SNP Links for Protein (Select 1034605037) - SNP

Select item 14909549141.

rs1490954914 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 18:70324701 (GRCh38)
18:67991937 (GRCh37)
Canonical SPDI:: NC_000018.10:70324700:A:G
Gene:: SOCS6 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: G=0.000111/1 (ALFA)
G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000018.10:g.70324701A>G, NC_000018.9:g.67991937A>G, XM_005266783.5:c.33A>G, XM_005266783.4:c.33A>G, XM_005266783.3:c.33A>G, XM_005266783.2:c.33A>G, XM_005266783.1:c.33A>G, NM_004232.4:c.33A>G, NM_004232.3:c.33A>G, XM_017026087.2:c.33A>G, XM_017026087.1:c.33A>G, XM_017026086.2:c.33A>G, XM_017026086.1:c.33A>G, XM_047437942.1:c.33A>G, XM_047437941.1:c.33A>G, XM_047437939.1:c.33A>G, XM_047437937.1:c.33A>G, XM_047437940.1:c.33A>G, XM_047437938.1:c.33A>G

Select item 14904645672.

rs1490464567 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 18:70325005 (GRCh38)
18:67992241 (GRCh37)
Canonical SPDI:: NC_000018.10:70325004:T:C
Gene:: SOCS6 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000018.10:g.70325005T>C, NC_000018.9:g.67992241T>C, XM_005266783.5:c.337T>C, XM_005266783.4:c.337T>C, XM_005266783.3:c.337T>C, XM_005266783.2:c.337T>C, XM_005266783.1:c.337T>C, NM_004232.4:c.337T>C, NM_004232.3:c.337T>C, XM_017026087.2:c.337T>C, XM_017026087.1:c.337T>C, XM_017026086.2:c.337T>C, XM_017026086.1:c.337T>C, XM_047437942.1:c.337T>C, XM_047437941.1:c.337T>C, XM_047437939.1:c.337T>C, XM_047437937.1:c.337T>C, XM_047437940.1:c.337T>C, XM_047437938.1:c.337T>C, XP_005266840.1:p.Phe113Leu, NP_004223.2:p.Phe113Leu, XP_016881576.1:p.Phe113Leu, XP_016881575.1:p.Phe113Leu, XP_047293898.1:p.Phe113Leu, XP_047293897.1:p.Phe113Leu, XP_047293895.1:p.Phe113Leu, XP_047293893.1:p.Phe113Leu, XP_047293896.1:p.Phe113Leu, XP_047293894.1:p.Phe113Leu

Select item 14899703723.

rs1489970372 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 18:70325269 (GRCh38)
18:67992505 (GRCh37)
Canonical SPDI:: NC_000018.10:70325268:C:T
Gene:: SOCS6 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000018.10:g.70325269C>T, NC_000018.9:g.67992505C>T, XM_005266783.5:c.601C>T, XM_005266783.4:c.601C>T, XM_005266783.3:c.601C>T, XM_005266783.2:c.601C>T, XM_005266783.1:c.601C>T, NM_004232.4:c.601C>T, NM_004232.3:c.601C>T, XM_017026087.2:c.601C>T, XM_017026087.1:c.601C>T, XM_017026086.2:c.601C>T, XM_017026086.1:c.601C>T, XM_047437942.1:c.601C>T, XM_047437941.1:c.601C>T, XM_047437939.1:c.601C>T, XM_047437937.1:c.601C>T, XM_047437940.1:c.601C>T, XM_047437938.1:c.601C>T

Select item 14896070984.

rs1489607098 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 18:70324747 (GRCh38)
18:67991983 (GRCh37)
Canonical SPDI:: NC_000018.10:70324746:G:T
Gene:: SOCS6 (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_000018.10:g.70324747G>T, NC_000018.9:g.67991983G>T, XM_005266783.5:c.79G>T, XM_005266783.4:c.79G>T, XM_005266783.3:c.79G>T, XM_005266783.2:c.79G>T, XM_005266783.1:c.79G>T, NM_004232.4:c.79G>T, NM_004232.3:c.79G>T, XM_017026087.2:c.79G>T, XM_017026087.1:c.79G>T, XM_017026086.2:c.79G>T, XM_017026086.1:c.79G>T, XM_047437942.1:c.79G>T, XM_047437941.1:c.79G>T, XM_047437939.1:c.79G>T, XM_047437937.1:c.79G>T, XM_047437940.1:c.79G>T, XM_047437938.1:c.79G>T, XP_005266840.1:p.Val27Leu, NP_004223.2:p.Val27Leu, XP_016881576.1:p.Val27Leu, XP_016881575.1:p.Val27Leu, XP_047293898.1:p.Val27Leu, XP_047293897.1:p.Val27Leu, XP_047293895.1:p.Val27Leu, XP_047293893.1:p.Val27Leu, XP_047293896.1:p.Val27Leu, XP_047293894.1:p.Val27Leu

