SNP Links for Protein (Select 19924163) - SNP

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Links from Protein

Items: 1 to 20 of 374

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Select item 14896296241.

rs1489629624 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:26067382 (GRCh38)
1:26393873 (GRCh37)
Canonical SPDI:: NC_000001.11:26067381:G:A
Gene:: TRIM63 (Varview)
Functional Consequence:: missense_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=0.000011/3 (TOPMED)
HGVS:: NC_000001.11:g.26067382G>A, NC_000001.10:g.26393873G>A, NG_033268.1:g.5253C>T, NM_032588.4:c.113C>T, NM_032588.3:c.113C>T, NP_115977.2:p.Pro38Leu

Select item 14882597382.

rs1488259738 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:26067392 (GRCh38)
1:26393883 (GRCh37)
Canonical SPDI:: NC_000001.11:26067391:C:T
Gene:: TRIM63 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
T=0.000014/2 (GnomAD)
HGVS:: NC_000001.11:g.26067392C>T, NC_000001.10:g.26393883C>T, NG_033268.1:g.5243G>A, NM_032588.4:c.103G>A, NM_032588.3:c.103G>A, NP_115977.2:p.Val35Ile

Select item 14811207023.

rs1481120702 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 1:26061186 (GRCh38)
1:26387677 (GRCh37)
Canonical SPDI:: NC_000001.11:26061185:T:G
Gene:: TRIM63 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.26061186T>G, NC_000001.10:g.26387677T>G, NG_033268.1:g.11449A>C, NM_032588.4:c.481A>C, NM_032588.3:c.481A>C, NP_115977.2:p.Ser161Arg

Select item 14804293474.

rs1480429347 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 1:26061230 (GRCh38)
1:26387721 (GRCh37)
Canonical SPDI:: NC_000001.11:26061229:T:G
Gene:: TRIM63 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: G=0.000071/1 (ALFA)
G=0.000026/7 (TOPMED)
HGVS:: NC_000001.11:g.26061230T>G, NC_000001.10:g.26387721T>G, NG_033268.1:g.11405A>C, NM_032588.4:c.437A>C, NM_032588.3:c.437A>C, NP_115977.2:p.Lys146Thr

Select item 14795528765.

rs1479552876 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C [Show Flanks]
Chromosome:: 1:26060309 (GRCh38)
1:26386800 (GRCh37)
Canonical SPDI:: NC_000001.11:26060308:T:A,NC_000001.11:26060308:T:C
Gene:: TRIM63 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
C=0.000007/1 (GnomAD)
A=0.000342/1 (KOREAN)
HGVS:: NC_000001.11:g.26060309T>A, NC_000001.11:g.26060309T>C, NC_000001.10:g.26386800T>A, NC_000001.10:g.26386800T>C, NG_033268.1:g.12326A>T, NG_033268.1:g.12326A>G, NM_032588.4:c.554A>T, NM_032588.4:c.554A>G, NM_032588.3:c.554A>T, NM_032588.3:c.554A>G, NP_115977.2:p.Gln185Leu, NP_115977.2:p.Gln185Arg

Select item 14768250396.

rs1476825039 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:26061195 (GRCh38)
1:26387686 (GRCh37)
Canonical SPDI:: NC_000001.11:26061194:G:A
Gene:: TRIM63 (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_000001.11:g.26061195G>A, NC_000001.10:g.26387686G>A, NG_033268.1:g.11440C>T, NM_032588.4:c.472C>T, NM_032588.3:c.472C>T, NP_115977.2:p.Pro158Ser

Select item 14767117517.

