SNP Links for Protein (Select 11128015) - SNP

Links from Protein

Items: 1 to 20 of 215

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Select item 14898132671.

rs1489813267 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 9:21350571 (GRCh38)
9:21350570 (GRCh37)
Canonical SPDI:: NC_000009.12:21350570:T:C
Gene:: IFNA6 (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=0.000007/1 (GnomAD)
C=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000009.12:g.21350571T>C, NC_000009.11:g.21350570T>C, NM_021002.2:c.317A>G, NP_066282.1:p.Asp106Gly

Select item 14877500522.

rs1487750052 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 9:21350627 (GRCh38)
9:21350626 (GRCh37)
Canonical SPDI:: NC_000009.12:21350626:G:A,NC_000009.12:21350626:G:C
Gene:: IFNA6 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000009.12:g.21350627G>A, NC_000009.12:g.21350627G>C, NC_000009.11:g.21350626G>A, NC_000009.11:g.21350626G>C, NM_021002.2:c.261C>T, NM_021002.2:c.261C>G

Select item 14870819963.

rs1487081996 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 9:21350796 (GRCh38)
9:21350795 (GRCh37)
Canonical SPDI:: NC_000009.12:21350795:C:T
Gene:: IFNA6 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: T=0.000071/1 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000009.12:g.21350796C>T, NC_000009.11:g.21350795C>T, NM_021002.2:c.92G>A, NP_066282.1:p.Ser31Asn

Select item 14833768754.

rs1483376875 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 9:21350698 (GRCh38)
9:21350697 (GRCh37)
Canonical SPDI:: NC_000009.12:21350697:C:A
Gene:: IFNA6 (Varview)
Functional Consequence:: coding_sequence_variant,stop_gained
Validated:: by frequency
MAF:: A=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000009.12:g.21350698C>A, NC_000009.11:g.21350697C>A, NM_021002.2:c.190G>T, NP_066282.1:p.Glu64Ter

Select item 14805935625.

rs1480593562 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 9:21350762 (GRCh38)
9:21350761 (GRCh37)
Canonical SPDI:: NC_000009.12:21350761:T:A
Gene:: IFNA6 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000009.12:g.21350762T>A, NC_000009.11:g.21350761T>A, NM_021002.2:c.126A>T

Select item 14775993556.

rs1477599355 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 9:21350879 (GRCh38)
9:21350878 (GRCh37)
Canonical SPDI:: NC_000009.12:21350878:C:T
Gene:: IFNA6 (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_000009.12:g.21350879C>T, NC_000009.11:g.21350878C>T, NM_021002.2:c.9G>A

Select item 14725364557.

rs1472536455 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 9:21350346 (GRCh38)
9:21350345 (GRCh37)
Canonical SPDI:: NC_000009.12:21350345:A:G
Gene:: IFNA6 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by cluster
MAF:: G=0.000004/1 (GnomAD_exomes)
G=0.000007/1 (GnomAD)
HGVS:: NC_000009.12:g.21350346A>G, NC_000009.11:g.21350345A>G, NM_021002.2:c.542T>C, NP_066282.1:p.Leu181Ser

Select item 14680541098.

rs1468054109 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 9:21350561 (GRCh38)
9:21350560 (GRCh37)
Canonical SPDI:: NC_000009.12:21350560:A:G
Gene:: IFNA6 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_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_000009.12:g.21350561A>G, NC_000009.11:g.21350560A>G, NM_021002.2:c.327T>C

Select item 14672049469.

rs1467204946 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 9:21350779 (GRCh38)
9:21350778 (GRCh37)
Canonical SPDI:: NC_000009.12:21350778:T:A
Gene:: IFNA6 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000009.12:g.21350779T>A, NC_000009.11:g.21350778T>A, NM_021002.2:c.109A>T, NP_066282.1:p.Thr37Ser

Select item 146460437710.

rs1464604377 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 9:21350510 (GRCh38)
9:21350509 (GRCh37)
Canonical SPDI:: NC_000009.12:21350509:C:A
Gene:: IFNA6 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
HGVS:: NC_000009.12:g.21350510C>A, NC_000009.11:g.21350509C>A, NM_021002.2:c.378G>T, NP_066282.1:p.Glu126Asp

Select item 145875246911.

rs1458752469 [Homo sapiens]

