SNP Links for Protein (Select 13994276) - SNP

Links from Protein

Items: 1 to 20 of 328

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Select item 14877977211.

rs1487797721 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 16:2713545 (GRCh38)
16:2763546 (GRCh37)
Canonical SPDI:: NC_000016.10:2713544:T:C
Gene:: PRSS27 (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)
C=0.000008/2 (TOPMED)
HGVS:: NC_000016.10:g.2713545T>C, NC_000016.9:g.2763546T>C, NM_031948.5:c.662A>G, NM_031948.4:c.662A>G, NM_031948.3:c.662A>G, XM_011522689.3:c.356A>G, XM_011522689.2:c.356A>G, XM_011522689.1:c.356A>G, NM_001318395.2:c.356A>G, NM_001318395.1:c.356A>G, NP_114154.1:p.Lys221Arg, XP_011520991.1:p.Lys119Arg, NP_001305324.1:p.Lys119Arg

Select item 14856130612.

rs1485613061 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 16:2713535 (GRCh38)
16:2763536 (GRCh37)
Canonical SPDI:: NC_000016.10:2713534:G:A
Gene:: PRSS27 (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_000016.10:g.2713535G>A, NC_000016.9:g.2763536G>A, NM_031948.5:c.672C>T, NM_031948.4:c.672C>T, NM_031948.3:c.672C>T, XM_011522689.3:c.366C>T, XM_011522689.2:c.366C>T, XM_011522689.1:c.366C>T, NM_001318395.2:c.366C>T, NM_001318395.1:c.366C>T

Select item 14845446153.

rs1484544615 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 16:2715825 (GRCh38)
16:2765826 (GRCh37)
Canonical SPDI:: NC_000016.10:2715824:C:T
Gene:: PRSS27 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,upstream_transcript_variant,intron_variant,synonymous_variant,coding_sequence_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_000016.10:g.2715825C>T, NC_000016.9:g.2765826C>T, NM_031948.5:c.129G>A, NM_031948.4:c.129G>A, NM_031948.3:c.129G>A

Select item 14829367574.

rs1482936757 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 16:2714322 (GRCh38)
16:2764323 (GRCh37)
Canonical SPDI:: NC_000016.10:2714321:G:C
Gene:: PRSS27 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,5_prime_UTR_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000016.10:g.2714322G>C, NC_000016.9:g.2764323G>C, NM_031948.5:c.251C>G, NM_031948.4:c.251C>G, NM_031948.3:c.251C>G, XM_011522689.3:c.-56C>G, XM_011522689.2:c.-56C>G, XM_011522689.1:c.-56C>G, NM_001318395.2:c.-56C>G, NM_001318395.1:c.-56C>G, NP_114154.1:p.Ser84Cys

Select item 14819976375.

rs1481997637 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 16:2715750 (GRCh38)
16:2765751 (GRCh37)
Canonical SPDI:: NC_000016.10:2715749:C:G,NC_000016.10:2715749:C:T
Gene:: PRSS27 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,upstream_transcript_variant,intron_variant,synonymous_variant,coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000016.10:g.2715750C>G, NC_000016.10:g.2715750C>T, NC_000016.9:g.2765751C>G, NC_000016.9:g.2765751C>T, NM_031948.5:c.204G>C, NM_031948.5:c.204G>A, NM_031948.4:c.204G>C, NM_031948.4:c.204G>A, NM_031948.3:c.204G>C, NM_031948.3:c.204G>A, NP_114154.1:p.Gln68His

Select item 14796073276.

rs1479607327 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 16:2715834 (GRCh38)
16:2765835 (GRCh37)
Canonical SPDI:: NC_000016.10:2715833:G:A
Gene:: PRSS27 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,upstream_transcript_variant,intron_variant,synonymous_variant,coding_sequence_variant
HGVS:: NC_000016.10:g.2715834G>A, NC_000016.9:g.2765835G>A, NM_031948.5:c.120C>T, NM_031948.4:c.120C>T, NM_031948.3:c.120C>T

Select item 14773627887.

rs1477362788 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 16:2712772 (GRCh38)
16:2762773 (GRCh37)
Canonical SPDI:: NC_000016.10:2712771:A:G
Gene:: PRSS27 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: G=0.000047/1 (ALFA)
G=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000016.10:g.2712772A>G, NC_000016.9:g.2762773A>G, NM_031948.5:c.721T>C, NM_031948.4:c.721T>C, NM_031948.3:c.721T>C, XM_011522689.3:c.415T>C, XM_011522689.2:c.415T>C, XM_011522689.1:c.415T>C, NM_001318395.2:c.415T>C, NM_001318395.1:c.415T>C, NP_114154.1:p.Trp241Arg, XP_011520991.1:p.Trp139Arg, NP_001305324.1:p.Trp139Arg

Select item 14684268958.

