SNP Links for Protein (Select 33695107) - SNP

Select item 14901369291.

rs1490136929 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G [Show Flanks]
Chromosome:: 2:230910931 (GRCh38)
2:231775646 (GRCh37)
Canonical SPDI:: NC_000002.12:230910930:A:C,NC_000002.12:230910930:A:G
Gene:: GPR55 (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)
HGVS:: NC_000002.12:g.230910931A>C, NC_000002.12:g.230910931A>G, NC_000002.11:g.231775646A>C, NC_000002.11:g.231775646A>G, NG_050956.1:g.55297T>G, NG_050956.1:g.55297T>C, NM_005683.4:c.32T>G, NM_005683.4:c.32T>C, NM_005683.3:c.32T>G, NM_005683.3:c.32T>C, XM_005246952.5:c.32T>G, XM_005246952.5:c.32T>C, XM_005246952.4:c.32T>G, XM_005246952.4:c.32T>C, XM_005246952.3:c.32T>G, XM_005246952.3:c.32T>C, XM_005246952.2:c.32T>G, XM_005246952.2:c.32T>C, XM_005246952.1:c.32T>G, XM_005246952.1:c.32T>C, XM_011512175.4:c.32T>G, XM_011512175.4:c.32T>C, XM_011512175.3:c.32T>G, XM_011512175.3:c.32T>C, XM_011512175.2:c.32T>G, XM_011512175.2:c.32T>C, XM_011512175.1:c.32T>G, XM_011512175.1:c.32T>C, XM_011512176.3:c.32T>G, XM_011512176.3:c.32T>C, XM_011512176.2:c.32T>G, XM_011512176.2:c.32T>C, XM_011512176.1:c.32T>G, XM_011512176.1:c.32T>C, NP_005674.2:p.Leu11Arg, NP_005674.2:p.Leu11Pro, XP_005247009.1:p.Leu11Arg, XP_005247009.1:p.Leu11Pro, XP_011510477.1:p.Leu11Arg, XP_011510477.1:p.Leu11Pro, XP_011510478.1:p.Leu11Arg, XP_011510478.1:p.Leu11Pro

Select item 14870830732.

rs1487083073 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 2:230910096 (GRCh38)
2:231774811 (GRCh37)
Canonical SPDI:: NC_000002.12:230910095:G:A
Gene:: GPR55 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000002.12:g.230910096G>A, NC_000002.11:g.231774811G>A, NG_050956.1:g.56132C>T, NM_005683.4:c.867C>T, NM_005683.3:c.867C>T, XM_005246952.5:c.867C>T, XM_005246952.4:c.867C>T, XM_005246952.3:c.867C>T, XM_005246952.2:c.867C>T, XM_005246952.1:c.867C>T, XM_011512175.4:c.867C>T, XM_011512175.3:c.867C>T, XM_011512175.2:c.867C>T, XM_011512175.1:c.867C>T, XM_011512176.3:c.867C>T, XM_011512176.2:c.867C>T, XM_011512176.1:c.867C>T

Select item 14859309393.

rs1485930939 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 2:230910533 (GRCh38)
2:231775248 (GRCh37)
Canonical SPDI:: NC_000002.12:230910532:T:C
Gene:: GPR55 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000002.12:g.230910533T>C, NC_000002.11:g.231775248T>C, NG_050956.1:g.55695A>G, NM_005683.4:c.430A>G, NM_005683.3:c.430A>G, XM_005246952.5:c.430A>G, XM_005246952.4:c.430A>G, XM_005246952.3:c.430A>G, XM_005246952.2:c.430A>G, XM_005246952.1:c.430A>G, XM_011512175.4:c.430A>G, XM_011512175.3:c.430A>G, XM_011512175.2:c.430A>G, XM_011512175.1:c.430A>G, XM_011512176.3:c.430A>G, XM_011512176.2:c.430A>G, XM_011512176.1:c.430A>G, NP_005674.2:p.Thr144Ala, XP_005247009.1:p.Thr144Ala, XP_011510477.1:p.Thr144Ala, XP_011510478.1:p.Thr144Ala

Select item 14829851444.

