM_002015.4:c.1415C>G, NM_002015.3:c.1415C>G, XM_011535010.3:c.704C>G, XM_011535010.2:c.704C>G, XM_011535010.1:c.704C>G, XM_011535008.3:c.872C>G, XM_011535008.2:c.872C>G, XM_011535008.1:c.872C>G, XM_047430204.1:c.704C>G, NP_002006.2:p.Pro472Arg, XP_011533312.1:p.Pro235Arg, XP_011533310.1:p.Pro291Arg, XP_047286160.1:p.Pro235Arg

Select item 147541955019.

rs1475419550 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 13:40560849 (GRCh38)
13:41134986 (GRCh37)
Canonical SPDI:: NC_000013.11:40560848:A:T
Gene:: FOXO1 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant,5_prime_UTR_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_000013.11:g.40560849A>T, NC_000013.10:g.41134986A>T, NG_023244.1:g.110749T>A, NM_002015.4:c.642T>A, NM_002015.3:c.642T>A, XM_011535010.3:c.-70T>A, XM_011535010.2:c.-70T>A, XM_011535010.1:c.-70T>A, XM_011535008.3:c.99T>A, XM_011535008.2:c.99T>A, XM_011535008.1:c.99T>A, XM_047430204.1:c.-70T>A

Select item 147406609220.

rs1474066092 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 13:40560300 (GRCh38)
13:41134437 (GRCh37)
Canonical SPDI:: NC_000013.11:40560299:G:A
Gene:: FOXO1 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000013.11:g.40560300G>A, NC_000013.10:g.41134437G>A, NG_023244.1:g.111298C>T, NM_002015.4:c.1191C>T, NM_002015.3:c.1191C>T, XM_011535010.3:c.480C>T, XM_011535010.2:c.480C>T, XM_011535010.1:c.480C>T, XM_011535008.3:c.648C>T, XM_011535008.2:c.648C>T, XM_011535008.1:c.648C>T, XM_047430204.1:c.480C>T

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