rs1476711751 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 1:26058473 (GRCh38)
1:26384964 (GRCh37)
Canonical SPDI:: NC_000001.11:26058472:G:A,NC_000001.11:26058472:G:C
Gene:: TRIM63 (Varview)
Functional Consequence:: stop_gained,coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
A=0.000342/1 (KOREAN)
HGVS:: NC_000001.11:g.26058473G>A, NC_000001.11:g.26058473G>C, NC_000001.10:g.26384964G>A, NC_000001.10:g.26384964G>C, NG_033268.1:g.14162C>T, NG_033268.1:g.14162C>G, NM_032588.4:c.748C>T, NM_032588.4:c.748C>G, NM_032588.3:c.748C>T, NM_032588.3:c.748C>G, NP_115977.2:p.Gln250Ter, NP_115977.2:p.Gln250Glu

Select item 14744011648.

rs1474401164 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:26057278 (GRCh38)
1:26383769 (GRCh37)
Canonical SPDI:: NC_000001.11:26057277:A:G
Gene:: TRIM63 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.26057278A>G, NC_000001.10:g.26383769A>G, NG_033268.1:g.15357T>C, NM_032588.4:c.904T>C, NM_032588.3:c.904T>C, NP_115977.2:p.Phe302Leu

Select item 14719978519.

rs1471997851 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 1:26053931 (GRCh38)
1:26380422 (GRCh37)
Canonical SPDI:: NC_000001.11:26053930:T:G
Gene:: TRIM63 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
HGVS:: NC_000001.11:g.26053931T>G, NC_000001.10:g.26380422T>G, NG_033268.1:g.18704A>C, NM_032588.4:c.1013A>C, NM_032588.3:c.1013A>C, NG_076259.1:g.74T>G, NP_115977.2:p.Asp338Ala

Select item 147164032210.

rs1471640322 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 1:26053946 (GRCh38)
1:26380437 (GRCh37)
Canonical SPDI:: NC_000001.11:26053945:A:T
Gene:: TRIM63 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
HGVS:: NC_000001.11:g.26053946A>T, NC_000001.10:g.26380437A>T, NG_033268.1:g.18689T>A, NM_032588.4:c.998T>A, NM_032588.3:c.998T>A, NG_076259.1:g.89A>T, NP_115977.2:p.Phe333Tyr

Select item 146937150311.

rs1469371503 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,G [Show Flanks]
Chromosome:: 1:26058535 (GRCh38)
1:26385026 (GRCh37)
Canonical SPDI:: NC_000001.11:26058534:T:A,NC_000001.11:26058534:T:G
Gene:: TRIM63 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
G=0.000004/1 (GnomAD_exomes)
A=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.26058535T>A, NC_000001.11:g.26058535T>G, NC_000001.10:g.26385026T>A, NC_000001.10:g.26385026T>G, NG_033268.1:g.14100A>T, NG_033268.1:g.14100A>C, NM_032588.4:c.686A>T, NM_032588.4:c.686A>C, NM_032588.3:c.686A>T, NM_032588.3:c.686A>C, NP_115977.2:p.Gln229Leu, NP_115977.2:p.Gln229Pro

Select item 146698318312.

rs1466983183 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 1:26067476 (GRCh38)
1:26393967 (GRCh37)
Canonical SPDI:: NC_000001.11:26067475:G:C
Gene:: TRIM63 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (GnomAD_exomes)
C=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.26067476G>C, NC_000001.10:g.26393967G>C, NG_033268.1:g.5159C>G, NM_032588.4:c.19C>G, NM_032588.3:c.19C>G, NP_115977.2:p.Leu7Val

Select item 146560310713.

rs1465603107 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 1:26066427 (GRCh38)
1:26392918 (GRCh37)
Canonical SPDI:: NC_000001.11:26066426:T:C
Gene:: TRIM63 (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_000001.11:g.26066427T>C, NC_000001.10:g.26392918T>C, NG_033268.1:g.6208A>G, NM_032588.4:c.173A>G, NM_032588.3:c.173A>G, NP_115977.2:p.Tyr58Cys

Select item 146534214814.

