SNP Links for Protein (Select 973353032) - SNP

Links from Protein

Items: 1 to 20 of 73

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Select item 14696647011.

rs1469664701 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:103066308 (GRCh38)
11:102937037 (GRCh37)
Canonical SPDI:: NC_000011.10:103066307:C:T
Gene:: DCUN1D5 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
HGVS:: NC_000011.10:g.103066308C>T, NC_000011.9:g.102937037C>T, NM_032299.4:c.516G>A, NM_032299.3:c.516G>A, NM_001318739.2:c.309G>A, NM_001318739.1:c.309G>A, NM_001318741.2:c.177G>A, NM_001318741.1:c.177G>A, NM_001318740.2:c.177G>A, NM_001318740.1:c.177G>A

Select item 14369791912.

rs1436979191 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:103064306 (GRCh38)
11:102935035 (GRCh37)
Canonical SPDI:: NC_000011.10:103064305:A:G
Gene:: DCUN1D5 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_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_000011.10:g.103064306A>G, NC_000011.9:g.102935035A>G, NM_032299.4:c.627T>C, NM_032299.3:c.627T>C, NM_001318739.2:c.420T>C, NM_001318739.1:c.420T>C, NM_001318741.2:c.288T>C, NM_001318741.1:c.288T>C, NM_001318740.2:c.288T>C, NM_001318740.1:c.288T>C

Select item 14340648393.

rs1434064839 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:103066272 (GRCh38)
11:102937001 (GRCh37)
Canonical SPDI:: NC_000011.10:103066271:C:T
Gene:: DCUN1D5 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by cluster
MAF:: T=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.103066272C>T, NC_000011.9:g.102937001C>T, NM_032299.4:c.552G>A, NM_032299.3:c.552G>A, NM_001318739.2:c.345G>A, NM_001318739.1:c.345G>A, NM_001318741.2:c.213G>A, NM_001318741.1:c.213G>A, NM_001318740.2:c.213G>A, NM_001318740.1:c.213G>A

Select item 14155480324.

rs1415548032 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:103066474 (GRCh38)
11:102937203 (GRCh37)
Canonical SPDI:: NC_000011.10:103066473:G:A
Gene:: DCUN1D5 (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=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.103066474G>A, NC_000011.9:g.102937203G>A, NM_032299.4:c.435C>T, NM_032299.3:c.435C>T, NM_001318739.2:c.228C>T, NM_001318739.1:c.228C>T, NM_001318741.2:c.96C>T, NM_001318741.1:c.96C>T, NM_001318740.2:c.96C>T, NM_001318740.1:c.96C>T

Select item 13732161215.

rs1373216121 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:103066338 (GRCh38)
11:102937067 (GRCh37)
Canonical SPDI:: NC_000011.10:103066337:A:G
Gene:: DCUN1D5 (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_000011.10:g.103066338A>G, NC_000011.9:g.102937067A>G, NM_032299.4:c.486T>C, NM_032299.3:c.486T>C, NM_001318739.2:c.279T>C, NM_001318739.1:c.279T>C, NM_001318741.2:c.147T>C, NM_001318741.1:c.147T>C, NM_001318740.2:c.147T>C, NM_001318740.1:c.147T>C

Select item 13578097826.

rs1357809782 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 11:103066498 (GRCh38)
11:102937227 (GRCh37)
Canonical SPDI:: NC_000011.10:103066497:T:C,NC_000011.10:103066497:T:G
Gene:: DCUN1D5 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.103066498T>C, NC_000011.10:g.103066498T>G, NC_000011.9:g.102937227T>C, NC_000011.9:g.102937227T>G, NM_032299.4:c.411A>G, NM_032299.4:c.411A>C, NM_032299.3:c.411A>G, NM_032299.3:c.411A>C, NM_001318739.2:c.204A>G, NM_001318739.2:c.204A>C, NM_001318739.1:c.204A>G, NM_001318739.1:c.204A>C, NM_001318741.2:c.72A>G, NM_001318741.2:c.72A>C, NM_001318741.1:c.72A>G, NM_001318741.1:c.72A>C, NM_001318740.2:c.72A>G, NM_001318740.2:c.72A>C, NM_001318740.1:c.72A>G, NM_001318740.1:c.72A>C

Select item 13406730607.

rs1340673060 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:103062409 (GRCh38)
11:102933138 (GRCh37)
Canonical SPDI:: NC_000011.10:103062408:C:T
Gene:: DCUN1D5 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.103062409C>T, NC_000011.9:g.102933138C>T, NM_032299.4:c.664G>A, NM_032299.3:c.664G>A, NM_001318739.2:c.457G>A, NM_001318739.1:c.457G>A, NM_001318741.2:c.325G>A, NM_001318741.1:c.325G>A, NM_001318740.2:c.325G>A, NM_001318740.1:c.325G>A, NP_115675.1:p.Val222Ile, NP_001305668.1:p.Val153Ile, NP_001305670.1:p.Val109Ile, NP_001305669.1:p.Val109Ile

Select item 13304506218.

