SNP Links for Protein (Select 61658636) - SNP

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Links from Protein

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Select item 14900175761.

rs1490017576 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 16:3069044 (GRCh38)
16:3119045 (GRCh37)
Canonical SPDI:: NC_000016.10:3069043:A:G
Gene:: IL32 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000011/3 (TOPMED)
HGVS:: NC_000016.10:g.3069044A>G, NC_000016.9:g.3119045A>G, NG_029254.1:g.8733A>G, NM_004221.7:c.256A>G, NM_004221.6:c.256A>G, NM_004221.5:c.256A>G, NM_004221.4:c.256A>G, NM_001308078.4:c.394A>G, NM_001308078.3:c.394A>G, NM_001308078.2:c.394A>G, NM_001308078.1:c.394A>G, NM_001012631.4:c.256A>G, NM_001012631.3:c.256A>G, NM_001012631.2:c.256A>G, NM_001012631.1:c.256A>G, NM_001012718.4:c.256A>G, NM_001012718.3:c.256A>G, NM_001012718.2:c.256A>G, NM_001012718.1:c.256A>G, NM_001012634.4:c.196A>G, NM_001012634.3:c.196A>G, NM_001012634.2:c.196A>G, NM_001012634.1:c.196A>G, NM_001012635.4:c.196A>G, NM_001012635.3:c.196A>G, NM_001012635.2:c.196A>G, NM_001012635.1:c.196A>G, NM_001012633.4:c.256A>G, NM_001012633.3:c.256A>G, NM_001012633.2:c.256A>G, NM_001012633.1:c.256A>G, NM_001369596.3:c.256A>G, NM_001369596.2:c.256A>G, NM_001369596.1:c.256A>G, NM_001369587.3:c.394A>G, NM_001369587.2:c.394A>G, NM_001369587.1:c.394A>G, NM_001369588.3:c.394A>G, NM_001369588.2:c.394A>G, NM_001369588.1:c.394A>G, NM_001369589.3:c.256A>G, NM_001369589.2:c.256A>G, NM_001369589.1:c.256A>G, NM_001012632.3:c.256A>G, NM_001012632.2:c.256A>G, NM_001012632.1:c.256A>G, NM_001369593.3:c.226A>G, NM_001369593.2:c.226A>G, NM_001369593.1:c.226A>G, NM_001369591.3:c.196A>G, NM_001369591.2:c.196A>G, NM_001369591.1:c.196A>G, NM_001369592.3:c.196A>G, NM_001369592.2:c.196A>G, NM_001369592.1:c.196A>G, NM_001369590.3:c.196A>G, NM_001369590.2:c.196A>G, NM_001369590.1:c.196A>G, NM_001369595.3:c.196A>G, NM_001369595.2:c.196A>G, NM_001369595.1:c.196A>G, NM_001012636.2:c.229A>G, NM_001012636.1:c.229A>G, NM_001376923.1:c.256A>G, NP_004212.4:p.Arg86Gly, NP_001295007.1:p.Arg132Gly, NP_001012649.1:p.Arg86Gly, NP_001012736.1:p.Arg86Gly, NP_001012652.1:p.Arg66Gly, NP_001012653.1:p.Arg66Gly, NP_001012651.1:p.Arg86Gly, NP_001356525.1:p.Arg86Gly, NP_001356516.1:p.Arg132Gly, NP_001356517.1:p.Arg132Gly, NP_001356518.1:p.Arg86Gly, NP_001012650.1:p.Arg86Gly, NP_001356522.1:p.Arg76Gly, NP_001356520.1:p.Arg66Gly, NP_001356521.1:p.Arg66Gly, NP_001356519.1:p.Arg66Gly, NP_001356524.1:p.Arg66Gly, NP_001012654.1:p.Arg77Gly, NP_001363852.1:p.Arg86Gly

Select item 14781468282.

rs1478146828 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,G,T [Show Flanks]
Chromosome:: 16:3069051 (GRCh38)
16:3119052 (GRCh37)
Canonical SPDI:: NC_000016.10:3069050:C:A,NC_000016.10:3069050:C:G,NC_000016.10:3069050:C:T
Gene:: IL32 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
A=0.000004/1 (TOPMED)
C=0.5/1 (SGDP_PRJ)
HGVS:: NC_000016.10:g.3069051C>A, NC_000016.10:g.3069051C>G, NC_000016.10:g.3069051C>T, NC_000016.9:g.3119052C>A, NC_000016.9:g.3119052C>G, NC_000016.9:g.3119052C>T, NG_029254.1:g.8740C>A, NG_029254.1:g.8740C>G, NG_029254.1:g.8740C>T, NM_004221.7:c.263C>A, NM_004221.7:c.263C>G, NM_004221.7:c.263C>T, NM_004221.6:c.263C>A, NM_004221.6:c.263C>G, NM_004221.6:c.263C>T, NM_004221.5:c.263C>A, NM_004221.5:c.263C>G, NM_004221.5:c.263C>T, NM_004221.4:c.263C>A, NM_004221.4:c.263C>G, NM_004221.4:c.263C>T, NM_001308078.4:c.401C>A, NM_001308078.4:c.401C>G, NM_001308078.4:c.401C>T, NM_001308078.3:c.401C>A, NM_001308078.3:c.401C>G, NM_001308078.3:c.401C>T, NM_001308078.2:c.401C>A, NM_001308078.2:c.401C>G, NM_001308078.2:c.401C>T, NM_001308078.1:c.401C>A, NM_001308078.1:c.401C>G, NM_001308078.1:c.401C>T, NM_001012631.4:c.263C>A, NM_001012631.4:c.263C>G, NM_001012631.4:c.263C>T, NM_001012631.3:c.263C>A, NM_001012631.3:c.263C>G, NM_001012631.3:c.263C>T, NM_001012631.2:c.263C>A, NM_001012631.2:c.263C>G, NM_001012631.2:c.263C>T, NM_001012631.1:c.263C>A, NM_001012631.1:c.263C>G, NM_001012631.1:c.263C>T, NM_001012718.4:c.263C>A, NM_001012718.4:c.263C>G, NM_001012718.4:c.263C>T, NM_001012718.3:c.263C>A, NM_001012718.3:c.263C>G, NM_001012718.3:c.263C>T, NM_001012718.2:c.263C>A, NM_001012718.2:c.263C>G, NM_001012718.2:c.263C>T, NM_001012718.1:c.263C>A, NM_001012718.1:c.263C>G, NM_001012718.1:c.263C>T, NM_001012634.4:c.203C>A, NM_001012634.4:c.203C>G, NM_001012634.4:c.203C>T, NM_001012634.3:c.203C>A, NM_001012634.3:c.203C>G, NM_001012634.3:c.203C>T, NM_001012634.2:c.203C>A, NM_001012634.2:c.203C>G, NM_001012634.2:c.203C>T, NM_001012634.1:c.203C>A, NM_001012634.1:c.203C>G, NM_001012634.1:c.203C>T, NM_001012635.4:c.203C>A, NM_001012635.4:c.203C>G, NM_001012635.4:c.203C>T, NM_001012635.3:c.203C>A, NM_001012635.3:c.203C>G, NM_001012635.3:c.203C>T, NM_001012635.2:c.203C>A, NM_001012635.2:c.203C>G, NM_001012635.2:c.203C>T, NM_001012635.1:c.203C>A, NM_001012635.1:c.203C>G, NM_001012635.1:c.203C>T, NM_001012633.4:c.263C>A, NM_001012633.4:c.263C>G, NM_001012633.4:c.263C>T, NM_001012633.3:c.263C>A, NM_001012633.3:c.263C>G, NM_001012633.3:c.263C>T, NM_001012633.2:c.263C>A, NM_001012633.2:c.263C>G, NM_001012633.2:c.263C>T, NM_001012633.1:c.263C>A, NM_001012633.1:c.263C>G, NM_001012633.1:c.263C>T, NM_001369596.3:c.263C>A, NM_001369596.3:c.263C>G, NM_001369596.3:c.263C>T, NM_001369596.2:c.263C>A, NM_001369596.2:c.263C>G, NM_001369596.2:c.263C>T, NM_001369596.1:c.263C>A, NM_001369596.1:c.263C>G, NM_001369596.1:c.263C>T, NM_001369587.3:c.401C>A, NM_001369587.3:c.401C>G, NM_001369587.3:c.401C>T, NM_001369587.2:c.401C>A, NM_001369587.2:c.401C>G, NM_001369587.2:c.401C>T, NM_001369587.1:c.401C>A, NM_001369587.1:c.401C>G, NM_001369587.1:c.401C>T, NM_001369588.3:c.401C>A, NM_001369588.3:c.401C>G, NM_001369588.3:c.401C>T, NM_001369588.2:c.401C>A, NM_001369588.2:c.401C>G, NM_001369588.2:c.401C>T, NM_001369588.1:c.401C>A, NM_001369588.1:c.401C>G, NM_001369588.1:c.401C>T, NM_001369589.3:c.263C>A, NM_001369589.3:c.263C>G, NM_001369589.3:c.263C>T, NM_001369589.2:c.263C>A, NM_001369589.2:c.263C>G, NM_001369589.2:c.263C>T, NM_001369589.1:c.263C>A, NM_001369589.1:c.263C>G, NM_001369589.1:c.263C>T, NM_001012632.3:c.263C>A, NM_001012632.3:c.263C>G, NM_001012632.3:c.263C>T, NM_001012632.2:c.263C>A, NM_001012632.2:c.263C>G, NM_001012632.2:c.263C>T, NM_001012632.1:c.263C>A, NM_001012632.1:c.263C>G, NM_001012632.1:c.263C>T, NM_001369593.3:c.233C>A, NM_001369593.3:c.233C>G, NM_001369593.3:c.233C>T, NM_001369593.2:c.233C>A, NM_001369593.2:c.233C>G, NM_001369593.2:c.233C>T, NM_001369593.1:c.233C>A, NM_001369593.1:c.233C>G, NM_001369593.1:c.233C>T, NM_001369591.3:c.203C>A, NM_001369591.3:c.203C>G, NM_001369591.3:c.203C>T, NM_001369591.2:c.203C>A, NM_001369591.2:c.203C>G, NM_001369591.2:c.203C>T, NM_001369591.1:c.203C>A, NM_001369591.1:c.203C>G, NM_001369591.1:c.203C>T, NM_001369592.3:c.203C>A, NM_001369592.3:c.203C>G, NM_001369592.3:c.203C>T, NM_001369592.2:c.203C>A, NM_001369592.2:c.203C>G, NM_001369592.2:c.203C>T, NM_001369592.1:c.203C>A, NM_001369592.1:c.203C>G, NM_001369592.1:c.203C>T, NM_001369590.3:c.203C>A, NM_001369590.3:c.203C>G, NM_001369590.3:c.203C>T, NM_001369590.2:c.203C>A, NM_001369590.2:c.203C>G, NM_001369590.2:c.203C>T, NM_001369590.1:c.203C>A, NM_001369590.1:c.203C>G, NM_001369590.1:c.203C>T, NM_001369595.3:c.203C>A, NM_001369595.3:c.203C>G, NM_001369595.3:c.203C>T, NM_001369595.2:c.203C>A, NM_001369595.2:c.203C>G, NM_001369595.2:c.203C>T, NM_001369595.1:c.203C>A, NM_001369595.1:c.203C>G, NM_001369595.1:c.203C>T, NM_001012636.2:c.236C>A, NM_001012636.2:c.236C>G, NM_001012636.2:c.236C>T, NM_001012636.1:c.236C>A, NM_001012636.1:c.236C>G, NM_001012636.1:c.236C>T, NM_001376923.1:c.263C>A, NM_001376923.1:c.263C>G, NM_001376923.1:c.263C>T, NP_004212.4:p.Pro88His, NP_004212.4:p.Pro88Arg, NP_004212.4:p.Pro88Leu, NP_001295007.1:p.Pro134His, NP_001295007.1:p.Pro134Arg, NP_001295007.1:p.Pro134Leu, NP_001012649.1:p.Pro88His, NP_001012649.1:p.Pro88Arg, NP_001012649.1:p.Pro88Leu, NP_001012736.1:p.Pro88His, NP_001012736.1:p.Pro88Arg, NP_001012736.1:p.Pro88Leu, NP_001012652.1:p.Pro68His, NP_001012652.1:p.Pro68Arg, NP_001012652.1:p.Pro68Leu, NP_001012653.1:p.Pro68His, NP_001012653.1:p.Pro68Arg, NP_001012653.1:p.Pro68Leu, NP_001012651.1:p.Pro88His, NP_001012651.1:p.Pro88Arg, NP_001012651.1:p.Pro88Leu, NP_001356525.1:p.Pro88His, NP_001356525.1:p.Pro88Arg, NP_001356525.1:p.Pro88Leu, NP_001356516.1:p.Pro134His, NP_001356516.1:p.Pro134Arg, NP_001356516.1:p.Pro134Leu, NP_001356517.1:p.Pro134His, NP_001356517.1:p.Pro134Arg, NP_001356517.1:p.Pro134Leu, NP_001356518.1:p.Pro88His, NP_001356518.1:p.Pro88Arg, NP_001356518.1:p.Pro88Leu, NP_001012650.1:p.Pro88His, NP_001012650.1:p.Pro88Arg, NP_001012650.1:p.Pro88Leu, NP_001356522.1:p.Pro78His, NP_001356522.1:p.Pro78Arg, NP_001356522.1:p.Pro78Leu, NP_001356520.1:p.Pro68His, NP_001356520.1:p.Pro68Arg, NP_001356520.1:p.Pro68Leu, NP_001356521.1:p.Pro68His, NP_001356521.1:p.Pro68Arg, NP_001356521.1:p.Pro68Leu, NP_001356519.1:p.Pro68His, NP_001356519.1:p.Pro68Arg, NP_001356519.1:p.Pro68Leu, NP_001356524.1:p.Pro68His, NP_001356524.1:p.Pro68Arg, NP_001356524.1:p.Pro68Leu, NP_001012654.1:p.Pro79His, NP_001012654.1:p.Pro79Arg, NP_001012654.1:p.Pro79Leu, NP_001363852.1:p.Pro88His, NP_001363852.1:p.Pro88Arg, NP_001363852.1:p.Pro88Leu

