SNP Links for Protein (Select 38201670) - SNP

Links from Protein

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Select item 14869717191.

rs1486971719 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G [Show Flanks]
Chromosome:: 12:6652412 (GRCh38)
12:6761578 (GRCh37)
Canonical SPDI:: NC_000012.12:6652411:A:C,NC_000012.12:6652411:A:G
Gene:: ING4 (Varview)
Functional Consequence:: intron_variant,coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000014/2 (GnomAD)
HGVS:: NC_000012.12:g.6652412A>C, NC_000012.12:g.6652412A>G, NC_000012.11:g.6761578A>C, NC_000012.11:g.6761578A>G, NG_047151.1:g.15738T>G, NG_047151.1:g.15738T>C, NM_016162.4:c.504T>G, NM_016162.4:c.504T>C, NM_016162.3:c.504T>G, NM_016162.3:c.504T>C, NM_001127582.2:c.507T>G, NM_001127582.2:c.507T>C, NM_001127582.1:c.507T>G, NM_001127582.1:c.507T>C, NM_001127583.2:c.498T>G, NM_001127583.2:c.498T>C, NM_001127583.1:c.498T>G, NM_001127583.1:c.498T>C, NM_001127584.2:c.495T>G, NM_001127584.2:c.495T>C, NM_001127584.1:c.495T>G, NM_001127584.1:c.495T>C, NM_001127585.2:c.435T>G, NM_001127585.2:c.435T>C, NM_001127585.1:c.435T>G, NM_001127585.1:c.435T>C, XM_011520965.4:c.426T>G, XM_011520965.4:c.426T>C, XM_011520965.3:c.426T>G, XM_011520965.3:c.426T>C, XM_011520965.2:c.426T>G, XM_011520965.2:c.426T>C, XM_011520965.1:c.426T>G, XM_011520965.1:c.426T>C, XM_011520964.3:c.432T>G, XM_011520964.3:c.432T>C, XM_011520964.2:c.432T>G, XM_011520964.2:c.432T>C, XM_011520964.1:c.432T>G, XM_011520964.1:c.432T>C, NM_198287.1:c.*636T>G, NM_198287.1:c.*636T>C, XM_047428932.1:c.360T>G, XM_047428932.1:c.360T>C, XM_047428931.1:c.426T>G, XM_047428931.1:c.426T>C

Select item 14869349092.

rs1486934909 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 12:6652767 (GRCh38)
12:6761933 (GRCh37)
Canonical SPDI:: NC_000012.12:6652766:C:A
Gene:: ING4 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
A=0.000008/2 (TOPMED)
HGVS:: NC_000012.12:g.6652767C>A, NC_000012.11:g.6761933C>A, NG_047151.1:g.15383G>T, NM_016162.4:c.392G>T, NM_016162.3:c.392G>T, NM_001127582.2:c.395G>T, NM_001127582.1:c.395G>T, NM_001127583.2:c.386G>T, NM_001127583.1:c.386G>T, NM_001127584.2:c.383G>T, NM_001127584.1:c.383G>T, NM_001127585.2:c.323G>T, NM_001127585.1:c.323G>T, NM_001127586.2:c.395G>T, NM_001127586.1:c.395G>T, XM_011520965.4:c.314G>T, XM_011520965.3:c.314G>T, XM_011520965.2:c.314G>T, XM_011520965.1:c.314G>T, XM_011520964.3:c.320G>T, XM_011520964.2:c.320G>T, XM_011520964.1:c.320G>T, NM_198287.1:c.*524G>T, XM_047428932.1:c.248G>T, XM_047428931.1:c.314G>T, NP_057246.2:p.Ser131Ile, NP_001121054.1:p.Gly132Val, NP_001121055.1:p.Gly129Val, NP_001121056.1:p.Gly128Val, NP_001121057.1:p.Gly108Val, NP_001121058.1:p.Gly132Val, XP_011519267.1:p.Gly105Val, XP_011519266.1:p.Ser107Ile, XP_047284888.1:p.Gly83Val, XP_047284887.1:p.Gly105Val

Select item 14858455843.

rs1485845584 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 12:6656797 (GRCh38)
12:6765963 (GRCh37)
Canonical SPDI:: NC_000012.12:6656796:A:G
Gene:: ING4 (Varview)
Functional Consequence:: 5_prime_UTR_variant,intron_variant,coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: G=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000012.12:g.6656797A>G, NC_000012.11:g.6765963A>G, NG_047151.1:g.11353T>C, NM_016162.4:c.39T>C, NM_016162.3:c.39T>C, NM_001127582.2:c.39T>C, NM_001127582.1:c.39T>C, NM_001127583.2:c.39T>C, NM_001127583.1:c.39T>C, NM_001127584.2:c.39T>C, NM_001127584.1:c.39T>C, NM_001127586.2:c.39T>C, NM_001127586.1:c.39T>C, XM_011520965.4:c.-43T>C, XM_011520965.3:c.-43T>C, XM_011520965.2:c.-43T>C, XM_011520965.1:c.-43T>C, NM_198287.1:c.39T>C, XM_047428932.1:c.-385T>C