rs1468426895 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 16:2715784 (GRCh38)
16:2765785 (GRCh37)
Canonical SPDI:: NC_000016.10:2715783:C:T
Gene:: PRSS27 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,upstream_transcript_variant,intron_variant,coding_sequence_variant,missense_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_000016.10:g.2715784C>T, NC_000016.9:g.2765785C>T, NM_031948.5:c.170G>A, NM_031948.4:c.170G>A, NM_031948.3:c.170G>A, NP_114154.1:p.Ser57Asn

Select item 14649580399.

rs1464958039 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,G [Show Flanks]
Chromosome:: 16:2712759 (GRCh38)
16:2762760 (GRCh37)
Canonical SPDI:: NC_000016.10:2712758:C:A,NC_000016.10:2712758:C:G
Gene:: PRSS27 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
A=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000016.10:g.2712759C>A, NC_000016.10:g.2712759C>G, NC_000016.9:g.2762760C>A, NC_000016.9:g.2762760C>G, NM_031948.5:c.734G>T, NM_031948.5:c.734G>C, NM_031948.4:c.734G>T, NM_031948.4:c.734G>C, NM_031948.3:c.734G>T, NM_031948.3:c.734G>C, XM_011522689.3:c.428G>T, XM_011522689.3:c.428G>C, XM_011522689.2:c.428G>T, XM_011522689.2:c.428G>C, XM_011522689.1:c.428G>T, XM_011522689.1:c.428G>C, NM_001318395.2:c.428G>T, NM_001318395.2:c.428G>C, NM_001318395.1:c.428G>T, NM_001318395.1:c.428G>C, NP_114154.1:p.Gly245Val, NP_114154.1:p.Gly245Ala, XP_011520991.1:p.Gly143Val, XP_011520991.1:p.Gly143Ala, NP_001305324.1:p.Gly143Val, NP_001305324.1:p.Gly143Ala

Select item 146458694010.

rs1464586940 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 16:2712766 (GRCh38)
16:2762767 (GRCh37)
Canonical SPDI:: NC_000016.10:2712765:G:A
Gene:: PRSS27 (Varview)
Functional Consequence:: stop_gained,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000014/2 (GnomAD)
A=0.000015/4 (TOPMED)
HGVS:: NC_000016.10:g.2712766G>A, NC_000016.9:g.2762767G>A, NM_031948.5:c.727C>T, NM_031948.4:c.727C>T, NM_031948.3:c.727C>T, XM_011522689.3:c.421C>T, XM_011522689.2:c.421C>T, XM_011522689.1:c.421C>T, NM_001318395.2:c.421C>T, NM_001318395.1:c.421C>T, NP_114154.1:p.Gln243Ter, XP_011520991.1:p.Gln141Ter, NP_001305324.1:p.Gln141Ter

Select item 145852242111.

rs1458522421 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 16:2713631 (GRCh38)
16:2763632 (GRCh37)
Canonical SPDI:: NC_000016.10:2713630:G:A
Gene:: PRSS27 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000016.10:g.2713631G>A, NC_000016.9:g.2763632G>A, NM_031948.5:c.576C>T, NM_031948.4:c.576C>T, NM_031948.3:c.576C>T, XM_011522689.3:c.270C>T, XM_011522689.2:c.270C>T, XM_011522689.1:c.270C>T, NM_001318395.2:c.270C>T, NM_001318395.1:c.270C>T

Select item 145671276412.

rs1456712764 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 16:2715845 (GRCh38)
16:2765846 (GRCh37)
Canonical SPDI:: NC_000016.10:2715844:C:A
Gene:: PRSS27 (Varview)
Functional Consequence:: coding_sequence_variant,intron_variant,upstream_transcript_variant,genic_upstream_transcript_variant,missense_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000016.10:g.2715845C>A, NC_000016.9:g.2765846C>A, NM_031948.5:c.109G>T, NM_031948.4:c.109G>T, NM_031948.3:c.109G>T, NP_114154.1:p.Gly37Cys

Select item 145046380513.

rs1450463805 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 16:2715730 (GRCh38)
16:2765731 (GRCh37)
Canonical SPDI:: NC_000016.10:2715729:T:C
Gene:: PRSS27 (Varview)
Functional Consequence:: coding_sequence_variant,intron_variant,upstream_transcript_variant,genic_upstream_transcript_variant,missense_variant
Validated:: by frequency
MAF:: C=0.000007/1 (GnomAD_exomes)
HGVS:: NC_000016.10:g.2715730T>C, NC_000016.9:g.2765731T>C, NM_031948.5:c.224A>G, NM_031948.4:c.224A>G, NM_031948.3:c.224A>G, NP_114154.1:p.His75Arg

Select item 144927201614.

rs1449272016 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 16:2715880 (GRCh38)
16:2765881 (GRCh37)
Canonical SPDI:: NC_000016.10:2715879:G:T
Gene:: PRSS27 (Varview)
Functional Consequence:: coding_sequence_variant,intron_variant,upstream_transcript_variant,genic_upstream_transcript_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000016.10:g.2715880G>T, NC_000016.9:g.2765881G>T, NM_031948.5:c.74C>A, NM_031948.4:c.74C>A, NM_031948.3:c.74C>A, NP_114154.1:p.Ala25Asp