Select item 14778211933.

rs1477821193 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 16:3069271 (GRCh38)
16:3119272 (GRCh37)
Canonical SPDI:: NC_000016.10:3069270:C:A,NC_000016.10:3069270:C:T
Gene:: IL32 (Varview)
Functional Consequence:: coding_sequence_variant,intron_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (GnomAD_exomes)
T=0.000011/3 (TOPMED)
HGVS:: NC_000016.10:g.3069271C>A, NC_000016.10:g.3069271C>T, NC_000016.9:g.3119272C>A, NC_000016.9:g.3119272C>T, NG_029254.1:g.8960C>A, NG_029254.1:g.8960C>T, NM_004221.7:c.483C>A, NM_004221.7:c.483C>T, NM_004221.6:c.483C>A, NM_004221.6:c.483C>T, NM_004221.5:c.483C>A, NM_004221.5:c.483C>T, NM_004221.4:c.483C>A, NM_004221.4:c.483C>T, NM_001308078.4:c.621C>A, NM_001308078.4:c.621C>T, NM_001308078.3:c.621C>A, NM_001308078.3:c.621C>T, NM_001308078.2:c.621C>A, NM_001308078.2:c.621C>T, NM_001308078.1:c.621C>A, NM_001308078.1:c.621C>T, NM_001012631.4:c.483C>A, NM_001012631.4:c.483C>T, NM_001012631.3:c.483C>A, NM_001012631.3:c.483C>T, NM_001012631.2:c.483C>A, NM_001012631.2:c.483C>T, NM_001012631.1:c.483C>A, NM_001012631.1:c.483C>T, NM_001012718.4:c.483C>A, NM_001012718.4:c.483C>T, NM_001012718.3:c.483C>A, NM_001012718.3:c.483C>T, NM_001012718.2:c.483C>A, NM_001012718.2:c.483C>T, NM_001012718.1:c.483C>A, NM_001012718.1:c.483C>T, NM_001012634.4:c.423C>A, NM_001012634.4:c.423C>T, NM_001012634.3:c.423C>A, NM_001012634.3:c.423C>T, NM_001012634.2:c.423C>A, NM_001012634.2:c.423C>T, NM_001012634.1:c.423C>A, NM_001012634.1:c.423C>T, NM_001012635.4:c.423C>A, NM_001012635.4:c.423C>T, NM_001012635.3:c.423C>A, NM_001012635.3:c.423C>T, NM_001012635.2:c.423C>A, NM_001012635.2:c.423C>T, NM_001012635.1:c.423C>A, NM_001012635.1:c.423C>T, NM_001369596.3:c.483C>A, NM_001369596.3:c.483C>T, NM_001369596.2:c.483C>A, NM_001369596.2:c.483C>T, NM_001369596.1:c.483C>A, NM_001369596.1:c.483C>T, NM_001369587.3:c.621C>A, NM_001369587.3:c.621C>T, NM_001369587.2:c.621C>A, NM_001369587.2:c.621C>T, NM_001369587.1:c.621C>A, NM_001369587.1:c.621C>T, NM_001369588.3:c.621C>A, NM_001369588.3:c.621C>T, NM_001369588.2:c.621C>A, NM_001369588.2:c.621C>T, NM_001369588.1:c.621C>A, NM_001369588.1:c.621C>T, NM_001369589.3:c.483C>A, NM_001369589.3:c.483C>T, NM_001369589.2:c.483C>A, NM_001369589.2:c.483C>T, NM_001369589.1:c.483C>A, NM_001369589.1:c.483C>T, NM_001012632.3:c.483C>A, NM_001012632.3:c.483C>T, NM_001012632.2:c.483C>A, NM_001012632.2:c.483C>T, NM_001012632.1:c.483C>A, NM_001012632.1:c.483C>T, NM_001369593.3:c.453C>A, NM_001369593.3:c.453C>T, NM_001369593.2:c.453C>A, NM_001369593.2:c.453C>T, NM_001369593.1:c.453C>A, NM_001369593.1:c.453C>T, NM_001369591.3:c.423C>A, NM_001369591.3:c.423C>T, NM_001369591.2:c.423C>A, NM_001369591.2:c.423C>T, NM_001369591.1:c.423C>A, NM_001369591.1:c.423C>T, NM_001369592.3:c.423C>A, NM_001369592.3:c.423C>T, NM_001369592.2:c.423C>A, NM_001369592.2:c.423C>T, NM_001369592.1:c.423C>A, NM_001369592.1:c.423C>T, NM_001369590.3:c.423C>A, NM_001369590.3:c.423C>T, NM_001369590.2:c.423C>A, NM_001369590.2:c.423C>T, NM_001369590.1:c.423C>A, NM_001369590.1:c.423C>T, NM_001012636.2:c.456C>A, NM_001012636.2:c.456C>T, NM_001012636.1:c.456C>A, NM_001012636.1:c.456C>T, NM_001376923.1:c.483C>A, NM_001376923.1:c.483C>T

Select item 14661555794.