Select item 14753213774.

rs1475321377 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 12:6653012 (GRCh38)
12:6762178 (GRCh37)
Canonical SPDI:: NC_000012.12:6653011:G:A
Gene:: ING4 (Varview)
Functional Consequence:: 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_000012.12:g.6653012G>A, NC_000012.11:g.6762178G>A, NG_047151.1:g.15138C>T, NM_016162.4:c.315C>T, NM_016162.3:c.315C>T, NM_001127582.2:c.315C>T, NM_001127582.1:c.315C>T, NM_001127583.2:c.315C>T, NM_001127583.1:c.315C>T, NM_001127584.2:c.315C>T, NM_001127584.1:c.315C>T, NM_001127585.2:c.243C>T, NM_001127585.1:c.243C>T, NM_001127586.2:c.315C>T, NM_001127586.1:c.315C>T, XM_011520965.4:c.234C>T, XM_011520965.3:c.234C>T, XM_011520965.2:c.234C>T, XM_011520965.1:c.234C>T, XM_011520964.3:c.243C>T, XM_011520964.2:c.243C>T, XM_011520964.1:c.243C>T, NM_198287.1:c.*447C>T, XM_047428932.1:c.168C>T, XM_047428931.1:c.243C>T

Select item 14720224445.

rs1472022444 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 12:6653253 (GRCh38)
12:6762419 (GRCh37)
Canonical SPDI:: NC_000012.12:6653252:G:A,NC_000012.12:6653252:G:C
Gene:: ING4 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000071/1 (ALFA)
C=0.000004/1 (GnomAD_exomes)
A=0.000007/1 (GnomAD)
HGVS:: NC_000012.12:g.6653253G>A, NC_000012.12:g.6653253G>C, NC_000012.11:g.6762419G>A, NC_000012.11:g.6762419G>C, NG_047151.1:g.14897C>T, NG_047151.1:g.14897C>G, NM_016162.4:c.253C>T, NM_016162.4:c.253C>G, NM_016162.3:c.253C>T, NM_016162.3:c.253C>G, NM_001127582.2:c.253C>T, NM_001127582.2:c.253C>G, NM_001127582.1:c.253C>T, NM_001127582.1:c.253C>G, NM_001127583.2:c.253C>T, NM_001127583.2:c.253C>G, NM_001127583.1:c.253C>T, NM_001127583.1:c.253C>G, NM_001127584.2:c.253C>T, NM_001127584.2:c.253C>G, NM_001127584.1:c.253C>T, NM_001127584.1:c.253C>G, NM_001127585.2:c.181C>T, NM_001127585.2:c.181C>G, NM_001127585.1:c.181C>T, NM_001127585.1:c.181C>G, NM_001127586.2:c.253C>T, NM_001127586.2:c.253C>G, NM_001127586.1:c.253C>T, NM_001127586.1:c.253C>G, XM_011520965.4:c.172C>T, XM_011520965.4:c.172C>G, XM_011520965.3:c.172C>T, XM_011520965.3:c.172C>G, XM_011520965.2:c.172C>T, XM_011520965.2:c.172C>G, XM_011520965.1:c.172C>T, XM_011520965.1:c.172C>G, XM_011520964.3:c.181C>T, XM_011520964.3:c.181C>G, XM_011520964.2:c.181C>T, XM_011520964.2:c.181C>G, XM_011520964.1:c.181C>T, XM_011520964.1:c.181C>G, NM_198287.1:c.*385C>T, NM_198287.1:c.*385C>G, XM_047428932.1:c.106C>T, XM_047428932.1:c.106C>G, XM_047428931.1:c.181C>T, XM_047428931.1:c.181C>G, NP_057246.2:p.Leu85Phe, NP_057246.2:p.Leu85Val, NP_001121054.1:p.Leu85Phe, NP_001121054.1:p.Leu85Val, NP_001121055.1:p.Leu85Phe, NP_001121055.1:p.Leu85Val, NP_001121056.1:p.Leu85Phe, NP_001121056.1:p.Leu85Val, NP_001121057.1:p.Leu61Phe, NP_001121057.1:p.Leu61Val, NP_001121058.1:p.Leu85Phe, NP_001121058.1:p.Leu85Val, XP_011519267.1:p.Leu58Phe, XP_011519267.1:p.Leu58Val, XP_011519266.1:p.Leu61Phe, XP_011519266.1:p.Leu61Val, XP_047284888.1:p.Leu36Phe, XP_047284888.1:p.Leu36Val, XP_047284887.1:p.Leu61Phe, XP_047284887.1:p.Leu61Val

