SNP Links for Protein (Select 16306487) - SNP

Links from Protein

Items: 1 to 20 of 707

<< First< Prev

Page of 36

Next >Last >>

Select item 14904298881.

rs1490429888 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 18:65880674 (GRCh38)
18:63547910 (GRCh37)
Canonical SPDI:: NC_000018.10:65880673:A:G
Gene:: CDH7 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,genic_downstream_transcript_variant
Validated:: by frequency,by cluster
MAF:: G=0.000004/1 (GnomAD_exomes)
G=0.000007/1 (GnomAD)
HGVS:: NC_000018.10:g.65880674A>G, NC_000018.9:g.63547910A>G, NM_004361.5:c.2138A>G, NM_004361.4:c.2138A>G, NM_004361.3:c.2138A>G, NM_004361.2:c.2138A>G, NM_033646.4:c.2138A>G, NM_033646.3:c.2138A>G, NM_033646.2:c.2138A>G, NM_033646.1:c.2138A>G, NM_001362438.2:c.2138A>G, NM_001362438.1:c.2138A>G, NP_004352.2:p.Glu713Gly, NP_387450.1:p.Glu713Gly, NP_001349367.1:p.Glu713Gly

Select item 14897376452.

rs1489737645 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 18:65824805 (GRCh38)
18:63492041 (GRCh37)
Canonical SPDI:: NC_000018.10:65824804:C:A
Gene:: CDH7 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
HGVS:: NC_000018.10:g.65824805C>A, NC_000018.9:g.63492041C>A, NM_004361.5:c.955C>A, NM_004361.4:c.955C>A, NM_004361.3:c.955C>A, NM_004361.2:c.955C>A, NM_033646.4:c.955C>A, NM_033646.3:c.955C>A, NM_033646.2:c.955C>A, NM_033646.1:c.955C>A, NM_001317214.3:c.955C>A, NM_001317214.2:c.955C>A, NM_001317214.1:c.955C>A, NM_001362438.2:c.955C>A, NM_001362438.1:c.955C>A, NP_004352.2:p.Gln319Lys, NP_387450.1:p.Gln319Lys, NP_001304143.1:p.Gln319Lys, NP_001349367.1:p.Gln319Lys

Select item 14854011253.

rs1485401125 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 18:65880535 (GRCh38)
18:63547771 (GRCh37)
Canonical SPDI:: NC_000018.10:65880534:G:C
Gene:: CDH7 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000018.10:g.65880535G>C, NC_000018.9:g.63547771G>C, NM_004361.5:c.1999G>C, NM_004361.4:c.1999G>C, NM_004361.3:c.1999G>C, NM_004361.2:c.1999G>C, NM_033646.4:c.1999G>C, NM_033646.3:c.1999G>C, NM_033646.2:c.1999G>C, NM_033646.1:c.1999G>C, NM_001362438.2:c.1999G>C, NM_001362438.1:c.1999G>C, NP_004352.2:p.Asp667His, NP_387450.1:p.Asp667His, NP_001349367.1:p.Asp667His

Select item 14822991254.

rs1482299125 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 18:65880685 (GRCh38)
18:63547921 (GRCh37)
Canonical SPDI:: NC_000018.10:65880684:G:A
Gene:: CDH7 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,genic_downstream_transcript_variant
HGVS:: NC_000018.10:g.65880685G>A, NC_000018.9:g.63547921G>A, NM_004361.5:c.2149G>A, NM_004361.4:c.2149G>A, NM_004361.3:c.2149G>A, NM_004361.2:c.2149G>A, NM_033646.4:c.2149G>A, NM_033646.3:c.2149G>A, NM_033646.2:c.2149G>A, NM_033646.1:c.2149G>A, NM_001362438.2:c.2149G>A, NM_001362438.1:c.2149G>A, NP_004352.2:p.Glu717Lys, NP_387450.1:p.Glu717Lys, NP_001349367.1:p.Glu717Lys

Select item 14820582845.