Select item 14895814115.

rs1489581411 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 18:70325381 (GRCh38)
18:67992617 (GRCh37)
Canonical SPDI:: NC_000018.10:70325380:G:A
Gene:: SOCS6 (Varview)
Functional Consequence:: missense_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)
A=0.000012/3 (GnomAD_exomes)
HGVS:: NC_000018.10:g.70325381G>A, NC_000018.9:g.67992617G>A, XM_005266783.5:c.713G>A, XM_005266783.4:c.713G>A, XM_005266783.3:c.713G>A, XM_005266783.2:c.713G>A, XM_005266783.1:c.713G>A, NM_004232.4:c.713G>A, NM_004232.3:c.713G>A, XM_017026087.2:c.713G>A, XM_017026087.1:c.713G>A, XM_017026086.2:c.713G>A, XM_017026086.1:c.713G>A, XM_047437942.1:c.713G>A, XM_047437941.1:c.713G>A, XM_047437939.1:c.713G>A, XM_047437937.1:c.713G>A, XM_047437940.1:c.713G>A, XM_047437938.1:c.713G>A, XP_005266840.1:p.Arg238Gln, NP_004223.2:p.Arg238Gln, XP_016881576.1:p.Arg238Gln, XP_016881575.1:p.Arg238Gln, XP_047293898.1:p.Arg238Gln, XP_047293897.1:p.Arg238Gln, XP_047293895.1:p.Arg238Gln, XP_047293893.1:p.Arg238Gln, XP_047293896.1:p.Arg238Gln, XP_047293894.1:p.Arg238Gln

Select item 14891671926.

rs1489167192 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 18:70325595 (GRCh38)
18:67992831 (GRCh37)
Canonical SPDI:: NC_000018.10:70325594:A:G
Gene:: SOCS6 (Varview)
Functional Consequence:: synonymous_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)
HGVS:: NC_000018.10:g.70325595A>G, NC_000018.9:g.67992831A>G, XM_005266783.5:c.927A>G, XM_005266783.4:c.927A>G, XM_005266783.3:c.927A>G, XM_005266783.2:c.927A>G, XM_005266783.1:c.927A>G, NM_004232.4:c.927A>G, NM_004232.3:c.927A>G, XM_017026087.2:c.927A>G, XM_017026087.1:c.927A>G, XM_017026086.2:c.927A>G, XM_017026086.1:c.927A>G, XM_047437942.1:c.927A>G, XM_047437941.1:c.927A>G, XM_047437939.1:c.927A>G, XM_047437937.1:c.927A>G, XM_047437940.1:c.927A>G, XM_047437938.1:c.927A>G

Select item 14891156677.

rs1489115667 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 18:70324942 (GRCh38)
18:67992178 (GRCh37)
Canonical SPDI:: NC_000018.10:70324941:G:A
Gene:: SOCS6 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000018.10:g.70324942G>A, NC_000018.9:g.67992178G>A, XM_005266783.5:c.274G>A, XM_005266783.4:c.274G>A, XM_005266783.3:c.274G>A, XM_005266783.2:c.274G>A, XM_005266783.1:c.274G>A, NM_004232.4:c.274G>A, NM_004232.3:c.274G>A, XM_017026087.2:c.274G>A, XM_017026087.1:c.274G>A, XM_017026086.2:c.274G>A, XM_017026086.1:c.274G>A, XM_047437942.1:c.274G>A, XM_047437941.1:c.274G>A, XM_047437939.1:c.274G>A, XM_047437937.1:c.274G>A, XM_047437940.1:c.274G>A, XM_047437938.1:c.274G>A, XP_005266840.1:p.Gly92Ser, NP_004223.2:p.Gly92Ser, XP_016881576.1:p.Gly92Ser, XP_016881575.1:p.Gly92Ser, XP_047293898.1:p.Gly92Ser, XP_047293897.1:p.Gly92Ser, XP_047293895.1:p.Gly92Ser, XP_047293893.1:p.Gly92Ser, XP_047293896.1:p.Gly92Ser, XP_047293894.1:p.Gly92Ser