Variant type:: DELINS
Alleles:: CTC>- [Show Flanks]
Chromosome:: 9:21350754 (GRCh38)
9:21350753 (GRCh37)
Canonical SPDI:: NC_000009.12:21350750:CTCCTC:CTC
Gene:: IFNA6 (Varview)
Functional Consequence:: coding_sequence_variant,inframe_deletion
Validated:: by frequency,by cluster
MAF:: -=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000009.12:g.21350751CTC[1], NC_000009.11:g.21350750CTC[1], NM_021002.2:c.132GAG[1], NP_066282.1:p.Arg46del

Select item 145080962912.

rs1450809629 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 9:21350780 (GRCh38)
9:21350779 (GRCh37)
Canonical SPDI:: NC_000009.12:21350779:C:A,NC_000009.12:21350779:C:T
Gene:: IFNA6 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000084/1 (ALFA)
A=0.000011/3 (TOPMED)
T=0.001638/3 (Korea1K)
HGVS:: NC_000009.12:g.21350780C>A, NC_000009.12:g.21350780C>T, NC_000009.11:g.21350779C>A, NC_000009.11:g.21350779C>T, NM_021002.2:c.108G>T, NM_021002.2:c.108G>A, NP_066282.1:p.Arg36Ser

Select item 144886269013.

rs1448862690 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 9:21350729 (GRCh38)
9:21350728 (GRCh37)
Canonical SPDI:: NC_000009.12:21350728:C:T
Gene:: IFNA6 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000009.12:g.21350729C>T, NC_000009.11:g.21350728C>T, NM_021002.2:c.159G>A

Select item 144813070014.

rs1448130700 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 9:21350468 (GRCh38)
9:21350467 (GRCh37)
Canonical SPDI:: NC_000009.12:21350467:G:A,NC_000009.12:21350467:G:C
Gene:: IFNA6 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
A=0.000008/2 (TOPMED)
C=0.000106/2 (TOMMO)
HGVS:: NC_000009.12:g.21350468G>A, NC_000009.12:g.21350468G>C, NC_000009.11:g.21350467G>A, NC_000009.11:g.21350467G>C, NM_021002.2:c.420C>T, NM_021002.2:c.420C>G, NP_066282.1:p.Ile140Met

Select item 144603731515.

rs1446037315 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 9:21350878 (GRCh38)
9:21350877 (GRCh37)
Canonical SPDI:: NC_000009.12:21350877:G:A,NC_000009.12:21350877:G:C
Gene:: IFNA6 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000031/1 (ALFA)
A=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000009.12:g.21350878G>A, NC_000009.12:g.21350878G>C, NC_000009.11:g.21350877G>A, NC_000009.11:g.21350877G>C, NM_021002.2:c.10C>T, NM_021002.2:c.10C>G, NP_066282.1:p.Pro4Ser, NP_066282.1:p.Pro4Ala

Select item 143774110316.

rs1437741103 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 9:21350827 (GRCh38)
9:21350826 (GRCh37)
Canonical SPDI:: NC_000009.12:21350826:A:G
Gene:: IFNA6 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000009.12:g.21350827A>G, NC_000009.11:g.21350826A>G, NM_021002.2:c.61T>C, NP_066282.1:p.Ser21Pro

Select item 142776401317.

rs1427764013 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 9:21350765 (GRCh38)
9:21350764 (GRCh37)
Canonical SPDI:: NC_000009.12:21350764:C:T
Gene:: IFNA6 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000009.12:g.21350765C>T, NC_000009.11:g.21350764C>T, NM_021002.2:c.123G>A

Select item 142369224518.

rs1423692245 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 9:21350507 (GRCh38)
9:21350506 (GRCh37)
Canonical SPDI:: NC_000009.12:21350506:C:A
Gene:: IFNA6 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
A=0.000004/1 (TOPMED)
HGVS:: NC_000009.12:g.21350507C>A, NC_000009.11:g.21350506C>A, NM_021002.2:c.381G>T

Select item 142330914019.

rs1423309140 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 9:21350650 (GRCh38)
9:21350649 (GRCh37)
Canonical SPDI:: NC_000009.12:21350649:G:A
Gene:: IFNA6 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000009.12:g.21350650G>A, NC_000009.11:g.21350649G>A, NM_021002.2:c.238C>T, NP_066282.1:p.Leu80Phe

Select item 142023185720.

rs1420231857 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 9:21350356 (GRCh38)
9:21350355 (GRCh37)
Canonical SPDI:: NC_000009.12:21350355:A:T
Gene:: IFNA6 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000009.12:g.21350356A>T, NC_000009.11:g.21350355A>T, NM_021002.2:c.532T>A, NP_066282.1:p.Ser178Thr

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