rs1482985144 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 2:230910188 (GRCh38)
2:231774903 (GRCh37)
Canonical SPDI:: NC_000002.12:230910187:C:G
Gene:: GPR55 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000002.12:g.230910188C>G, NC_000002.11:g.231774903C>G, NG_050956.1:g.56040G>C, NM_005683.4:c.775G>C, NM_005683.3:c.775G>C, XM_005246952.5:c.775G>C, XM_005246952.4:c.775G>C, XM_005246952.3:c.775G>C, XM_005246952.2:c.775G>C, XM_005246952.1:c.775G>C, XM_011512175.4:c.775G>C, XM_011512175.3:c.775G>C, XM_011512175.2:c.775G>C, XM_011512175.1:c.775G>C, XM_011512176.3:c.775G>C, XM_011512176.2:c.775G>C, XM_011512176.1:c.775G>C, NP_005674.2:p.Glu259Gln, XP_005247009.1:p.Glu259Gln, XP_011510477.1:p.Glu259Gln, XP_011510478.1:p.Glu259Gln

Select item 14817059705.

rs1481705970 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 2:230910397 (GRCh38)
2:231775112 (GRCh37)
Canonical SPDI:: NC_000002.12:230910396:C:T
Gene:: GPR55 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000011/3 (TOPMED)
T=0.000014/2 (GnomAD)
HGVS:: NC_000002.12:g.230910397C>T, NC_000002.11:g.231775112C>T, NG_050956.1:g.55831G>A, NM_005683.4:c.566G>A, NM_005683.3:c.566G>A, XM_005246952.5:c.566G>A, XM_005246952.4:c.566G>A, XM_005246952.3:c.566G>A, XM_005246952.2:c.566G>A, XM_005246952.1:c.566G>A, XM_011512175.4:c.566G>A, XM_011512175.3:c.566G>A, XM_011512175.2:c.566G>A, XM_011512175.1:c.566G>A, XM_011512176.3:c.566G>A, XM_011512176.2:c.566G>A, XM_011512176.1:c.566G>A, NP_005674.2:p.Gly189Asp, XP_005247009.1:p.Gly189Asp, XP_011510477.1:p.Gly189Asp, XP_011510478.1:p.Gly189Asp

Select item 14766514586.

rs1476651458 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 2:230910640 (GRCh38)
2:231775355 (GRCh37)
Canonical SPDI:: NC_000002.12:230910639:C:T
Gene:: GPR55 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (GnomAD_exomes)
T=0.000004/1 (TOPMED)
T=0.000212/4 (TOMMO)
T=0.000546/1 (Korea1K)
HGVS:: NC_000002.12:g.230910640C>T, NC_000002.11:g.231775355C>T, NG_050956.1:g.55588G>A, NM_005683.4:c.323G>A, NM_005683.3:c.323G>A, XM_005246952.5:c.323G>A, XM_005246952.4:c.323G>A, XM_005246952.3:c.323G>A, XM_005246952.2:c.323G>A, XM_005246952.1:c.323G>A, XM_011512175.4:c.323G>A, XM_011512175.3:c.323G>A, XM_011512175.2:c.323G>A, XM_011512175.1:c.323G>A, XM_011512176.3:c.323G>A, XM_011512176.2:c.323G>A, XM_011512176.1:c.323G>A, NP_005674.2:p.Ser108Asn, XP_005247009.1:p.Ser108Asn, XP_011510477.1:p.Ser108Asn, XP_011510478.1:p.Ser108Asn

Select item 14742795157.

rs1474279515 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 2:230910065 (GRCh38)
2:231774780 (GRCh37)
Canonical SPDI:: NC_000002.12:230910064:T:C
Gene:: GPR55 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
HGVS:: NC_000002.12:g.230910065T>C, NC_000002.11:g.231774780T>C, NG_050956.1:g.56163A>G, NM_005683.4:c.898A>G, NM_005683.3:c.898A>G, XM_005246952.5:c.898A>G, XM_005246952.4:c.898A>G, XM_005246952.3:c.898A>G, XM_005246952.2:c.898A>G, XM_005246952.1:c.898A>G, XM_011512175.4:c.898A>G, XM_011512175.3:c.898A>G, XM_011512175.2:c.898A>G, XM_011512175.1:c.898A>G, XM_011512176.3:c.898A>G, XM_011512176.2:c.898A>G, XM_011512176.1:c.898A>G, NP_005674.2:p.Arg300Gly, XP_005247009.1:p.Arg300Gly, XP_011510477.1:p.Arg300Gly, XP_011510478.1:p.Arg300Gly