rs1482058284 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 18:65862763 (GRCh38)
18:63529999 (GRCh37)
Canonical SPDI:: NC_000018.10:65862762:C:T
Gene:: CDH7 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by cluster
MAF:: T=0./0 (KOREAN)
T=0.000004/1 (GnomAD_exomes)
T=0.00006/1 (TOMMO)
HGVS:: NC_000018.10:g.65862763C>T, NC_000018.9:g.63529999C>T, NM_004361.5:c.1710C>T, NM_004361.4:c.1710C>T, NM_004361.3:c.1710C>T, NM_004361.2:c.1710C>T, NM_033646.4:c.1710C>T, NM_033646.3:c.1710C>T, NM_033646.2:c.1710C>T, NM_033646.1:c.1710C>T, NM_001317214.3:c.1710C>T, NM_001317214.2:c.1710C>T, NM_001317214.1:c.1710C>T, NM_001362438.2:c.1710C>T, NM_001362438.1:c.1710C>T

Select item 14780418326.

rs1478041832 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 18:65843937 (GRCh38)
18:63511173 (GRCh37)
Canonical SPDI:: NC_000018.10:65843936:A:G
Gene:: CDH7 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000018.10:g.65843937A>G, NC_000018.9:g.63511173A>G, NM_004361.5:c.1107A>G, NM_004361.4:c.1107A>G, NM_004361.3:c.1107A>G, NM_004361.2:c.1107A>G, NM_033646.4:c.1107A>G, NM_033646.3:c.1107A>G, NM_033646.2:c.1107A>G, NM_033646.1:c.1107A>G, NM_001317214.3:c.1107A>G, NM_001317214.2:c.1107A>G, NM_001317214.1:c.1107A>G, NM_001362438.2:c.1107A>G, NM_001362438.1:c.1107A>G

Select item 14761972447.

rs1476197244 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 18:65880540 (GRCh38)
18:63547776 (GRCh37)
Canonical SPDI:: NC_000018.10:65880539:G:A
Gene:: CDH7 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,genic_downstream_transcript_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000018.10:g.65880540G>A, NC_000018.9:g.63547776G>A, NM_004361.5:c.2004G>A, NM_004361.4:c.2004G>A, NM_004361.3:c.2004G>A, NM_004361.2:c.2004G>A, NM_033646.4:c.2004G>A, NM_033646.3:c.2004G>A, NM_033646.2:c.2004G>A, NM_033646.1:c.2004G>A, NM_001362438.2:c.2004G>A, NM_001362438.1:c.2004G>A, NP_004352.2:p.Met668Ile, NP_387450.1:p.Met668Ile, NP_001349367.1:p.Met668Ile

Select item 14748868918.

rs1474886891 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 18:65880626 (GRCh38)
18:63547862 (GRCh37)
Canonical SPDI:: NC_000018.10:65880625:C:G
Gene:: CDH7 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000018.10:g.65880626C>G, NC_000018.9:g.63547862C>G, NM_004361.5:c.2090C>G, NM_004361.4:c.2090C>G, NM_004361.3:c.2090C>G, NM_004361.2:c.2090C>G, NM_033646.4:c.2090C>G, NM_033646.3:c.2090C>G, NM_033646.2:c.2090C>G, NM_033646.1:c.2090C>G, NM_001362438.2:c.2090C>G, NM_001362438.1:c.2090C>G, NP_004352.2:p.Ala697Gly, NP_387450.1:p.Ala697Gly, NP_001349367.1:p.Ala697Gly

Select item 14746385089.

rs1474638508 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 18:65762959 (GRCh38)
18:63430195 (GRCh37)
Canonical SPDI:: NC_000018.10:65762958:A:G
Gene:: CDH7 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000018.10:g.65762959A>G, NC_000018.9:g.63430195A>G, NM_004361.5:c.117A>G, NM_004361.4:c.117A>G, NM_004361.3:c.117A>G, NM_004361.2:c.117A>G, NM_033646.4:c.117A>G, NM_033646.3:c.117A>G, NM_033646.2:c.117A>G, NM_033646.1:c.117A>G, NM_001317214.3:c.117A>G, NM_001317214.2:c.117A>G, NM_001317214.1:c.117A>G, NM_001362438.2:c.117A>G, NM_001362438.1:c.117A>G

