SNP Links for Protein (Select 7706451) - SNP

Links from Protein

Items: 1 to 20 of 423

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Select item 14855794591.

rs1485579459 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 16:19872115 (GRCh38)
16:19883437 (GRCh37)
Canonical SPDI:: NC_000016.10:19872114:A:G
Gene:: GPRC5B (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000102/2 (ALFA)
G=0.000007/1 (GnomAD)
G=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000016.10:g.19872115A>G, NC_000016.9:g.19883437A>G, XM_006721052.3:c.731T>C, XM_006721052.2:c.731T>C, XM_006721052.1:c.731T>C, NM_016235.3:c.731T>C, NM_016235.2:c.731T>C, NM_016235.1:c.731T>C, NM_001304771.1:c.1124T>C, XP_006721115.1:p.Val244Ala, NP_057319.1:p.Val244Ala, NP_001291700.1:p.Val375Ala

Select item 14836331892.

rs1483633189 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 16:19872097 (GRCh38)
16:19883419 (GRCh37)
Canonical SPDI:: NC_000016.10:19872096:C:A
Gene:: GPRC5B (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000016.10:g.19872097C>A, NC_000016.9:g.19883419C>A, XM_006721052.3:c.749G>T, XM_006721052.2:c.749G>T, XM_006721052.1:c.749G>T, NM_016235.3:c.749G>T, NM_016235.2:c.749G>T, NM_016235.1:c.749G>T, NM_001304771.1:c.1142G>T, XP_006721115.1:p.Trp250Leu, NP_057319.1:p.Trp250Leu, NP_001291700.1:p.Trp381Leu

Select item 14827229853.

rs1482722985 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 16:19872804 (GRCh38)
16:19884126 (GRCh37)
Canonical SPDI:: NC_000016.10:19872803:C:A
Gene:: GPRC5B (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
HGVS:: NC_000016.10:g.19872804C>A, NC_000016.9:g.19884126C>A, XM_006721052.3:c.42G>T, XM_006721052.2:c.42G>T, XM_006721052.1:c.42G>T, NM_016235.3:c.42G>T, NM_016235.2:c.42G>T, NM_016235.1:c.42G>T, NM_001304771.1:c.435G>T

Select item 14752249254.

rs1475224925 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 16:19871819 (GRCh38)
16:19883141 (GRCh37)
Canonical SPDI:: NC_000016.10:19871818:C:T
Gene:: GPRC5B (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000016.10:g.19871819C>T, NC_000016.9:g.19883141C>T, XM_006721052.3:c.1027G>A, XM_006721052.2:c.1027G>A, XM_006721052.1:c.1027G>A, NM_016235.3:c.1027G>A, NM_016235.2:c.1027G>A, NM_016235.1:c.1027G>A, NM_001304771.1:c.1420G>A, XP_006721115.1:p.Ala343Thr, NP_057319.1:p.Ala343Thr, NP_001291700.1:p.Ala474Thr

Select item 14732209895.

rs1473220989 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 16:19872026 (GRCh38)
16:19883348 (GRCh37)
Canonical SPDI:: NC_000016.10:19872025:T:A
Gene:: GPRC5B (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
HGVS:: NC_000016.10:g.19872026T>A, NC_000016.9:g.19883348T>A, XM_006721052.3:c.820A>T, XM_006721052.2:c.820A>T, XM_006721052.1:c.820A>T, NM_016235.3:c.820A>T, NM_016235.2:c.820A>T, NM_016235.1:c.820A>T, NM_001304771.1:c.1213A>T, XP_006721115.1:p.Ile274Phe, NP_057319.1:p.Ile274Phe, NP_001291700.1:p.Ile405Phe

Select item 14722272486.

rs1472227248 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 16:19872366 (GRCh38)
16:19883688 (GRCh37)
Canonical SPDI:: NC_000016.10:19872365:C:T
Gene:: GPRC5B (Varview)
Functional Consequence:: coding_sequence_variant,stop_gained
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000016.10:g.19872366C>T, NC_000016.9:g.19883688C>T, XM_006721052.3:c.480G>A, XM_006721052.2:c.480G>A, XM_006721052.1:c.480G>A, NM_016235.3:c.480G>A, NM_016235.2:c.480G>A, NM_016235.1:c.480G>A, NM_001304771.1:c.873G>A, XP_006721115.1:p.Trp160Ter, NP_057319.1:p.Trp160Ter, NP_001291700.1:p.Trp291Ter

Select item 14705149217.

rs1470514921 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 16:19872786 (GRCh38)
16:19884108 (GRCh37)
Canonical SPDI:: NC_000016.10:19872785:G:T
Gene:: GPRC5B (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: T=0.000071/1 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000016.10:g.19872786G>T, NC_000016.9:g.19884108G>T, XM_006721052.3:c.60C>A, XM_006721052.2:c.60C>A, XM_006721052.1:c.60C>A, NM_016235.3:c.60C>A, NM_016235.2:c.60C>A, NM_016235.1:c.60C>A, NM_001304771.1:c.453C>A

Select item 14644704068.

