SNP Links for Protein (Select 4503835) - SNP

Links from Protein

Items: 1 to 20 of 492

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Select item 14891073051.

rs1489107305 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 7:73434410 (GRCh38)
7:72848740 (GRCh37)
Canonical SPDI:: NC_000007.14:73434409:G:T
Gene:: FZD9 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000006/1 (GnomAD_exomes)
T=0.000007/1 (GnomAD)
T=0.000015/4 (TOPMED)
HGVS:: NC_000007.14:g.73434410G>T, NC_000007.13:g.72848740G>T, NG_012028.1:g.5632G>T, NM_003508.3:c.403G>T, NM_003508.2:c.403G>T, NW_003871064.1:g.963646G>T, NP_003499.1:p.Asp135Tyr

Select item 14874356482.

rs1487435648 [Homo sapiens]

Variant type:: DELINS
Alleles:: C>- [Show Flanks]
Chromosome:: 7:73434856 (GRCh38)
7:72849186 (GRCh37)
Canonical SPDI:: NC_000007.14:73434855:CC:C
Gene:: FZD9 (Varview)
Functional Consequence:: frameshift_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: CC=0./0 (ALFA)
-=0.000034/9 (TOPMED)
-=0.000036/5 (GnomAD)
HGVS:: NC_000007.14:g.73434857del, NC_000007.13:g.72849187del, NG_012028.1:g.6079del, NM_003508.3:c.850del, NM_003508.2:c.850del, NW_003871064.1:g.964093del, NP_003499.1:p.Arg284fs

Select item 14871402153.

rs1487140215 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 7:73435367 (GRCh38)
7:72849697 (GRCh37)
Canonical SPDI:: NC_000007.14:73435366:C:G,NC_000007.14:73435366:C:T
Gene:: FZD9 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
HGVS:: NC_000007.14:g.73435367C>G, NC_000007.14:g.73435367C>T, NC_000007.13:g.72849697C>G, NC_000007.13:g.72849697C>T, NG_012028.1:g.6589C>G, NG_012028.1:g.6589C>T, NM_003508.3:c.1360C>G, NM_003508.3:c.1360C>T, NM_003508.2:c.1360C>G, NM_003508.2:c.1360C>T, NG_078353.1:g.49C>G, NG_078353.1:g.49C>T, NW_003871064.1:g.964603C>G, NW_003871064.1:g.964603C>T, NP_003499.1:p.Leu454Val, NP_003499.1:p.Leu454Phe

Select item 14858698864.

rs1485869886 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 7:73435770 (GRCh38)
7:72850100 (GRCh37)
Canonical SPDI:: NC_000007.14:73435769:C:T
Gene:: FZD9 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000071/1 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000014/2 (GnomAD)
HGVS:: NC_000007.14:g.73435770C>T, NC_000007.13:g.72850100C>T, NG_012028.1:g.6992C>T, NM_003508.3:c.1763C>T, NM_003508.2:c.1763C>T, NG_078353.1:g.452C>T, NW_003871064.1:g.965006C>T, NP_003499.1:p.Pro588Leu

Select item 14795479925.

rs1479547992 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 7:73434014 (GRCh38)
7:72848344 (GRCh37)
Canonical SPDI:: NC_000007.14:73434013:G:A
Gene:: FZD9 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000007.14:g.73434014G>A, NC_000007.13:g.72848344G>A, NG_012028.1:g.5236G>A, NM_003508.3:c.7G>A, NM_003508.2:c.7G>A, NW_003871064.1:g.963250G>A, NP_003499.1:p.Val3Met

Select item 14785665116.

rs1478566511 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 7:73434477 (GRCh38)
7:72848807 (GRCh37)
Canonical SPDI:: NC_000007.14:73434476:A:T
Gene:: FZD9 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000011/3 (TOPMED)
T=0.000014/2 (GnomAD)
HGVS:: NC_000007.14:g.73434477A>T, NC_000007.13:g.72848807A>T, NG_012028.1:g.5699A>T, NM_003508.3:c.470A>T, NM_003508.2:c.470A>T, NW_003871064.1:g.963713A>T, NP_003499.1:p.Glu157Val

Select item 14778876537.

rs1477887653 [Homo sapiens]

Variant type:: DELINS
Alleles:: G>- [Show Flanks]
Chromosome:: 7:73434499 (GRCh38)
7:72848829 (GRCh37)
Canonical SPDI:: NC_000007.14:73434498:GG:G
Gene:: FZD9 (Varview)
Functional Consequence:: frameshift_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: GG=0./0 (ALFA)
-=0.000004/1 (TOPMED)
HGVS:: NC_000007.14:g.73434500del, NC_000007.13:g.72848830del, NG_012028.1:g.5722del, NM_003508.3:c.493del, NM_003508.2:c.493del, NW_003871064.1:g.963736del, NP_003499.1:p.Glu165fs