rs1466155579 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 16:3069015 (GRCh38)
16:3119016 (GRCh37)
Canonical SPDI:: NC_000016.10:3069014:A:G
Gene:: IL32 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000005/1 (GnomAD_exomes)
G=0.000008/2 (TOPMED)
HGVS:: NC_000016.10:g.3069015A>G, NC_000016.9:g.3119016A>G, NG_029254.1:g.8704A>G, NM_004221.7:c.227A>G, NM_004221.6:c.227A>G, NM_004221.5:c.227A>G, NM_004221.4:c.227A>G, NM_001308078.4:c.365A>G, NM_001308078.3:c.365A>G, NM_001308078.2:c.365A>G, NM_001308078.1:c.365A>G, NM_001012631.4:c.227A>G, NM_001012631.3:c.227A>G, NM_001012631.2:c.227A>G, NM_001012631.1:c.227A>G, NM_001012718.4:c.227A>G, NM_001012718.3:c.227A>G, NM_001012718.2:c.227A>G, NM_001012718.1:c.227A>G, NM_001012634.4:c.167A>G, NM_001012634.3:c.167A>G, NM_001012634.2:c.167A>G, NM_001012634.1:c.167A>G, NM_001012635.4:c.167A>G, NM_001012635.3:c.167A>G, NM_001012635.2:c.167A>G, NM_001012635.1:c.167A>G, NM_001012633.4:c.227A>G, NM_001012633.3:c.227A>G, NM_001012633.2:c.227A>G, NM_001012633.1:c.227A>G, NM_001369596.3:c.227A>G, NM_001369596.2:c.227A>G, NM_001369596.1:c.227A>G, NM_001369587.3:c.365A>G, NM_001369587.2:c.365A>G, NM_001369587.1:c.365A>G, NM_001369588.3:c.365A>G, NM_001369588.2:c.365A>G, NM_001369588.1:c.365A>G, NM_001369589.3:c.227A>G, NM_001369589.2:c.227A>G, NM_001369589.1:c.227A>G, NM_001012632.3:c.227A>G, NM_001012632.2:c.227A>G, NM_001012632.1:c.227A>G, NM_001369593.3:c.197A>G, NM_001369593.2:c.197A>G, NM_001369593.1:c.197A>G, NM_001369591.3:c.167A>G, NM_001369591.2:c.167A>G, NM_001369591.1:c.167A>G, NM_001369592.3:c.167A>G, NM_001369592.2:c.167A>G, NM_001369592.1:c.167A>G, NM_001369590.3:c.167A>G, NM_001369590.2:c.167A>G, NM_001369590.1:c.167A>G, NM_001369595.3:c.167A>G, NM_001369595.2:c.167A>G, NM_001369595.1:c.167A>G, NM_001012636.2:c.200A>G, NM_001012636.1:c.200A>G, NM_001376923.1:c.227A>G, NP_004212.4:p.Glu76Gly, NP_001295007.1:p.Glu122Gly, NP_001012649.1:p.Glu76Gly, NP_001012736.1:p.Glu76Gly, NP_001012652.1:p.Glu56Gly, NP_001012653.1:p.Glu56Gly, NP_001012651.1:p.Glu76Gly, NP_001356525.1:p.Glu76Gly, NP_001356516.1:p.Glu122Gly, NP_001356517.1:p.Glu122Gly, NP_001356518.1:p.Glu76Gly, NP_001012650.1:p.Glu76Gly, NP_001356522.1:p.Glu66Gly, NP_001356520.1:p.Glu56Gly, NP_001356521.1:p.Glu56Gly, NP_001356519.1:p.Glu56Gly, NP_001356524.1:p.Glu56Gly, NP_001012654.1:p.Glu67Gly, NP_001363852.1:p.Glu76Gly

Select item 14631947155.

rs1463194715 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 16:3069162 (GRCh38)
16:3119163 (GRCh37)
Canonical SPDI:: NC_000016.10:3069161:G:A
Gene:: IL32 (Varview)
Functional Consequence:: intron_variant,missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000016.10:g.3069162G>A, NC_000016.9:g.3119163G>A, NG_029254.1:g.8851G>A, NM_004221.7:c.374G>A, NM_004221.6:c.374G>A, NM_004221.5:c.374G>A, NM_004221.4:c.374G>A, NM_001308078.4:c.512G>A, NM_001308078.3:c.512G>A, NM_001308078.2:c.512G>A, NM_001308078.1:c.512G>A, NM_001012631.4:c.374G>A, NM_001012631.3:c.374G>A, NM_001012631.2:c.374G>A, NM_001012631.1:c.374G>A, NM_001012718.4:c.374G>A, NM_001012718.3:c.374G>A, NM_001012718.2:c.374G>A, NM_001012718.1:c.374G>A, NM_001012634.4:c.314G>A, NM_001012634.3:c.314G>A, NM_001012634.2:c.314G>A, NM_001012634.1:c.314G>A, NM_001012635.4:c.314G>A, NM_001012635.3:c.314G>A, NM_001012635.2:c.314G>A, NM_001012635.1:c.314G>A, NM_001369596.3:c.374G>A, NM_001369596.2:c.374G>A, NM_001369596.1:c.374G>A, NM_001369587.3:c.512G>A, NM_001369587.2:c.512G>A, NM_001369587.1:c.512G>A, NM_001369588.3:c.512G>A, NM_001369588.2:c.512G>A, NM_001369588.1:c.512G>A, NM_001369589.3:c.374G>A, NM_001369589.2:c.374G>A, NM_001369589.1:c.374G>A, NM_001012632.3:c.374G>A, NM_001012632.2:c.374G>A, NM_001012632.1:c.374G>A, NM_001369593.3:c.344G>A, NM_001369593.2:c.344G>A, NM_001369593.1:c.344G>A, NM_001369591.3:c.314G>A, NM_001369591.2:c.314G>A, NM_001369591.1:c.314G>A, NM_001369592.3:c.314G>A, NM_001369592.2:c.314G>A, NM_001369592.1:c.314G>A, NM_001369590.3:c.314G>A, NM_001369590.2:c.314G>A, NM_001369590.1:c.314G>A, NM_001012636.2:c.347G>A, NM_001012636.1:c.347G>A, NM_001376923.1:c.374G>A, NP_004212.4:p.Gly125Glu, NP_001295007.1:p.Gly171Glu, NP_001012649.1:p.Gly125Glu, NP_001012736.1:p.Gly125Glu, NP_001012652.1:p.Gly105Glu, NP_001012653.1:p.Gly105Glu, NP_001356525.1:p.Gly125Glu, NP_001356516.1:p.Gly171Glu, NP_001356517.1:p.Gly171Glu, NP_001356518.1:p.Gly125Glu, NP_001012650.1:p.Gly125Glu, NP_001356522.1:p.Gly115Glu, NP_001356520.1:p.Gly105Glu, NP_001356521.1:p.Gly105Glu, NP_001356519.1:p.Gly105Glu, NP_001012654.1:p.Gly116Glu, NP_001363852.1:p.Gly125Glu

Select item 14589186246.

rs1458918624 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 16:3069168 (GRCh38)
16:3119169 (GRCh37)
Canonical SPDI:: NC_000016.10:3069167:T:C
Gene:: IL32 (Varview)
Functional Consequence:: intron_variant,missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.00005/7 (GnomAD)
HGVS:: NC_000016.10:g.3069168T>C, NC_000016.9:g.3119169T>C, NG_029254.1:g.8857T>C, NM_004221.7:c.380T>C, NM_004221.6:c.380T>C, NM_004221.5:c.380T>C, NM_004221.4:c.380T>C, NM_001308078.4:c.518T>C, NM_001308078.3:c.518T>C, NM_001308078.2:c.518T>C, NM_001308078.1:c.518T>C, NM_001012631.4:c.380T>C, NM_001012631.3:c.380T>C, NM_001012631.2:c.380T>C, NM_001012631.1:c.380T>C, NM_001012718.4:c.380T>C, NM_001012718.3:c.380T>C, NM_001012718.2:c.380T>C, NM_001012718.1:c.380T>C, NM_001012634.4:c.320T>C, NM_001012634.3:c.320T>C, NM_001012634.2:c.320T>C, NM_001012634.1:c.320T>C, NM_001012635.4:c.320T>C, NM_001012635.3:c.320T>C, NM_001012635.2:c.320T>C, NM_001012635.1:c.320T>C, NM_001369596.3:c.380T>C, NM_001369596.2:c.380T>C, NM_001369596.1:c.380T>C, NM_001369587.3:c.518T>C, NM_001369587.2:c.518T>C, NM_001369587.1:c.518T>C, NM_001369588.3:c.518T>C, NM_001369588.2:c.518T>C, NM_001369588.1:c.518T>C, NM_001369589.3:c.380T>C, NM_001369589.2:c.380T>C, NM_001369589.1:c.380T>C, NM_001012632.3:c.380T>C, NM_001012632.2:c.380T>C, NM_001012632.1:c.380T>C, NM_001369593.3:c.350T>C, NM_001369593.2:c.350T>C, NM_001369593.1:c.350T>C, NM_001369591.3:c.320T>C, NM_001369591.2:c.320T>C, NM_001369591.1:c.320T>C, NM_001369592.3:c.320T>C, NM_001369592.2:c.320T>C, NM_001369592.1:c.320T>C, NM_001369590.3:c.320T>C, NM_001369590.2:c.320T>C, NM_001369590.1:c.320T>C, NM_001012636.2:c.353T>C, NM_001012636.1:c.353T>C, NM_001376923.1:c.380T>C, NP_004212.4:p.Leu127Pro, NP_001295007.1:p.Leu173Pro, NP_001012649.1:p.Leu127Pro, NP_001012736.1:p.Leu127Pro, NP_001012652.1:p.Leu107Pro, NP_001012653.1:p.Leu107Pro, NP_001356525.1:p.Leu127Pro, NP_001356516.1:p.Leu173Pro, NP_001356517.1:p.Leu173Pro, NP_001356518.1:p.Leu127Pro, NP_001012650.1:p.Leu127Pro, NP_001356522.1:p.Leu117Pro, NP_001356520.1:p.Leu107Pro, NP_001356521.1:p.Leu107Pro, NP_001356519.1:p.Leu107Pro, NP_001012654.1:p.Leu118Pro, NP_001363852.1:p.Leu127Pro

Select item 14522653647.

