SNP Links for Protein (Select 68160922) - SNP

Links from Protein

Items: 1 to 20 of 89

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Select item 14740505031.

rs1474050503 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 5:150446816 (GRCh38)
5:149826379 (GRCh37)
Canonical SPDI:: NC_000005.10:150446815:G:A
Gene:: RPS14 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000005.10:g.150446816G>A, NC_000005.9:g.149826379G>A, NG_042287.1:g.7941C>T, NM_005617.4:c.297C>T, NM_005617.3:c.297C>T, NM_001025071.2:c.297C>T, NM_001025071.1:c.297C>T, NM_001025070.2:c.297C>T, NM_001025070.1:c.297C>T

Select item 14646212242.

rs1464621224 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 5:150444339 (GRCh38)
5:149823902 (GRCh37)
Canonical SPDI:: NC_000005.10:150444338:T:C
Gene:: RPS14 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000015/4 (TOPMED)
HGVS:: NC_000005.10:g.150444339T>C, NC_000005.9:g.149823902T>C, NG_042287.1:g.10418A>G, NM_005617.4:c.403A>G, NM_005617.3:c.403A>G, NM_001025071.2:c.403A>G, NM_001025071.1:c.403A>G, NM_001025070.2:c.403A>G, NM_001025070.1:c.403A>G, NP_005608.1:p.Ile135Val, NP_001020242.1:p.Ile135Val, NP_001020241.1:p.Ile135Val

Select item 14521418843.

rs1452141884 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 5:150446875 (GRCh38)
5:149826438 (GRCh37)
Canonical SPDI:: NC_000005.10:150446874:C:T
Gene:: RPS14 (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=0.000007/1 (GnomAD)
HGVS:: NC_000005.10:g.150446875C>T, NC_000005.9:g.149826438C>T, NG_042287.1:g.7882G>A, NM_005617.4:c.238G>A, NM_005617.3:c.238G>A, NM_001025071.2:c.238G>A, NM_001025071.1:c.238G>A, NM_001025070.2:c.238G>A, NM_001025070.1:c.238G>A, NP_005608.1:p.Asp80Asn, NP_001020242.1:p.Asp80Asn, NP_001020241.1:p.Asp80Asn

Select item 14494180954.

rs1449418095 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 5:150444313 (GRCh38)
5:149823876 (GRCh37)
Canonical SPDI:: NC_000005.10:150444312:C:A
Gene:: RPS14 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: A=0.00005/1 (ALFA)
HGVS:: NC_000005.10:g.150444313C>A, NC_000005.9:g.149823876C>A, NG_042287.1:g.10444G>T, NM_005617.4:c.429G>T, NM_005617.3:c.429G>T, NM_001025071.2:c.429G>T, NM_001025071.1:c.429G>T, NM_001025070.2:c.429G>T, NM_001025070.1:c.429G>T, NP_005608.1:p.Lys143Asn, NP_001020242.1:p.Lys143Asn, NP_001020241.1:p.Lys143Asn

Select item 14304459655.

rs1430445965 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 5:150446836 (GRCh38)
5:149826399 (GRCh37)
Canonical SPDI:: NC_000005.10:150446835:G:A
Gene:: RPS14 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000005.10:g.150446836G>A, NC_000005.9:g.149826399G>A, NG_042287.1:g.7921C>T, NM_005617.4:c.277C>T, NM_005617.3:c.277C>T, NM_001025071.2:c.277C>T, NM_001025071.1:c.277C>T, NM_001025070.2:c.277C>T, NM_001025070.1:c.277C>T

Select item 14129742296.

rs1412974229 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 5:150447705 (GRCh38)
5:149827268 (GRCh37)
Canonical SPDI:: NC_000005.10:150447704:T:C
Gene:: RPS14 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000005.10:g.150447705T>C, NC_000005.9:g.149827268T>C, NG_042287.1:g.7052A>G, NM_005617.4:c.29A>G, NM_005617.3:c.29A>G, NM_001025071.2:c.29A>G, NM_001025071.1:c.29A>G, NM_001025070.2:c.29A>G, NM_001025070.1:c.29A>G, NP_005608.1:p.Lys10Arg, NP_001020242.1:p.Lys10Arg, NP_001020241.1:p.Lys10Arg

Select item 14051545987.