Select item 14759346708.

rs1475934670 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 7:73435468 (GRCh38)
7:72849798 (GRCh37)
Canonical SPDI:: NC_000007.14:73435467:G:A,NC_000007.14:73435467:G:T
Gene:: FZD9 (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=0.000008/2 (TOPMED)
HGVS:: NC_000007.14:g.73435468G>A, NC_000007.14:g.73435468G>T, NC_000007.13:g.72849798G>A, NC_000007.13:g.72849798G>T, NG_012028.1:g.6690G>A, NG_012028.1:g.6690G>T, NM_003508.3:c.1461G>A, NM_003508.3:c.1461G>T, NM_003508.2:c.1461G>A, NM_003508.2:c.1461G>T, NG_078353.1:g.150G>A, NG_078353.1:g.150G>T, NW_003871064.1:g.964704G>A, NW_003871064.1:g.964704G>T

Select item 14698172069.

rs1469817206 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 7:73434964 (GRCh38)
7:72849294 (GRCh37)
Canonical SPDI:: NC_000007.14:73434963:G:A
Gene:: FZD9 (Varview)
Functional Consequence:: synonymous_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=0.000032/8 (GnomAD_exomes)
HGVS:: NC_000007.14:g.73434964G>A, NC_000007.13:g.72849294G>A, NG_012028.1:g.6186G>A, NM_003508.3:c.957G>A, NM_003508.2:c.957G>A, NW_003871064.1:g.964200G>A

Select item 146676167110.

rs1466761671 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,G [Show Flanks]
Chromosome:: 7:73434556 (GRCh38)
7:72848886 (GRCh37)
Canonical SPDI:: NC_000007.14:73434555:C:A,NC_000007.14:73434555:C:G
Gene:: FZD9 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
G=0.000014/2 (GnomAD)
HGVS:: NC_000007.14:g.73434556C>A, NC_000007.14:g.73434556C>G, NC_000007.13:g.72848886C>A, NC_000007.13:g.72848886C>G, NG_012028.1:g.5778C>A, NG_012028.1:g.5778C>G, NM_003508.3:c.549C>A, NM_003508.3:c.549C>G, NM_003508.2:c.549C>A, NM_003508.2:c.549C>G, NW_003871064.1:g.963792C>A, NW_003871064.1:g.963792C>G

Select item 145911849911.

rs1459118499 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 7:73434596 (GRCh38)
7:72848926 (GRCh37)
Canonical SPDI:: NC_000007.14:73434595:G:C
Gene:: FZD9 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000071/1 (ALFA)
C=0.000008/2 (TOPMED)
C=0.000014/2 (GnomAD)
HGVS:: NC_000007.14:g.73434596G>C, NC_000007.13:g.72848926G>C, NG_012028.1:g.5818G>C, NM_003508.3:c.589G>C, NM_003508.2:c.589G>C, NW_003871064.1:g.963832G>C, NP_003499.1:p.Glu197Gln

Select item 145820247312.

rs1458202473 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->GGCAGCTGC [Show Flanks]
Chromosome:: 7:73434044 (GRCh38)
7:72848375 (GRCh37)
Canonical SPDI:: NC_000007.14:73434044:GGCAGCTGC:GGCAGCTGCGGCAGCTGC
Gene:: FZD9 (Varview)
Functional Consequence:: coding_sequence_variant,inframe_insertion
Validated:: by frequency,by alfa,by cluster
MAF:: GGCAGCTGCGGCAGCTGC=0./0 (ALFA)
GGCAGCTGC=0.000004/1 (TOPMED)
GGCAGCTGC=0.000029/4 (GnomAD)
HGVS:: NC_000007.14:g.73434045_73434053dup, NC_000007.13:g.72848375_72848383dup, NG_012028.1:g.5267_5275dup, NM_003508.3:c.38_46dup, NM_003508.2:c.38_46dup, NW_003871064.1:g.963281_963289dup, NP_003499.1:p.Leu16_Ala17insArgGlnLeu

Select item 145575683813.

rs1455756838 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 7:73434801 (GRCh38)
7:72849131 (GRCh37)
Canonical SPDI:: NC_000007.14:73434800:G:T
Gene:: FZD9 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (GnomAD_exomes)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000007.14:g.73434801G>T, NC_000007.13:g.72849131G>T, NG_012028.1:g.6023G>T, NM_003508.3:c.794G>T, NM_003508.2:c.794G>T, NW_003871064.1:g.964037G>T, NP_003499.1:p.Arg265Leu

Select item 145549851714.