rs1452265364 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 16:3069022 (GRCh38)
16:3119023 (GRCh37)
Canonical SPDI:: NC_000016.10:3069021:T:C,NC_000016.10:3069021:T:G
Gene:: IL32 (Varview)
Functional Consequence:: synonymous_variant,missense_variant,coding_sequence_variant
Validated:: by frequency,by cluster
MAF:: C=0.00004/1 (TOMMO)
HGVS:: NC_000016.10:g.3069022T>C, NC_000016.10:g.3069022T>G, NC_000016.9:g.3119023T>C, NC_000016.9:g.3119023T>G, NG_029254.1:g.8711T>C, NG_029254.1:g.8711T>G, NM_004221.7:c.234T>C, NM_004221.7:c.234T>G, NM_004221.6:c.234T>C, NM_004221.6:c.234T>G, NM_004221.5:c.234T>C, NM_004221.5:c.234T>G, NM_004221.4:c.234T>C, NM_004221.4:c.234T>G, NM_001308078.4:c.372T>C, NM_001308078.4:c.372T>G, NM_001308078.3:c.372T>C, NM_001308078.3:c.372T>G, NM_001308078.2:c.372T>C, NM_001308078.2:c.372T>G, NM_001308078.1:c.372T>C, NM_001308078.1:c.372T>G, NM_001012631.4:c.234T>C, NM_001012631.4:c.234T>G, NM_001012631.3:c.234T>C, NM_001012631.3:c.234T>G, NM_001012631.2:c.234T>C, NM_001012631.2:c.234T>G, NM_001012631.1:c.234T>C, NM_001012631.1:c.234T>G, NM_001012718.4:c.234T>C, NM_001012718.4:c.234T>G, NM_001012718.3:c.234T>C, NM_001012718.3:c.234T>G, NM_001012718.2:c.234T>C, NM_001012718.2:c.234T>G, NM_001012718.1:c.234T>C, NM_001012718.1:c.234T>G, NM_001012634.4:c.174T>C, NM_001012634.4:c.174T>G, NM_001012634.3:c.174T>C, NM_001012634.3:c.174T>G, NM_001012634.2:c.174T>C, NM_001012634.2:c.174T>G, NM_001012634.1:c.174T>C, NM_001012634.1:c.174T>G, NM_001012635.4:c.174T>C, NM_001012635.4:c.174T>G, NM_001012635.3:c.174T>C, NM_001012635.3:c.174T>G, NM_001012635.2:c.174T>C, NM_001012635.2:c.174T>G, NM_001012635.1:c.174T>C, NM_001012635.1:c.174T>G, NM_001012633.4:c.234T>C, NM_001012633.4:c.234T>G, NM_001012633.3:c.234T>C, NM_001012633.3:c.234T>G, NM_001012633.2:c.234T>C, NM_001012633.2:c.234T>G, NM_001012633.1:c.234T>C, NM_001012633.1:c.234T>G, NM_001369596.3:c.234T>C, NM_001369596.3:c.234T>G, NM_001369596.2:c.234T>C, NM_001369596.2:c.234T>G, NM_001369596.1:c.234T>C, NM_001369596.1:c.234T>G, NM_001369587.3:c.372T>C, NM_001369587.3:c.372T>G, NM_001369587.2:c.372T>C, NM_001369587.2:c.372T>G, NM_001369587.1:c.372T>C, NM_001369587.1:c.372T>G, NM_001369588.3:c.372T>C, NM_001369588.3:c.372T>G, NM_001369588.2:c.372T>C, NM_001369588.2:c.372T>G, NM_001369588.1:c.372T>C, NM_001369588.1:c.372T>G, NM_001369589.3:c.234T>C, NM_001369589.3:c.234T>G, NM_001369589.2:c.234T>C, NM_001369589.2:c.234T>G, NM_001369589.1:c.234T>C, NM_001369589.1:c.234T>G, NM_001012632.3:c.234T>C, NM_001012632.3:c.234T>G, NM_001012632.2:c.234T>C, NM_001012632.2:c.234T>G, NM_001012632.1:c.234T>C, NM_001012632.1:c.234T>G, NM_001369593.3:c.204T>C, NM_001369593.3:c.204T>G, NM_001369593.2:c.204T>C, NM_001369593.2:c.204T>G, NM_001369593.1:c.204T>C, NM_001369593.1:c.204T>G, NM_001369591.3:c.174T>C, NM_001369591.3:c.174T>G, NM_001369591.2:c.174T>C, NM_001369591.2:c.174T>G, NM_001369591.1:c.174T>C, NM_001369591.1:c.174T>G, NM_001369592.3:c.174T>C, NM_001369592.3:c.174T>G, NM_001369592.2:c.174T>C, NM_001369592.2:c.174T>G, NM_001369592.1:c.174T>C, NM_001369592.1:c.174T>G, NM_001369590.3:c.174T>C, NM_001369590.3:c.174T>G, NM_001369590.2:c.174T>C, NM_001369590.2:c.174T>G, NM_001369590.1:c.174T>C, NM_001369590.1:c.174T>G, NM_001369595.3:c.174T>C, NM_001369595.3:c.174T>G, NM_001369595.2:c.174T>C, NM_001369595.2:c.174T>G, NM_001369595.1:c.174T>C, NM_001369595.1:c.174T>G, NM_001012636.2:c.207T>C, NM_001012636.2:c.207T>G, NM_001012636.1:c.207T>C, NM_001012636.1:c.207T>G, NM_001376923.1:c.234T>C, NM_001376923.1:c.234T>G, NP_004212.4:p.Asp78Glu, NP_001295007.1:p.Asp124Glu, NP_001012649.1:p.Asp78Glu, NP_001012736.1:p.Asp78Glu, NP_001012652.1:p.Asp58Glu, NP_001012653.1:p.Asp58Glu, NP_001012651.1:p.Asp78Glu, NP_001356525.1:p.Asp78Glu, NP_001356516.1:p.Asp124Glu, NP_001356517.1:p.Asp124Glu, NP_001356518.1:p.Asp78Glu, NP_001012650.1:p.Asp78Glu, NP_001356522.1:p.Asp68Glu, NP_001356520.1:p.Asp58Glu, NP_001356521.1:p.Asp58Glu, NP_001356519.1:p.Asp58Glu, NP_001356524.1:p.Asp58Glu, NP_001012654.1:p.Asp69Glu, NP_001363852.1:p.Asp78Glu

Select item 14331414268.

rs1433141426 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 16:3067391 (GRCh38)
16:3117392 (GRCh37)
Canonical SPDI:: NC_000016.10:3067390:C:T
Gene:: IL32 (Varview)
Functional Consequence:: 5_prime_UTR_variant,synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000016.10:g.3067391C>T, NC_000016.9:g.3117392C>T, NG_029254.1:g.7080C>T, NM_004221.7:c.30C>T, NM_004221.6:c.30C>T, NM_004221.5:c.30C>T, NM_004221.4:c.30C>T, NM_001308078.4:c.30C>T, NM_001308078.3:c.30C>T, NM_001308078.2:c.30C>T, NM_001308078.1:c.30C>T, NM_001012631.4:c.30C>T, NM_001012631.3:c.30C>T, NM_001012631.2:c.30C>T, NM_001012631.1:c.30C>T, NM_001012718.4:c.30C>T, NM_001012718.3:c.30C>T, NM_001012718.2:c.30C>T, NM_001012718.1:c.30C>T, NM_001012634.4:c.30C>T, NM_001012634.3:c.30C>T, NM_001012634.2:c.30C>T, NM_001012634.1:c.30C>T, NM_001012635.4:c.30C>T, NM_001012635.3:c.30C>T, NM_001012635.2:c.30C>T, NM_001012635.1:c.30C>T, NM_001012633.4:c.30C>T, NM_001012633.3:c.30C>T, NM_001012633.2:c.30C>T, NM_001012633.1:c.30C>T, NM_001369596.3:c.30C>T, NM_001369596.2:c.30C>T, NM_001369596.1:c.30C>T, NM_001369587.3:c.30C>T, NM_001369587.2:c.30C>T, NM_001369587.1:c.30C>T, NM_001369588.3:c.30C>T, NM_001369588.2:c.30C>T, NM_001369588.1:c.30C>T, NM_001369589.3:c.30C>T, NM_001369589.2:c.30C>T, NM_001369589.1:c.30C>T, NM_001012632.3:c.30C>T, NM_001012632.2:c.30C>T, NM_001012632.1:c.30C>T, NM_001369593.3:c.-1C>T, NM_001369593.2:c.-1C>T, NM_001369593.1:c.-1C>T, NM_001369591.3:c.30C>T, NM_001369591.2:c.30C>T, NM_001369591.1:c.30C>T, NM_001369592.3:c.30C>T, NM_001369592.2:c.30C>T, NM_001369592.1:c.30C>T, NM_001369590.3:c.30C>T, NM_001369590.2:c.30C>T, NM_001369590.1:c.30C>T, NM_001369595.3:c.30C>T, NM_001369595.2:c.30C>T, NM_001369595.1:c.30C>T, NM_001012636.2:c.30C>T, NM_001012636.1:c.30C>T, NM_001376923.1:c.30C>T

Select item 14291051019.