Select item 14714004286.

rs1471400428 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 12:6653346 (GRCh38)
12:6762512 (GRCh37)
Canonical SPDI:: NC_000012.12:6653345:G:A,NC_000012.12:6653345:G:C
Gene:: ING4 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000043/1 (ALFA)
C=0.000007/1 (GnomAD)
A=0.000012/3 (GnomAD_exomes)
HGVS:: NC_000012.12:g.6653346G>A, NC_000012.12:g.6653346G>C, NC_000012.11:g.6762512G>A, NC_000012.11:g.6762512G>C, NG_047151.1:g.14804C>T, NG_047151.1:g.14804C>G, NM_016162.4:c.160C>T, NM_016162.4:c.160C>G, NM_016162.3:c.160C>T, NM_016162.3:c.160C>G, NM_001127582.2:c.160C>T, NM_001127582.2:c.160C>G, NM_001127582.1:c.160C>T, NM_001127582.1:c.160C>G, NM_001127583.2:c.160C>T, NM_001127583.2:c.160C>G, NM_001127583.1:c.160C>T, NM_001127583.1:c.160C>G, NM_001127584.2:c.160C>T, NM_001127584.2:c.160C>G, NM_001127584.1:c.160C>T, NM_001127584.1:c.160C>G, NM_001127585.2:c.88C>T, NM_001127585.2:c.88C>G, NM_001127585.1:c.88C>T, NM_001127585.1:c.88C>G, NM_001127586.2:c.160C>T, NM_001127586.2:c.160C>G, NM_001127586.1:c.160C>T, NM_001127586.1:c.160C>G, XM_011520965.4:c.79C>T, XM_011520965.4:c.79C>G, XM_011520965.3:c.79C>T, XM_011520965.3:c.79C>G, XM_011520965.2:c.79C>T, XM_011520965.2:c.79C>G, XM_011520965.1:c.79C>T, XM_011520965.1:c.79C>G, XM_011520964.3:c.88C>T, XM_011520964.3:c.88C>G, XM_011520964.2:c.88C>T, XM_011520964.2:c.88C>G, XM_011520964.1:c.88C>T, XM_011520964.1:c.88C>G, NM_198287.1:c.*292C>T, NM_198287.1:c.*292C>G, XM_047428932.1:c.13C>T, XM_047428932.1:c.13C>G, XM_047428931.1:c.88C>T, XM_047428931.1:c.88C>G, NP_057246.2:p.Arg54Cys, NP_057246.2:p.Arg54Gly, NP_001121054.1:p.Arg54Cys, NP_001121054.1:p.Arg54Gly, NP_001121055.1:p.Arg54Cys, NP_001121055.1:p.Arg54Gly, NP_001121056.1:p.Arg54Cys, NP_001121056.1:p.Arg54Gly, NP_001121057.1:p.Arg30Cys, NP_001121057.1:p.Arg30Gly, NP_001121058.1:p.Arg54Cys, NP_001121058.1:p.Arg54Gly, XP_011519267.1:p.Arg27Cys, XP_011519267.1:p.Arg27Gly, XP_011519266.1:p.Arg30Cys, XP_011519266.1:p.Arg30Gly, XP_047284888.1:p.Arg5Cys, XP_047284888.1:p.Arg5Gly, XP_047284887.1:p.Arg30Cys, XP_047284887.1:p.Arg30Gly

Select item 14660836727.