Select item 14742511448.

rs1474251144 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 2:230910692 (GRCh38)
2:231775407 (GRCh37)
Canonical SPDI:: NC_000002.12:230910691:G:A
Gene:: GPR55 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
HGVS:: NC_000002.12:g.230910692G>A, NC_000002.11:g.231775407G>A, NG_050956.1:g.55536C>T, NM_005683.4:c.271C>T, NM_005683.3:c.271C>T, XM_005246952.5:c.271C>T, XM_005246952.4:c.271C>T, XM_005246952.3:c.271C>T, XM_005246952.2:c.271C>T, XM_005246952.1:c.271C>T, XM_011512175.4:c.271C>T, XM_011512175.3:c.271C>T, XM_011512175.2:c.271C>T, XM_011512175.1:c.271C>T, XM_011512176.3:c.271C>T, XM_011512176.2:c.271C>T, XM_011512176.1:c.271C>T, NP_005674.2:p.Pro91Ser, XP_005247009.1:p.Pro91Ser, XP_011510477.1:p.Pro91Ser, XP_011510478.1:p.Pro91Ser

Select item 14711765689.

rs1471176568 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 2:230910880 (GRCh38)
2:231775595 (GRCh37)
Canonical SPDI:: NC_000002.12:230910879:A:G
Gene:: GPR55 (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_000002.12:g.230910880A>G, NC_000002.11:g.231775595A>G, NG_050956.1:g.55348T>C, NM_005683.4:c.83T>C, NM_005683.3:c.83T>C, XM_005246952.5:c.83T>C, XM_005246952.4:c.83T>C, XM_005246952.3:c.83T>C, XM_005246952.2:c.83T>C, XM_005246952.1:c.83T>C, XM_011512175.4:c.83T>C, XM_011512175.3:c.83T>C, XM_011512175.2:c.83T>C, XM_011512175.1:c.83T>C, XM_011512176.3:c.83T>C, XM_011512176.2:c.83T>C, XM_011512176.1:c.83T>C, NP_005674.2:p.Ile28Thr, XP_005247009.1:p.Ile28Thr, XP_011510477.1:p.Ile28Thr, XP_011510478.1:p.Ile28Thr

Select item 147096685210.

rs1470966852 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 2:230910538 (GRCh38)
2:231775253 (GRCh37)
Canonical SPDI:: NC_000002.12:230910537:C:T
Gene:: GPR55 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000002.12:g.230910538C>T, NC_000002.11:g.231775253C>T, NG_050956.1:g.55690G>A, NM_005683.4:c.425G>A, NM_005683.3:c.425G>A, XM_005246952.5:c.425G>A, XM_005246952.4:c.425G>A, XM_005246952.3:c.425G>A, XM_005246952.2:c.425G>A, XM_005246952.1:c.425G>A, XM_011512175.4:c.425G>A, XM_011512175.3:c.425G>A, XM_011512175.2:c.425G>A, XM_011512175.1:c.425G>A, XM_011512176.3:c.425G>A, XM_011512176.2:c.425G>A, XM_011512176.1:c.425G>A, NP_005674.2:p.Cys142Tyr, XP_005247009.1:p.Cys142Tyr, XP_011510477.1:p.Cys142Tyr, XP_011510478.1:p.Cys142Tyr

Select item 147037638911.

