SNP Links for Protein (Select 289547754) - SNP

Links from Protein

Items: 1 to 20 of 497

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Select item 14896752501.

rs1489675250 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 16:1079383 (GRCh38)
16:1129383 (GRCh37)
Canonical SPDI:: NC_000016.10:1079382:T:A
Gene:: SSTR5 (Varview), SSTR5-AS1 (Varview)
Functional Consequence:: coding_sequence_variant,2KB_upstream_variant,missense_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000011/3 (TOPMED)
A=0.000014/2 (GnomAD)
HGVS:: NC_000016.10:g.1079383T>A, NC_000016.9:g.1129383T>A, NG_016744.1:g.11628T>A, NM_001053.4:c.515T>A, NM_001053.3:c.515T>A, NM_001172560.3:c.515T>A, NM_001172560.2:c.515T>A, NM_001172560.1:c.515T>A, NM_001172572.1:c.515T>A, NM_001172573.1:c.515T>A, NP_001044.1:p.Leu172Gln, NP_001166031.1:p.Leu172Gln

Select item 14889577822.

rs1488957782 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 16:1079331 (GRCh38)
16:1129331 (GRCh37)
Canonical SPDI:: NC_000016.10:1079330:G:A,NC_000016.10:1079330:G:T
Gene:: SSTR5 (Varview), SSTR5-AS1 (Varview)
Functional Consequence:: coding_sequence_variant,2KB_upstream_variant,missense_variant,upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
T=0.000004/1 (TOPMED)
HGVS:: NC_000016.10:g.1079331G>A, NC_000016.10:g.1079331G>T, NC_000016.9:g.1129331G>A, NC_000016.9:g.1129331G>T, NG_016744.1:g.11576G>A, NG_016744.1:g.11576G>T, NM_001053.4:c.463G>A, NM_001053.4:c.463G>T, NM_001053.3:c.463G>A, NM_001053.3:c.463G>T, NM_001172560.3:c.463G>A, NM_001172560.3:c.463G>T, NM_001172560.2:c.463G>A, NM_001172560.2:c.463G>T, NM_001172560.1:c.463G>A, NM_001172560.1:c.463G>T, NM_001172572.1:c.463G>A, NM_001172572.1:c.463G>T, NM_001172573.1:c.463G>A, NM_001172573.1:c.463G>T, NP_001044.1:p.Val155Met, NP_001044.1:p.Val155Leu, NP_001166031.1:p.Val155Met, NP_001166031.1:p.Val155Leu

Select item 14886426963.

rs1488642696 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 16:1079126 (GRCh38)
16:1129126 (GRCh37)
Canonical SPDI:: NC_000016.10:1079125:C:T
Gene:: SSTR5 (Varview), SSTR5-AS1 (Varview)
Functional Consequence:: coding_sequence_variant,2KB_upstream_variant,upstream_transcript_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
T=0.000021/3 (GnomAD)
HGVS:: NC_000016.10:g.1079126C>T, NC_000016.9:g.1129126C>T, NG_016744.1:g.11371C>T, NM_001053.4:c.258C>T, NM_001053.3:c.258C>T, NM_001172560.3:c.258C>T, NM_001172560.2:c.258C>T, NM_001172560.1:c.258C>T, NM_001172572.1:c.258C>T, NM_001172573.1:c.258C>T

Select item 14873393154.

rs1487339315 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 16:1079380 (GRCh38)
16:1129380 (GRCh37)
Canonical SPDI:: NC_000016.10:1079379:C:T
Gene:: SSTR5 (Varview), SSTR5-AS1 (Varview)
Functional Consequence:: coding_sequence_variant,upstream_transcript_variant,missense_variant,2KB_upstream_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000016.10:g.1079380C>T, NC_000016.9:g.1129380C>T, NG_016744.1:g.11625C>T, NM_001053.4:c.512C>T, NM_001053.3:c.512C>T, NM_001172560.3:c.512C>T, NM_001172560.2:c.512C>T, NM_001172560.1:c.512C>T, NM_001172572.1:c.512C>T, NM_001172573.1:c.512C>T, NP_001044.1:p.Ser171Leu, NP_001166031.1:p.Ser171Leu

Select item 14728106125.