rs1466083672 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 12:6653356 (GRCh38)
12:6762522 (GRCh37)
Canonical SPDI:: NC_000012.12:6653355:C:G,NC_000012.12:6653355:C:T
Gene:: ING4 (Varview)
Functional Consequence:: initiator_codon_variant,coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000012.12:g.6653356C>G, NC_000012.12:g.6653356C>T, NC_000012.11:g.6762522C>G, NC_000012.11:g.6762522C>T, NG_047151.1:g.14794G>C, NG_047151.1:g.14794G>A, NM_016162.4:c.150G>C, NM_016162.4:c.150G>A, NM_016162.3:c.150G>C, NM_016162.3:c.150G>A, NM_001127582.2:c.150G>C, NM_001127582.2:c.150G>A, NM_001127582.1:c.150G>C, NM_001127582.1:c.150G>A, NM_001127583.2:c.150G>C, NM_001127583.2:c.150G>A, NM_001127583.1:c.150G>C, NM_001127583.1:c.150G>A, NM_001127584.2:c.150G>C, NM_001127584.2:c.150G>A, NM_001127584.1:c.150G>C, NM_001127584.1:c.150G>A, NM_001127585.2:c.78G>C, NM_001127585.2:c.78G>A, NM_001127585.1:c.78G>C, NM_001127585.1:c.78G>A, NM_001127586.2:c.150G>C, NM_001127586.2:c.150G>A, NM_001127586.1:c.150G>C, NM_001127586.1:c.150G>A, XM_011520965.4:c.69G>C, XM_011520965.4:c.69G>A, XM_011520965.3:c.69G>C, XM_011520965.3:c.69G>A, XM_011520965.2:c.69G>C, XM_011520965.2:c.69G>A, XM_011520965.1:c.69G>C, XM_011520965.1:c.69G>A, XM_011520964.3:c.78G>C, XM_011520964.3:c.78G>A, XM_011520964.2:c.78G>C, XM_011520964.2:c.78G>A, XM_011520964.1:c.78G>C, XM_011520964.1:c.78G>A, NM_198287.1:c.*282G>C, NM_198287.1:c.*282G>A, XM_047428932.1:c.3G>C, XM_047428932.1:c.3G>A, XM_047428931.1:c.78G>C, XM_047428931.1:c.78G>A, NP_057246.2:p.Met50Ile, NP_057246.2:p.Met50Ile, NP_001121054.1:p.Met50Ile, NP_001121054.1:p.Met50Ile, NP_001121055.1:p.Met50Ile, NP_001121055.1:p.Met50Ile, NP_001121056.1:p.Met50Ile, NP_001121056.1:p.Met50Ile, NP_001121057.1:p.Met26Ile, NP_001121057.1:p.Met26Ile, NP_001121058.1:p.Met50Ile, NP_001121058.1:p.Met50Ile, XP_011519267.1:p.Met23Ile, XP_011519267.1:p.Met23Ile, XP_011519266.1:p.Met26Ile, XP_011519266.1:p.Met26Ile, XP_047284888.1:p.Met1Ile, XP_047284888.1:p.Met1Ile, XP_047284887.1:p.Met26Ile, XP_047284887.1:p.Met26Ile

Select item 14647055368.

rs1464705536 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G [Show Flanks]
Chromosome:: 12:6653373 (GRCh38)
12:6762539 (GRCh37)
Canonical SPDI:: NC_000012.12:6653372:A:C,NC_000012.12:6653372:A:G
Gene:: ING4 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant,5_prime_UTR_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
C=0.000008/2 (TOPMED)
C=0.000021/3 (GnomAD)
HGVS:: NC_000012.12:g.6653373A>C, NC_000012.12:g.6653373A>G, NC_000012.11:g.6762539A>C, NC_000012.11:g.6762539A>G, NG_047151.1:g.14777T>G, NG_047151.1:g.14777T>C, NM_016162.4:c.133T>G, NM_016162.4:c.133T>C, NM_016162.3:c.133T>G, NM_016162.3:c.133T>C, NM_001127582.2:c.133T>G, NM_001127582.2:c.133T>C, NM_001127582.1:c.133T>G, NM_001127582.1:c.133T>C, NM_001127583.2:c.133T>G, NM_001127583.2:c.133T>C, NM_001127583.1:c.133T>G, NM_001127583.1:c.133T>C, NM_001127584.2:c.133T>G, NM_001127584.2:c.133T>C, NM_001127584.1:c.133T>G, NM_001127584.1:c.133T>C, NM_001127585.2:c.61T>G, NM_001127585.2:c.61T>C, NM_001127585.1:c.61T>G, NM_001127585.1:c.61T>C, NM_001127586.2:c.133T>G, NM_001127586.2:c.133T>C, NM_001127586.1:c.133T>G, NM_001127586.1:c.133T>C, XM_011520965.4:c.52T>G, XM_011520965.4:c.52T>C, XM_011520965.3:c.52T>G, XM_011520965.3:c.52T>C, XM_011520965.2:c.52T>G, XM_011520965.2:c.52T>C, XM_011520965.1:c.52T>G, XM_011520965.1:c.52T>C, XM_011520964.3:c.61T>G, XM_011520964.3:c.61T>C, XM_011520964.2:c.61T>G, XM_011520964.2:c.61T>C, XM_011520964.1:c.61T>G, XM_011520964.1:c.61T>C, NM_198287.1:c.*265T>G, NM_198287.1:c.*265T>C, XM_047428932.1:c.-15T>G, XM_047428932.1:c.-15T>C, XM_047428931.1:c.61T>G, XM_047428931.1:c.61T>C, NP_057246.2:p.Leu45Val, NP_001121054.1:p.Leu45Val, NP_001121055.1:p.Leu45Val, NP_001121056.1:p.Leu45Val, NP_001121057.1:p.Leu21Val, NP_001121058.1:p.Leu45Val, XP_011519267.1:p.Leu18Val, XP_011519266.1:p.Leu21Val, XP_047284887.1:p.Leu21Val