rs1470376389 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 2:230910810 (GRCh38)
2:231775525 (GRCh37)
Canonical SPDI:: NC_000002.12:230910809:G:C
Gene:: GPR55 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
HGVS:: NC_000002.12:g.230910810G>C, NC_000002.11:g.231775525G>C, NG_050956.1:g.55418C>G, NM_005683.4:c.153C>G, NM_005683.3:c.153C>G, XM_005246952.5:c.153C>G, XM_005246952.4:c.153C>G, XM_005246952.3:c.153C>G, XM_005246952.2:c.153C>G, XM_005246952.1:c.153C>G, XM_011512175.4:c.153C>G, XM_011512175.3:c.153C>G, XM_011512175.2:c.153C>G, XM_011512175.1:c.153C>G, XM_011512176.3:c.153C>G, XM_011512176.2:c.153C>G, XM_011512176.1:c.153C>G, NP_005674.2:p.Asn51Lys, XP_005247009.1:p.Asn51Lys, XP_011510477.1:p.Asn51Lys, XP_011510478.1:p.Asn51Lys

Select item 146294931812.

rs1462949318 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 2:230910609 (GRCh38)
2:231775324 (GRCh37)
Canonical SPDI:: NC_000002.12:230910608:G:A,NC_000002.12:230910608:G:T
Gene:: GPR55 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000002.12:g.230910609G>A, NC_000002.12:g.230910609G>T, NC_000002.11:g.231775324G>A, NC_000002.11:g.231775324G>T, NG_050956.1:g.55619C>T, NG_050956.1:g.55619C>A, NM_005683.4:c.354C>T, NM_005683.4:c.354C>A, NM_005683.3:c.354C>T, NM_005683.3:c.354C>A, XM_005246952.5:c.354C>T, XM_005246952.5:c.354C>A, XM_005246952.4:c.354C>T, XM_005246952.4:c.354C>A, XM_005246952.3:c.354C>T, XM_005246952.3:c.354C>A, XM_005246952.2:c.354C>T, XM_005246952.2:c.354C>A, XM_005246952.1:c.354C>T, XM_005246952.1:c.354C>A, XM_011512175.4:c.354C>T, XM_011512175.4:c.354C>A, XM_011512175.3:c.354C>T, XM_011512175.3:c.354C>A, XM_011512175.2:c.354C>T, XM_011512175.2:c.354C>A, XM_011512175.1:c.354C>T, XM_011512175.1:c.354C>A, XM_011512176.3:c.354C>T, XM_011512176.3:c.354C>A, XM_011512176.2:c.354C>T, XM_011512176.2:c.354C>A, XM_011512176.1:c.354C>T, XM_011512176.1:c.354C>A, NP_005674.2:p.Asp118Glu, XP_005247009.1:p.Asp118Glu, XP_011510477.1:p.Asp118Glu, XP_011510478.1:p.Asp118Glu

Select item 145570897913.

rs1455708979 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 2:230910287 (GRCh38)
2:231775002 (GRCh37)
Canonical SPDI:: NC_000002.12:230910286:A:G
Gene:: GPR55 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000002.12:g.230910287A>G, NC_000002.11:g.231775002A>G, NG_050956.1:g.55941T>C, NM_005683.4:c.676T>C, NM_005683.3:c.676T>C, XM_005246952.5:c.676T>C, XM_005246952.4:c.676T>C, XM_005246952.3:c.676T>C, XM_005246952.2:c.676T>C, XM_005246952.1:c.676T>C, XM_011512175.4:c.676T>C, XM_011512175.3:c.676T>C, XM_011512175.2:c.676T>C, XM_011512175.1:c.676T>C, XM_011512176.3:c.676T>C, XM_011512176.2:c.676T>C, XM_011512176.1:c.676T>C, NP_005674.2:p.Tyr226His, XP_005247009.1:p.Tyr226His, XP_011510477.1:p.Tyr226His, XP_011510478.1:p.Tyr226His

Select item 145446557314.

rs1454465573 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 2:230910138 (GRCh38)
2:231774853 (GRCh37)
Canonical SPDI:: NC_000002.12:230910137:A:G
Gene:: GPR55 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000002.12:g.230910138A>G, NC_000002.11:g.231774853A>G, NG_050956.1:g.56090T>C, NM_005683.4:c.825T>C, NM_005683.3:c.825T>C, XM_005246952.5:c.825T>C, XM_005246952.4:c.825T>C, XM_005246952.3:c.825T>C, XM_005246952.2:c.825T>C, XM_005246952.1:c.825T>C, XM_011512175.4:c.825T>C, XM_011512175.3:c.825T>C, XM_011512175.2:c.825T>C, XM_011512175.1:c.825T>C, XM_011512176.3:c.825T>C, XM_011512176.2:c.825T>C, XM_011512176.1:c.825T>C