Select item 14879364788.

rs1487936478 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->AAA [Show Flanks]
Chromosome:: 18:70324716 (GRCh38)
18:67991953 (GRCh37)
Canonical SPDI:: NC_000018.10:70324716:AAAA:AAAAAAA
Gene:: SOCS6 (Varview)
Functional Consequence:: inframe_insertion,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAA=0./0 (ALFA)
AAA=0.000004/1 (TOPMED)
AAA=0.000014/2 (GnomAD)
HGVS:: NC_000018.10:g.70324718_70324720dup, NC_000018.9:g.67991954_67991956dup, XM_005266783.5:c.50_52dup, XM_005266783.4:c.50_52dup, XM_005266783.3:c.50_52dup, XM_005266783.2:c.50_52dup, XM_005266783.1:c.50_52dup, NM_004232.4:c.50_52dup, NM_004232.3:c.50_52dup, XM_017026087.2:c.50_52dup, XM_017026087.1:c.50_52dup, XM_017026086.2:c.50_52dup, XM_017026086.1:c.50_52dup, XM_047437942.1:c.50_52dup, XM_047437941.1:c.50_52dup, XM_047437939.1:c.50_52dup, XM_047437937.1:c.50_52dup, XM_047437940.1:c.50_52dup, XM_047437938.1:c.50_52dup, XP_005266840.1:p.Lys17dup, NP_004223.2:p.Lys17dup, XP_016881576.1:p.Lys17dup, XP_016881575.1:p.Lys17dup, XP_047293898.1:p.Lys17dup, XP_047293897.1:p.Lys17dup, XP_047293895.1:p.Lys17dup, XP_047293893.1:p.Lys17dup, XP_047293896.1:p.Lys17dup, XP_047293894.1:p.Lys17dup

Select item 14848440379.

rs1484844037 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 18:70324865 (GRCh38)
18:67992101 (GRCh37)
Canonical SPDI:: NC_000018.10:70324864:A:G
Gene:: SOCS6 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000018.10:g.70324865A>G, NC_000018.9:g.67992101A>G, XM_005266783.5:c.197A>G, XM_005266783.4:c.197A>G, XM_005266783.3:c.197A>G, XM_005266783.2:c.197A>G, XM_005266783.1:c.197A>G, NM_004232.4:c.197A>G, NM_004232.3:c.197A>G, XM_017026087.2:c.197A>G, XM_017026087.1:c.197A>G, XM_017026086.2:c.197A>G, XM_017026086.1:c.197A>G, XM_047437942.1:c.197A>G, XM_047437941.1:c.197A>G, XM_047437939.1:c.197A>G, XM_047437937.1:c.197A>G, XM_047437940.1:c.197A>G, XM_047437938.1:c.197A>G, XP_005266840.1:p.Asn66Ser, NP_004223.2:p.Asn66Ser, XP_016881576.1:p.Asn66Ser, XP_016881575.1:p.Asn66Ser, XP_047293898.1:p.Asn66Ser, XP_047293897.1:p.Asn66Ser, XP_047293895.1:p.Asn66Ser, XP_047293893.1:p.Asn66Ser, XP_047293896.1:p.Asn66Ser, XP_047293894.1:p.Asn66Ser

Select item 147956487810.

rs1479564878 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 18:70325212 (GRCh38)
18:67992448 (GRCh37)
Canonical SPDI:: NC_000018.10:70325211:A:G
Gene:: SOCS6 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000018.10:g.70325212A>G, NC_000018.9:g.67992448A>G, XM_005266783.5:c.544A>G, XM_005266783.4:c.544A>G, XM_005266783.3:c.544A>G, XM_005266783.2:c.544A>G, XM_005266783.1:c.544A>G, NM_004232.4:c.544A>G, NM_004232.3:c.544A>G, XM_017026087.2:c.544A>G, XM_017026087.1:c.544A>G, XM_017026086.2:c.544A>G, XM_017026086.1:c.544A>G, XM_047437942.1:c.544A>G, XM_047437941.1:c.544A>G, XM_047437939.1:c.544A>G, XM_047437937.1:c.544A>G, XM_047437940.1:c.544A>G, XM_047437938.1:c.544A>G, XP_005266840.1:p.Thr182Ala, NP_004223.2:p.Thr182Ala, XP_016881576.1:p.Thr182Ala, XP_016881575.1:p.Thr182Ala, XP_047293898.1:p.Thr182Ala, XP_047293897.1:p.Thr182Ala, XP_047293895.1:p.Thr182Ala, XP_047293893.1:p.Thr182Ala, XP_047293896.1:p.Thr182Ala, XP_047293894.1:p.Thr182Ala