rs1330450621 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 11:103064377 (GRCh38)
11:102935106 (GRCh37)
Canonical SPDI:: NC_000011.10:103064376:G:C
Gene:: DCUN1D5 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000023/6 (TOPMED)
HGVS:: NC_000011.10:g.103064377G>C, NC_000011.9:g.102935106G>C, NM_032299.4:c.556C>G, NM_032299.3:c.556C>G, NM_001318739.2:c.349C>G, NM_001318739.1:c.349C>G, NM_001318741.2:c.217C>G, NM_001318741.1:c.217C>G, NM_001318740.2:c.217C>G, NM_001318740.1:c.217C>G, NP_115675.1:p.Gln186Glu, NP_001305668.1:p.Gln117Glu, NP_001305670.1:p.Gln73Glu, NP_001305669.1:p.Gln73Glu

Select item 12964864929.

rs1296486492 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:103064317 (GRCh38)
11:102935046 (GRCh37)
Canonical SPDI:: NC_000011.10:103064316:T:C
Gene:: DCUN1D5 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.103064317T>C, NC_000011.9:g.102935046T>C, NM_032299.4:c.616A>G, NM_032299.3:c.616A>G, NM_001318739.2:c.409A>G, NM_001318739.1:c.409A>G, NM_001318741.2:c.277A>G, NM_001318741.1:c.277A>G, NM_001318740.2:c.277A>G, NM_001318740.1:c.277A>G, NP_115675.1:p.Thr206Ala, NP_001305668.1:p.Thr137Ala, NP_001305670.1:p.Thr93Ala, NP_001305669.1:p.Thr93Ala

Select item 128435982210.

rs1284359822 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:103062373 (GRCh38)
11:102933102 (GRCh37)
Canonical SPDI:: NC_000011.10:103062372:G:A
Gene:: DCUN1D5 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000011.10:g.103062373G>A, NC_000011.9:g.102933102G>A, NM_032299.4:c.700C>T, NM_032299.3:c.700C>T, NM_001318739.2:c.493C>T, NM_001318739.1:c.493C>T, NM_001318741.2:c.361C>T, NM_001318741.1:c.361C>T, NM_001318740.2:c.361C>T, NM_001318740.1:c.361C>T, NP_115675.1:p.Arg234Cys, NP_001305668.1:p.Arg165Cys, NP_001305670.1:p.Arg121Cys, NP_001305669.1:p.Arg121Cys

Select item 127873179211.

rs1278731792 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 11:103066555 (GRCh38)
11:102937284 (GRCh37)
Canonical SPDI:: NC_000011.10:103066554:T:G
Gene:: DCUN1D5 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.103066555T>G, NC_000011.9:g.102937284T>G, NM_032299.4:c.354A>C, NM_032299.3:c.354A>C, NM_001318739.2:c.147A>C, NM_001318739.1:c.147A>C, NM_001318741.2:c.15A>C, NM_001318741.1:c.15A>C, NM_001318740.2:c.15A>C, NM_001318740.1:c.15A>C

Select item 127307648512.

rs1273076485 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:103062391 (GRCh38)
11:102933120 (GRCh37)
Canonical SPDI:: NC_000011.10:103062390:C:T
Gene:: DCUN1D5 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.103062391C>T, NC_000011.9:g.102933120C>T, NM_032299.4:c.682G>A, NM_032299.3:c.682G>A, NM_001318739.2:c.475G>A, NM_001318739.1:c.475G>A, NM_001318741.2:c.343G>A, NM_001318741.1:c.343G>A, NM_001318740.2:c.343G>A, NM_001318740.1:c.343G>A, NP_115675.1:p.Val228Ile, NP_001305668.1:p.Val159Ile, NP_001305670.1:p.Val115Ile, NP_001305669.1:p.Val115Ile

Select item 126210299313.

rs1262102993 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 11:103064307 (GRCh38)
11:102935036 (GRCh37)
Canonical SPDI:: NC_000011.10:103064306:G:C
Gene:: DCUN1D5 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.103064307G>C, NC_000011.9:g.102935036G>C, NM_032299.4:c.626C>G, NM_032299.3:c.626C>G, NM_001318739.2:c.419C>G, NM_001318739.1:c.419C>G, NM_001318741.2:c.287C>G, NM_001318741.1:c.287C>G, NM_001318740.2:c.287C>G, NM_001318740.1:c.287C>G, NP_115675.1:p.Ala209Gly, NP_001305668.1:p.Ala140Gly, NP_001305670.1:p.Ala96Gly, NP_001305669.1:p.Ala96Gly

Select item 125386163614.

rs1253861636 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:103064276 (GRCh38)
11:102935005 (GRCh37)
Canonical SPDI:: NC_000011.10:103064275:A:G
Gene:: DCUN1D5 (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_000011.10:g.103064276A>G, NC_000011.9:g.102935005A>G, NM_032299.4:c.657T>C, NM_032299.3:c.657T>C, NM_001318739.2:c.450T>C, NM_001318739.1:c.450T>C, NM_001318741.2:c.318T>C, NM_001318741.1:c.318T>C, NM_001318740.2:c.318T>C, NM_001318740.1:c.318T>C

Select item 123423060615.

