SNP Links for Protein (Select 20070199) - SNP

Links from Protein

Items: 1 to 20 of 463

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Select item 14906675581.

rs1490667558 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 19:17232526 (GRCh38)
19:17343335 (GRCh37)
Canonical SPDI:: NC_000019.10:17232525:G:A
Gene:: NR2F6 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000019.10:g.17232526G>A, NC_000019.9:g.17343335G>A, NM_005234.4:c.1041C>T, NM_005234.3:c.1041C>T

Select item 14905851362.

rs1490585136 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 19:17235541 (GRCh38)
19:17346350 (GRCh37)
Canonical SPDI:: NC_000019.10:17235540:C:A,NC_000019.10:17235540:C:T
Gene:: NR2F6 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000019.10:g.17235541C>A, NC_000019.10:g.17235541C>T, NC_000019.9:g.17346350C>A, NC_000019.9:g.17346350C>T, NM_005234.4:c.898G>T, NM_005234.4:c.898G>A, NM_005234.3:c.898G>T, NM_005234.3:c.898G>A, NP_005225.2:p.Ala300Ser, NP_005225.2:p.Ala300Thr

Select item 14871321803.

rs1487132180 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 19:17232475 (GRCh38)
19:17343284 (GRCh37)
Canonical SPDI:: NC_000019.10:17232474:A:T
Gene:: NR2F6 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000019.10:g.17232475A>T, NC_000019.9:g.17343284A>T, NM_005234.4:c.1092T>A, NM_005234.3:c.1092T>A

Select item 14854201234.

rs1485420123 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 19:17235893 (GRCh38)
19:17346702 (GRCh37)
Canonical SPDI:: NC_000019.10:17235892:C:T
Gene:: NR2F6 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
T=0.000035/1 (TOMMO)
HGVS:: NC_000019.10:g.17235893C>T, NC_000019.9:g.17346702C>T, NM_005234.4:c.546G>A, NM_005234.3:c.546G>A

Select item 14853931725.

rs1485393172 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 19:17245155 (GRCh38)
19:17355964 (GRCh37)
Canonical SPDI:: NC_000019.10:17245154:G:A
Gene:: NR2F6 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000071/1 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000023/6 (TOPMED)
A=0.002762/46 (TOMMO)
A=0.002888/8 (KOREAN)
A=0.00454/8 (Korea1K)
HGVS:: NC_000019.10:g.17245155G>A, NC_000019.9:g.17355964G>A, NM_005234.4:c.66C>T, NM_005234.3:c.66C>T

Select item 14813240956.

rs1481324095 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 19:17235764 (GRCh38)
19:17346573 (GRCh37)
Canonical SPDI:: NC_000019.10:17235763:C:T
Gene:: NR2F6 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
HGVS:: NC_000019.10:g.17235764C>T, NC_000019.9:g.17346573C>T, NM_005234.4:c.675G>A, NM_005234.3:c.675G>A

Select item 14805617037.

rs1480561703 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 19:17235673 (GRCh38)
19:17346482 (GRCh37)
Canonical SPDI:: NC_000019.10:17235672:T:C
Gene:: NR2F6 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: C=0.00001/1 (GnomAD_exomes)
HGVS:: NC_000019.10:g.17235673T>C, NC_000019.9:g.17346482T>C, NM_005234.4:c.766A>G, NM_005234.3:c.766A>G, NP_005225.2:p.Thr256Ala

Select item 14792242798.

rs1479224279 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 19:17235778 (GRCh38)
19:17346587 (GRCh37)
Canonical SPDI:: NC_000019.10:17235777:G:A
Gene:: NR2F6 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: A=0.00001/1 (GnomAD_exomes)
HGVS:: NC_000019.10:g.17235778G>A, NC_000019.9:g.17346587G>A, NM_005234.4:c.661C>T, NM_005234.3:c.661C>T, NP_005225.2:p.Pro221Ser

Select item 14779195899.

rs1477919589 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 19:17235926 (GRCh38)
19:17346735 (GRCh37)
Canonical SPDI:: NC_000019.10:17235925:C:A
Gene:: NR2F6 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
HGVS:: NC_000019.10:g.17235926C>A, NC_000019.9:g.17346735C>A, NM_005234.4:c.513G>T, NM_005234.3:c.513G>T

Select item 147442152210.

rs1474421522 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 19:17235785 (GRCh38)
19:17346594 (GRCh37)
Canonical SPDI:: NC_000019.10:17235784:G:A
Gene:: NR2F6 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000011/3 (TOPMED)
HGVS:: NC_000019.10:g.17235785G>A, NC_000019.9:g.17346594G>A, NM_005234.4:c.654C>T, NM_005234.3:c.654C>T

Select item 146961740511.