rs1464470406 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 16:19872486 (GRCh38)
16:19883808 (GRCh37)
Canonical SPDI:: NC_000016.10:19872485:G:A
Gene:: GPRC5B (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_000016.10:g.19872486G>A, NC_000016.9:g.19883808G>A, XM_006721052.3:c.360C>T, XM_006721052.2:c.360C>T, XM_006721052.1:c.360C>T, NM_016235.3:c.360C>T, NM_016235.2:c.360C>T, NM_016235.1:c.360C>T, NM_001304771.1:c.753C>T

Select item 14581400969.

rs1458140096 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 16:19871974 (GRCh38)
16:19883296 (GRCh37)
Canonical SPDI:: NC_000016.10:19871973:T:C
Gene:: GPRC5B (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000016.10:g.19871974T>C, NC_000016.9:g.19883296T>C, XM_006721052.3:c.872A>G, XM_006721052.2:c.872A>G, XM_006721052.1:c.872A>G, NM_016235.3:c.872A>G, NM_016235.2:c.872A>G, NM_016235.1:c.872A>G, NM_001304771.1:c.1265A>G, XP_006721115.1:p.Glu291Gly, NP_057319.1:p.Glu291Gly, NP_001291700.1:p.Glu422Gly

Select item 145745213210.

rs1457452132 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 16:19872611 (GRCh38)
16:19883933 (GRCh37)
Canonical SPDI:: NC_000016.10:19872610:C:A
Gene:: GPRC5B (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000016.10:g.19872611C>A, NC_000016.9:g.19883933C>A, XM_006721052.3:c.235G>T, XM_006721052.2:c.235G>T, XM_006721052.1:c.235G>T, NM_016235.3:c.235G>T, NM_016235.2:c.235G>T, NM_016235.1:c.235G>T, NM_001304771.1:c.628G>T, XP_006721115.1:p.Val79Leu, NP_057319.1:p.Val79Leu, NP_001291700.1:p.Val210Leu

Select item 145486666811.

rs1454866668 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 16:19872337 (GRCh38)
16:19883659 (GRCh37)
Canonical SPDI:: NC_000016.10:19872336:A:G
Gene:: GPRC5B (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
HGVS:: NC_000016.10:g.19872337A>G, NC_000016.9:g.19883659A>G, XM_006721052.3:c.509T>C, XM_006721052.2:c.509T>C, XM_006721052.1:c.509T>C, NM_016235.3:c.509T>C, NM_016235.2:c.509T>C, NM_016235.1:c.509T>C, NM_001304771.1:c.902T>C, XP_006721115.1:p.Met170Thr, NP_057319.1:p.Met170Thr, NP_001291700.1:p.Met301Thr

Select item 145271650712.

rs1452716507 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 16:19871900 (GRCh38)
16:19883222 (GRCh37)
Canonical SPDI:: NC_000016.10:19871899:G:A
Gene:: GPRC5B (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by cluster
HGVS:: NC_000016.10:g.19871900G>A, NC_000016.9:g.19883222G>A, XM_006721052.3:c.946C>T, XM_006721052.2:c.946C>T, XM_006721052.1:c.946C>T, NM_016235.3:c.946C>T, NM_016235.2:c.946C>T, NM_016235.1:c.946C>T, NM_001304771.1:c.1339C>T, XP_006721115.1:p.Arg316Trp, NP_057319.1:p.Arg316Trp, NP_001291700.1:p.Arg447Trp

Select item 144841917013.

rs1448419170 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 16:19872163 (GRCh38)
16:19883485 (GRCh37)
Canonical SPDI:: NC_000016.10:19872162:C:G,NC_000016.10:19872162:C:T
Gene:: GPRC5B (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
G=0.000004/1 (GnomAD_exomes)
T=0.000004/1 (TOPMED)
HGVS:: NC_000016.10:g.19872163C>G, NC_000016.10:g.19872163C>T, NC_000016.9:g.19883485C>G, NC_000016.9:g.19883485C>T, XM_006721052.3:c.683G>C, XM_006721052.3:c.683G>A, XM_006721052.2:c.683G>C, XM_006721052.2:c.683G>A, XM_006721052.1:c.683G>C, XM_006721052.1:c.683G>A, NM_016235.3:c.683G>C, NM_016235.3:c.683G>A, NM_016235.2:c.683G>C, NM_016235.2:c.683G>A, NM_016235.1:c.683G>C, NM_016235.1:c.683G>A, NM_001304771.1:c.1076G>C, NM_001304771.1:c.1076G>A, XP_006721115.1:p.Arg228Thr, XP_006721115.1:p.Arg228Lys, NP_057319.1:p.Arg228Thr, NP_057319.1:p.Arg228Lys, NP_001291700.1:p.Arg359Thr, NP_001291700.1:p.Arg359Lys

Select item 144238590214.