Select item 147531252711.

rs1475312527 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 18:70325142 (GRCh38)
18:67992378 (GRCh37)
Canonical SPDI:: NC_000018.10:70325141:G:T
Gene:: SOCS6 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000018.10:g.70325142G>T, NC_000018.9:g.67992378G>T, XM_005266783.5:c.474G>T, XM_005266783.4:c.474G>T, XM_005266783.3:c.474G>T, XM_005266783.2:c.474G>T, XM_005266783.1:c.474G>T, NM_004232.4:c.474G>T, NM_004232.3:c.474G>T, XM_017026087.2:c.474G>T, XM_017026087.1:c.474G>T, XM_017026086.2:c.474G>T, XM_017026086.1:c.474G>T, XM_047437942.1:c.474G>T, XM_047437941.1:c.474G>T, XM_047437939.1:c.474G>T, XM_047437937.1:c.474G>T, XM_047437940.1:c.474G>T, XM_047437938.1:c.474G>T, XP_005266840.1:p.Leu158Phe, NP_004223.2:p.Leu158Phe, XP_016881576.1:p.Leu158Phe, XP_016881575.1:p.Leu158Phe, XP_047293898.1:p.Leu158Phe, XP_047293897.1:p.Leu158Phe, XP_047293895.1:p.Leu158Phe, XP_047293893.1:p.Leu158Phe, XP_047293896.1:p.Leu158Phe, XP_047293894.1:p.Leu158Phe

Select item 147334743212.

rs1473347432 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 18:70325763 (GRCh38)
18:67992999 (GRCh37)
Canonical SPDI:: NC_000018.10:70325762:T:G
Gene:: SOCS6 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (GnomAD_exomes)
G=0.000008/2 (TOPMED)
HGVS:: NC_000018.10:g.70325763T>G, NC_000018.9:g.67992999T>G, XM_005266783.5:c.1095T>G, XM_005266783.4:c.1095T>G, XM_005266783.3:c.1095T>G, XM_005266783.2:c.1095T>G, XM_005266783.1:c.1095T>G, NM_004232.4:c.1095T>G, NM_004232.3:c.1095T>G, XM_017026087.2:c.1095T>G, XM_017026087.1:c.1095T>G, XM_017026086.2:c.1095T>G, XM_017026086.1:c.1095T>G, XM_047437942.1:c.1095T>G, XM_047437941.1:c.1095T>G, XM_047437939.1:c.1095T>G, XM_047437937.1:c.1095T>G, XM_047437940.1:c.1095T>G, XM_047437938.1:c.1095T>G

Select item 147271595713.

rs1472715957 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 18:70325148 (GRCh38)
18:67992384 (GRCh37)
Canonical SPDI:: NC_000018.10:70325147:C:G
Gene:: SOCS6 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000018.10:g.70325148C>G, NC_000018.9:g.67992384C>G, XM_005266783.5:c.480C>G, XM_005266783.4:c.480C>G, XM_005266783.3:c.480C>G, XM_005266783.2:c.480C>G, XM_005266783.1:c.480C>G, NM_004232.4:c.480C>G, NM_004232.3:c.480C>G, XM_017026087.2:c.480C>G, XM_017026087.1:c.480C>G, XM_017026086.2:c.480C>G, XM_017026086.1:c.480C>G, XM_047437942.1:c.480C>G, XM_047437941.1:c.480C>G, XM_047437939.1:c.480C>G, XM_047437937.1:c.480C>G, XM_047437940.1:c.480C>G, XM_047437938.1:c.480C>G, XP_005266840.1:p.His160Gln, NP_004223.2:p.His160Gln, XP_016881576.1:p.His160Gln, XP_016881575.1:p.His160Gln, XP_047293898.1:p.His160Gln, XP_047293897.1:p.His160Gln, XP_047293895.1:p.His160Gln, XP_047293893.1:p.His160Gln, XP_047293896.1:p.His160Gln, XP_047293894.1:p.His160Gln

Select item 146960943914.