Select item 145213720215.

rs1452137202 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 2:230910590 (GRCh38)
2:231775305 (GRCh37)
Canonical SPDI:: NC_000002.12:230910589:A:G
Gene:: GPR55 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000071/1 (ALFA)
G=0.000004/1 (GnomAD_exomes)
G=0.000011/3 (TOPMED)
G=0.000021/3 (GnomAD)
HGVS:: NC_000002.12:g.230910590A>G, NC_000002.11:g.231775305A>G, NG_050956.1:g.55638T>C, NM_005683.4:c.373T>C, NM_005683.3:c.373T>C, XM_005246952.5:c.373T>C, XM_005246952.4:c.373T>C, XM_005246952.3:c.373T>C, XM_005246952.2:c.373T>C, XM_005246952.1:c.373T>C, XM_011512175.4:c.373T>C, XM_011512175.3:c.373T>C, XM_011512175.2:c.373T>C, XM_011512175.1:c.373T>C, XM_011512176.3:c.373T>C, XM_011512176.2:c.373T>C, XM_011512176.1:c.373T>C, NP_005674.2:p.Tyr125His, XP_005247009.1:p.Tyr125His, XP_011510477.1:p.Tyr125His, XP_011510478.1:p.Tyr125His

Select item 144760261616.

rs1447602616 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 2:230910302 (GRCh38)
2:231775017 (GRCh37)
Canonical SPDI:: NC_000002.12:230910301:G:A
Gene:: GPR55 (Varview)
Functional Consequence:: stop_gained,coding_sequence_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000002.12:g.230910302G>A, NC_000002.11:g.231775017G>A, NG_050956.1:g.55926C>T, NM_005683.4:c.661C>T, NM_005683.3:c.661C>T, XM_005246952.5:c.661C>T, XM_005246952.4:c.661C>T, XM_005246952.3:c.661C>T, XM_005246952.2:c.661C>T, XM_005246952.1:c.661C>T, XM_011512175.4:c.661C>T, XM_011512175.3:c.661C>T, XM_011512175.2:c.661C>T, XM_011512175.1:c.661C>T, XM_011512176.3:c.661C>T, XM_011512176.2:c.661C>T, XM_011512176.1:c.661C>T, NP_005674.2:p.Gln221Ter, XP_005247009.1:p.Gln221Ter, XP_011510477.1:p.Gln221Ter, XP_011510478.1:p.Gln221Ter

Select item 143962479217.

rs1439624792 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 2:230910936 (GRCh38)
2:231775651 (GRCh37)
Canonical SPDI:: NC_000002.12:230910935:G:T
Gene:: GPR55 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: T=0.000111/1 (ALFA)
T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000002.12:g.230910936G>T, NC_000002.11:g.231775651G>T, NG_050956.1:g.55292C>A, NM_005683.4:c.27C>A, NM_005683.3:c.27C>A, XM_005246952.5:c.27C>A, XM_005246952.4:c.27C>A, XM_005246952.3:c.27C>A, XM_005246952.2:c.27C>A, XM_005246952.1:c.27C>A, XM_011512175.4:c.27C>A, XM_011512175.3:c.27C>A, XM_011512175.2:c.27C>A, XM_011512175.1:c.27C>A, XM_011512176.3:c.27C>A, XM_011512176.2:c.27C>A, XM_011512176.1:c.27C>A, NP_005674.2:p.Asp9Glu, XP_005247009.1:p.Asp9Glu, XP_011510477.1:p.Asp9Glu, XP_011510478.1:p.Asp9Glu

Select item 143889807718.