Select item 147458950910.

rs1474589509 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 18:65880512 (GRCh38)
18:63547748 (GRCh37)
Canonical SPDI:: NC_000018.10:65880511:G:T
Gene:: CDH7 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000018.10:g.65880512G>T, NC_000018.9:g.63547748G>T, NM_004361.5:c.1976G>T, NM_004361.4:c.1976G>T, NM_004361.3:c.1976G>T, NM_004361.2:c.1976G>T, NM_033646.4:c.1976G>T, NM_033646.3:c.1976G>T, NM_033646.2:c.1976G>T, NM_033646.1:c.1976G>T, NM_001362438.2:c.1976G>T, NM_001362438.1:c.1976G>T, NP_004352.2:p.Gly659Val, NP_387450.1:p.Gly659Val, NP_001349367.1:p.Gly659Val

Select item 147190649811.

rs1471906498 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 18:65880611 (GRCh38)
18:63547847 (GRCh37)
Canonical SPDI:: NC_000018.10:65880610:T:C
Gene:: CDH7 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,genic_downstream_transcript_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000018.10:g.65880611T>C, NC_000018.9:g.63547847T>C, NM_004361.5:c.2075T>C, NM_004361.4:c.2075T>C, NM_004361.3:c.2075T>C, NM_004361.2:c.2075T>C, NM_033646.4:c.2075T>C, NM_033646.3:c.2075T>C, NM_033646.2:c.2075T>C, NM_033646.1:c.2075T>C, NM_001362438.2:c.2075T>C, NM_001362438.1:c.2075T>C, NP_004352.2:p.Phe692Ser, NP_387450.1:p.Phe692Ser, NP_001349367.1:p.Phe692Ser

Select item 147148867612.

rs1471488676 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 18:65762960 (GRCh38)
18:63430196 (GRCh37)
Canonical SPDI:: NC_000018.10:65762959:T:C
Gene:: CDH7 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000018.10:g.65762960T>C, NC_000018.9:g.63430196T>C, NM_004361.5:c.118T>C, NM_004361.4:c.118T>C, NM_004361.3:c.118T>C, NM_004361.2:c.118T>C, NM_033646.4:c.118T>C, NM_033646.3:c.118T>C, NM_033646.2:c.118T>C, NM_033646.1:c.118T>C, NM_001317214.3:c.118T>C, NM_001317214.2:c.118T>C, NM_001317214.1:c.118T>C, NM_001362438.2:c.118T>C, NM_001362438.1:c.118T>C, NP_004352.2:p.Ser40Pro, NP_387450.1:p.Ser40Pro, NP_001304143.1:p.Ser40Pro, NP_001349367.1:p.Ser40Pro

Select item 147140604913.

rs1471406049 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 18:65880696 (GRCh38)
18:63547932 (GRCh37)
Canonical SPDI:: NC_000018.10:65880695:T:C
Gene:: CDH7 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0.000094/2 (ALFA)
C=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000018.10:g.65880696T>C, NC_000018.9:g.63547932T>C, NM_004361.5:c.2160T>C, NM_004361.4:c.2160T>C, NM_004361.3:c.2160T>C, NM_004361.2:c.2160T>C, NM_033646.4:c.2160T>C, NM_033646.3:c.2160T>C, NM_033646.2:c.2160T>C, NM_033646.1:c.2160T>C, NM_001362438.2:c.2160T>C, NM_001362438.1:c.2160T>C

Select item 147085609014.