rs1469609439 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 18:70326034 (GRCh38)
18:67993270 (GRCh37)
Canonical SPDI:: NC_000018.10:70326033:G:T
Gene:: SOCS6 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000021/3 (GnomAD)
T=0.000023/6 (TOPMED)
HGVS:: NC_000018.10:g.70326034G>T, NC_000018.9:g.67993270G>T, XM_005266783.5:c.1366G>T, XM_005266783.4:c.1366G>T, XM_005266783.3:c.1366G>T, XM_005266783.2:c.1366G>T, XM_005266783.1:c.1366G>T, NM_004232.4:c.1366G>T, NM_004232.3:c.1366G>T, XM_017026087.2:c.1366G>T, XM_017026087.1:c.1366G>T, XM_017026086.2:c.1366G>T, XM_017026086.1:c.1366G>T, XM_047437942.1:c.1366G>T, XM_047437941.1:c.1366G>T, XM_047437939.1:c.1366G>T, XM_047437937.1:c.1366G>T, XM_047437940.1:c.1366G>T, XM_047437938.1:c.1366G>T, XP_005266840.1:p.Asp456Tyr, NP_004223.2:p.Asp456Tyr, XP_016881576.1:p.Asp456Tyr, XP_016881575.1:p.Asp456Tyr, XP_047293898.1:p.Asp456Tyr, XP_047293897.1:p.Asp456Tyr, XP_047293895.1:p.Asp456Tyr, XP_047293893.1:p.Asp456Tyr, XP_047293896.1:p.Asp456Tyr, XP_047293894.1:p.Asp456Tyr

Select item 146849406115.

rs1468494061 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 18:70325160 (GRCh38)
18:67992396 (GRCh37)
Canonical SPDI:: NC_000018.10:70325159:G:A
Gene:: SOCS6 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
A=0.000007/1 (GnomAD)
A=0.000015/4 (TOPMED)
HGVS:: NC_000018.10:g.70325160G>A, NC_000018.9:g.67992396G>A, XM_005266783.5:c.492G>A, XM_005266783.4:c.492G>A, XM_005266783.3:c.492G>A, XM_005266783.2:c.492G>A, XM_005266783.1:c.492G>A, NM_004232.4:c.492G>A, NM_004232.3:c.492G>A, XM_017026087.2:c.492G>A, XM_017026087.1:c.492G>A, XM_017026086.2:c.492G>A, XM_017026086.1:c.492G>A, XM_047437942.1:c.492G>A, XM_047437941.1:c.492G>A, XM_047437939.1:c.492G>A, XM_047437937.1:c.492G>A, XM_047437940.1:c.492G>A, XM_047437938.1:c.492G>A

Select item 146379883616.

rs1463798836 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 18:70326200 (GRCh38)
18:67993436 (GRCh37)
Canonical SPDI:: NC_000018.10:70326199:A:T
Gene:: SOCS6 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000018.10:g.70326200A>T, NC_000018.9:g.67993436A>T, XM_005266783.5:c.1532A>T, XM_005266783.4:c.1532A>T, XM_005266783.3:c.1532A>T, XM_005266783.2:c.1532A>T, XM_005266783.1:c.1532A>T, NM_004232.4:c.1532A>T, NM_004232.3:c.1532A>T, XM_017026087.2:c.1532A>T, XM_017026087.1:c.1532A>T, XM_017026086.2:c.1532A>T, XM_017026086.1:c.1532A>T, XM_047437942.1:c.1532A>T, XM_047437941.1:c.1532A>T, XM_047437939.1:c.1532A>T, XM_047437937.1:c.1532A>T, XM_047437940.1:c.1532A>T, XM_047437938.1:c.1532A>T, XP_005266840.1:p.Tyr511Phe, NP_004223.2:p.Tyr511Phe, XP_016881576.1:p.Tyr511Phe, XP_016881575.1:p.Tyr511Phe, XP_047293898.1:p.Tyr511Phe, XP_047293897.1:p.Tyr511Phe, XP_047293895.1:p.Tyr511Phe, XP_047293893.1:p.Tyr511Phe, XP_047293896.1:p.Tyr511Phe, XP_047293894.1:p.Tyr511Phe

Select item 146203020617.