rs1429105101 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 16:3069031 (GRCh38)
16:3119032 (GRCh37)
Canonical SPDI:: NC_000016.10:3069030:G:C
Gene:: IL32 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000005/1 (GnomAD_exomes)
C=0.000014/2 (GnomAD)
HGVS:: NC_000016.10:g.3069031G>C, NC_000016.9:g.3119032G>C, NG_029254.1:g.8720G>C, NM_004221.7:c.243G>C, NM_004221.6:c.243G>C, NM_004221.5:c.243G>C, NM_004221.4:c.243G>C, NM_001308078.4:c.381G>C, NM_001308078.3:c.381G>C, NM_001308078.2:c.381G>C, NM_001308078.1:c.381G>C, NM_001012631.4:c.243G>C, NM_001012631.3:c.243G>C, NM_001012631.2:c.243G>C, NM_001012631.1:c.243G>C, NM_001012718.4:c.243G>C, NM_001012718.3:c.243G>C, NM_001012718.2:c.243G>C, NM_001012718.1:c.243G>C, NM_001012634.4:c.183G>C, NM_001012634.3:c.183G>C, NM_001012634.2:c.183G>C, NM_001012634.1:c.183G>C, NM_001012635.4:c.183G>C, NM_001012635.3:c.183G>C, NM_001012635.2:c.183G>C, NM_001012635.1:c.183G>C, NM_001012633.4:c.243G>C, NM_001012633.3:c.243G>C, NM_001012633.2:c.243G>C, NM_001012633.1:c.243G>C, NM_001369596.3:c.243G>C, NM_001369596.2:c.243G>C, NM_001369596.1:c.243G>C, NM_001369587.3:c.381G>C, NM_001369587.2:c.381G>C, NM_001369587.1:c.381G>C, NM_001369588.3:c.381G>C, NM_001369588.2:c.381G>C, NM_001369588.1:c.381G>C, NM_001369589.3:c.243G>C, NM_001369589.2:c.243G>C, NM_001369589.1:c.243G>C, NM_001012632.3:c.243G>C, NM_001012632.2:c.243G>C, NM_001012632.1:c.243G>C, NM_001369593.3:c.213G>C, NM_001369593.2:c.213G>C, NM_001369593.1:c.213G>C, NM_001369591.3:c.183G>C, NM_001369591.2:c.183G>C, NM_001369591.1:c.183G>C, NM_001369592.3:c.183G>C, NM_001369592.2:c.183G>C, NM_001369592.1:c.183G>C, NM_001369590.3:c.183G>C, NM_001369590.2:c.183G>C, NM_001369590.1:c.183G>C, NM_001369595.3:c.183G>C, NM_001369595.2:c.183G>C, NM_001369595.1:c.183G>C, NM_001012636.2:c.216G>C, NM_001012636.1:c.216G>C, NM_001376923.1:c.243G>C

Select item 142870010910.

rs1428700109 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 16:3069032 (GRCh38)
16:3119033 (GRCh37)
Canonical SPDI:: NC_000016.10:3069031:T:A
Gene:: IL32 (Varview)
Functional Consequence:: coding_sequence_variant,missense_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.3069032T>A, NC_000016.9:g.3119033T>A, NG_029254.1:g.8721T>A, NM_004221.7:c.244T>A, NM_004221.6:c.244T>A, NM_004221.5:c.244T>A, NM_004221.4:c.244T>A, NM_001308078.4:c.382T>A, NM_001308078.3:c.382T>A, NM_001308078.2:c.382T>A, NM_001308078.1:c.382T>A, NM_001012631.4:c.244T>A, NM_001012631.3:c.244T>A, NM_001012631.2:c.244T>A, NM_001012631.1:c.244T>A, NM_001012718.4:c.244T>A, NM_001012718.3:c.244T>A, NM_001012718.2:c.244T>A, NM_001012718.1:c.244T>A, NM_001012634.4:c.184T>A, NM_001012634.3:c.184T>A, NM_001012634.2:c.184T>A, NM_001012634.1:c.184T>A, NM_001012635.4:c.184T>A, NM_001012635.3:c.184T>A, NM_001012635.2:c.184T>A, NM_001012635.1:c.184T>A, NM_001012633.4:c.244T>A, NM_001012633.3:c.244T>A, NM_001012633.2:c.244T>A, NM_001012633.1:c.244T>A, NM_001369596.3:c.244T>A, NM_001369596.2:c.244T>A, NM_001369596.1:c.244T>A, NM_001369587.3:c.382T>A, NM_001369587.2:c.382T>A, NM_001369587.1:c.382T>A, NM_001369588.3:c.382T>A, NM_001369588.2:c.382T>A, NM_001369588.1:c.382T>A, NM_001369589.3:c.244T>A, NM_001369589.2:c.244T>A, NM_001369589.1:c.244T>A, NM_001012632.3:c.244T>A, NM_001012632.2:c.244T>A, NM_001012632.1:c.244T>A, NM_001369593.3:c.214T>A, NM_001369593.2:c.214T>A, NM_001369593.1:c.214T>A, NM_001369591.3:c.184T>A, NM_001369591.2:c.184T>A, NM_001369591.1:c.184T>A, NM_001369592.3:c.184T>A, NM_001369592.2:c.184T>A, NM_001369592.1:c.184T>A, NM_001369590.3:c.184T>A, NM_001369590.2:c.184T>A, NM_001369590.1:c.184T>A, NM_001369595.3:c.184T>A, NM_001369595.2:c.184T>A, NM_001369595.1:c.184T>A, NM_001012636.2:c.217T>A, NM_001012636.1:c.217T>A, NM_001376923.1:c.244T>A, NP_004212.4:p.Cys82Ser, NP_001295007.1:p.Cys128Ser, NP_001012649.1:p.Cys82Ser, NP_001012736.1:p.Cys82Ser, NP_001012652.1:p.Cys62Ser, NP_001012653.1:p.Cys62Ser, NP_001012651.1:p.Cys82Ser, NP_001356525.1:p.Cys82Ser, NP_001356516.1:p.Cys128Ser, NP_001356517.1:p.Cys128Ser, NP_001356518.1:p.Cys82Ser, NP_001012650.1:p.Cys82Ser, NP_001356522.1:p.Cys72Ser, NP_001356520.1:p.Cys62Ser, NP_001356521.1:p.Cys62Ser, NP_001356519.1:p.Cys62Ser, NP_001356524.1:p.Cys62Ser, NP_001012654.1:p.Cys73Ser, NP_001363852.1:p.Cys82Ser

Select item 142735068311.

rs1427350683 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 16:3069053 (GRCh38)
16:3119054 (GRCh37)
Canonical SPDI:: NC_000016.10:3069052:G:A
Gene:: IL32 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000009/2 (GnomAD_exomes)
HGVS:: NC_000016.10:g.3069053G>A, NC_000016.9:g.3119054G>A, NG_029254.1:g.8742G>A, NM_004221.7:c.265G>A, NM_004221.6:c.265G>A, NM_004221.5:c.265G>A, NM_004221.4:c.265G>A, NM_001308078.4:c.403G>A, NM_001308078.3:c.403G>A, NM_001308078.2:c.403G>A, NM_001308078.1:c.403G>A, NM_001012631.4:c.265G>A, NM_001012631.3:c.265G>A, NM_001012631.2:c.265G>A, NM_001012631.1:c.265G>A, NM_001012718.4:c.265G>A, NM_001012718.3:c.265G>A, NM_001012718.2:c.265G>A, NM_001012718.1:c.265G>A, NM_001012634.4:c.205G>A, NM_001012634.3:c.205G>A, NM_001012634.2:c.205G>A, NM_001012634.1:c.205G>A, NM_001012635.4:c.205G>A, NM_001012635.3:c.205G>A, NM_001012635.2:c.205G>A, NM_001012635.1:c.205G>A, NM_001012633.4:c.265G>A, NM_001012633.3:c.265G>A, NM_001012633.2:c.265G>A, NM_001012633.1:c.265G>A, NM_001369596.3:c.265G>A, NM_001369596.2:c.265G>A, NM_001369596.1:c.265G>A, NM_001369587.3:c.403G>A, NM_001369587.2:c.403G>A, NM_001369587.1:c.403G>A, NM_001369588.3:c.403G>A, NM_001369588.2:c.403G>A, NM_001369588.1:c.403G>A, NM_001369589.3:c.265G>A, NM_001369589.2:c.265G>A, NM_001369589.1:c.265G>A, NM_001012632.3:c.265G>A, NM_001012632.2:c.265G>A, NM_001012632.1:c.265G>A, NM_001369593.3:c.235G>A, NM_001369593.2:c.235G>A, NM_001369593.1:c.235G>A, NM_001369591.3:c.205G>A, NM_001369591.2:c.205G>A, NM_001369591.1:c.205G>A, NM_001369592.3:c.205G>A, NM_001369592.2:c.205G>A, NM_001369592.1:c.205G>A, NM_001369590.3:c.205G>A, NM_001369590.2:c.205G>A, NM_001369590.1:c.205G>A, NM_001369595.3:c.205G>A, NM_001369595.2:c.205G>A, NM_001369595.1:c.205G>A, NM_001012636.2:c.238G>A, NM_001012636.1:c.238G>A, NM_001376923.1:c.265G>A, NP_004212.4:p.Val89Ile, NP_001295007.1:p.Val135Ile, NP_001012649.1:p.Val89Ile, NP_001012736.1:p.Val89Ile, NP_001012652.1:p.Val69Ile, NP_001012653.1:p.Val69Ile, NP_001012651.1:p.Val89Ile, NP_001356525.1:p.Val89Ile, NP_001356516.1:p.Val135Ile, NP_001356517.1:p.Val135Ile, NP_001356518.1:p.Val89Ile, NP_001012650.1:p.Val89Ile, NP_001356522.1:p.Val79Ile, NP_001356520.1:p.Val69Ile, NP_001356521.1:p.Val69Ile, NP_001356519.1:p.Val69Ile, NP_001356524.1:p.Val69Ile, NP_001012654.1:p.Val80Ile, NP_001363852.1:p.Val89Ile

Select item 142202442312.

