SNP Links for Protein (Select 18491024) - SNP

Links from Protein

Items: 1 to 20 of 785

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Select item 14894348981.

rs1489434898 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:66491272 (GRCh38)
11:66258743 (GRCh37)
Canonical SPDI:: NC_000011.10:66491271:G:A
Gene:: DPP3 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.66491272G>A, NC_000011.9:g.66258743G>A, NG_032068.1:g.15864G>A, NM_005700.5:c.687G>A, NM_005700.4:c.687G>A, NM_130443.4:c.687G>A, NM_130443.3:c.687G>A, NM_001256670.2:c.597G>A, NM_001256670.1:c.597G>A

Select item 14874444942.

rs1487444494 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 11:66497300 (GRCh38)
11:66264771 (GRCh37)
Canonical SPDI:: NC_000011.10:66497299:C:G
Gene:: DPP3 (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.66497300C>G, NC_000011.9:g.66264771C>G, NG_032068.1:g.21892C>G, NM_005700.5:c.1701C>G, NM_005700.4:c.1701C>G, NM_130443.4:c.1701C>G, NM_130443.3:c.1701C>G, NM_001256670.2:c.1611C>G, NM_001256670.1:c.1611C>G

Select item 14859563293.

rs1485956329 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:66493576 (GRCh38)
11:66261047 (GRCh37)
Canonical SPDI:: NC_000011.10:66493575:T:C
Gene:: DPP3 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000031/1 (ALFA)
C=0./0 (GnomAD)
C=0.000004/1 (GnomAD_exomes)
C=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.66493576T>C, NC_000011.9:g.66261047T>C, NG_032068.1:g.18168T>C, NM_005700.5:c.1332T>C, NM_005700.4:c.1332T>C, NM_130443.4:c.1332T>C, NM_130443.3:c.1332T>C, NM_001256670.2:c.1242T>C, NM_001256670.1:c.1242T>C

Select item 14843704814.

rs1484370481 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:66486577 (GRCh38)
11:66254048 (GRCh37)
Canonical SPDI:: NC_000011.10:66486576:C:T
Gene:: DPP3 (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_000011.10:g.66486577C>T, NC_000011.9:g.66254048C>T, NG_032068.1:g.11169C>T, NM_005700.5:c.398C>T, NM_005700.4:c.398C>T, NM_130443.4:c.398C>T, NM_130443.3:c.398C>T, NM_001256670.2:c.308C>T, NM_001256670.1:c.308C>T, NP_005691.2:p.Ala133Val, NP_569710.2:p.Ala133Val, NP_001243599.1:p.Ala103Val

Select item 14836138875.

rs1483613887 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:66486663 (GRCh38)
11:66254134 (GRCh37)
Canonical SPDI:: NC_000011.10:66486662:G:A
Gene:: DPP3 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.66486663G>A, NC_000011.9:g.66254134G>A, NG_032068.1:g.11255G>A, NM_005700.5:c.484G>A, NM_005700.4:c.484G>A, NM_130443.4:c.484G>A, NM_130443.3:c.484G>A, NM_001256670.2:c.394G>A, NM_001256670.1:c.394G>A, NP_005691.2:p.Gly162Arg, NP_569710.2:p.Gly162Arg, NP_001243599.1:p.Gly132Arg

Select item 14797125686.

rs1479712568 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:66491619 (GRCh38)
11:66259090 (GRCh37)
Canonical SPDI:: NC_000011.10:66491618:G:A
Gene:: DPP3 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.66491619G>A, NC_000011.9:g.66259090G>A, NG_032068.1:g.16211G>A, NM_005700.5:c.924G>A, NM_005700.4:c.924G>A, NM_130443.4:c.924G>A, NM_130443.3:c.924G>A, NM_001256670.2:c.834G>A, NM_001256670.1:c.834G>A

Select item 14780065597.

rs1478006559 [Homo sapiens]

Variant type:: INS
Alleles:: ->GAGTAGGTAGGG [Show Flanks]
Chromosome:: 11:66495734 (GRCh38)
11:66263206 (GRCh37)
Canonical SPDI:: NC_000011.10:66495734::GAGTAGGTAGGG
Gene:: DPP3 (Varview)
Functional Consequence:: inframe_insertion,coding_sequence_variant,stop_gained
Validated:: by frequency,by cluster
MAF:: GAGTAGGTAGGG=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.66495734_66495735insGAGTAGGTAGGG, NC_000011.9:g.66263205_66263206insGAGTAGGTAGGG, NG_032068.1:g.20326_20327insGAGTAGGTAGGG, NM_005700.5:c.1682_1683insGAGTAGGTAGGG, NM_005700.4:c.1682_1683insGAGTAGGTAGGG, NM_130443.4:c.1682_1683insGAGTAGGTAGGG, NM_130443.3:c.1682_1683insGAGTAGGTAGGG, NM_001256670.2:c.1592_1593insGAGTAGGTAGGG, NM_001256670.1:c.1592_1593insGAGTAGGTAGGG, NP_005691.2:p.Phe562_Asn563insSerArgTer, NP_569710.2:p.Phe562_Asn563insSerArgTer, NP_001243599.1:p.Phe532_Asn533insSerArgTer