rs1442385902 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 16:19872194 (GRCh38)
16:19883516 (GRCh37)
Canonical SPDI:: NC_000016.10:19872193:C:A,NC_000016.10:19872193:C:T
Gene:: GPRC5B (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000016.10:g.19872194C>A, NC_000016.10:g.19872194C>T, NC_000016.9:g.19883516C>A, NC_000016.9:g.19883516C>T, XM_006721052.3:c.652G>T, XM_006721052.3:c.652G>A, XM_006721052.2:c.652G>T, XM_006721052.2:c.652G>A, XM_006721052.1:c.652G>T, XM_006721052.1:c.652G>A, NM_016235.3:c.652G>T, NM_016235.3:c.652G>A, NM_016235.2:c.652G>T, NM_016235.2:c.652G>A, NM_016235.1:c.652G>T, NM_016235.1:c.652G>A, NM_001304771.1:c.1045G>T, NM_001304771.1:c.1045G>A, XP_006721115.1:p.Ala218Ser, XP_006721115.1:p.Ala218Thr, NP_057319.1:p.Ala218Ser, NP_057319.1:p.Ala218Thr, NP_001291700.1:p.Ala349Ser, NP_001291700.1:p.Ala349Thr

Select item 144210579315.

rs1442105793 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 16:19861949 (GRCh38)
16:19873271 (GRCh37)
Canonical SPDI:: NC_000016.10:19861948:T:C
Gene:: GPRC5B (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=0.000008/2 (TOPMED)
HGVS:: NC_000016.10:g.19861949T>C, NC_000016.9:g.19873271T>C, XM_006721052.3:c.1055A>G, XM_006721052.2:c.1055A>G, XM_006721052.1:c.1055A>G, NM_016235.3:c.1055A>G, NM_016235.2:c.1055A>G, NM_016235.1:c.1055A>G, NM_001304771.1:c.1448A>G, XP_006721115.1:p.Asn352Ser, NP_057319.1:p.Asn352Ser, NP_001291700.1:p.Asn483Ser

Select item 144166855316.

rs1441668553 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 16:19861887 (GRCh38)
16:19873209 (GRCh37)
Canonical SPDI:: NC_000016.10:19861886:T:A
Gene:: GPRC5B (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000016.10:g.19861887T>A, NC_000016.9:g.19873209T>A, XM_006721052.3:c.1117A>T, XM_006721052.2:c.1117A>T, XM_006721052.1:c.1117A>T, NM_016235.3:c.1117A>T, NM_016235.2:c.1117A>T, NM_016235.1:c.1117A>T, NM_001304771.1:c.1510A>T, XP_006721115.1:p.Ser373Cys, NP_057319.1:p.Ser373Cys, NP_001291700.1:p.Ser504Cys

Select item 143542793917.

rs1435427939 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 16:19872659 (GRCh38)
16:19883981 (GRCh37)
Canonical SPDI:: NC_000016.10:19872658:C:T
Gene:: GPRC5B (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
HGVS:: NC_000016.10:g.19872659C>T, NC_000016.9:g.19883981C>T, XM_006721052.3:c.187G>A, XM_006721052.2:c.187G>A, XM_006721052.1:c.187G>A, NM_016235.3:c.187G>A, NM_016235.2:c.187G>A, NM_016235.1:c.187G>A, NM_001304771.1:c.580G>A, XP_006721115.1:p.Ala63Thr, NP_057319.1:p.Ala63Thr, NP_001291700.1:p.Ala194Thr

Select item 143541040818.

rs1435410408 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 16:19871961 (GRCh38)
16:19883283 (GRCh37)
Canonical SPDI:: NC_000016.10:19871960:G:A
Gene:: GPRC5B (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000016.10:g.19871961G>A, NC_000016.9:g.19883283G>A, XM_006721052.3:c.885C>T, XM_006721052.2:c.885C>T, XM_006721052.1:c.885C>T, NM_016235.3:c.885C>T, NM_016235.2:c.885C>T, NM_016235.1:c.885C>T, NM_001304771.1:c.1278C>T

Select item 143513842119.

rs1435138421 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 16:19872542 (GRCh38)
16:19883864 (GRCh37)
Canonical SPDI:: NC_000016.10:19872541:C:A
Gene:: GPRC5B (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
HGVS:: NC_000016.10:g.19872542C>A, NC_000016.9:g.19883864C>A, XM_006721052.3:c.304G>T, XM_006721052.2:c.304G>T, XM_006721052.1:c.304G>T, NM_016235.3:c.304G>T, NM_016235.2:c.304G>T, NM_016235.1:c.304G>T, NM_001304771.1:c.697G>T, XP_006721115.1:p.Gly102Trp, NP_057319.1:p.Gly102Trp, NP_001291700.1:p.Gly233Trp

Select item 143196286820.

rs1431962868 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 16:19872083 (GRCh38)
16:19883405 (GRCh37)
Canonical SPDI:: NC_000016.10:19872082:G:A
Gene:: GPRC5B (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_000016.10:g.19872083G>A, NC_000016.9:g.19883405G>A, XM_006721052.3:c.763C>T, XM_006721052.2:c.763C>T, XM_006721052.1:c.763C>T, NM_016235.3:c.763C>T, NM_016235.2:c.763C>T, NM_016235.1:c.763C>T, NM_001304771.1:c.1156C>T, XP_006721115.1:p.Leu255Phe, NP_057319.1:p.Leu255Phe, NP_001291700.1:p.Leu386Phe

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