rs1470856090 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 18:65862890 (GRCh38)
18:63530126 (GRCh37)
Canonical SPDI:: NC_000018.10:65862889:A:G
Gene:: CDH7 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by cluster
MAF:: G=0.000004/1 (GnomAD_exomes)
G=0.000071/1 (TOMMO)
G=0.000342/1 (KOREAN)
HGVS:: NC_000018.10:g.65862890A>G, NC_000018.9:g.63530126A>G, NM_004361.5:c.1837A>G, NM_004361.4:c.1837A>G, NM_004361.3:c.1837A>G, NM_004361.2:c.1837A>G, NM_033646.4:c.1837A>G, NM_033646.3:c.1837A>G, NM_033646.2:c.1837A>G, NM_033646.1:c.1837A>G, NM_001317214.3:c.1837A>G, NM_001317214.2:c.1837A>G, NM_001317214.1:c.1837A>G, NM_001362438.2:c.1837A>G, NM_001362438.1:c.1837A>G, NP_004352.2:p.Ile613Val, NP_387450.1:p.Ile613Val, NP_001304143.1:p.Ile613Val, NP_001349367.1:p.Ile613Val

Select item 146973365415.

rs1469733654 [Homo sapiens]

Variant type:: DELINS
Alleles:: ACA>- [Show Flanks]
Chromosome:: 18:65857869 (GRCh38)
18:63525105 (GRCh37)
Canonical SPDI:: NC_000018.10:65857866:CAACA:CA
Gene:: CDH7 (Varview)
Functional Consequence:: coding_sequence_variant,inframe_deletion
Validated:: by frequency,by alfa
MAF:: CA=0./0 (ALFA)
HGVS:: NC_000018.10:g.65857869_65857871del, NC_000018.9:g.63525105_63525107del, NM_004361.5:c.1289_1291del, NM_004361.4:c.1289_1291del, NM_004361.3:c.1289_1291del, NM_004361.2:c.1289_1291del, NM_033646.4:c.1289_1291del, NM_033646.3:c.1289_1291del, NM_033646.2:c.1289_1291del, NM_033646.1:c.1289_1291del, NM_001317214.3:c.1289_1291del, NM_001317214.2:c.1289_1291del, NM_001317214.1:c.1289_1291del, NM_001362438.2:c.1289_1291del, NM_001362438.1:c.1289_1291del, NP_004352.2:p.Asn430del, NP_387450.1:p.Asn430del, NP_001304143.1:p.Asn430del, NP_001349367.1:p.Asn430del

Select item 146948945416.

rs1469489454 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 18:65843949 (GRCh38)
18:63511185 (GRCh37)
Canonical SPDI:: NC_000018.10:65843948:G:A
Gene:: CDH7 (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=0.000014/2 (GnomAD)
HGVS:: NC_000018.10:g.65843949G>A, NC_000018.9:g.63511185G>A, NM_004361.5:c.1119G>A, NM_004361.4:c.1119G>A, NM_004361.3:c.1119G>A, NM_004361.2:c.1119G>A, NM_033646.4:c.1119G>A, NM_033646.3:c.1119G>A, NM_033646.2:c.1119G>A, NM_033646.1:c.1119G>A, NM_001317214.3:c.1119G>A, NM_001317214.2:c.1119G>A, NM_001317214.1:c.1119G>A, NM_001362438.2:c.1119G>A, NM_001362438.1:c.1119G>A

Select item 146903837117.

rs1469038371 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 18:65843956 (GRCh38)
18:63511192 (GRCh37)
Canonical SPDI:: NC_000018.10:65843955:G:A
Gene:: CDH7 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by cluster
MAF:: A=0.000007/1 (GnomAD)
HGVS:: NC_000018.10:g.65843956G>A, NC_000018.9:g.63511192G>A, NM_004361.5:c.1126G>A, NM_004361.4:c.1126G>A, NM_004361.3:c.1126G>A, NM_004361.2:c.1126G>A, NM_033646.4:c.1126G>A, NM_033646.3:c.1126G>A, NM_033646.2:c.1126G>A, NM_033646.1:c.1126G>A, NM_001317214.3:c.1126G>A, NM_001317214.2:c.1126G>A, NM_001317214.1:c.1126G>A, NM_001362438.2:c.1126G>A, NM_001362438.1:c.1126G>A, NP_004352.2:p.Val376Met, NP_387450.1:p.Val376Met, NP_001304143.1:p.Val376Met, NP_001349367.1:p.Val376Met

Select item 146777487618.

