SNP Links for Protein (Select 543583770) - SNP

Links from Protein

Items: 1 to 20 of 249

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Select item 14810528781.

rs1481052878 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 15:101277376 (GRCh38)
15:101817581 (GRCh37)
Canonical SPDI:: NC_000015.10:101277375:C:A,NC_000015.10:101277375:C:T
Gene:: SELENOS (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
HGVS:: NC_000015.10:g.101277376C>A, NC_000015.10:g.101277376C>T, NC_000015.9:g.101817581C>A, NC_000015.9:g.101817581C>T, NG_013322.1:g.5120G>T, NG_013322.1:g.5120G>A, NM_018445.6:c.42G>T, NM_018445.6:c.42G>A, NM_018445.5:c.42G>T, NM_018445.5:c.42G>A, NM_018445.4:c.42G>T, NM_018445.4:c.42G>A, NM_203472.3:c.42G>T, NM_203472.3:c.42G>A, NM_203472.2:c.42G>T, NM_203472.2:c.42G>A, NM_203472.1:c.42G>T, NM_203472.1:c.42G>A

Select item 14795502262.

rs1479550226 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 15:101275309 (GRCh38)
15:101815514 (GRCh37)
Canonical SPDI:: NC_000015.10:101275308:T:C
Gene:: SELENOS (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000015.10:g.101275309T>C, NC_000015.9:g.101815514T>C, NG_013322.1:g.7187A>G, NM_018445.6:c.264A>G, NM_018445.5:c.264A>G, NM_018445.4:c.264A>G, NM_203472.3:c.264A>G, NM_203472.2:c.264A>G, NM_203472.1:c.264A>G

Select item 14786799643.

rs1478679964 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 15:101276585 (GRCh38)
15:101816790 (GRCh37)
Canonical SPDI:: NC_000015.10:101276584:C:G,NC_000015.10:101276584:C:T
Gene:: SELENOS (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000015.10:g.101276585C>G, NC_000015.10:g.101276585C>T, NC_000015.9:g.101816790C>G, NC_000015.9:g.101816790C>T, NG_013322.1:g.5911G>C, NG_013322.1:g.5911G>A, NM_018445.6:c.167G>C, NM_018445.6:c.167G>A, NM_018445.5:c.167G>C, NM_018445.5:c.167G>A, NM_018445.4:c.167G>C, NM_018445.4:c.167G>A, NM_203472.3:c.167G>C, NM_203472.3:c.167G>A, NM_203472.2:c.167G>C, NM_203472.2:c.167G>A, NM_203472.1:c.167G>C, NM_203472.1:c.167G>A, NP_060915.2:p.Arg56Thr, NP_060915.2:p.Arg56Lys, NP_982298.2:p.Arg56Thr, NP_982298.2:p.Arg56Lys

Select item 14776268514.

rs1477626851 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 15:101274478 (GRCh38)
15:101814683 (GRCh37)
Canonical SPDI:: NC_000015.10:101274477:C:T
Gene:: SELENOS (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000015.10:g.101274478C>T, NC_000015.9:g.101814683C>T, NG_013322.1:g.8018G>A, NM_018445.6:c.426G>A, NM_018445.5:c.426G>A, NM_018445.4:c.426G>A, NM_203472.3:c.426G>A, NM_203472.2:c.426G>A, NM_203472.1:c.426G>A

Select item 14756733405.

rs1475673340 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 15:101276640 (GRCh38)
15:101816845 (GRCh37)
Canonical SPDI:: NC_000015.10:101276639:C:T
Gene:: SELENOS (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000008/2 (GnomAD_exomes)
T=0.000008/2 (TOPMED)
HGVS:: NC_000015.10:g.101276640C>T, NC_000015.9:g.101816845C>T, NG_013322.1:g.5856G>A, NM_018445.6:c.112G>A, NM_018445.5:c.112G>A, NM_018445.4:c.112G>A, NM_203472.3:c.112G>A, NM_203472.2:c.112G>A, NM_203472.1:c.112G>A, NP_060915.2:p.Val38Ile, NP_982298.2:p.Val38Ile

Select item 14750213386.

rs1475021338 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 15:101277412 (GRCh38)
15:101817617 (GRCh37)
Canonical SPDI:: NC_000015.10:101277411:T:G
Gene:: SELENOS (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
HGVS:: NC_000015.10:g.101277412T>G, NC_000015.9:g.101817617T>G, NG_013322.1:g.5084A>C, NM_018445.6:c.6A>C, NM_018445.5:c.6A>C, NM_018445.4:c.6A>C, NM_203472.3:c.6A>C, NM_203472.2:c.6A>C, NM_203472.1:c.6A>C, NP_060915.2:p.Glu2Asp, NP_982298.2:p.Glu2Asp

Select item 14741105067.