rs1422024423 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 16:3069126 (GRCh38)
16:3119127 (GRCh37)
Canonical SPDI:: NC_000016.10:3069125:A:G
Gene:: IL32 (Varview)
Functional Consequence:: missense_variant,intron_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000071/1 (ALFA)
G=0.000004/1 (GnomAD_exomes)
G=0.000011/3 (TOPMED)
HGVS:: NC_000016.10:g.3069126A>G, NC_000016.9:g.3119127A>G, NG_029254.1:g.8815A>G, NM_004221.7:c.338A>G, NM_004221.6:c.338A>G, NM_004221.5:c.338A>G, NM_004221.4:c.338A>G, NM_001308078.4:c.476A>G, NM_001308078.3:c.476A>G, NM_001308078.2:c.476A>G, NM_001308078.1:c.476A>G, NM_001012631.4:c.338A>G, NM_001012631.3:c.338A>G, NM_001012631.2:c.338A>G, NM_001012631.1:c.338A>G, NM_001012718.4:c.338A>G, NM_001012718.3:c.338A>G, NM_001012718.2:c.338A>G, NM_001012718.1:c.338A>G, NM_001012634.4:c.278A>G, NM_001012634.3:c.278A>G, NM_001012634.2:c.278A>G, NM_001012634.1:c.278A>G, NM_001012635.4:c.278A>G, NM_001012635.3:c.278A>G, NM_001012635.2:c.278A>G, NM_001012635.1:c.278A>G, NM_001369596.3:c.338A>G, NM_001369596.2:c.338A>G, NM_001369596.1:c.338A>G, NM_001369587.3:c.476A>G, NM_001369587.2:c.476A>G, NM_001369587.1:c.476A>G, NM_001369588.3:c.476A>G, NM_001369588.2:c.476A>G, NM_001369588.1:c.476A>G, NM_001369589.3:c.338A>G, NM_001369589.2:c.338A>G, NM_001369589.1:c.338A>G, NM_001012632.3:c.338A>G, NM_001012632.2:c.338A>G, NM_001012632.1:c.338A>G, NM_001369593.3:c.308A>G, NM_001369593.2:c.308A>G, NM_001369593.1:c.308A>G, NM_001369591.3:c.278A>G, NM_001369591.2:c.278A>G, NM_001369591.1:c.278A>G, NM_001369592.3:c.278A>G, NM_001369592.2:c.278A>G, NM_001369592.1:c.278A>G, NM_001369590.3:c.278A>G, NM_001369590.2:c.278A>G, NM_001369590.1:c.278A>G, NM_001012636.2:c.311A>G, NM_001012636.1:c.311A>G, NM_001376923.1:c.338A>G, NP_004212.4:p.Gln113Arg, NP_001295007.1:p.Gln159Arg, NP_001012649.1:p.Gln113Arg, NP_001012736.1:p.Gln113Arg, NP_001012652.1:p.Gln93Arg, NP_001012653.1:p.Gln93Arg, NP_001356525.1:p.Gln113Arg, NP_001356516.1:p.Gln159Arg, NP_001356517.1:p.Gln159Arg, NP_001356518.1:p.Gln113Arg, NP_001012650.1:p.Gln113Arg, NP_001356522.1:p.Gln103Arg, NP_001356520.1:p.Gln93Arg, NP_001356521.1:p.Gln93Arg, NP_001356519.1:p.Gln93Arg, NP_001012654.1:p.Gln104Arg, NP_001363852.1:p.Gln113Arg

Select item 141181141513.

rs1411811415 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 16:3065821 (GRCh38)
16:3115822 (GRCh37)
Canonical SPDI:: NC_000016.10:3065820:C:T
Gene:: IL32 (Varview)
Functional Consequence:: missense_variant,intron_variant,coding_sequence_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000016.10:g.3065821C>T, NC_000016.9:g.3115822C>T, NG_029254.1:g.5510C>T, NM_004221.7:c.10C>T, NM_004221.6:c.10C>T, NM_004221.5:c.10C>T, NM_004221.4:c.10C>T, NM_001308078.4:c.10C>T, NM_001308078.3:c.10C>T, NM_001308078.2:c.10C>T, NM_001308078.1:c.10C>T, NM_001012631.4:c.10C>T, NM_001012631.3:c.10C>T, NM_001012631.2:c.10C>T, NM_001012631.1:c.10C>T, NM_001012718.4:c.10C>T, NM_001012718.3:c.10C>T, NM_001012718.2:c.10C>T, NM_001012718.1:c.10C>T, NM_001012634.4:c.10C>T, NM_001012634.3:c.10C>T, NM_001012634.2:c.10C>T, NM_001012634.1:c.10C>T, NM_001012635.4:c.10C>T, NM_001012635.3:c.10C>T, NM_001012635.2:c.10C>T, NM_001012635.1:c.10C>T, NM_001012633.4:c.10C>T, NM_001012633.3:c.10C>T, NM_001012633.2:c.10C>T, NM_001012633.1:c.10C>T, NM_001369596.3:c.10C>T, NM_001369596.2:c.10C>T, NM_001369596.1:c.10C>T, NM_001369587.3:c.10C>T, NM_001369587.2:c.10C>T, NM_001369587.1:c.10C>T, NM_001369588.3:c.10C>T, NM_001369588.2:c.10C>T, NM_001369588.1:c.10C>T, NM_001369589.3:c.10C>T, NM_001369589.2:c.10C>T, NM_001369589.1:c.10C>T, NM_001012632.3:c.10C>T, NM_001012632.2:c.10C>T, NM_001012632.1:c.10C>T, NM_001369591.3:c.10C>T, NM_001369591.2:c.10C>T, NM_001369591.1:c.10C>T, NM_001369592.3:c.10C>T, NM_001369592.2:c.10C>T, NM_001369592.1:c.10C>T, NM_001369590.3:c.10C>T, NM_001369590.2:c.10C>T, NM_001369590.1:c.10C>T, NM_001369595.3:c.10C>T, NM_001369595.2:c.10C>T, NM_001369595.1:c.10C>T, NM_001012636.2:c.10C>T, NM_001012636.1:c.10C>T, NM_001376923.1:c.10C>T, NP_004212.4:p.Pro4Ser, NP_001295007.1:p.Pro4Ser, NP_001012649.1:p.Pro4Ser, NP_001012736.1:p.Pro4Ser, NP_001012652.1:p.Pro4Ser, NP_001012653.1:p.Pro4Ser, NP_001012651.1:p.Pro4Ser, NP_001356525.1:p.Pro4Ser, NP_001356516.1:p.Pro4Ser, NP_001356517.1:p.Pro4Ser, NP_001356518.1:p.Pro4Ser, NP_001012650.1:p.Pro4Ser, NP_001356520.1:p.Pro4Ser, NP_001356521.1:p.Pro4Ser, NP_001356519.1:p.Pro4Ser, NP_001356524.1:p.Pro4Ser, NP_001012654.1:p.Pro4Ser, NP_001363852.1:p.Pro4Ser

Select item 140245803914.

rs1402458039 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 16:3069074 (GRCh38)
16:3119075 (GRCh37)
Canonical SPDI:: NC_000016.10:3069073:G:A
Gene:: IL32 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000016.10:g.3069074G>A, NC_000016.9:g.3119075G>A, NG_029254.1:g.8763G>A, NM_004221.7:c.286G>A, NM_004221.6:c.286G>A, NM_004221.5:c.286G>A, NM_004221.4:c.286G>A, NM_001308078.4:c.424G>A, NM_001308078.3:c.424G>A, NM_001308078.2:c.424G>A, NM_001308078.1:c.424G>A, NM_001012631.4:c.286G>A, NM_001012631.3:c.286G>A, NM_001012631.2:c.286G>A, NM_001012631.1:c.286G>A, NM_001012718.4:c.286G>A, NM_001012718.3:c.286G>A, NM_001012718.2:c.286G>A, NM_001012718.1:c.286G>A, NM_001012634.4:c.226G>A, NM_001012634.3:c.226G>A, NM_001012634.2:c.226G>A, NM_001012634.1:c.226G>A, NM_001012635.4:c.226G>A, NM_001012635.3:c.226G>A, NM_001012635.2:c.226G>A, NM_001012635.1:c.226G>A, NM_001012633.4:c.286G>A, NM_001012633.3:c.286G>A, NM_001012633.2:c.286G>A, NM_001012633.1:c.286G>A, NM_001369596.3:c.286G>A, NM_001369596.2:c.286G>A, NM_001369596.1:c.286G>A, NM_001369587.3:c.424G>A, NM_001369587.2:c.424G>A, NM_001369587.1:c.424G>A, NM_001369588.3:c.424G>A, NM_001369588.2:c.424G>A, NM_001369588.1:c.424G>A, NM_001369589.3:c.286G>A, NM_001369589.2:c.286G>A, NM_001369589.1:c.286G>A, NM_001012632.3:c.286G>A, NM_001012632.2:c.286G>A, NM_001012632.1:c.286G>A, NM_001369593.3:c.256G>A, NM_001369593.2:c.256G>A, NM_001369593.1:c.256G>A, NM_001369591.3:c.226G>A, NM_001369591.2:c.226G>A, NM_001369591.1:c.226G>A, NM_001369592.3:c.226G>A, NM_001369592.2:c.226G>A, NM_001369592.1:c.226G>A, NM_001369590.3:c.226G>A, NM_001369590.2:c.226G>A, NM_001369590.1:c.226G>A, NM_001369595.3:c.226G>A, NM_001369595.2:c.226G>A, NM_001369595.1:c.226G>A, NM_001012636.2:c.259G>A, NM_001012636.1:c.259G>A, NM_001376923.1:c.286G>A, NP_004212.4:p.Ala96Thr, NP_001295007.1:p.Ala142Thr, NP_001012649.1:p.Ala96Thr, NP_001012736.1:p.Ala96Thr, NP_001012652.1:p.Ala76Thr, NP_001012653.1:p.Ala76Thr, NP_001012651.1:p.Ala96Thr, NP_001356525.1:p.Ala96Thr, NP_001356516.1:p.Ala142Thr, NP_001356517.1:p.Ala142Thr, NP_001356518.1:p.Ala96Thr, NP_001012650.1:p.Ala96Thr, NP_001356522.1:p.Ala86Thr, NP_001356520.1:p.Ala76Thr, NP_001356521.1:p.Ala76Thr, NP_001356519.1:p.Ala76Thr, NP_001356524.1:p.Ala76Thr, NP_001012654.1:p.Ala87Thr, NP_001363852.1:p.Ala96Thr