Select item 14516749219.

rs1451674921 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 12:6652691 (GRCh38)
12:6761857 (GRCh37)
Canonical SPDI:: NC_000012.12:6652690:A:G
Gene:: ING4 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000011/3 (TOPMED)
HGVS:: NC_000012.12:g.6652691A>G, NC_000012.11:g.6761857A>G, NG_047151.1:g.15459T>C, NM_016162.4:c.468T>C, NM_016162.3:c.468T>C, NM_001127582.2:c.471T>C, NM_001127582.1:c.471T>C, NM_001127583.2:c.462T>C, NM_001127583.1:c.462T>C, NM_001127584.2:c.459T>C, NM_001127584.1:c.459T>C, NM_001127585.2:c.399T>C, NM_001127585.1:c.399T>C, NM_001127586.2:c.471T>C, NM_001127586.1:c.471T>C, XM_011520965.4:c.390T>C, XM_011520965.3:c.390T>C, XM_011520965.2:c.390T>C, XM_011520965.1:c.390T>C, XM_011520964.3:c.396T>C, XM_011520964.2:c.396T>C, XM_011520964.1:c.396T>C, NM_198287.1:c.*600T>C, XM_047428932.1:c.324T>C, XM_047428931.1:c.390T>C

Select item 144296704310.

rs1442967043 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 12:6651357 (GRCh38)
12:6760523 (GRCh37)
Canonical SPDI:: NC_000012.12:6651356:C:T
Gene:: ING4 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000012.12:g.6651357C>T, NC_000012.11:g.6760523C>T, NG_047151.1:g.16793G>A, NM_016162.4:c.674G>A, NM_016162.3:c.674G>A, NM_001127582.2:c.677G>A, NM_001127582.1:c.677G>A, NM_001127583.2:c.668G>A, NM_001127583.1:c.668G>A, NM_001127584.2:c.665G>A, NM_001127584.1:c.665G>A, NM_001127585.2:c.605G>A, NM_001127585.1:c.605G>A, NM_001127586.2:c.529G>A, NM_001127586.1:c.529G>A, XM_011520965.4:c.596G>A, XM_011520965.3:c.596G>A, XM_011520965.2:c.596G>A, XM_011520965.1:c.596G>A, XM_011520964.3:c.602G>A, XM_011520964.2:c.602G>A, XM_011520964.1:c.602G>A, NM_198287.1:c.*806G>A, XM_047428932.1:c.530G>A, XM_047428931.1:c.596G>A, NP_057246.2:p.Cys225Tyr, NP_001121054.1:p.Cys226Tyr, NP_001121055.1:p.Cys223Tyr, NP_001121056.1:p.Cys222Tyr, NP_001121057.1:p.Cys202Tyr, NP_001121058.1:p.Val177Met, XP_011519267.1:p.Cys199Tyr, XP_011519266.1:p.Cys201Tyr, XP_047284888.1:p.Cys177Tyr, XP_047284887.1:p.Cys199Tyr

Select item 144112865611.

rs1441128656 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 12:6652982 (GRCh38)
12:6762148 (GRCh37)
Canonical SPDI:: NC_000012.12:6652981:C:A
Gene:: ING4 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000012.12:g.6652982C>A, NC_000012.11:g.6762148C>A, NG_047151.1:g.15168G>T, NM_016162.4:c.345G>T, NM_016162.3:c.345G>T, NM_001127582.2:c.345G>T, NM_001127582.1:c.345G>T, NM_001127583.2:c.345G>T, NM_001127583.1:c.345G>T, NM_001127584.2:c.345G>T, NM_001127584.1:c.345G>T, NM_001127585.2:c.273G>T, NM_001127585.1:c.273G>T, NM_001127586.2:c.345G>T, NM_001127586.1:c.345G>T, XM_011520965.4:c.264G>T, XM_011520965.3:c.264G>T, XM_011520965.2:c.264G>T, XM_011520965.1:c.264G>T, XM_011520964.3:c.273G>T, XM_011520964.2:c.273G>T, XM_011520964.1:c.273G>T, NM_198287.1:c.*477G>T, XM_047428932.1:c.198G>T, XM_047428931.1:c.273G>T, NP_057246.2:p.Gln115His, NP_001121054.1:p.Gln115His, NP_001121055.1:p.Gln115His, NP_001121056.1:p.Gln115His, NP_001121057.1:p.Gln91His, NP_001121058.1:p.Gln115His, XP_011519267.1:p.Gln88His, XP_011519266.1:p.Gln91His, XP_047284888.1:p.Gln66His, XP_047284887.1:p.Gln91His

