SNP Links for Protein (Select 4507545) - SNP

Links from Protein

Items: 1 to 20 of 462

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Select item 14885262361.

rs1488526236 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 1:236142739 (GRCh38)
1:236306039 (GRCh37)
Canonical SPDI:: NC_000001.11:236142738:C:A,NC_000001.11:236142738:C:T
Gene:: GPR137B (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
C=0.5/1 (SGDP_PRJ)
HGVS:: NC_000001.11:g.236142739C>A, NC_000001.11:g.236142739C>T, NC_000001.10:g.236306039C>A, NC_000001.10:g.236306039C>T, NM_003272.4:c.117C>A, NM_003272.4:c.117C>T, NM_003272.3:c.117C>A, NM_003272.3:c.117C>T, XM_017002209.3:c.117C>A, XM_017002209.3:c.117C>T, XM_017002209.2:c.117C>A, XM_017002209.2:c.117C>T, XM_017002209.1:c.117C>A, XM_017002209.1:c.117C>T

Select item 14860990572.

rs1486099057 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 1:236143031 (GRCh38)
1:236306331 (GRCh37)
Canonical SPDI:: NC_000001.11:236143030:A:C
Gene:: GPR137B (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.236143031A>C, NC_000001.10:g.236306331A>C, NM_003272.4:c.409A>C, NM_003272.3:c.409A>C, XM_017002209.3:c.409A>C, XM_017002209.2:c.409A>C, XM_017002209.1:c.409A>C, NP_003263.1:p.Thr137Pro, XP_016857698.1:p.Thr137Pro

Select item 14838147123.

rs1483814712 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:236142645 (GRCh38)
1:236305945 (GRCh37)
Canonical SPDI:: NC_000001.11:236142644:C:T
Gene:: GPR137B (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_000001.11:g.236142645C>T, NC_000001.10:g.236305945C>T, NM_003272.4:c.23C>T, NM_003272.3:c.23C>T, XM_017002209.3:c.23C>T, XM_017002209.2:c.23C>T, XM_017002209.1:c.23C>T, NP_003263.1:p.Pro8Leu, XP_016857698.1:p.Pro8Leu

Select item 14815118284.

rs1481511828 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:236142748 (GRCh38)
1:236306048 (GRCh37)
Canonical SPDI:: NC_000001.11:236142747:G:A
Gene:: GPR137B (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0./0 (GnomAD)
A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.236142748G>A, NC_000001.10:g.236306048G>A, NM_003272.4:c.126G>A, NM_003272.3:c.126G>A, XM_017002209.3:c.126G>A, XM_017002209.2:c.126G>A, XM_017002209.1:c.126G>A

Select item 14782312665.

rs1478231266 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 1:236142825 (GRCh38)
1:236306125 (GRCh37)
Canonical SPDI:: NC_000001.11:236142824:T:A
Gene:: GPR137B (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: A=0.000071/1 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.236142825T>A, NC_000001.10:g.236306125T>A, NM_003272.4:c.203T>A, NM_003272.3:c.203T>A, XM_017002209.3:c.203T>A, XM_017002209.2:c.203T>A, XM_017002209.1:c.203T>A, NP_003263.1:p.Leu68Gln, XP_016857698.1:p.Leu68Gln

Select item 14769322746.

rs1476932274 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 1:236178498 (GRCh38)
1:236341798 (GRCh37)
Canonical SPDI:: NC_000001.11:236178497:A:C
Gene:: GPR137B (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_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_000001.11:g.236178498A>C, NC_000001.10:g.236341798A>C, NM_003272.4:c.549A>C, NM_003272.3:c.549A>C, XM_017002209.3:c.549A>C, XM_017002209.2:c.549A>C, XM_017002209.1:c.549A>C

Select item 14758028727.

rs1475802872 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:236178432 (GRCh38)
1:236341732 (GRCh37)
Canonical SPDI:: NC_000001.11:236178431:C:T
Gene:: GPR137B (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000011/3 (TOPMED)
HGVS:: NC_000001.11:g.236178432C>T, NC_000001.10:g.236341732C>T, NM_003272.4:c.483C>T, NM_003272.3:c.483C>T, XM_017002209.3:c.483C>T, XM_017002209.2:c.483C>T, XM_017002209.1:c.483C>T

Select item 14746294008.