Select item 139925850315.

rs1399258503 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 16:3069065 (GRCh38)
16:3119066 (GRCh37)
Canonical SPDI:: NC_000016.10:3069064:G:C
Gene:: IL32 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000016.10:g.3069065G>C, NC_000016.9:g.3119066G>C, NG_029254.1:g.8754G>C, NM_004221.7:c.277G>C, NM_004221.6:c.277G>C, NM_004221.5:c.277G>C, NM_004221.4:c.277G>C, NM_001308078.4:c.415G>C, NM_001308078.3:c.415G>C, NM_001308078.2:c.415G>C, NM_001308078.1:c.415G>C, NM_001012631.4:c.277G>C, NM_001012631.3:c.277G>C, NM_001012631.2:c.277G>C, NM_001012631.1:c.277G>C, NM_001012718.4:c.277G>C, NM_001012718.3:c.277G>C, NM_001012718.2:c.277G>C, NM_001012718.1:c.277G>C, NM_001012634.4:c.217G>C, NM_001012634.3:c.217G>C, NM_001012634.2:c.217G>C, NM_001012634.1:c.217G>C, NM_001012635.4:c.217G>C, NM_001012635.3:c.217G>C, NM_001012635.2:c.217G>C, NM_001012635.1:c.217G>C, NM_001012633.4:c.277G>C, NM_001012633.3:c.277G>C, NM_001012633.2:c.277G>C, NM_001012633.1:c.277G>C, NM_001369596.3:c.277G>C, NM_001369596.2:c.277G>C, NM_001369596.1:c.277G>C, NM_001369587.3:c.415G>C, NM_001369587.2:c.415G>C, NM_001369587.1:c.415G>C, NM_001369588.3:c.415G>C, NM_001369588.2:c.415G>C, NM_001369588.1:c.415G>C, NM_001369589.3:c.277G>C, NM_001369589.2:c.277G>C, NM_001369589.1:c.277G>C, NM_001012632.3:c.277G>C, NM_001012632.2:c.277G>C, NM_001012632.1:c.277G>C, NM_001369593.3:c.247G>C, NM_001369593.2:c.247G>C, NM_001369593.1:c.247G>C, NM_001369591.3:c.217G>C, NM_001369591.2:c.217G>C, NM_001369591.1:c.217G>C, NM_001369592.3:c.217G>C, NM_001369592.2:c.217G>C, NM_001369592.1:c.217G>C, NM_001369590.3:c.217G>C, NM_001369590.2:c.217G>C, NM_001369590.1:c.217G>C, NM_001369595.3:c.217G>C, NM_001369595.2:c.217G>C, NM_001369595.1:c.217G>C, NM_001012636.2:c.250G>C, NM_001012636.1:c.250G>C, NM_001376923.1:c.277G>C, NP_004212.4:p.Glu93Gln, NP_001295007.1:p.Glu139Gln, NP_001012649.1:p.Glu93Gln, NP_001012736.1:p.Glu93Gln, NP_001012652.1:p.Glu73Gln, NP_001012653.1:p.Glu73Gln, NP_001012651.1:p.Glu93Gln, NP_001356525.1:p.Glu93Gln, NP_001356516.1:p.Glu139Gln, NP_001356517.1:p.Glu139Gln, NP_001356518.1:p.Glu93Gln, NP_001012650.1:p.Glu93Gln, NP_001356522.1:p.Glu83Gln, NP_001356520.1:p.Glu73Gln, NP_001356521.1:p.Glu73Gln, NP_001356519.1:p.Glu73Gln, NP_001356524.1:p.Glu73Gln, NP_001012654.1:p.Glu84Gln, NP_001363852.1:p.Glu93Gln

Select item 139196098416.

rs1391960984 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 16:3069145 (GRCh38)
16:3119146 (GRCh37)
Canonical SPDI:: NC_000016.10:3069144:G:A
Gene:: IL32 (Varview)
Functional Consequence:: intron_variant,coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000016.10:g.3069145G>A, NC_000016.9:g.3119146G>A, NG_029254.1:g.8834G>A, NM_004221.7:c.357G>A, NM_004221.6:c.357G>A, NM_004221.5:c.357G>A, NM_004221.4:c.357G>A, NM_001308078.4:c.495G>A, NM_001308078.3:c.495G>A, NM_001308078.2:c.495G>A, NM_001308078.1:c.495G>A, NM_001012631.4:c.357G>A, NM_001012631.3:c.357G>A, NM_001012631.2:c.357G>A, NM_001012631.1:c.357G>A, NM_001012718.4:c.357G>A, NM_001012718.3:c.357G>A, NM_001012718.2:c.357G>A, NM_001012718.1:c.357G>A, NM_001012634.4:c.297G>A, NM_001012634.3:c.297G>A, NM_001012634.2:c.297G>A, NM_001012634.1:c.297G>A, NM_001012635.4:c.297G>A, NM_001012635.3:c.297G>A, NM_001012635.2:c.297G>A, NM_001012635.1:c.297G>A, NM_001369596.3:c.357G>A, NM_001369596.2:c.357G>A, NM_001369596.1:c.357G>A, NM_001369587.3:c.495G>A, NM_001369587.2:c.495G>A, NM_001369587.1:c.495G>A, NM_001369588.3:c.495G>A, NM_001369588.2:c.495G>A, NM_001369588.1:c.495G>A, NM_001369589.3:c.357G>A, NM_001369589.2:c.357G>A, NM_001369589.1:c.357G>A, NM_001012632.3:c.357G>A, NM_001012632.2:c.357G>A, NM_001012632.1:c.357G>A, NM_001369593.3:c.327G>A, NM_001369593.2:c.327G>A, NM_001369593.1:c.327G>A, NM_001369591.3:c.297G>A, NM_001369591.2:c.297G>A, NM_001369591.1:c.297G>A, NM_001369592.3:c.297G>A, NM_001369592.2:c.297G>A, NM_001369592.1:c.297G>A, NM_001369590.3:c.297G>A, NM_001369590.2:c.297G>A, NM_001369590.1:c.297G>A, NM_001012636.2:c.330G>A, NM_001012636.1:c.330G>A, NM_001376923.1:c.357G>A

Select item 138742960017.

rs1387429600 [Homo sapiens]

Variant type:: DEL
Alleles:: CCGGATGT>- [Show Flanks]
Chromosome:: 16:3069056 (GRCh38)
16:3119057 (GRCh37)
Canonical SPDI:: NC_000016.10:3069055:CCGGATGT:
Gene:: IL32 (Varview)
Functional Consequence:: stop_gained,coding_sequence_variant
HGVS:: NC_000016.10:g.3069056_3069063del, NC_000016.9:g.3119057_3119064del, NG_029254.1:g.8745_8752del, NM_004221.7:c.268_275del, NM_004221.6:c.268_275del, NM_004221.5:c.268_275del, NM_004221.4:c.268_275del, NM_001308078.4:c.406_413del, NM_001308078.3:c.406_413del, NM_001308078.2:c.406_413del, NM_001308078.1:c.406_413del, NM_001012631.4:c.268_275del, NM_001012631.3:c.268_275del, NM_001012631.2:c.268_275del, NM_001012631.1:c.268_275del, NM_001012718.4:c.268_275del, NM_001012718.3:c.268_275del, NM_001012718.2:c.268_275del, NM_001012718.1:c.268_275del, NM_001012634.4:c.208_215del, NM_001012634.3:c.208_215del, NM_001012634.2:c.208_215del, NM_001012634.1:c.208_215del, NM_001012635.4:c.208_215del, NM_001012635.3:c.208_215del, NM_001012635.2:c.208_215del, NM_001012635.1:c.208_215del, NM_001012633.4:c.268_275del, NM_001012633.3:c.268_275del, NM_001012633.2:c.268_275del, NM_001012633.1:c.268_275del, NM_001369596.3:c.268_275del, NM_001369596.2:c.268_275del, NM_001369596.1:c.268_275del, NM_001369587.3:c.406_413del, NM_001369587.2:c.406_413del, NM_001369587.1:c.406_413del, NM_001369588.3:c.406_413del, NM_001369588.2:c.406_413del, NM_001369588.1:c.406_413del, NM_001369589.3:c.268_275del, NM_001369589.2:c.268_275del, NM_001369589.1:c.268_275del, NM_001012632.3:c.268_275del, NM_001012632.2:c.268_275del, NM_001012632.1:c.268_275del, NM_001369593.3:c.238_245del, NM_001369593.2:c.238_245del, NM_001369593.1:c.238_245del, NM_001369591.3:c.208_215del, NM_001369591.2:c.208_215del, NM_001369591.1:c.208_215del, NM_001369592.3:c.208_215del, NM_001369592.2:c.208_215del, NM_001369592.1:c.208_215del, NM_001369590.3:c.208_215del, NM_001369590.2:c.208_215del, NM_001369590.1:c.208_215del, NM_001369595.3:c.208_215del, NM_001369595.2:c.208_215del, NM_001369595.1:c.208_215del, NM_001012636.2:c.241_248del, NM_001012636.1:c.241_248del, NM_001376923.1:c.268_275del, NP_004212.4:p.Val89_Pro90insTer, NP_001295007.1:p.Val135_Pro136insTer, NP_001012649.1:p.Val89_Pro90insTer, NP_001012736.1:p.Val89_Pro90insTer, NP_001012652.1:p.Val69_Pro70insTer, NP_001012653.1:p.Val69_Pro70insTer, NP_001012651.1:p.Val89_Pro90insTer, NP_001356525.1:p.Val89_Pro90insTer, NP_001356516.1:p.Val135_Pro136insTer, NP_001356517.1:p.Val135_Pro136insTer, NP_001356518.1:p.Val89_Pro90insTer, NP_001012650.1:p.Val89_Pro90insTer, NP_001356522.1:p.Val79_Pro80insTer, NP_001356520.1:p.Val69_Pro70insTer, NP_001356521.1:p.Val69_Pro70insTer, NP_001356519.1:p.Val69_Pro70insTer, NP_001356524.1:p.Val69_Pro70insTer, NP_001012654.1:p.Val80_Pro81insTer, NP_001363852.1:p.Val89_Pro90insTer