rs1467774876 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,G [Show Flanks]
Chromosome:: 18:65824652 (GRCh38)
18:63491888 (GRCh37)
Canonical SPDI:: NC_000018.10:65824651:C:A,NC_000018.10:65824651:C:G
Gene:: CDH7 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by cluster
MAF:: G=0.000004/1 (GnomAD_exomes)
A=0.000035/1 (TOMMO)
HGVS:: NC_000018.10:g.65824652C>A, NC_000018.10:g.65824652C>G, NC_000018.9:g.63491888C>A, NC_000018.9:g.63491888C>G, NM_004361.5:c.802C>A, NM_004361.5:c.802C>G, NM_004361.4:c.802C>A, NM_004361.4:c.802C>G, NM_004361.3:c.802C>A, NM_004361.3:c.802C>G, NM_004361.2:c.802C>A, NM_004361.2:c.802C>G, NM_033646.4:c.802C>A, NM_033646.4:c.802C>G, NM_033646.3:c.802C>A, NM_033646.3:c.802C>G, NM_033646.2:c.802C>A, NM_033646.2:c.802C>G, NM_033646.1:c.802C>A, NM_033646.1:c.802C>G, NM_001317214.3:c.802C>A, NM_001317214.3:c.802C>G, NM_001317214.2:c.802C>A, NM_001317214.2:c.802C>G, NM_001317214.1:c.802C>A, NM_001317214.1:c.802C>G, NM_001362438.2:c.802C>A, NM_001362438.2:c.802C>G, NM_001362438.1:c.802C>A, NM_001362438.1:c.802C>G, NP_004352.2:p.Gln268Lys, NP_004352.2:p.Gln268Glu, NP_387450.1:p.Gln268Lys, NP_387450.1:p.Gln268Glu, NP_001304143.1:p.Gln268Lys, NP_001304143.1:p.Gln268Glu, NP_001349367.1:p.Gln268Lys, NP_001349367.1:p.Gln268Glu

Select item 146737155919.

rs1467371559 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 18:65824801 (GRCh38)
18:63492037 (GRCh37)
Canonical SPDI:: NC_000018.10:65824800:A:G
Gene:: CDH7 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000018.10:g.65824801A>G, NC_000018.9:g.63492037A>G, NM_004361.5:c.951A>G, NM_004361.4:c.951A>G, NM_004361.3:c.951A>G, NM_004361.2:c.951A>G, NM_033646.4:c.951A>G, NM_033646.3:c.951A>G, NM_033646.2:c.951A>G, NM_033646.1:c.951A>G, NM_001317214.3:c.951A>G, NM_001317214.2:c.951A>G, NM_001317214.1:c.951A>G, NM_001362438.2:c.951A>G, NM_001362438.1:c.951A>G

Select item 146632713420.

rs1466327134 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 18:65862684 (GRCh38)
18:63529920 (GRCh37)
Canonical SPDI:: NC_000018.10:65862683:T:G
Gene:: CDH7 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000018.10:g.65862684T>G, NC_000018.9:g.63529920T>G, NM_004361.5:c.1631T>G, NM_004361.4:c.1631T>G, NM_004361.3:c.1631T>G, NM_004361.2:c.1631T>G, NM_033646.4:c.1631T>G, NM_033646.3:c.1631T>G, NM_033646.2:c.1631T>G, NM_033646.1:c.1631T>G, NM_001317214.3:c.1631T>G, NM_001317214.2:c.1631T>G, NM_001317214.1:c.1631T>G, NM_001362438.2:c.1631T>G, NM_001362438.1:c.1631T>G, NP_004352.2:p.Leu544Arg, NP_387450.1:p.Leu544Arg, NP_001304143.1:p.Leu544Arg, NP_001349367.1:p.Leu544Arg

dbSNP

Result Filters

Clinical Significance

Validation Status

Function Class

Variation Class

Annotation

Global MAF

Custom range

Additional filters

Display Settings:

Send to:

Links from Protein

Items: 1 to 20 of 707

Display Settings:

Send to:

Supplemental Content

Find related data

Recent activity