Select item 14773467128.

rs1477346712 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:66482269 (GRCh38)
11:66249740 (GRCh37)
Canonical SPDI:: NC_000011.10:66482268:C:T
Gene:: DPP3 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.66482269C>T, NC_000011.9:g.66249740C>T, NG_032068.1:g.6861C>T, NM_005700.5:c.69C>T, NM_005700.4:c.69C>T, NM_130443.4:c.69C>T, NM_130443.3:c.69C>T, NM_001256670.2:c.69C>T, NM_001256670.1:c.69C>T

Select item 14766250439.

rs1476625043 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:66497357 (GRCh38)
11:66264828 (GRCh37)
Canonical SPDI:: NC_000011.10:66497356:C:T
Gene:: DPP3 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (GnomAD_exomes)
T=0.000014/2 (GnomAD)
T=0.000035/1 (TOMMO)
HGVS:: NC_000011.10:g.66497357C>T, NC_000011.9:g.66264828C>T, NG_032068.1:g.21949C>T, NM_005700.5:c.1758C>T, NM_005700.4:c.1758C>T, NM_130443.4:c.1758C>T, NM_130443.3:c.1758C>T, NM_001256670.2:c.1668C>T, NM_001256670.1:c.1668C>T

Select item 147653075410.

rs1476530754 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 11:66495249 (GRCh38)
11:66262720 (GRCh37)
Canonical SPDI:: NC_000011.10:66495248:A:C
Gene:: DPP3 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.66495249A>C, NC_000011.9:g.66262720A>C, NG_032068.1:g.19841A>C, NM_005700.5:c.1433A>C, NM_005700.4:c.1433A>C, NM_130443.4:c.1433A>C, NM_130443.3:c.1433A>C, NM_001256670.2:c.1343A>C, NM_001256670.1:c.1343A>C, NP_005691.2:p.Asn478Thr, NP_569710.2:p.Asn478Thr, NP_001243599.1:p.Asn448Thr

Select item 147424626411.

rs1474246264 [Homo sapiens]

Variant type:: DELINS
Alleles:: GAG>- [Show Flanks]
Chromosome:: 11:66482462 (GRCh38)
11:66249933 (GRCh37)
Canonical SPDI:: NC_000011.10:66482455:GAGGAGGAG:GAGGAG
Gene:: DPP3 (Varview)
Functional Consequence:: inframe_deletion,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GAGGAG=0./0 (ALFA)
-=0.000004/1 (GnomAD_exomes)
-=0.000007/1 (GnomAD)
-=0.000008/2 (TOPMED)
HGVS:: NC_000011.10:g.66482456GAG[2], NC_000011.9:g.66249927GAG[2], NG_032068.1:g.7048GAG[2], NM_005700.5:c.256GAG[2], NM_005700.4:c.256GAG[2], NM_130443.4:c.256GAG[2], NM_130443.3:c.256GAG[2], NM_001256670.2:c.256GAG[2], NM_001256670.1:c.256GAG[2], NP_005691.2:p.Glu88del, NP_569710.2:p.Glu88del, NP_001243599.1:p.Glu88del

Select item 147360679012.

rs1473606790 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:66509168 (GRCh38)
11:66276639 (GRCh37)
Canonical SPDI:: NC_000011.10:66509167:T:C
Gene:: BBS1 (Varview), DPP3 (Varview)
Functional Consequence:: upstream_transcript_variant,coding_sequence_variant,2KB_upstream_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
HGVS:: NC_000011.10:g.66509168T>C, NC_000011.9:g.66276639T>C, NG_032068.1:g.33760T>C, NM_005700.5:c.2131T>C, NM_005700.4:c.2131T>C, NM_130443.4:c.2131T>C, NM_130443.3:c.2131T>C, NM_001256670.2:c.2041T>C, NM_001256670.1:c.2041T>C, NG_009093.1:g.3521T>C

Select item 147320057813.

rs1473200578 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 11:66486594 (GRCh38)
11:66254065 (GRCh37)
Canonical SPDI:: NC_000011.10:66486593:G:T
Gene:: DPP3 (Varview)
Functional Consequence:: coding_sequence_variant,stop_gained
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000155/4 (ALFA)
T=0.000014/2 (GnomAD)
T=0.00067/3 (Estonian)
HGVS:: NC_000011.10:g.66486594G>T, NC_000011.9:g.66254065G>T, NG_032068.1:g.11186G>T, NM_005700.5:c.415G>T, NM_005700.4:c.415G>T, NM_130443.4:c.415G>T, NM_130443.3:c.415G>T, NM_001256670.2:c.325G>T, NM_001256670.1:c.325G>T, NP_005691.2:p.Glu139Ter, NP_569710.2:p.Glu139Ter, NP_001243599.1:p.Glu109Ter

Select item 147256462314.