Select item 138723257418.

rs1387232574 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 16:3069237 (GRCh38)
16:3119238 (GRCh37)
Canonical SPDI:: NC_000016.10:3069236:G:C
Gene:: IL32 (Varview)
Functional Consequence:: intron_variant,missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000016.10:g.3069237G>C, NC_000016.9:g.3119238G>C, NG_029254.1:g.8926G>C, NM_004221.7:c.449G>C, NM_004221.6:c.449G>C, NM_004221.5:c.449G>C, NM_004221.4:c.449G>C, NM_001308078.4:c.587G>C, NM_001308078.3:c.587G>C, NM_001308078.2:c.587G>C, NM_001308078.1:c.587G>C, NM_001012631.4:c.449G>C, NM_001012631.3:c.449G>C, NM_001012631.2:c.449G>C, NM_001012631.1:c.449G>C, NM_001012718.4:c.449G>C, NM_001012718.3:c.449G>C, NM_001012718.2:c.449G>C, NM_001012718.1:c.449G>C, NM_001012634.4:c.389G>C, NM_001012634.3:c.389G>C, NM_001012634.2:c.389G>C, NM_001012634.1:c.389G>C, NM_001012635.4:c.389G>C, NM_001012635.3:c.389G>C, NM_001012635.2:c.389G>C, NM_001012635.1:c.389G>C, NM_001369596.3:c.449G>C, NM_001369596.2:c.449G>C, NM_001369596.1:c.449G>C, NM_001369587.3:c.587G>C, NM_001369587.2:c.587G>C, NM_001369587.1:c.587G>C, NM_001369588.3:c.587G>C, NM_001369588.2:c.587G>C, NM_001369588.1:c.587G>C, NM_001369589.3:c.449G>C, NM_001369589.2:c.449G>C, NM_001369589.1:c.449G>C, NM_001012632.3:c.449G>C, NM_001012632.2:c.449G>C, NM_001012632.1:c.449G>C, NM_001369593.3:c.419G>C, NM_001369593.2:c.419G>C, NM_001369593.1:c.419G>C, NM_001369591.3:c.389G>C, NM_001369591.2:c.389G>C, NM_001369591.1:c.389G>C, NM_001369592.3:c.389G>C, NM_001369592.2:c.389G>C, NM_001369592.1:c.389G>C, NM_001369590.3:c.389G>C, NM_001369590.2:c.389G>C, NM_001369590.1:c.389G>C, NM_001012636.2:c.422G>C, NM_001012636.1:c.422G>C, NM_001376923.1:c.449G>C, NP_004212.4:p.Ser150Thr, NP_001295007.1:p.Ser196Thr, NP_001012649.1:p.Ser150Thr, NP_001012736.1:p.Ser150Thr, NP_001012652.1:p.Ser130Thr, NP_001012653.1:p.Ser130Thr, NP_001356525.1:p.Ser150Thr, NP_001356516.1:p.Ser196Thr, NP_001356517.1:p.Ser196Thr, NP_001356518.1:p.Ser150Thr, NP_001012650.1:p.Ser150Thr, NP_001356522.1:p.Ser140Thr, NP_001356520.1:p.Ser130Thr, NP_001356521.1:p.Ser130Thr, NP_001356519.1:p.Ser130Thr, NP_001012654.1:p.Ser141Thr, NP_001363852.1:p.Ser150Thr

Select item 138527435519.

rs1385274355 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 16:3067997 (GRCh38)
16:3117998 (GRCh37)
Canonical SPDI:: NC_000016.10:3067996:T:G
Gene:: IL32 (Varview)
Functional Consequence:: intron_variant,missense_variant,coding_sequence_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_000016.10:g.3067997T>G, NC_000016.9:g.3117998T>G, NG_029254.1:g.7686T>G, NM_004221.7:c.128T>G, NM_004221.6:c.128T>G, NM_004221.5:c.128T>G, NM_004221.4:c.128T>G, NM_001308078.4:c.266T>G, NM_001308078.3:c.266T>G, NM_001308078.2:c.266T>G, NM_001308078.1:c.266T>G, NM_001012631.4:c.128T>G, NM_001012631.3:c.128T>G, NM_001012631.2:c.128T>G, NM_001012631.1:c.128T>G, NM_001012718.4:c.128T>G, NM_001012718.3:c.128T>G, NM_001012718.2:c.128T>G, NM_001012718.1:c.128T>G, NM_001012634.4:c.68T>G, NM_001012634.3:c.68T>G, NM_001012634.2:c.68T>G, NM_001012634.1:c.68T>G, NM_001012635.4:c.68T>G, NM_001012635.3:c.68T>G, NM_001012635.2:c.68T>G, NM_001012635.1:c.68T>G, NM_001012633.4:c.128T>G, NM_001012633.3:c.128T>G, NM_001012633.2:c.128T>G, NM_001012633.1:c.128T>G, NM_001369596.3:c.128T>G, NM_001369596.2:c.128T>G, NM_001369596.1:c.128T>G, NM_001369587.3:c.266T>G, NM_001369587.2:c.266T>G, NM_001369587.1:c.266T>G, NM_001369588.3:c.266T>G, NM_001369588.2:c.266T>G, NM_001369588.1:c.266T>G, NM_001369589.3:c.128T>G, NM_001369589.2:c.128T>G, NM_001369589.1:c.128T>G, NM_001012632.3:c.128T>G, NM_001012632.2:c.128T>G, NM_001012632.1:c.128T>G, NM_001369593.3:c.98T>G, NM_001369593.2:c.98T>G, NM_001369593.1:c.98T>G, NM_001369591.3:c.68T>G, NM_001369591.2:c.68T>G, NM_001369591.1:c.68T>G, NM_001369592.3:c.68T>G, NM_001369592.2:c.68T>G, NM_001369592.1:c.68T>G, NM_001369590.3:c.128T>G, NM_001369590.2:c.128T>G, NM_001369590.1:c.128T>G, NM_001369595.3:c.68T>G, NM_001369595.2:c.68T>G, NM_001369595.1:c.68T>G, NM_001376923.1:c.128T>G, NP_004212.4:p.Leu43Arg, NP_001295007.1:p.Leu89Arg, NP_001012649.1:p.Leu43Arg, NP_001012736.1:p.Leu43Arg, NP_001012652.1:p.Leu23Arg, NP_001012653.1:p.Leu23Arg, NP_001012651.1:p.Leu43Arg, NP_001356525.1:p.Leu43Arg, NP_001356516.1:p.Leu89Arg, NP_001356517.1:p.Leu89Arg, NP_001356518.1:p.Leu43Arg, NP_001012650.1:p.Leu43Arg, NP_001356522.1:p.Leu33Arg, NP_001356520.1:p.Leu23Arg, NP_001356521.1:p.Leu23Arg, NP_001356519.1:p.Leu43Arg, NP_001356524.1:p.Leu23Arg, NP_001363852.1:p.Leu43Arg

Select item 138332779020.

rs1383327790 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 16:3069295 (GRCh38)
16:3119296 (GRCh37)
Canonical SPDI:: NC_000016.10:3069294:A:G
Gene:: IL32 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
HGVS:: NC_000016.10:g.3069295A>G, NC_000016.9:g.3119296A>G, NG_029254.1:g.8984A>G, NM_004221.7:c.507A>G, NM_004221.6:c.507A>G, NM_004221.5:c.507A>G, NM_004221.4:c.507A>G, NM_001308078.4:c.645A>G, NM_001308078.3:c.645A>G, NM_001308078.2:c.645A>G, NM_001308078.1:c.645A>G, NM_001012631.4:c.507A>G, NM_001012631.3:c.507A>G, NM_001012631.2:c.507A>G, NM_001012631.1:c.507A>G, NM_001012718.4:c.507A>G, NM_001012718.3:c.507A>G, NM_001012718.2:c.507A>G, NM_001012718.1:c.507A>G, NM_001012634.4:c.447A>G, NM_001012634.3:c.447A>G, NM_001012634.2:c.447A>G, NM_001012634.1:c.447A>G, NM_001012635.4:c.447A>G, NM_001012635.3:c.447A>G, NM_001012635.2:c.447A>G, NM_001012635.1:c.447A>G, NM_001012633.4:c.336A>G, NM_001012633.3:c.336A>G, NM_001012633.2:c.336A>G, NM_001012633.1:c.336A>G, NM_001369596.3:c.507A>G, NM_001369596.2:c.507A>G, NM_001369596.1:c.507A>G, NM_001369587.3:c.645A>G, NM_001369587.2:c.645A>G, NM_001369587.1:c.645A>G, NM_001369588.3:c.645A>G, NM_001369588.2:c.645A>G, NM_001369588.1:c.645A>G, NM_001369589.3:c.507A>G, NM_001369589.2:c.507A>G, NM_001369589.1:c.507A>G, NM_001012632.3:c.507A>G, NM_001012632.2:c.507A>G, NM_001012632.1:c.507A>G, NM_001369593.3:c.477A>G, NM_001369593.2:c.477A>G, NM_001369593.1:c.477A>G, NM_001369591.3:c.447A>G, NM_001369591.2:c.447A>G, NM_001369591.1:c.447A>G, NM_001369592.3:c.447A>G, NM_001369592.2:c.447A>G, NM_001369592.1:c.447A>G, NM_001369590.3:c.447A>G, NM_001369590.2:c.447A>G, NM_001369590.1:c.447A>G, NM_001369595.3:c.276A>G, NM_001369595.2:c.276A>G, NM_001369595.1:c.276A>G, NM_001012636.2:c.480A>G, NM_001012636.1:c.480A>G, NM_001376923.1:c.507A>G

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