rs1474110506 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 15:101277380 (GRCh38)
15:101817585 (GRCh37)
Canonical SPDI:: NC_000015.10:101277379:G:A,NC_000015.10:101277379:G:T
Gene:: SELENOS (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.00001/1 (GnomAD_exomes)
HGVS:: NC_000015.10:g.101277380G>A, NC_000015.10:g.101277380G>T, NC_000015.9:g.101817585G>A, NC_000015.9:g.101817585G>T, NG_013322.1:g.5116C>T, NG_013322.1:g.5116C>A, NM_018445.6:c.38C>T, NM_018445.6:c.38C>A, NM_018445.5:c.38C>T, NM_018445.5:c.38C>A, NM_018445.4:c.38C>T, NM_018445.4:c.38C>A, NM_203472.3:c.38C>T, NM_203472.3:c.38C>A, NM_203472.2:c.38C>T, NM_203472.2:c.38C>A, NM_203472.1:c.38C>T, NM_203472.1:c.38C>A, NP_060915.2:p.Ala13Val, NP_060915.2:p.Ala13Asp, NP_982298.2:p.Ala13Val, NP_982298.2:p.Ala13Asp

Select item 14646604058.

rs1464660405 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->AGCCA [Show Flanks]
Chromosome:: 15:101276648 (GRCh38)
15:101816854 (GRCh37)
Canonical SPDI:: NC_000015.10:101276648:AGCCA:AGCCAAGCCA
Gene:: SELENOS (Varview)
Functional Consequence:: coding_sequence_variant,frameshift_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AGCCAAGCCA=0./0 (ALFA)
AGCCA=0.000004/1 (TOPMED)
AGCCA=0.000014/2 (GnomAD)
HGVS:: NC_000015.10:g.101276649_101276653dup, NC_000015.9:g.101816854_101816858dup, NG_013322.1:g.5843_5847dup, NM_018445.6:c.99_103dup, NM_018445.5:c.99_103dup, NM_018445.4:c.99_103dup, NM_203472.3:c.99_103dup, NM_203472.2:c.99_103dup, NM_203472.1:c.99_103dup, NP_060915.2:p.Trp35fs, NP_982298.2:p.Trp35fs

Select item 14569712169.

rs1456971216 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 15:101274603 (GRCh38)
15:101814808 (GRCh37)
Canonical SPDI:: NC_000015.10:101274602:T:C
Gene:: SELENOS (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000014/2 (GnomAD)
HGVS:: NC_000015.10:g.101274603T>C, NC_000015.9:g.101814808T>C, NG_013322.1:g.7893A>G, NM_018445.6:c.397A>G, NM_018445.5:c.397A>G, NM_018445.4:c.397A>G, NM_203472.3:c.397A>G, NM_203472.2:c.397A>G, NM_203472.1:c.397A>G, NP_060915.2:p.Lys133Glu, NP_982298.2:p.Lys133Glu

Select item 145625013310.

rs1456250133 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 15:101274669 (GRCh38)
15:101814874 (GRCh37)
Canonical SPDI:: NC_000015.10:101274668:T:C
Gene:: SELENOS (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
HGVS:: NC_000015.10:g.101274669T>C, NC_000015.9:g.101814874T>C, NG_013322.1:g.7827A>G, NM_018445.6:c.331A>G, NM_018445.5:c.331A>G, NM_018445.4:c.331A>G, NM_203472.3:c.331A>G, NM_203472.2:c.331A>G, NM_203472.1:c.331A>G, NP_060915.2:p.Lys111Glu, NP_982298.2:p.Lys111Glu

Select item 145271718711.

rs1452717187 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 15:101276569 (GRCh38)
15:101816774 (GRCh37)
Canonical SPDI:: NC_000015.10:101276568:C:A
Gene:: SELENOS (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: A=0.000071/1 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000015.10:g.101276569C>A, NC_000015.9:g.101816774C>A, NG_013322.1:g.5927G>T, NM_018445.6:c.183G>T, NM_018445.5:c.183G>T, NM_018445.4:c.183G>T, NM_203472.3:c.183G>T, NM_203472.2:c.183G>T, NM_203472.1:c.183G>T, NP_060915.2:p.Arg61Ser, NP_982298.2:p.Arg61Ser

Select item 144973207912.

rs1449732079 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 15:101274671 (GRCh38)
15:101814876 (GRCh37)
Canonical SPDI:: NC_000015.10:101274670:T:G
Gene:: SELENOS (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000057/2 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000015.10:g.101274671T>G, NC_000015.9:g.101814876T>G, NG_013322.1:g.7825A>C, NM_018445.6:c.329A>C, NM_018445.5:c.329A>C, NM_018445.4:c.329A>C, NM_203472.3:c.329A>C, NM_203472.2:c.329A>C, NM_203472.1:c.329A>C, NP_060915.2:p.Glu110Ala, NP_982298.2:p.Glu110Ala

Select item 144407340213.

rs1444073402 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 15:101276596 (GRCh38)
15:101816801 (GRCh37)
Canonical SPDI:: NC_000015.10:101276595:G:A
Gene:: SELENOS (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000034/9 (TOPMED)
HGVS:: NC_000015.10:g.101276596G>A, NC_000015.9:g.101816801G>A, NG_013322.1:g.5900C>T, NM_018445.6:c.156C>T, NM_018445.5:c.156C>T, NM_018445.4:c.156C>T, NM_203472.3:c.156C>T, NM_203472.2:c.156C>T, NM_203472.1:c.156C>T

