SNP Links for Protein (Select 28416913) - SNP

Links from Protein

Items: 1 to 20 of 241

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Select item 14856615771.

rs1485661577 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 16:28499889 (GRCh38)
16:28511210 (GRCh37)
Canonical SPDI:: NC_000016.10:28499888:T:C
Gene:: IL27 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
HGVS:: NC_000016.10:g.28499889T>C, NC_000016.9:g.28511210T>C, NM_145659.3:c.494A>G, NP_663634.2:p.Glu165Gly

Select item 14842808492.

rs1484280849 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 16:28499878 (GRCh38)
16:28511199 (GRCh37)
Canonical SPDI:: NC_000016.10:28499877:C:G,NC_000016.10:28499877:C:T
Gene:: IL27 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000016.10:g.28499878C>G, NC_000016.10:g.28499878C>T, NC_000016.9:g.28511199C>G, NC_000016.9:g.28511199C>T, NM_145659.3:c.505G>C, NM_145659.3:c.505G>A, NP_663634.2:p.Glu169Gln, NP_663634.2:p.Glu169Lys

Select item 14786452293.

rs1478645229 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,G [Show Flanks]
Chromosome:: 16:28502050 (GRCh38)
16:28513371 (GRCh37)
Canonical SPDI:: NC_000016.10:28502049:T:A,NC_000016.10:28502049:T:G
Gene:: IL27 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by cluster
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000016.10:g.28502050T>A, NC_000016.10:g.28502050T>G, NC_000016.9:g.28513371T>A, NC_000016.9:g.28513371T>G, NM_145659.3:c.388A>T, NM_145659.3:c.388A>C, NP_663634.2:p.Thr130Ser, NP_663634.2:p.Thr130Pro

Select item 14776726674.

rs1477672667 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 16:28499833 (GRCh38)
16:28511154 (GRCh37)
Canonical SPDI:: NC_000016.10:28499832:C:T
Gene:: IL27 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
HGVS:: NC_000016.10:g.28499833C>T, NC_000016.9:g.28511154C>T, NM_145659.3:c.550G>A, NP_663634.2:p.Ala184Thr

Select item 14713884955.

rs1471388495 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 16:28499890 (GRCh38)
16:28511211 (GRCh37)
Canonical SPDI:: NC_000016.10:28499889:C:G
Gene:: IL27 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000016.10:g.28499890C>G, NC_000016.9:g.28511211C>G, NM_145659.3:c.493G>C, NP_663634.2:p.Glu165Gln

Select item 14654697326.

rs1465469732 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 16:28499791 (GRCh38)
16:28511112 (GRCh37)
Canonical SPDI:: NC_000016.10:28499790:G:T
Gene:: IL27 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
HGVS:: NC_000016.10:g.28499791G>T, NC_000016.9:g.28511112G>T, NM_145659.3:c.592C>A, NP_663634.2:p.Pro198Thr

Select item 14620743567.

rs1462074356 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 16:28506786 (GRCh38)
16:28518107 (GRCh37)
Canonical SPDI:: NC_000016.10:28506785:C:A
Gene:: IL27 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
HGVS:: NC_000016.10:g.28506786C>A, NC_000016.9:g.28518107C>A, NM_145659.3:c.26G>T, NP_663634.2:p.Gly9Val

Select item 14616494468.

rs1461649446 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 16:28499751 (GRCh38)
16:28511072 (GRCh37)
Canonical SPDI:: NC_000016.10:28499750:T:G
Gene:: IL27 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000016.10:g.28499751T>G, NC_000016.9:g.28511072T>G, NM_145659.3:c.632A>C, NP_663634.2:p.Glu211Ala

Select item 14607454949.

rs1460745494 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 16:28503786 (GRCh38)
16:28515107 (GRCh37)
Canonical SPDI:: NC_000016.10:28503785:G:A
Gene:: IL27 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000016.10:g.28503786G>A, NC_000016.9:g.28515107G>A, NM_145659.3:c.212C>T, NP_663634.2:p.Ser71Phe

Select item 145885417510.

rs1458854175 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 16:28499848 (GRCh38)
16:28511169 (GRCh37)
Canonical SPDI:: NC_000016.10:28499847:C:A
Gene:: IL27 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
HGVS:: NC_000016.10:g.28499848C>A, NC_000016.9:g.28511169C>A, NM_145659.3:c.535G>T, NP_663634.2:p.Gly179Trp