rs1405154598 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 5:150447595 (GRCh38)
5:149827158 (GRCh37)
Canonical SPDI:: NC_000005.10:150447594:G:T
Gene:: RPS14 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000005.10:g.150447595G>T, NC_000005.9:g.149827158G>T, NG_042287.1:g.7162C>A, NM_005617.4:c.139C>A, NM_005617.3:c.139C>A, NM_001025071.2:c.139C>A, NM_001025071.1:c.139C>A, NM_001025070.2:c.139C>A, NM_001025070.1:c.139C>A, NP_005608.1:p.Leu47Ile, NP_001020242.1:p.Leu47Ile, NP_001020241.1:p.Leu47Ile

Select item 13913709498.

rs1391370949 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 5:150445615 (GRCh38)
5:149825178 (GRCh37)
Canonical SPDI:: NC_000005.10:150445614:G:A
Gene:: RPS14 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000005.10:g.150445615G>A, NC_000005.9:g.149825178G>A, NG_042287.1:g.9142C>T, NM_005617.4:c.382C>T, NM_005617.3:c.382C>T, NM_001025071.2:c.382C>T, NM_001025071.1:c.382C>T, NM_001025070.2:c.382C>T, NM_001025070.1:c.382C>T, NP_005608.1:p.Arg128Trp, NP_001020242.1:p.Arg128Trp, NP_001020241.1:p.Arg128Trp

Select item 13910837869.

rs1391083786 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 5:150446848 (GRCh38)
5:149826411 (GRCh37)
Canonical SPDI:: NC_000005.10:150446847:C:G
Gene:: RPS14 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000005.10:g.150446848C>G, NC_000005.9:g.149826411C>G, NG_042287.1:g.7909G>C, NM_005617.4:c.265G>C, NM_005617.3:c.265G>C, NM_001025071.2:c.265G>C, NM_001025071.1:c.265G>C, NM_001025070.2:c.265G>C, NM_001025070.1:c.265G>C, NP_005608.1:p.Gly89Arg, NP_001020242.1:p.Gly89Arg, NP_001020241.1:p.Gly89Arg

Select item 138516121410.

rs1385161214 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 5:150446833 (GRCh38)
5:149826396 (GRCh37)
Canonical SPDI:: NC_000005.10:150446832:G:A
Gene:: RPS14 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
HGVS:: NC_000005.10:g.150446833G>A, NC_000005.9:g.149826396G>A, NG_042287.1:g.7924C>T, NM_005617.4:c.280C>T, NM_005617.3:c.280C>T, NM_001025071.2:c.280C>T, NM_001025071.1:c.280C>T, NM_001025070.2:c.280C>T, NM_001025070.1:c.280C>T, NP_005608.1:p.His94Tyr, NP_001020242.1:p.His94Tyr, NP_001020241.1:p.His94Tyr

Select item 137980303111.

rs1379803031 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 5:150446939 (GRCh38)
5:149826502 (GRCh37)
Canonical SPDI:: NC_000005.10:150446938:A:G
Gene:: RPS14 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000005.10:g.150446939A>G, NC_000005.9:g.149826502A>G, NG_042287.1:g.7818T>C, NM_005617.4:c.174T>C, NM_005617.3:c.174T>C, NM_001025071.2:c.174T>C, NM_001025071.1:c.174T>C, NM_001025070.2:c.174T>C, NM_001025070.1:c.174T>C

Select item 137951262512.

rs1379512625 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 5:150444322 (GRCh38)
5:149823885 (GRCh37)
Canonical SPDI:: NC_000005.10:150444321:A:C
Gene:: RPS14 (Varview)
Functional Consequence:: synonymous_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_000005.10:g.150444322A>C, NC_000005.9:g.149823885A>C, NG_042287.1:g.10435T>G, NM_005617.4:c.420T>G, NM_005617.3:c.420T>G, NM_001025071.2:c.420T>G, NM_001025071.1:c.420T>G, NM_001025070.2:c.420T>G, NM_001025070.1:c.420T>G

Select item 133703574913.

rs1337035749 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 5:150446954 (GRCh38)
5:149826517 (GRCh37)
Canonical SPDI:: NC_000005.10:150446953:G:A
Gene:: RPS14 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000005.10:g.150446954G>A, NC_000005.9:g.149826517G>A, NG_042287.1:g.7803C>T, NM_005617.4:c.159C>T, NM_005617.3:c.159C>T, NM_001025071.2:c.159C>T, NM_001025071.1:c.159C>T, NM_001025070.2:c.159C>T, NM_001025070.1:c.159C>T

Select item 133140540714.