Select item 144238185414.

rs1442381854 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 15:101276544 (GRCh38)
15:101816749 (GRCh37)
Canonical SPDI:: NC_000015.10:101276543:C:T
Gene:: SELENOS (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000015.10:g.101276544C>T, NC_000015.9:g.101816749C>T, NG_013322.1:g.5952G>A, NM_018445.6:c.208G>A, NM_018445.5:c.208G>A, NM_018445.4:c.208G>A, NM_203472.3:c.208G>A, NM_203472.2:c.208G>A, NM_203472.1:c.208G>A, NP_060915.2:p.Val70Met, NP_982298.2:p.Val70Met

Select item 144091080415.

rs1440910804 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 15:101277348 (GRCh38)
15:101817553 (GRCh37)
Canonical SPDI:: NC_000015.10:101277347:T:C
Gene:: SELENOS (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
HGVS:: NC_000015.10:g.101277348T>C, NC_000015.9:g.101817553T>C, NG_013322.1:g.5148A>G, NM_018445.6:c.70A>G, NM_018445.5:c.70A>G, NM_018445.4:c.70A>G, NM_203472.3:c.70A>G, NM_203472.2:c.70A>G, NM_203472.1:c.70A>G, NP_060915.2:p.Thr24Ala, NP_982298.2:p.Thr24Ala

Select item 143916128116.

rs1439161281 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 15:101275323 (GRCh38)
15:101815528 (GRCh37)
Canonical SPDI:: NC_000015.10:101275322:C:T
Gene:: SELENOS (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
HGVS:: NC_000015.10:g.101275323C>T, NC_000015.9:g.101815528C>T, NG_013322.1:g.7173G>A, NM_018445.6:c.250G>A, NM_018445.5:c.250G>A, NM_018445.4:c.250G>A, NM_203472.3:c.250G>A, NM_203472.2:c.250G>A, NM_203472.1:c.250G>A, NP_060915.2:p.Ala84Thr, NP_982298.2:p.Ala84Thr

Select item 142592068117.

rs1425920681 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 15:101275298 (GRCh38)
15:101815503 (GRCh37)
Canonical SPDI:: NC_000015.10:101275297:T:C
Gene:: SELENOS (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)
C=0.000007/1 (GnomAD)
HGVS:: NC_000015.10:g.101275298T>C, NC_000015.9:g.101815503T>C, NG_013322.1:g.7198A>G, NM_018445.6:c.275A>G, NM_018445.5:c.275A>G, NM_018445.4:c.275A>G, NM_203472.3:c.275A>G, NM_203472.2:c.275A>G, NM_203472.1:c.275A>G, NP_060915.2:p.Glu92Gly, NP_982298.2:p.Glu92Gly

Select item 142545598818.

rs1425455988 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 15:101274430 (GRCh38)
15:101814635 (GRCh37)
Canonical SPDI:: NC_000015.10:101274429:C:A,NC_000015.10:101274429:C:T
Gene:: SELENOS (Varview)
Functional Consequence:: synonymous_variant,missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
T=0.000004/1 (GnomAD_exomes)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000015.10:g.101274430C>A, NC_000015.10:g.101274430C>T, NC_000015.9:g.101814635C>A, NC_000015.9:g.101814635C>T, NG_013322.1:g.8066G>T, NG_013322.1:g.8066G>A, NM_018445.6:c.474G>T, NM_018445.6:c.474G>A, NM_018445.5:c.474G>T, NM_018445.5:c.474G>A, NM_018445.4:c.474G>T, NM_018445.4:c.474G>A, NM_203472.3:c.474G>T, NM_203472.3:c.474G>A, NM_203472.2:c.474G>T, NM_203472.2:c.474G>A, NM_203472.1:c.474G>T, NM_203472.1:c.474G>A, NP_060915.2:p.Leu158Phe, NP_982298.2:p.Leu158Phe

Select item 142538364619.

rs1425383646 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 15:101274490 (GRCh38)
15:101814695 (GRCh37)
Canonical SPDI:: NC_000015.10:101274489:T:C
Gene:: SELENOS (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000011/3 (TOPMED)
HGVS:: NC_000015.10:g.101274490T>C, NC_000015.9:g.101814695T>C, NG_013322.1:g.8006A>G, NM_018445.6:c.414A>G, NM_018445.5:c.414A>G, NM_018445.4:c.414A>G, NM_203472.3:c.414A>G, NM_203472.2:c.414A>G, NM_203472.1:c.414A>G

Select item 142356599020.

rs1423565990 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 15:101276593 (GRCh38)
15:101816798 (GRCh37)
Canonical SPDI:: NC_000015.10:101276592:G:C
Gene:: SELENOS (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000015.10:g.101276593G>C, NC_000015.9:g.101816798G>C, NG_013322.1:g.5903C>G, NM_018445.6:c.159C>G, NM_018445.5:c.159C>G, NM_018445.4:c.159C>G, NM_203472.3:c.159C>G, NM_203472.2:c.159C>G, NM_203472.1:c.159C>G

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