Select item 144056395212.

rs1440563952 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 12:6653290 (GRCh38)
12:6762456 (GRCh37)
Canonical SPDI:: NC_000012.12:6653289:A:G
Gene:: ING4 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000008/2 (TOPMED)
HGVS:: NC_000012.12:g.6653290A>G, NC_000012.11:g.6762456A>G, NG_047151.1:g.14860T>C, NM_016162.4:c.216T>C, NM_016162.3:c.216T>C, NM_001127582.2:c.216T>C, NM_001127582.1:c.216T>C, NM_001127583.2:c.216T>C, NM_001127583.1:c.216T>C, NM_001127584.2:c.216T>C, NM_001127584.1:c.216T>C, NM_001127585.2:c.144T>C, NM_001127585.1:c.144T>C, NM_001127586.2:c.216T>C, NM_001127586.1:c.216T>C, XM_011520965.4:c.135T>C, XM_011520965.3:c.135T>C, XM_011520965.2:c.135T>C, XM_011520965.1:c.135T>C, XM_011520964.3:c.144T>C, XM_011520964.2:c.144T>C, XM_011520964.1:c.144T>C, NM_198287.1:c.*348T>C, XM_047428932.1:c.69T>C, XM_047428931.1:c.144T>C

Select item 143581600713.

rs1435816007 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 12:6653349 (GRCh38)
12:6762515 (GRCh37)
Canonical SPDI:: NC_000012.12:6653348:C:A
Gene:: ING4 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: A=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000012.12:g.6653349C>A, NC_000012.11:g.6762515C>A, NG_047151.1:g.14801G>T, NM_016162.4:c.157G>T, NM_016162.3:c.157G>T, NM_001127582.2:c.157G>T, NM_001127582.1:c.157G>T, NM_001127583.2:c.157G>T, NM_001127583.1:c.157G>T, NM_001127584.2:c.157G>T, NM_001127584.1:c.157G>T, NM_001127585.2:c.85G>T, NM_001127585.1:c.85G>T, NM_001127586.2:c.157G>T, NM_001127586.1:c.157G>T, XM_011520965.4:c.76G>T, XM_011520965.3:c.76G>T, XM_011520965.2:c.76G>T, XM_011520965.1:c.76G>T, XM_011520964.3:c.85G>T, XM_011520964.2:c.85G>T, XM_011520964.1:c.85G>T, NM_198287.1:c.*289G>T, XM_047428932.1:c.10G>T, XM_047428931.1:c.85G>T, NP_057246.2:p.Ala53Ser, NP_001121054.1:p.Ala53Ser, NP_001121055.1:p.Ala53Ser, NP_001121056.1:p.Ala53Ser, NP_001121057.1:p.Ala29Ser, NP_001121058.1:p.Ala53Ser, XP_011519267.1:p.Ala26Ser, XP_011519266.1:p.Ala29Ser, XP_047284888.1:p.Ala4Ser, XP_047284887.1:p.Ala29Ser

Select item 143397526214.

rs1433975262 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 12:6663080 (GRCh38)
12:6772246 (GRCh37)
Canonical SPDI:: NC_000012.12:6663079:C:T
Gene:: ING4 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,5_prime_UTR_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0.0002/2 (ALFA)
HGVS:: NC_000012.12:g.6663080C>T, NC_000012.11:g.6772246C>T, NG_047151.1:g.5070G>A, NM_016162.4:c.22G>A, NM_016162.3:c.22G>A, NM_001127582.2:c.22G>A, NM_001127582.1:c.22G>A, NM_001127583.2:c.22G>A, NM_001127583.1:c.22G>A, NM_001127584.2:c.22G>A, NM_001127584.1:c.22G>A, NM_001127585.2:c.22G>A, NM_001127585.1:c.22G>A, NM_001127586.2:c.22G>A, NM_001127586.1:c.22G>A, XM_011520965.4:c.-77G>A, XM_011520965.1:c.-77G>A, XM_011520964.3:c.22G>A, XM_011520964.2:c.22G>A, XM_011520964.1:c.22G>A, NM_198287.1:c.22G>A, XM_047428931.1:c.22G>A, NP_057246.2:p.Glu8Lys, NP_001121054.1:p.Glu8Lys, NP_001121055.1:p.Glu8Lys, NP_001121056.1:p.Glu8Lys, NP_001121057.1:p.Glu8Lys, NP_001121058.1:p.Glu8Lys, XP_011519266.1:p.Glu8Lys, XP_047284887.1:p.Glu8Lys

Select item 141553967115.