rs1472810612 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 16:1079254 (GRCh38)
16:1129254 (GRCh37)
Canonical SPDI:: NC_000016.10:1079253:G:A
Gene:: SSTR5 (Varview), SSTR5-AS1 (Varview)
Functional Consequence:: coding_sequence_variant,upstream_transcript_variant,missense_variant,2KB_upstream_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000016.10:g.1079254G>A, NC_000016.9:g.1129254G>A, NG_016744.1:g.11499G>A, NM_001053.4:c.386G>A, NM_001053.3:c.386G>A, NM_001172560.3:c.386G>A, NM_001172560.2:c.386G>A, NM_001172560.1:c.386G>A, NM_001172572.1:c.386G>A, NM_001172573.1:c.386G>A, NP_001044.1:p.Cys129Tyr, NP_001166031.1:p.Cys129Tyr

Select item 14704969876.

rs1470496987 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 16:1079445 (GRCh38)
16:1129445 (GRCh37)
Canonical SPDI:: NC_000016.10:1079444:C:T
Gene:: SSTR5 (Varview), SSTR5-AS1 (Varview)
Functional Consequence:: coding_sequence_variant,upstream_transcript_variant,missense_variant,2KB_upstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000008/2 (TOPMED)
HGVS:: NC_000016.10:g.1079445C>T, NC_000016.9:g.1129445C>T, NG_016744.1:g.11690C>T, NM_001053.4:c.577C>T, NM_001053.3:c.577C>T, NM_001172560.3:c.577C>T, NM_001172560.2:c.577C>T, NM_001172560.1:c.577C>T, NM_001172572.1:c.577C>T, NP_001044.1:p.Pro193Ser, NP_001166031.1:p.Pro193Ser

Select item 14668548467.

rs1466854846 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 16:1079264 (GRCh38)
16:1129264 (GRCh37)
Canonical SPDI:: NC_000016.10:1079263:C:T
Gene:: SSTR5 (Varview), SSTR5-AS1 (Varview)
Functional Consequence:: coding_sequence_variant,upstream_transcript_variant,synonymous_variant,2KB_upstream_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000016.10:g.1079264C>T, NC_000016.9:g.1129264C>T, NG_016744.1:g.11509C>T, NM_001053.4:c.396C>T, NM_001053.3:c.396C>T, NM_001172560.3:c.396C>T, NM_001172560.2:c.396C>T, NM_001172560.1:c.396C>T, NM_001172572.1:c.396C>T, NM_001172573.1:c.396C>T

Select item 14645280808.

rs1464528080 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 16:1079827 (GRCh38)
16:1129827 (GRCh37)
Canonical SPDI:: NC_000016.10:1079826:G:C
Gene:: SSTR5 (Varview), SSTR5-AS1 (Varview)
Functional Consequence:: upstream_transcript_variant,missense_variant,2KB_upstream_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (GnomAD_exomes)
C=0.000008/2 (TOPMED)
HGVS:: NC_000016.10:g.1079827G>C, NC_000016.9:g.1129827G>C, NG_016744.1:g.12072G>C, NM_001053.4:c.959G>C, NM_001053.3:c.959G>C, NM_001172560.3:c.959G>C, NM_001172560.2:c.959G>C, NM_001172560.1:c.959G>C, NP_001044.1:p.Cys320Ser, NP_001166031.1:p.Cys320Ser

Select item 14617160549.

rs1461716054 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 16:1078985 (GRCh38)
16:1128985 (GRCh37)
Canonical SPDI:: NC_000016.10:1078984:G:A,NC_000016.10:1078984:G:T
Gene:: SSTR5 (Varview), SSTR5-AS1 (Varview)
Functional Consequence:: upstream_transcript_variant,synonymous_variant,2KB_upstream_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)
HGVS:: NC_000016.10:g.1078985G>A, NC_000016.10:g.1078985G>T, NC_000016.9:g.1128985G>A, NC_000016.9:g.1128985G>T, NG_016744.1:g.11230G>A, NG_016744.1:g.11230G>T, NM_001053.4:c.117G>A, NM_001053.4:c.117G>T, NM_001053.3:c.117G>A, NM_001053.3:c.117G>T, NM_001172560.3:c.117G>A, NM_001172560.3:c.117G>T, NM_001172560.2:c.117G>A, NM_001172560.2:c.117G>T, NM_001172560.1:c.117G>A, NM_001172560.1:c.117G>T, NM_001172572.1:c.117G>A, NM_001172572.1:c.117G>T, NM_001172573.1:c.117G>A, NM_001172573.1:c.117G>T

Select item 146162372310.