rs1472564623 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:66486671 (GRCh38)
11:66254142 (GRCh37)
Canonical SPDI:: NC_000011.10:66486670:G:A
Gene:: DPP3 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000011.10:g.66486671G>A, NC_000011.9:g.66254142G>A, NG_032068.1:g.11263G>A, NM_005700.5:c.492G>A, NM_005700.4:c.492G>A, NM_130443.4:c.492G>A, NM_130443.3:c.492G>A, NM_001256670.2:c.402G>A, NM_001256670.1:c.402G>A

Select item 147196744915.

rs1471967449 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:66495698 (GRCh38)
11:66263169 (GRCh37)
Canonical SPDI:: NC_000011.10:66495697:C:T
Gene:: DPP3 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.66495698C>T, NC_000011.9:g.66263169C>T, NG_032068.1:g.20290C>T, NM_005700.5:c.1646C>T, NM_005700.4:c.1646C>T, NM_130443.4:c.1646C>T, NM_130443.3:c.1646C>T, NM_001256670.2:c.1556C>T, NM_001256670.1:c.1556C>T, NP_005691.2:p.Ala549Val, NP_569710.2:p.Ala549Val, NP_001243599.1:p.Ala519Val

Select item 147166515216.

rs1471665152 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:66492799 (GRCh38)
11:66260270 (GRCh37)
Canonical SPDI:: NC_000011.10:66492798:C:T
Gene:: DPP3 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000011.10:g.66492799C>T, NC_000011.9:g.66260270C>T, NG_032068.1:g.17391C>T, NM_005700.5:c.1072C>T, NM_005700.4:c.1072C>T, NM_130443.4:c.1072C>T, NM_130443.3:c.1072C>T, NM_001256670.2:c.982C>T, NM_001256670.1:c.982C>T, NP_005691.2:p.Pro358Ser, NP_569710.2:p.Pro358Ser, NP_001243599.1:p.Pro328Ser

Select item 146820063317.

rs1468200633 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:66491300 (GRCh38)
11:66258771 (GRCh37)
Canonical SPDI:: NC_000011.10:66491299:T:C
Gene:: DPP3 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (GnomAD_exomes)
C=0.000007/1 (GnomAD)
C=0.000015/4 (TOPMED)
HGVS:: NC_000011.10:g.66491300T>C, NC_000011.9:g.66258771T>C, NG_032068.1:g.15892T>C, NM_005700.5:c.715T>C, NM_005700.4:c.715T>C, NM_130443.4:c.715T>C, NM_130443.3:c.715T>C, NM_001256670.2:c.625T>C, NM_001256670.1:c.625T>C, NP_005691.2:p.Phe239Leu, NP_569710.2:p.Phe239Leu, NP_001243599.1:p.Phe209Leu

Select item 146639524718.

rs1466395247 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 11:66504662 (GRCh38)
11:66272133 (GRCh37)
Canonical SPDI:: NC_000011.10:66504661:G:A,NC_000011.10:66504661:G:T
Gene:: DPP3 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.66504662G>A, NC_000011.10:g.66504662G>T, NC_000011.9:g.66272133G>A, NC_000011.9:g.66272133G>T, NG_032068.1:g.29254G>A, NG_032068.1:g.29254G>T, NM_005700.5:c.1929G>A, NM_005700.5:c.1929G>T, NM_005700.4:c.1929G>A, NM_005700.4:c.1929G>T, NM_130443.4:c.1929G>A, NM_130443.4:c.1929G>T, NM_130443.3:c.1929G>A, NM_130443.3:c.1929G>T, NM_001256670.2:c.1839G>A, NM_001256670.2:c.1839G>T, NM_001256670.1:c.1839G>A, NM_001256670.1:c.1839G>T

Select item 146266758719.

rs1462667587 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 11:66495487 (GRCh38)
11:66262958 (GRCh37)
Canonical SPDI:: NC_000011.10:66495486:G:A
Gene:: DPP3 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: A=0.000047/1 (ALFA)
A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.66495487G>A, NC_000011.9:g.66262958G>A, NG_032068.1:g.20079G>A, NM_005700.5:c.1575G>A, NM_005700.4:c.1575G>A, NM_130443.4:c.1575G>A, NM_130443.3:c.1575G>A, NM_001256670.2:c.1485G>A, NM_001256670.1:c.1485G>A

Select item 146258323320.

rs1462583233 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 11:66493542 (GRCh38)
11:66261013 (GRCh37)
Canonical SPDI:: NC_000011.10:66493541:A:G
Gene:: DPP3 (Varview)
Functional Consequence:: coding_sequence_variant,missense_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.66493542A>G, NC_000011.9:g.66261013A>G, NG_032068.1:g.18134A>G, NM_005700.5:c.1298A>G, NM_005700.4:c.1298A>G, NM_130443.4:c.1298A>G, NM_130443.3:c.1298A>G, NM_001256670.2:c.1208A>G, NM_001256670.1:c.1208A>G, NP_005691.2:p.Asp433Gly, NP_569710.2:p.Asp433Gly, NP_001243599.1:p.Asp403Gly

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