Select item 144621906015.

rs1446219060 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 16:2712665 (GRCh38)
16:2762666 (GRCh37)
Canonical SPDI:: NC_000016.10:2712664:G:A,NC_000016.10:2712664:G:T
Gene:: PRSS27 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000016.10:g.2712665G>A, NC_000016.10:g.2712665G>T, NC_000016.9:g.2762666G>A, NC_000016.9:g.2762666G>T, NM_031948.5:c.828C>T, NM_031948.5:c.828C>A, NM_031948.4:c.828C>T, NM_031948.4:c.828C>A, NM_031948.3:c.828C>T, NM_031948.3:c.828C>A, XM_011522689.3:c.522C>T, XM_011522689.3:c.522C>A, XM_011522689.2:c.522C>T, XM_011522689.2:c.522C>A, XM_011522689.1:c.522C>T, XM_011522689.1:c.522C>A, NM_001318395.2:c.522C>T, NM_001318395.2:c.522C>A, NM_001318395.1:c.522C>T, NM_001318395.1:c.522C>A

Select item 144619129516.

rs1446191295 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 16:2712752 (GRCh38)
16:2762753 (GRCh37)
Canonical SPDI:: NC_000016.10:2712751:G:A
Gene:: PRSS27 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
HGVS:: NC_000016.10:g.2712752G>A, NC_000016.9:g.2762753G>A, NM_031948.5:c.741C>T, NM_031948.4:c.741C>T, NM_031948.3:c.741C>T, XM_011522689.3:c.435C>T, XM_011522689.2:c.435C>T, XM_011522689.1:c.435C>T, NM_001318395.2:c.435C>T, NM_001318395.1:c.435C>T

Select item 143866105817.

rs1438661058 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 16:2713604 (GRCh38)
16:2763605 (GRCh37)
Canonical SPDI:: NC_000016.10:2713603:A:C
Gene:: PRSS27 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000016.10:g.2713604A>C, NC_000016.9:g.2763605A>C, NM_031948.5:c.603T>G, NM_031948.4:c.603T>G, NM_031948.3:c.603T>G, XM_011522689.3:c.297T>G, XM_011522689.2:c.297T>G, XM_011522689.1:c.297T>G, NM_001318395.2:c.297T>G, NM_001318395.1:c.297T>G, NP_114154.1:p.Phe201Leu, XP_011520991.1:p.Phe99Leu, NP_001305324.1:p.Phe99Leu

Select item 143681164018.

rs1436811640 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 16:2713576 (GRCh38)
16:2763577 (GRCh37)
Canonical SPDI:: NC_000016.10:2713575:C:T
Gene:: PRSS27 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000012/3 (GnomAD_exomes)
HGVS:: NC_000016.10:g.2713576C>T, NC_000016.9:g.2763577C>T, NM_031948.5:c.631G>A, NM_031948.4:c.631G>A, NM_031948.3:c.631G>A, XM_011522689.3:c.325G>A, XM_011522689.2:c.325G>A, XM_011522689.1:c.325G>A, NM_001318395.2:c.325G>A, NM_001318395.1:c.325G>A, NP_114154.1:p.Asp211Asn, XP_011520991.1:p.Asp109Asn, NP_001305324.1:p.Asp109Asn

Select item 143598679719.

rs1435986797 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 16:2715842 (GRCh38)
16:2765843 (GRCh37)
Canonical SPDI:: NC_000016.10:2715841:C:A,NC_000016.10:2715841:C:T
Gene:: PRSS27 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,upstream_transcript_variant,intron_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
HGVS:: NC_000016.10:g.2715842C>A, NC_000016.10:g.2715842C>T, NC_000016.9:g.2765843C>A, NC_000016.9:g.2765843C>T, NM_031948.5:c.112G>T, NM_031948.5:c.112G>A, NM_031948.4:c.112G>T, NM_031948.4:c.112G>A, NM_031948.3:c.112G>T, NM_031948.3:c.112G>A, NP_114154.1:p.Gly38Trp, NP_114154.1:p.Gly38Arg

Select item 143592717320.

rs1435927173 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 16:2712781 (GRCh38)
16:2762782 (GRCh37)
Canonical SPDI:: NC_000016.10:2712780:C:T
Gene:: PRSS27 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
HGVS:: NC_000016.10:g.2712781C>T, NC_000016.9:g.2762782C>T, NM_031948.5:c.712G>A, NM_031948.4:c.712G>A, NM_031948.3:c.712G>A, XM_011522689.3:c.406G>A, XM_011522689.2:c.406G>A, XM_011522689.1:c.406G>A, NM_001318395.2:c.406G>A, NM_001318395.1:c.406G>A, NP_114154.1:p.Gly238Ser, XP_011520991.1:p.Gly136Ser, NP_001305324.1:p.Gly136Ser

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