rs1465342148 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 1:26066327 (GRCh38)
1:26392818 (GRCh37)
Canonical SPDI:: NC_000001.11:26066326:G:T
Gene:: TRIM63 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.26066327G>T, NC_000001.10:g.26392818G>T, NG_033268.1:g.6308C>A, NM_032588.4:c.273C>A, NM_032588.3:c.273C>A

Select item 146321604315.

rs1463216043 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 1:26051881 (GRCh38)
1:26378372 (GRCh37)
Canonical SPDI:: NC_000001.11:26051880:G:A,NC_000001.11:26051880:G:T
Gene:: TRIM63 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.26051881G>A, NC_000001.11:g.26051881G>T, NC_000001.10:g.26378372G>A, NC_000001.10:g.26378372G>T, NG_033268.1:g.20754C>T, NG_033268.1:g.20754C>A, NM_032588.4:c.1054C>T, NM_032588.4:c.1054C>A, NM_032588.3:c.1054C>T, NM_032588.3:c.1054C>A, NP_115977.2:p.His352Tyr, NP_115977.2:p.His352Asn

Select item 146115026016.

rs1461150260 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 1:26061263 (GRCh38)
1:26387754 (GRCh37)
Canonical SPDI:: NC_000001.11:26061262:A:G
Gene:: TRIM63 (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=0.000008/2 (TOPMED)
HGVS:: NC_000001.11:g.26061263A>G, NC_000001.10:g.26387754A>G, NG_033268.1:g.11372T>C, NM_032588.4:c.404T>C, NM_032588.3:c.404T>C, NP_115977.2:p.Leu135Pro

Select item 145981999617.

rs1459819996 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,T [Show Flanks]
Chromosome:: 1:26066349 (GRCh38)
1:26392840 (GRCh37)
Canonical SPDI:: NC_000001.11:26066348:A:C,NC_000001.11:26066348:A:T
Gene:: TRIM63 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
T=0.000004/1 (GnomAD_exomes)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.26066349A>C, NC_000001.11:g.26066349A>T, NC_000001.10:g.26392840A>C, NC_000001.10:g.26392840A>T, NG_033268.1:g.6286T>G, NG_033268.1:g.6286T>A, NM_032588.4:c.251T>G, NM_032588.4:c.251T>A, NM_032588.3:c.251T>G, NM_032588.3:c.251T>A, NP_115977.2:p.Met84Arg, NP_115977.2:p.Met84Lys

Select item 145964528318.

rs1459645283 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 1:26061244 (GRCh38)
1:26387735 (GRCh37)
Canonical SPDI:: NC_000001.11:26061243:G:A,NC_000001.11:26061243:G:T
Gene:: TRIM63 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
T=0.000029/4 (GnomAD)
HGVS:: NC_000001.11:g.26061244G>A, NC_000001.11:g.26061244G>T, NC_000001.10:g.26387735G>A, NC_000001.10:g.26387735G>T, NG_033268.1:g.11391C>T, NG_033268.1:g.11391C>A, NM_032588.4:c.423C>T, NM_032588.4:c.423C>A, NM_032588.3:c.423C>T, NM_032588.3:c.423C>A

Select item 145693804519.

rs1456938045 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:26058599 (GRCh38)
1:26385090 (GRCh37)
Canonical SPDI:: NC_000001.11:26058598:C:T
Gene:: TRIM63 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
HGVS:: NC_000001.11:g.26058599C>T, NC_000001.10:g.26385090C>T, NG_033268.1:g.14036G>A, NM_032588.4:c.622G>A, NM_032588.3:c.622G>A, NP_115977.2:p.Glu208Lys

Select item 145484750320.

rs1454847503 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 1:26057242 (GRCh38)
1:26383733 (GRCh37)
Canonical SPDI:: NC_000001.11:26057241:G:C
Gene:: TRIM63 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.26057242G>C, NC_000001.10:g.26383733G>C, NG_033268.1:g.15393C>G, NM_032588.4:c.940C>G, NM_032588.3:c.940C>G, NP_115977.2:p.His314Asp

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