Select item 145772805911.

rs1457728059 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 16:28504032 (GRCh38)
16:28515353 (GRCh37)
Canonical SPDI:: NC_000016.10:28504031:A:G
Gene:: IL27 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000016.10:g.28504032A>G, NC_000016.9:g.28515353A>G, NM_145659.3:c.50T>C, NP_663634.2:p.Leu17Pro

Select item 145524310912.

rs1455243109 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 16:28499696 (GRCh38)
16:28511017 (GRCh37)
Canonical SPDI:: NC_000016.10:28499695:G:A,NC_000016.10:28499695:G:C
Gene:: IL27 (Varview)
Functional Consequence:: synonymous_variant,missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.00003/8 (TOPMED)
HGVS:: NC_000016.10:g.28499696G>A, NC_000016.10:g.28499696G>C, NC_000016.9:g.28511017G>A, NC_000016.9:g.28511017G>C, NM_145659.3:c.687C>T, NM_145659.3:c.687C>G, NP_663634.2:p.His229Gln

Select item 145106587513.

rs1451065875 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 16:28503716 (GRCh38)
16:28515037 (GRCh37)
Canonical SPDI:: NC_000016.10:28503715:G:A
Gene:: IL27 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000016.10:g.28503716G>A, NC_000016.9:g.28515037G>A, NM_145659.3:c.282C>T

Select item 144584679914.

rs1445846799 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 16:28503992 (GRCh38)
16:28515313 (GRCh37)
Canonical SPDI:: NC_000016.10:28503991:T:A
Gene:: IL27 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000016.10:g.28503992T>A, NC_000016.9:g.28515313T>A, NM_145659.3:c.90A>T

Select item 144339977315.

rs1443399773 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 16:28503999 (GRCh38)
16:28515320 (GRCh37)
Canonical SPDI:: NC_000016.10:28503998:C:A
Gene:: IL27 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000008/2 (TOPMED)
HGVS:: NC_000016.10:g.28503999C>A, NC_000016.9:g.28515320C>A, NM_145659.3:c.83G>T, NP_663634.2:p.Gly28Val

Select item 142479574916.

rs1424795749 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 16:28499896 (GRCh38)
16:28511217 (GRCh37)
Canonical SPDI:: NC_000016.10:28499895:G:A
Gene:: IL27 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000016.10:g.28499896G>A, NC_000016.9:g.28511217G>A, NM_145659.3:c.487C>T, NP_663634.2:p.Pro163Ser

Select item 142476107217.

rs1424761072 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 16:28499785 (GRCh38)
16:28511106 (GRCh37)
Canonical SPDI:: NC_000016.10:28499784:G:A,NC_000016.10:28499784:G:C
Gene:: IL27 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000016.10:g.28499785G>A, NC_000016.10:g.28499785G>C, NC_000016.9:g.28511106G>A, NC_000016.9:g.28511106G>C, NM_145659.3:c.598C>T, NM_145659.3:c.598C>G, NP_663634.2:p.Leu200Phe, NP_663634.2:p.Leu200Val

Select item 140805618618.

rs1408056186 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 16:28502080 (GRCh38)
16:28513401 (GRCh37)
Canonical SPDI:: NC_000016.10:28502079:G:T
Gene:: IL27 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000016.10:g.28502080G>T, NC_000016.9:g.28513401G>T, NM_145659.3:c.358C>A, NP_663634.2:p.Leu120Met

Select item 140454743619.

rs1404547436 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 16:28502019 (GRCh38)
16:28513340 (GRCh37)
Canonical SPDI:: NC_000016.10:28502018:A:G
Gene:: IL27 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (GnomAD_exomes)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000016.10:g.28502019A>G, NC_000016.9:g.28513340A>G, NM_145659.3:c.419T>C, NP_663634.2:p.Met140Thr

Select item 140381930420.

rs1403819304 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 16:28506806 (GRCh38)
16:28518127 (GRCh37)
Canonical SPDI:: NC_000016.10:28506805:G:A
Gene:: IL27 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000016.10:g.28506806G>A, NC_000016.9:g.28518127G>A, NM_145659.3:c.6C>T

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