rs1438898077 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 2:230910611 (GRCh38)
2:231775326 (GRCh37)
Canonical SPDI:: NC_000002.12:230910610:C:T
Gene:: GPR55 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
HGVS:: NC_000002.12:g.230910611C>T, NC_000002.11:g.231775326C>T, NG_050956.1:g.55617G>A, NM_005683.4:c.352G>A, NM_005683.3:c.352G>A, XM_005246952.5:c.352G>A, XM_005246952.4:c.352G>A, XM_005246952.3:c.352G>A, XM_005246952.2:c.352G>A, XM_005246952.1:c.352G>A, XM_011512175.4:c.352G>A, XM_011512175.3:c.352G>A, XM_011512175.2:c.352G>A, XM_011512175.1:c.352G>A, XM_011512176.3:c.352G>A, XM_011512176.2:c.352G>A, XM_011512176.1:c.352G>A, NP_005674.2:p.Asp118Asn, XP_005247009.1:p.Asp118Asn, XP_011510477.1:p.Asp118Asn, XP_011510478.1:p.Asp118Asn

Select item 143643580319.

rs1436435803 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 2:230910833 (GRCh38)
2:231775548 (GRCh37)
Canonical SPDI:: NC_000002.12:230910832:C:T
Gene:: GPR55 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000047/1 (ALFA)
T=0.000004/1 (GnomAD_exomes)
T=0.000035/1 (TOMMO)
HGVS:: NC_000002.12:g.230910833C>T, NC_000002.11:g.231775548C>T, NG_050956.1:g.55395G>A, NM_005683.4:c.130G>A, NM_005683.3:c.130G>A, XM_005246952.5:c.130G>A, XM_005246952.4:c.130G>A, XM_005246952.3:c.130G>A, XM_005246952.2:c.130G>A, XM_005246952.1:c.130G>A, XM_011512175.4:c.130G>A, XM_011512175.3:c.130G>A, XM_011512175.2:c.130G>A, XM_011512175.1:c.130G>A, XM_011512176.3:c.130G>A, XM_011512176.2:c.130G>A, XM_011512176.1:c.130G>A, NP_005674.2:p.Gly44Ser, XP_005247009.1:p.Gly44Ser, XP_011510477.1:p.Gly44Ser, XP_011510478.1:p.Gly44Ser

Select item 143632206420.

rs1436322064 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G [Show Flanks]
Chromosome:: 2:230910211 (GRCh38)
2:231774926 (GRCh37)
Canonical SPDI:: NC_000002.12:230910210:A:C,NC_000002.12:230910210:A:G
Gene:: GPR55 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by cluster
MAF:: G=0.000004/1 (GnomAD_exomes)
C=0.000035/1 (TOMMO)
HGVS:: NC_000002.12:g.230910211A>C, NC_000002.12:g.230910211A>G, NC_000002.11:g.231774926A>C, NC_000002.11:g.231774926A>G, NG_050956.1:g.56017T>G, NG_050956.1:g.56017T>C, NM_005683.4:c.752T>G, NM_005683.4:c.752T>C, NM_005683.3:c.752T>G, NM_005683.3:c.752T>C, XM_005246952.5:c.752T>G, XM_005246952.5:c.752T>C, XM_005246952.4:c.752T>G, XM_005246952.4:c.752T>C, XM_005246952.3:c.752T>G, XM_005246952.3:c.752T>C, XM_005246952.2:c.752T>G, XM_005246952.2:c.752T>C, XM_005246952.1:c.752T>G, XM_005246952.1:c.752T>C, XM_011512175.4:c.752T>G, XM_011512175.4:c.752T>C, XM_011512175.3:c.752T>G, XM_011512175.3:c.752T>C, XM_011512175.2:c.752T>G, XM_011512175.2:c.752T>C, XM_011512175.1:c.752T>G, XM_011512175.1:c.752T>C, XM_011512176.3:c.752T>G, XM_011512176.3:c.752T>C, XM_011512176.2:c.752T>G, XM_011512176.2:c.752T>C, XM_011512176.1:c.752T>G, XM_011512176.1:c.752T>C, NP_005674.2:p.Leu251Arg, NP_005674.2:p.Leu251Pro, XP_005247009.1:p.Leu251Arg, XP_005247009.1:p.Leu251Pro, XP_011510477.1:p.Leu251Arg, XP_011510477.1:p.Leu251Pro, XP_011510478.1:p.Leu251Arg, XP_011510478.1:p.Leu251Pro

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Result Filters

Clinical Significance

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Items: 1 to 20 of 325

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