rs1331405407 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 5:150445643 (GRCh38)
5:149825206 (GRCh37)
Canonical SPDI:: NC_000005.10:150445642:G:A
Gene:: RPS14 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000005.10:g.150445643G>A, NC_000005.9:g.149825206G>A, NG_042287.1:g.9114C>T, NM_005617.4:c.354C>T, NM_005617.3:c.354C>T, NM_001025071.2:c.354C>T, NM_001025071.1:c.354C>T, NM_001025070.2:c.354C>T, NM_001025070.1:c.354C>T

Select item 133087141015.

rs1330871410 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 5:150445654 (GRCh38)
5:149825217 (GRCh37)
Canonical SPDI:: NC_000005.10:150445653:C:T
Gene:: RPS14 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000005.10:g.150445654C>T, NC_000005.9:g.149825217C>T, NG_042287.1:g.9103G>A, NM_005617.4:c.343G>A, NM_005617.3:c.343G>A, NM_001025071.2:c.343G>A, NM_001025071.1:c.343G>A, NM_001025070.2:c.343G>A, NM_001025070.1:c.343G>A, NP_005608.1:p.Ala115Thr, NP_001020242.1:p.Ala115Thr, NP_001020241.1:p.Ala115Thr

Select item 129796195616.

rs1297961956 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 5:150444297 (GRCh38)
5:149823860 (GRCh37)
Canonical SPDI:: NC_000005.10:150444296:G:A
Gene:: RPS14 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000005.10:g.150444297G>A, NC_000005.9:g.149823860G>A, NG_042287.1:g.10460C>T, NM_005617.4:c.445C>T, NM_005617.3:c.445C>T, NM_001025071.2:c.445C>T, NM_001025071.1:c.445C>T, NM_001025070.2:c.445C>T, NM_001025070.1:c.445C>T, NP_005608.1:p.Arg149Cys, NP_001020242.1:p.Arg149Cys, NP_001020241.1:p.Arg149Cys

Select item 129476738317.

rs1294767383 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 5:150446839 (GRCh38)
5:149826402 (GRCh37)
Canonical SPDI:: NC_000005.10:150446838:C:T
Gene:: RPS14 (Varview)
Functional Consequence:: coding_sequence_variant,missense_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_000005.10:g.150446839C>T, NC_000005.9:g.149826402C>T, NG_042287.1:g.7918G>A, NM_005617.4:c.274G>A, NM_005617.3:c.274G>A, NM_001025071.2:c.274G>A, NM_001025071.1:c.274G>A, NM_001025070.2:c.274G>A, NM_001025070.1:c.274G>A, NP_005608.1:p.Ala92Thr, NP_001020242.1:p.Ala92Thr, NP_001020241.1:p.Ala92Thr

Select item 128909979418.

rs1289099794 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 5:150444328 (GRCh38)
5:149823891 (GRCh37)
Canonical SPDI:: NC_000005.10:150444327:G:A
Gene:: RPS14 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000071/1 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000005.10:g.150444328G>A, NC_000005.9:g.149823891G>A, NG_042287.1:g.10429C>T, NM_005617.4:c.414C>T, NM_005617.3:c.414C>T, NM_001025071.2:c.414C>T, NM_001025071.1:c.414C>T, NM_001025070.2:c.414C>T, NM_001025070.1:c.414C>T

Select item 128279853719.

rs1282798537 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 5:150444321 (GRCh38)
5:149823884 (GRCh37)
Canonical SPDI:: NC_000005.10:150444320:G:A
Gene:: RPS14 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000005.10:g.150444321G>A, NC_000005.9:g.149823884G>A, NG_042287.1:g.10436C>T, NM_005617.4:c.421C>T, NM_005617.3:c.421C>T, NM_001025071.2:c.421C>T, NM_001025071.1:c.421C>T, NM_001025070.2:c.421C>T, NM_001025070.1:c.421C>T, NP_005608.1:p.Arg141Cys, NP_001020242.1:p.Arg141Cys, NP_001020241.1:p.Arg141Cys

Select item 127335012220.

rs1273350122 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 5:150447671 (GRCh38)
5:149827234 (GRCh37)
Canonical SPDI:: NC_000005.10:150447670:C:G
Gene:: RPS14 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
HGVS:: NC_000005.10:g.150447671C>G, NC_000005.9:g.149827234C>G, NG_042287.1:g.7086G>C, NM_005617.4:c.63G>C, NM_005617.3:c.63G>C, NM_001025071.2:c.63G>C, NM_001025071.1:c.63G>C, NM_001025070.2:c.63G>C, NM_001025070.1:c.63G>C

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