rs1461623723 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 16:1079697 (GRCh38)
16:1129697 (GRCh37)
Canonical SPDI:: NC_000016.10:1079696:C:A
Gene:: SSTR5 (Varview), SSTR5-AS1 (Varview)
Functional Consequence:: upstream_transcript_variant,missense_variant,2KB_upstream_variant,coding_sequence_variant
HGVS:: NC_000016.10:g.1079697C>A, NC_000016.9:g.1129697C>A, NG_016744.1:g.11942C>A, NM_001053.4:c.829C>A, NM_001053.3:c.829C>A, NM_001172560.3:c.829C>A, NM_001172560.2:c.829C>A, NM_001172560.1:c.829C>A, NP_001044.1:p.Pro277Thr, NP_001166031.1:p.Pro277Thr

Select item 146071370511.

rs1460713705 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 16:1078885 (GRCh38)
16:1128885 (GRCh37)
Canonical SPDI:: NC_000016.10:1078884:C:T
Gene:: SSTR5 (Varview), SSTR5-AS1 (Varview)
Functional Consequence:: upstream_transcript_variant,missense_variant,2KB_upstream_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.1078885C>T, NC_000016.9:g.1128885C>T, NG_016744.1:g.11130C>T, NM_001053.4:c.17C>T, NM_001053.3:c.17C>T, NM_001172560.3:c.17C>T, NM_001172560.2:c.17C>T, NM_001172560.1:c.17C>T, NM_001172572.1:c.17C>T, NM_001172573.1:c.17C>T, NP_001044.1:p.Pro6Leu, NP_001166031.1:p.Pro6Leu

Select item 145827137412.

rs1458271374 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 16:1078930 (GRCh38)
16:1128930 (GRCh37)
Canonical SPDI:: NC_000016.10:1078929:C:A
Gene:: SSTR5 (Varview), SSTR5-AS1 (Varview)
Functional Consequence:: upstream_transcript_variant,missense_variant,2KB_upstream_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000016.10:g.1078930C>A, NC_000016.9:g.1128930C>A, NG_016744.1:g.11175C>A, NM_001053.4:c.62C>A, NM_001053.3:c.62C>A, NM_001172560.3:c.62C>A, NM_001172560.2:c.62C>A, NM_001172560.1:c.62C>A, NM_001172572.1:c.62C>A, NM_001172573.1:c.62C>A, NP_001044.1:p.Ser21Tyr, NP_001166031.1:p.Ser21Tyr

Select item 145715512513.

rs1457155125 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 16:1079440 (GRCh38)
16:1129440 (GRCh37)
Canonical SPDI:: NC_000016.10:1079439:C:T
Gene:: SSTR5 (Varview), SSTR5-AS1 (Varview)
Functional Consequence:: upstream_transcript_variant,missense_variant,2KB_upstream_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000108/2 (ALFA)
T=0.000008/2 (TOPMED)
T=0.000014/2 (GnomAD)
T=0.000446/2 (Estonian)
HGVS:: NC_000016.10:g.1079440C>T, NC_000016.9:g.1129440C>T, NG_016744.1:g.11685C>T, NM_001053.4:c.572C>T, NM_001053.3:c.572C>T, NM_001172560.3:c.572C>T, NM_001172560.2:c.572C>T, NM_001172560.1:c.572C>T, NM_001172572.1:c.572C>T, NP_001044.1:p.Pro191Leu, NP_001166031.1:p.Pro191Leu

Select item 145697402214.

rs1456974022 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 16:1079199 (GRCh38)
16:1129199 (GRCh37)
Canonical SPDI:: NC_000016.10:1079198:C:T
Gene:: SSTR5 (Varview), SSTR5-AS1 (Varview)
Functional Consequence:: upstream_transcript_variant,synonymous_variant,2KB_upstream_variant,coding_sequence_variant
Validated:: by frequency,by cluster
MAF:: T=0.000007/1 (GnomAD)
HGVS:: NC_000016.10:g.1079199C>T, NC_000016.9:g.1129199C>T, NG_016744.1:g.11444C>T, NM_001053.4:c.331C>T, NM_001053.3:c.331C>T, NM_001172560.3:c.331C>T, NM_001172560.2:c.331C>T, NM_001172560.1:c.331C>T, NM_001172572.1:c.331C>T, NM_001172573.1:c.331C>T

Select item 145229971015.