rs1474629400 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 1:236142678 (GRCh38)
1:236305978 (GRCh37)
Canonical SPDI:: NC_000001.11:236142677:C:A,NC_000001.11:236142677:C:T
Gene:: GPR137B (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
HGVS:: NC_000001.11:g.236142678C>A, NC_000001.11:g.236142678C>T, NC_000001.10:g.236305978C>A, NC_000001.10:g.236305978C>T, NM_003272.4:c.56C>A, NM_003272.4:c.56C>T, NM_003272.3:c.56C>A, NM_003272.3:c.56C>T, XM_017002209.3:c.56C>A, XM_017002209.3:c.56C>T, XM_017002209.2:c.56C>A, XM_017002209.2:c.56C>T, XM_017002209.1:c.56C>A, XM_017002209.1:c.56C>T, NP_003263.1:p.Pro19Gln, NP_003263.1:p.Pro19Leu, XP_016857698.1:p.Pro19Gln, XP_016857698.1:p.Pro19Leu

Select item 14743814899.

rs1474381489 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 1:236205230 (GRCh38)
1:236368530 (GRCh37)
Canonical SPDI:: NC_000001.11:236205229:C:A
Gene:: GPR137B (Varview)
Functional Consequence:: synonymous_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_000001.11:g.236205230C>A, NC_000001.10:g.236368530C>A, NM_003272.4:c.1071C>A, NM_003272.3:c.1071C>A, XM_017002209.3:c.1071C>A, XM_017002209.2:c.1071C>A, XM_017002209.1:c.1071C>A

Select item 146792599510.

rs1467925995 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:236205249 (GRCh38)
1:236368549 (GRCh37)
Canonical SPDI:: NC_000001.11:236205248:G:A
Gene:: GPR137B (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.236205249G>A, NC_000001.10:g.236368549G>A, NM_003272.4:c.1090G>A, NM_003272.3:c.1090G>A, XM_017002209.3:c.1090G>A, XM_017002209.2:c.1090G>A, XM_017002209.1:c.1090G>A, NP_003263.1:p.Gly364Ser, XP_016857698.1:p.Gly364Arg

Select item 146635320611.

rs1466353206 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:236142898 (GRCh38)
1:236306198 (GRCh37)
Canonical SPDI:: NC_000001.11:236142897:G:A
Gene:: GPR137B (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000008/2 (TOPMED)
HGVS:: NC_000001.11:g.236142898G>A, NC_000001.10:g.236306198G>A, NM_003272.4:c.276G>A, NM_003272.3:c.276G>A, XM_017002209.3:c.276G>A, XM_017002209.2:c.276G>A, XM_017002209.1:c.276G>A

Select item 146550078612.

rs1465500786 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 1:236179909 (GRCh38)
1:236343209 (GRCh37)
Canonical SPDI:: NC_000001.11:236179908:G:A
Gene:: GPR137B (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)
A=0.000007/1 (GnomAD)
A=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000001.11:g.236179909G>A, NC_000001.10:g.236343209G>A, NM_003272.4:c.718G>A, NM_003272.3:c.718G>A, XM_017002209.3:c.718G>A, XM_017002209.2:c.718G>A, XM_017002209.1:c.718G>A, NP_003263.1:p.Gly240Ser, XP_016857698.1:p.Gly240Ser

Select item 146255736413.

rs1462557364 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 1:236142947 (GRCh38)
1:236306247 (GRCh37)
Canonical SPDI:: NC_000001.11:236142946:C:A
Gene:: GPR137B (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000071/1 (ALFA)
A=0.000004/1 (GnomAD_exomes)
A=0.000007/1 (GnomAD)
A=0.000026/7 (TOPMED)
HGVS:: NC_000001.11:g.236142947C>A, NC_000001.10:g.236306247C>A, NM_003272.4:c.325C>A, NM_003272.3:c.325C>A, XM_017002209.3:c.325C>A, XM_017002209.2:c.325C>A, XM_017002209.1:c.325C>A, NP_003263.1:p.Leu109Ile, XP_016857698.1:p.Leu109Ile

Select item 146142112814.

rs1461421128 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:236142666 (GRCh38)
1:236305966 (GRCh37)
Canonical SPDI:: NC_000001.11:236142665:C:T
Gene:: GPR137B (Varview)
Functional Consequence:: missense_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)
T=0.000007/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.236142666C>T, NC_000001.10:g.236305966C>T, NM_003272.4:c.44C>T, NM_003272.3:c.44C>T, XM_017002209.3:c.44C>T, XM_017002209.2:c.44C>T, XM_017002209.1:c.44C>T, NP_003263.1:p.Pro15Leu, XP_016857698.1:p.Pro15Leu

Select item 145504538415.

rs1455045384 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:236142888 (GRCh38)
1:236306188 (GRCh37)
Canonical SPDI:: NC_000001.11:236142887:C:T
Gene:: GPR137B (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=0.000035/1 (TOMMO)
HGVS:: NC_000001.11:g.236142888C>T, NC_000001.10:g.236306188C>T, NM_003272.4:c.266C>T, NM_003272.3:c.266C>T, XM_017002209.3:c.266C>T, XM_017002209.2:c.266C>T, XM_017002209.1:c.266C>T, NP_003263.1:p.Ala89Val, XP_016857698.1:p.Ala89Val