rs1415539671 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 12:6653294 (GRCh38)
12:6762460 (GRCh37)
Canonical SPDI:: NC_000012.12:6653293:G:C
Gene:: ING4 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (GnomAD_exomes)
C=0.000007/1 (GnomAD)
C=0.000019/5 (TOPMED)
C=0.000354/6 (TOMMO)
C=0.000546/1 (Korea1K)
HGVS:: NC_000012.12:g.6653294G>C, NC_000012.11:g.6762460G>C, NG_047151.1:g.14856C>G, NM_016162.4:c.212C>G, NM_016162.3:c.212C>G, NM_001127582.2:c.212C>G, NM_001127582.1:c.212C>G, NM_001127583.2:c.212C>G, NM_001127583.1:c.212C>G, NM_001127584.2:c.212C>G, NM_001127584.1:c.212C>G, NM_001127585.2:c.140C>G, NM_001127585.1:c.140C>G, NM_001127586.2:c.212C>G, NM_001127586.1:c.212C>G, XM_011520965.4:c.131C>G, XM_011520965.3:c.131C>G, XM_011520965.2:c.131C>G, XM_011520965.1:c.131C>G, XM_011520964.3:c.140C>G, XM_011520964.2:c.140C>G, XM_011520964.1:c.140C>G, NM_198287.1:c.*344C>G, XM_047428932.1:c.65C>G, XM_047428931.1:c.140C>G, NP_057246.2:p.Ala71Gly, NP_001121054.1:p.Ala71Gly, NP_001121055.1:p.Ala71Gly, NP_001121056.1:p.Ala71Gly, NP_001121057.1:p.Ala47Gly, NP_001121058.1:p.Ala71Gly, XP_011519267.1:p.Ala44Gly, XP_011519266.1:p.Ala47Gly, XP_047284888.1:p.Ala22Gly, XP_047284887.1:p.Ala47Gly

Select item 140932824716.

rs1409328247 [Homo sapiens]

Variant type:: DELINS
Alleles:: G>- [Show Flanks]
Chromosome:: 12:6653248 (GRCh38)
12:6762414 (GRCh37)
Canonical SPDI:: NC_000012.12:6653247:GG:G
Gene:: ING4 (Varview)
Functional Consequence:: coding_sequence_variant,frameshift_variant
Validated:: by frequency
MAF:: -=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000012.12:g.6653249del, NC_000012.11:g.6762415del, NG_047151.1:g.14902del, NM_016162.4:c.258del, NM_016162.3:c.258del, NM_001127582.2:c.258del, NM_001127582.1:c.258del, NM_001127583.2:c.258del, NM_001127583.1:c.258del, NM_001127584.2:c.258del, NM_001127584.1:c.258del, NM_001127585.2:c.186del, NM_001127585.1:c.186del, NM_001127586.2:c.258del, NM_001127586.1:c.258del, XM_011520965.4:c.177del, XM_011520965.3:c.177del, XM_011520965.2:c.177del, XM_011520965.1:c.177del, XM_011520964.3:c.186del, XM_011520964.2:c.186del, XM_011520964.1:c.186del, NM_198287.1:c.*390del, XM_047428932.1:c.111del, XM_047428931.1:c.186del, NP_057246.2:p.Met87fs, NP_001121054.1:p.Met87fs, NP_001121055.1:p.Met87fs, NP_001121056.1:p.Met87fs, NP_001121057.1:p.Met63fs, NP_001121058.1:p.Met87fs, XP_011519267.1:p.Met60fs, XP_011519266.1:p.Met63fs, XP_047284888.1:p.Met38fs, XP_047284887.1:p.Met63fs

Select item 140550866217.

rs1405508662 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 12:6651208 (GRCh38)
12:6760374 (GRCh37)
Canonical SPDI:: NC_000012.12:6651207:C:T
Gene:: ING4 (Varview)
Functional Consequence:: 3_prime_UTR_variant,missense_variant,coding_sequence_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=0.000014/2 (GnomAD)
HGVS:: NC_000012.12:g.6651208C>T, NC_000012.11:g.6760374C>T, NG_047151.1:g.16942G>A, NM_016162.4:c.734G>A, NM_016162.3:c.734G>A, NM_001127582.2:c.737G>A, NM_001127582.1:c.737G>A, NM_001127583.2:c.728G>A, NM_001127583.1:c.728G>A, NM_001127584.2:c.725G>A, NM_001127584.1:c.725G>A, NM_001127585.2:c.665G>A, NM_001127585.1:c.665G>A, NM_001127586.2:c.*49G>A, NM_001127586.1:c.*49G>A, XM_011520965.4:c.656G>A, XM_011520965.3:c.656G>A, XM_011520965.2:c.656G>A, XM_011520965.1:c.656G>A, XM_011520964.3:c.662G>A, XM_011520964.2:c.662G>A, XM_011520964.1:c.662G>A, NM_198287.1:c.*866G>A, XM_047428932.1:c.590G>A, XM_047428931.1:c.656G>A, NP_057246.2:p.Arg245Gln, NP_001121054.1:p.Arg246Gln, NP_001121055.1:p.Arg243Gln, NP_001121056.1:p.Arg242Gln, NP_001121057.1:p.Arg222Gln, XP_011519267.1:p.Arg219Gln, XP_011519266.1:p.Arg221Gln, XP_047284888.1:p.Arg197Gln, XP_047284887.1:p.Arg219Gln