rs1462030206 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 18:70324780 (GRCh38)
18:67992016 (GRCh37)
Canonical SPDI:: NC_000018.10:70324779:A:C
Gene:: SOCS6 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000014/2 (GnomAD)
C=0.000023/6 (TOPMED)
HGVS:: NC_000018.10:g.70324780A>C, NC_000018.9:g.67992016A>C, XM_005266783.5:c.112A>C, XM_005266783.4:c.112A>C, XM_005266783.3:c.112A>C, XM_005266783.2:c.112A>C, XM_005266783.1:c.112A>C, NM_004232.4:c.112A>C, NM_004232.3:c.112A>C, XM_017026087.2:c.112A>C, XM_017026087.1:c.112A>C, XM_017026086.2:c.112A>C, XM_017026086.1:c.112A>C, XM_047437942.1:c.112A>C, XM_047437941.1:c.112A>C, XM_047437939.1:c.112A>C, XM_047437937.1:c.112A>C, XM_047437940.1:c.112A>C, XM_047437938.1:c.112A>C, XP_005266840.1:p.Lys38Gln, NP_004223.2:p.Lys38Gln, XP_016881576.1:p.Lys38Gln, XP_016881575.1:p.Lys38Gln, XP_047293898.1:p.Lys38Gln, XP_047293897.1:p.Lys38Gln, XP_047293895.1:p.Lys38Gln, XP_047293893.1:p.Lys38Gln, XP_047293896.1:p.Lys38Gln, XP_047293894.1:p.Lys38Gln

Select item 146072726418.

rs1460727264 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 18:70325306 (GRCh38)
18:67992542 (GRCh37)
Canonical SPDI:: NC_000018.10:70325305:T:C
Gene:: SOCS6 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000018.10:g.70325306T>C, NC_000018.9:g.67992542T>C, XM_005266783.5:c.638T>C, XM_005266783.4:c.638T>C, XM_005266783.3:c.638T>C, XM_005266783.2:c.638T>C, XM_005266783.1:c.638T>C, NM_004232.4:c.638T>C, NM_004232.3:c.638T>C, XM_017026087.2:c.638T>C, XM_017026087.1:c.638T>C, XM_017026086.2:c.638T>C, XM_017026086.1:c.638T>C, XM_047437942.1:c.638T>C, XM_047437941.1:c.638T>C, XM_047437939.1:c.638T>C, XM_047437937.1:c.638T>C, XM_047437940.1:c.638T>C, XM_047437938.1:c.638T>C, XP_005266840.1:p.Ile213Thr, NP_004223.2:p.Ile213Thr, XP_016881576.1:p.Ile213Thr, XP_016881575.1:p.Ile213Thr, XP_047293898.1:p.Ile213Thr, XP_047293897.1:p.Ile213Thr, XP_047293895.1:p.Ile213Thr, XP_047293893.1:p.Ile213Thr, XP_047293896.1:p.Ile213Thr, XP_047293894.1:p.Ile213Thr

Select item 146012122419.

rs1460121224 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 18:70325415 (GRCh38)
18:67992651 (GRCh37)
Canonical SPDI:: NC_000018.10:70325414:A:G
Gene:: SOCS6 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
HGVS:: NC_000018.10:g.70325415A>G, NC_000018.9:g.67992651A>G, XM_005266783.5:c.747A>G, XM_005266783.4:c.747A>G, XM_005266783.3:c.747A>G, XM_005266783.2:c.747A>G, XM_005266783.1:c.747A>G, NM_004232.4:c.747A>G, NM_004232.3:c.747A>G, XM_017026087.2:c.747A>G, XM_017026087.1:c.747A>G, XM_017026086.2:c.747A>G, XM_017026086.1:c.747A>G, XM_047437942.1:c.747A>G, XM_047437941.1:c.747A>G, XM_047437939.1:c.747A>G, XM_047437937.1:c.747A>G, XM_047437940.1:c.747A>G, XM_047437938.1:c.747A>G

Select item 145960784520.

rs1459607845 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 18:70324809 (GRCh38)
18:67992045 (GRCh37)
Canonical SPDI:: NC_000018.10:70324808:T:C
Gene:: SOCS6 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000018.10:g.70324809T>C, NC_000018.9:g.67992045T>C, XM_005266783.5:c.141T>C, XM_005266783.4:c.141T>C, XM_005266783.3:c.141T>C, XM_005266783.2:c.141T>C, XM_005266783.1:c.141T>C, NM_004232.4:c.141T>C, NM_004232.3:c.141T>C, XM_017026087.2:c.141T>C, XM_017026087.1:c.141T>C, XM_017026086.2:c.141T>C, XM_017026086.1:c.141T>C, XM_047437942.1:c.141T>C, XM_047437941.1:c.141T>C, XM_047437939.1:c.141T>C, XM_047437937.1:c.141T>C, XM_047437940.1:c.141T>C, XM_047437938.1:c.141T>C

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Result Filters

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Items: 1 to 20 of 504

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