rs1455498517 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 7:73435099 (GRCh38)
7:72849429 (GRCh37)
Canonical SPDI:: NC_000007.14:73435098:C:A,NC_000007.14:73435098:C:T
Gene:: FZD9 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
T=0.000004/1 (GnomAD_exomes)
A=0.000008/2 (TOPMED)
HGVS:: NC_000007.14:g.73435099C>A, NC_000007.14:g.73435099C>T, NC_000007.13:g.72849429C>A, NC_000007.13:g.72849429C>T, NG_012028.1:g.6321C>A, NG_012028.1:g.6321C>T, NM_003508.3:c.1092C>A, NM_003508.3:c.1092C>T, NM_003508.2:c.1092C>A, NM_003508.2:c.1092C>T, NW_003871064.1:g.964335C>A, NW_003871064.1:g.964335C>T

Select item 145154182115.

rs1451541821 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 7:73435475 (GRCh38)
7:72849805 (GRCh37)
Canonical SPDI:: NC_000007.14:73435474:G:T
Gene:: FZD9 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000007.14:g.73435475G>T, NC_000007.13:g.72849805G>T, NG_012028.1:g.6697G>T, NM_003508.3:c.1468G>T, NM_003508.2:c.1468G>T, NG_078353.1:g.157G>T, NW_003871064.1:g.964711G>T, NP_003499.1:p.Gly490Trp

Select item 144804444816.

rs1448044448 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 7:73435375 (GRCh38)
7:72849705 (GRCh37)
Canonical SPDI:: NC_000007.14:73435374:G:A,NC_000007.14:73435374:G:T
Gene:: FZD9 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
A=0.000008/2 (GnomAD_exomes)
T=0.000008/2 (TOPMED)
HGVS:: NC_000007.14:g.73435375G>A, NC_000007.14:g.73435375G>T, NC_000007.13:g.72849705G>A, NC_000007.13:g.72849705G>T, NG_012028.1:g.6597G>A, NG_012028.1:g.6597G>T, NM_003508.3:c.1368G>A, NM_003508.3:c.1368G>T, NM_003508.2:c.1368G>A, NM_003508.2:c.1368G>T, NG_078353.1:g.57G>A, NG_078353.1:g.57G>T, NW_003871064.1:g.964611G>A, NW_003871064.1:g.964611G>T

Select item 144668212717.

rs1446682127 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 7:73434106 (GRCh38)
7:72848436 (GRCh37)
Canonical SPDI:: NC_000007.14:73434105:G:A,NC_000007.14:73434105:G:C
Gene:: FZD9 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.001299/19 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000008/2 (TOPMED)
HGVS:: NC_000007.14:g.73434106G>A, NC_000007.14:g.73434106G>C, NC_000007.13:g.72848436G>A, NC_000007.13:g.72848436G>C, NG_012028.1:g.5328G>A, NG_012028.1:g.5328G>C, NM_003508.3:c.99G>A, NM_003508.3:c.99G>C, NM_003508.2:c.99G>A, NM_003508.2:c.99G>C, NW_003871064.1:g.963342G>A, NW_003871064.1:g.963342G>C

Select item 144650831718.

rs1446508317 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 7:73434229 (GRCh38)
7:72848559 (GRCh37)
Canonical SPDI:: NC_000007.14:73434228:G:A,NC_000007.14:73434228:G:T
Gene:: FZD9 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
T=0.00001/2 (GnomAD_exomes)
HGVS:: NC_000007.14:g.73434229G>A, NC_000007.14:g.73434229G>T, NC_000007.13:g.72848559G>A, NC_000007.13:g.72848559G>T, NG_012028.1:g.5451G>A, NG_012028.1:g.5451G>T, NM_003508.3:c.222G>A, NM_003508.3:c.222G>T, NM_003508.2:c.222G>A, NM_003508.2:c.222G>T, NW_003871064.1:g.963465G>A, NW_003871064.1:g.963465G>T

Select item 144440060819.

rs1444400608 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 7:73434546 (GRCh38)
7:72848876 (GRCh37)
Canonical SPDI:: NC_000007.14:73434545:C:G
Gene:: FZD9 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000071/1 (ALFA)
G=0.000019/5 (TOPMED)
G=0.000027/1 (GnomAD_exomes)
G=0.000029/4 (GnomAD)
HGVS:: NC_000007.14:g.73434546C>G, NC_000007.13:g.72848876C>G, NG_012028.1:g.5768C>G, NM_003508.3:c.539C>G, NM_003508.2:c.539C>G, NW_003871064.1:g.963782C>G, NP_003499.1:p.Ala180Gly

Select item 144385180320.

rs1443851803 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 7:73435697 (GRCh38)
7:72850027 (GRCh37)
Canonical SPDI:: NC_000007.14:73435696:G:A
Gene:: FZD9 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: A=0.000028/1 (ALFA)
A=0.000019/5 (TOPMED)
HGVS:: NC_000007.14:g.73435697G>A, NC_000007.13:g.72850027G>A, NG_012028.1:g.6919G>A, NM_003508.3:c.1690G>A, NM_003508.2:c.1690G>A, NG_078353.1:g.379G>A, NW_003871064.1:g.964933G>A, NP_003499.1:p.Gly564Ser

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