Select item 140209995718.

rs1402099957 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 12:6653302 (GRCh38)
12:6762468 (GRCh37)
Canonical SPDI:: NC_000012.12:6653301:G:A
Gene:: ING4 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_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_000012.12:g.6653302G>A, NC_000012.11:g.6762468G>A, NG_047151.1:g.14848C>T, NM_016162.4:c.204C>T, NM_016162.3:c.204C>T, NM_001127582.2:c.204C>T, NM_001127582.1:c.204C>T, NM_001127583.2:c.204C>T, NM_001127583.1:c.204C>T, NM_001127584.2:c.204C>T, NM_001127584.1:c.204C>T, NM_001127585.2:c.132C>T, NM_001127585.1:c.132C>T, NM_001127586.2:c.204C>T, NM_001127586.1:c.204C>T, XM_011520965.4:c.123C>T, XM_011520965.3:c.123C>T, XM_011520965.2:c.123C>T, XM_011520965.1:c.123C>T, XM_011520964.3:c.132C>T, XM_011520964.2:c.132C>T, XM_011520964.1:c.132C>T, NM_198287.1:c.*336C>T, XM_047428932.1:c.57C>T, XM_047428931.1:c.132C>T

Select item 138601375219.

rs1386013752 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 12:6651214 (GRCh38)
12:6760380 (GRCh37)
Canonical SPDI:: NC_000012.12:6651213:T:G
Gene:: ING4 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,3_prime_UTR_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000012.12:g.6651214T>G, NC_000012.11:g.6760380T>G, NG_047151.1:g.16936A>C, NM_016162.4:c.728A>C, NM_016162.3:c.728A>C, NM_001127582.2:c.731A>C, NM_001127582.1:c.731A>C, NM_001127583.2:c.722A>C, NM_001127583.1:c.722A>C, NM_001127584.2:c.719A>C, NM_001127584.1:c.719A>C, NM_001127585.2:c.659A>C, NM_001127585.1:c.659A>C, NM_001127586.2:c.*43A>C, NM_001127586.1:c.*43A>C, XM_011520965.4:c.650A>C, XM_011520965.3:c.650A>C, XM_011520965.2:c.650A>C, XM_011520965.1:c.650A>C, XM_011520964.3:c.656A>C, XM_011520964.2:c.656A>C, XM_011520964.1:c.656A>C, NM_198287.1:c.*860A>C, XM_047428932.1:c.584A>C, XM_047428931.1:c.650A>C, NP_057246.2:p.Gln243Pro, NP_001121054.1:p.Gln244Pro, NP_001121055.1:p.Gln241Pro, NP_001121056.1:p.Gln240Pro, NP_001121057.1:p.Gln220Pro, XP_011519267.1:p.Gln217Pro, XP_011519266.1:p.Gln219Pro, XP_047284888.1:p.Gln195Pro, XP_047284887.1:p.Gln217Pro

Select item 138267557720.

rs1382675577 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 12:6656728 (GRCh38)
12:6765894 (GRCh37)
Canonical SPDI:: NC_000012.12:6656727:C:T
Gene:: ING4 (Varview)
Functional Consequence:: 5_prime_UTR_variant,coding_sequence_variant,intron_variant,synonymous_variant
Validated:: by frequency
MAF:: T=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000012.12:g.6656728C>T, NC_000012.11:g.6765894C>T, NG_047151.1:g.11422G>A, NM_016162.4:c.108G>A, NM_016162.3:c.108G>A, NM_001127582.2:c.108G>A, NM_001127582.1:c.108G>A, NM_001127583.2:c.108G>A, NM_001127583.1:c.108G>A, NM_001127584.2:c.108G>A, NM_001127584.1:c.108G>A, NM_001127586.2:c.108G>A, NM_001127586.1:c.108G>A, XM_011520965.4:c.27G>A, XM_011520965.3:c.27G>A, XM_011520965.2:c.27G>A, XM_011520965.1:c.27G>A, NM_198287.1:c.108G>A, XM_047428932.1:c.-316G>A

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