rs1452299710 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 16:1079865 (GRCh38)
16:1129865 (GRCh37)
Canonical SPDI:: NC_000016.10:1079864:A:C
Gene:: SSTR5 (Varview), SSTR5-AS1 (Varview)
Functional Consequence:: upstream_transcript_variant,missense_variant,2KB_upstream_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (GnomAD_exomes)
C=0.000004/1 (TOPMED)
HGVS:: NC_000016.10:g.1079865A>C, NC_000016.9:g.1129865A>C, NG_016744.1:g.12110A>C, NM_001053.4:c.997A>C, NM_001053.3:c.997A>C, NM_001172560.3:c.997A>C, NM_001172560.2:c.997A>C, NM_001172560.1:c.997A>C, NP_001044.1:p.Thr333Pro, NP_001166031.1:p.Thr333Pro

Select item 144863991016.

rs1448639910 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 16:1079210 (GRCh38)
16:1129210 (GRCh37)
Canonical SPDI:: NC_000016.10:1079209:G:A
Gene:: SSTR5 (Varview), SSTR5-AS1 (Varview)
Functional Consequence:: upstream_transcript_variant,synonymous_variant,2KB_upstream_variant,coding_sequence_variant
HGVS:: NC_000016.10:g.1079210G>A, NC_000016.9:g.1129210G>A, NG_016744.1:g.11455G>A, NM_001053.4:c.342G>A, NM_001053.3:c.342G>A, NM_001172560.3:c.342G>A, NM_001172560.2:c.342G>A, NM_001172560.1:c.342G>A, NM_001172572.1:c.342G>A, NM_001172573.1:c.342G>A

Select item 144361980217.

rs1443619802 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 16:1079465 (GRCh38)
16:1129465 (GRCh37)
Canonical SPDI:: NC_000016.10:1079464:C:T
Gene:: SSTR5 (Varview), SSTR5-AS1 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant,synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000094/1 (ALFA)
T=0.000004/1 (GnomAD_exomes)
T=0.000011/3 (TOPMED)
HGVS:: NC_000016.10:g.1079465C>T, NC_000016.9:g.1129465C>T, NG_016744.1:g.11710C>T, NM_001053.4:c.597C>T, NM_001053.3:c.597C>T, NM_001172560.3:c.597C>T, NM_001172560.2:c.597C>T, NM_001172560.1:c.597C>T, NM_001172572.1:c.597C>T

Select item 144251345918.

rs1442513459 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 16:1079295 (GRCh38)
16:1129295 (GRCh37)
Canonical SPDI:: NC_000016.10:1079294:C:T
Gene:: SSTR5 (Varview), SSTR5-AS1 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant,coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000016.10:g.1079295C>T, NC_000016.9:g.1129295C>T, NG_016744.1:g.11540C>T, NM_001053.4:c.427C>T, NM_001053.3:c.427C>T, NM_001172560.3:c.427C>T, NM_001172560.2:c.427C>T, NM_001172560.1:c.427C>T, NM_001172572.1:c.427C>T, NM_001172573.1:c.427C>T, NP_001044.1:p.His143Tyr, NP_001166031.1:p.His143Tyr

Select item 143899265919.

rs1438992659 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 16:1079871 (GRCh38)
16:1129871 (GRCh37)
Canonical SPDI:: NC_000016.10:1079870:C:T
Gene:: SSTR5 (Varview), SSTR5-AS1 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant,coding_sequence_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.1079871C>T, NC_000016.9:g.1129871C>T, NG_016744.1:g.12116C>T, NM_001053.4:c.1003C>T, NM_001053.3:c.1003C>T, NM_001172560.3:c.1003C>T, NM_001172560.2:c.1003C>T, NM_001172560.1:c.1003C>T, NP_001044.1:p.Pro335Ser, NP_001166031.1:p.Pro335Ser

Select item 143842987320.

rs1438429873 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 16:1079680 (GRCh38)
16:1129680 (GRCh37)
Canonical SPDI:: NC_000016.10:1079679:A:G
Gene:: SSTR5 (Varview), SSTR5-AS1 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant,coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (GnomAD_exomes)
G=0.000004/1 (TOPMED)
HGVS:: NC_000016.10:g.1079680A>G, NC_000016.9:g.1129680A>G, NG_016744.1:g.11925A>G, NM_001053.4:c.812A>G, NM_001053.3:c.812A>G, NM_001172560.3:c.812A>G, NM_001172560.2:c.812A>G, NM_001172560.1:c.812A>G, NP_001044.1:p.Asn271Ser, NP_001166031.1:p.Asn271Ser

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