rs1234230606 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 11:103066553 (GRCh38)
11:102937282 (GRCh37)
Canonical SPDI:: NC_000011.10:103066552:T:A
Gene:: DCUN1D5 (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)
HGVS:: NC_000011.10:g.103066553T>A, NC_000011.9:g.102937282T>A, NM_032299.4:c.356A>T, NM_032299.3:c.356A>T, NM_001318739.2:c.149A>T, NM_001318739.1:c.149A>T, NM_001318741.2:c.17A>T, NM_001318741.1:c.17A>T, NM_001318740.2:c.17A>T, NM_001318740.1:c.17A>T, NP_115675.1:p.Glu119Val, NP_001305668.1:p.Glu50Val, NP_001305670.1:p.Glu6Val, NP_001305669.1:p.Glu6Val

Select item 122963037816.

rs1229630378 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:103066468 (GRCh38)
11:102937197 (GRCh37)
Canonical SPDI:: NC_000011.10:103066467:A:G
Gene:: DCUN1D5 (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_000011.10:g.103066468A>G, NC_000011.9:g.102937197A>G, NM_032299.4:c.441T>C, NM_032299.3:c.441T>C, NM_001318739.2:c.234T>C, NM_001318739.1:c.234T>C, NM_001318741.2:c.102T>C, NM_001318741.1:c.102T>C, NM_001318740.2:c.102T>C, NM_001318740.1:c.102T>C

Select item 122044514317.

rs1220445143 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C [Show Flanks]
Chromosome:: 11:103066537 (GRCh38)
11:102937266 (GRCh37)
Canonical SPDI:: NC_000011.10:103066536:T:A,NC_000011.10:103066536:T:C
Gene:: DCUN1D5 (Varview)
Functional Consequence:: missense_variant,synonymous_variant,coding_sequence_variant
Validated:: by frequency,by cluster
MAF:: C=0.000004/1 (GnomAD_exomes)
A=0.000177/3 (TOMMO)
HGVS:: NC_000011.10:g.103066537T>A, NC_000011.10:g.103066537T>C, NC_000011.9:g.102937266T>A, NC_000011.9:g.102937266T>C, NM_032299.4:c.372A>T, NM_032299.4:c.372A>G, NM_032299.3:c.372A>T, NM_032299.3:c.372A>G, NM_001318739.2:c.165A>T, NM_001318739.2:c.165A>G, NM_001318739.1:c.165A>T, NM_001318739.1:c.165A>G, NM_001318741.2:c.33A>T, NM_001318741.2:c.33A>G, NM_001318741.1:c.33A>T, NM_001318741.1:c.33A>G, NM_001318740.2:c.33A>T, NM_001318740.2:c.33A>G, NM_001318740.1:c.33A>T, NM_001318740.1:c.33A>G, NP_115675.1:p.Lys124Asn, NP_001305668.1:p.Lys55Asn, NP_001305670.1:p.Lys11Asn, NP_001305669.1:p.Lys11Asn

Select item 118160371218.

rs1181603712 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:103064324 (GRCh38)
11:102935053 (GRCh37)
Canonical SPDI:: NC_000011.10:103064323:G:A
Gene:: DCUN1D5 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.103064324G>A, NC_000011.9:g.102935053G>A, NM_032299.4:c.609C>T, NM_032299.3:c.609C>T, NM_001318739.2:c.402C>T, NM_001318739.1:c.402C>T, NM_001318741.2:c.270C>T, NM_001318741.1:c.270C>T, NM_001318740.2:c.270C>T, NM_001318740.1:c.270C>T

Select item 117978242819.

rs1179782428 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:103064283 (GRCh38)
11:102935012 (GRCh37)
Canonical SPDI:: NC_000011.10:103064282:T:C
Gene:: DCUN1D5 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000015/4 (TOPMED)
C=0.000021/3 (GnomAD)
HGVS:: NC_000011.10:g.103064283T>C, NC_000011.9:g.102935012T>C, NM_032299.4:c.650A>G, NM_032299.3:c.650A>G, NM_001318739.2:c.443A>G, NM_001318739.1:c.443A>G, NM_001318741.2:c.311A>G, NM_001318741.1:c.311A>G, NM_001318740.2:c.311A>G, NM_001318740.1:c.311A>G, NP_115675.1:p.Asp217Gly, NP_001305668.1:p.Asp148Gly, NP_001305670.1:p.Asp104Gly, NP_001305669.1:p.Asp104Gly

Select item 117028836720.

rs1170288367 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:103066477 (GRCh38)
11:102937206 (GRCh37)
Canonical SPDI:: NC_000011.10:103066476:A:G
Gene:: DCUN1D5 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: G=0.000111/1 (ALFA)
G=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000011.10:g.103066477A>G, NC_000011.9:g.102937206A>G, NM_032299.4:c.432T>C, NM_032299.3:c.432T>C, NM_001318739.2:c.225T>C, NM_001318739.1:c.225T>C, NM_001318741.2:c.93T>C, NM_001318741.1:c.93T>C, NM_001318740.2:c.93T>C, NM_001318740.1:c.93T>C

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