rs1469617405 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 19:17236046 (GRCh38)
19:17346855 (GRCh37)
Canonical SPDI:: NC_000019.10:17236045:G:A,NC_000019.10:17236045:G:T
Gene:: NR2F6 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
HGVS:: NC_000019.10:g.17236046G>A, NC_000019.10:g.17236046G>T, NC_000019.9:g.17346855G>A, NC_000019.9:g.17346855G>T, NM_005234.4:c.393C>T, NM_005234.4:c.393C>A, NM_005234.3:c.393C>T, NM_005234.3:c.393C>A

Select item 146884182712.

rs1468841827 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 19:17236043 (GRCh38)
19:17346852 (GRCh37)
Canonical SPDI:: NC_000019.10:17236042:C:G,NC_000019.10:17236042:C:T
Gene:: NR2F6 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.0002/1 (ALFA)
G=0.0002/1 (Estonian)
HGVS:: NC_000019.10:g.17236043C>G, NC_000019.10:g.17236043C>T, NC_000019.9:g.17346852C>G, NC_000019.9:g.17346852C>T, NM_005234.4:c.396G>C, NM_005234.4:c.396G>A, NM_005234.3:c.396G>C, NM_005234.3:c.396G>A

Select item 146804032613.

rs1468040326 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 19:17235699 (GRCh38)
19:17346508 (GRCh37)
Canonical SPDI:: NC_000019.10:17235698:G:A
Gene:: NR2F6 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000047/1 (ALFA)
A=0.000008/2 (TOPMED)
A=0.000034/3 (GnomAD_exomes)
HGVS:: NC_000019.10:g.17235699G>A, NC_000019.9:g.17346508G>A, NM_005234.4:c.740C>T, NM_005234.3:c.740C>T, NP_005225.2:p.Ala247Val

Select item 146401942014.

rs1464019420 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 19:17235500 (GRCh38)
19:17346309 (GRCh37)
Canonical SPDI:: NC_000019.10:17235499:G:A
Gene:: NR2F6 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: A=0.00001/2 (GnomAD_exomes)
HGVS:: NC_000019.10:g.17235500G>A, NC_000019.9:g.17346309G>A, NM_005234.4:c.939C>T, NM_005234.3:c.939C>T

Select item 146165962715.

rs1461659627 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 19:17245035 (GRCh38)
19:17355844 (GRCh37)
Canonical SPDI:: NC_000019.10:17245034:C:T
Gene:: NR2F6 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000008/2 (TOPMED)
T=0.001121/2 (Korea1K)
HGVS:: NC_000019.10:g.17245035C>T, NC_000019.9:g.17355844C>T, NM_005234.4:c.186G>A, NM_005234.3:c.186G>A

Select item 146138477216.

rs1461384772 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 19:17235710 (GRCh38)
19:17346519 (GRCh37)
Canonical SPDI:: NC_000019.10:17235709:G:A
Gene:: NR2F6 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
HGVS:: NC_000019.10:g.17235710G>A, NC_000019.9:g.17346519G>A, NM_005234.4:c.729C>T, NM_005234.3:c.729C>T

Select item 146040518817.

rs1460405188 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 19:17235626 (GRCh38)
19:17346435 (GRCh37)
Canonical SPDI:: NC_000019.10:17235625:G:A,NC_000019.10:17235625:G:T
Gene:: NR2F6 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
A=0.000014/2 (GnomAD_exomes)
HGVS:: NC_000019.10:g.17235626G>A, NC_000019.10:g.17235626G>T, NC_000019.9:g.17346435G>A, NC_000019.9:g.17346435G>T, NM_005234.4:c.813C>T, NM_005234.4:c.813C>A, NM_005234.3:c.813C>T, NM_005234.3:c.813C>A

Select item 146024214818.

rs1460242148 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 19:17235868 (GRCh38)
19:17346677 (GRCh37)
Canonical SPDI:: NC_000019.10:17235867:C:T
Gene:: NR2F6 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000008/2 (TOPMED)
HGVS:: NC_000019.10:g.17235868C>T, NC_000019.9:g.17346677C>T, NM_005234.4:c.571G>A, NM_005234.3:c.571G>A, NP_005225.2:p.Gly191Ser

Select item 145996089319.

rs1459960893 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 19:17232477 (GRCh38)
19:17343286 (GRCh37)
Canonical SPDI:: NC_000019.10:17232476:G:A
Gene:: NR2F6 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000071/1 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000014/2 (GnomAD)
HGVS:: NC_000019.10:g.17232477G>A, NC_000019.9:g.17343286G>A, NM_005234.4:c.1090C>T, NM_005234.3:c.1090C>T, NP_005225.2:p.Pro364Ser

Select item 145923522120.

rs1459235221 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 19:17240721 (GRCh38)
19:17351530 (GRCh37)
Canonical SPDI:: NC_000019.10:17240720:C:T
Gene:: NR2F6 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000019.10:g.17240721C>T, NC_000019.9:g.17351530C>T, NM_005234.4:c.323G>A, NM_005234.3:c.323G>A, NP_005225.2:p.Cys108Tyr

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Items: 1 to 20 of 463

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