Select item 145463408216.

rs1454634082 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 1:236142636 (GRCh38)
1:236305936 (GRCh37)
Canonical SPDI:: NC_000001.11:236142635:G:T
Gene:: GPR137B (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000071/1 (ALFA)
T=0.000011/1 (GnomAD_exomes)
T=0.000014/2 (GnomAD)
T=0.000019/5 (TOPMED)
T=0.000142/2 (TOMMO)
T=0.000567/1 (Korea1K)
T=0.001059/3 (KOREAN)
HGVS:: NC_000001.11:g.236142636G>T, NC_000001.10:g.236305936G>T, NM_003272.4:c.14G>T, NM_003272.3:c.14G>T, XM_017002209.3:c.14G>T, XM_017002209.2:c.14G>T, XM_017002209.1:c.14G>T, NP_003263.1:p.Arg5Leu, XP_016857698.1:p.Arg5Leu

Select item 145174404517.

rs1451744045 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 1:236142854 (GRCh38)
1:236306154 (GRCh37)
Canonical SPDI:: NC_000001.11:236142853:C:T
Gene:: GPR137B (Varview)
Functional Consequence:: coding_sequence_variant,stop_gained
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000001.11:g.236142854C>T, NC_000001.10:g.236306154C>T, NM_003272.4:c.232C>T, NM_003272.3:c.232C>T, XM_017002209.3:c.232C>T, XM_017002209.2:c.232C>T, XM_017002209.1:c.232C>T, NP_003263.1:p.Gln78Ter, XP_016857698.1:p.Gln78Ter

Select item 144799694618.

rs1447996946 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 1:236205224 (GRCh38)
1:236368524 (GRCh37)
Canonical SPDI:: NC_000001.11:236205223:C:G,NC_000001.11:236205223:C:T
Gene:: GPR137B (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (GnomAD_exomes)
T=0.000004/1 (TOPMED)
G=0.000035/1 (TOMMO)
HGVS:: NC_000001.11:g.236205224C>G, NC_000001.11:g.236205224C>T, NC_000001.10:g.236368524C>G, NC_000001.10:g.236368524C>T, NM_003272.4:c.1065C>G, NM_003272.4:c.1065C>T, NM_003272.3:c.1065C>G, NM_003272.3:c.1065C>T, XM_017002209.3:c.1065C>G, XM_017002209.3:c.1065C>T, XM_017002209.2:c.1065C>G, XM_017002209.2:c.1065C>T, XM_017002209.1:c.1065C>G, XM_017002209.1:c.1065C>T, NP_003263.1:p.Asn355Lys, XP_016857698.1:p.Asn355Lys

Select item 144698757619.

rs1446987576 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 1:236178451 (GRCh38)
1:236341751 (GRCh37)
Canonical SPDI:: NC_000001.11:236178450:G:A,NC_000001.11:236178450:G:C
Gene:: GPR137B (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
C=0.000004/1 (TOPMED)
HGVS:: NC_000001.11:g.236178451G>A, NC_000001.11:g.236178451G>C, NC_000001.10:g.236341751G>A, NC_000001.10:g.236341751G>C, NM_003272.4:c.502G>A, NM_003272.4:c.502G>C, NM_003272.3:c.502G>A, NM_003272.3:c.502G>C, XM_017002209.3:c.502G>A, XM_017002209.3:c.502G>C, XM_017002209.2:c.502G>A, XM_017002209.2:c.502G>C, XM_017002209.1:c.502G>A, XM_017002209.1:c.502G>C, NP_003263.1:p.Val168Ile, NP_003263.1:p.Val168Leu, XP_016857698.1:p.Val168Ile, XP_016857698.1:p.Val168Leu

Select item 144638352520.

rs1446383525 [Homo sapiens]

Variant type:: DELINS
Alleles:: ACT>- [Show Flanks]
Chromosome:: 1:236142975 (GRCh38)
1:236306275 (GRCh37)
Canonical SPDI:: NC_000001.11:236142972:CTACT:CT
Gene:: GPR137B (Varview)
Functional Consequence:: coding_sequence_variant,inframe_deletion
Validated:: by frequency
MAF:: -=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000001.11:g.236142975_236142977del, NC_000001.10:g.236306275_236306277del, NM_003272.4:c.353_355del, NM_003272.3:c.353_355del, XM_017002209.3:c.353_355del, XM_017002209.2:c.353_355del, XM_017002209.1:c.353_355del, NP_003263.1:p.Tyr118del, XP_016857698.1:p.Tyr118del

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