SNP Links for Protein (Select 53828712) - SNP

Links from Protein

Items: 1 to 20 of 451

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Select item 14899310401.

rs1489931040 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 14:19781181 (GRCh38)
14:20249340 (GRCh37)
Canonical SPDI:: NC_000014.9:19781180:A:G
Gene:: OR4M1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000014.9:g.19781181A>G, NC_000014.8:g.20249340A>G, NM_001005500.2:c.859A>G, NM_001005500.1:c.859A>G, NP_001005500.1:p.Ile287Val

Select item 14881076082.

rs1488107608 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 14:19780418 (GRCh38)
14:20248577 (GRCh37)
Canonical SPDI:: NC_000014.9:19780417:A:G
Gene:: OR4M1 (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)
HGVS:: NC_000014.9:g.19780418A>G, NC_000014.8:g.20248577A>G, NM_001005500.2:c.96A>G, NM_001005500.1:c.96A>G

Select item 14846535623.

rs1484653562 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 14:19780613 (GRCh38)
14:20248772 (GRCh37)
Canonical SPDI:: NC_000014.9:19780612:C:A
Gene:: OR4M1 (Varview)
Functional Consequence:: coding_sequence_variant,stop_gained
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000224/1 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000014.9:g.19780613C>A, NC_000014.8:g.20248772C>A, NM_001005500.2:c.291C>A, NM_001005500.1:c.291C>A, NP_001005500.1:p.Cys97Ter

Select item 14822224754.

rs1482222475 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 14:19780782 (GRCh38)
14:20248941 (GRCh37)
Canonical SPDI:: NC_000014.9:19780781:A:G
Gene:: OR4M1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
HGVS:: NC_000014.9:g.19780782A>G, NC_000014.8:g.20248941A>G, NM_001005500.2:c.460A>G, NM_001005500.1:c.460A>G, NP_001005500.1:p.Ile154Val

Select item 14791727685.

rs1479172768 [Homo sapiens]

Variant type:: DELINS
Alleles:: T>- [Show Flanks]
Chromosome:: 14:19780602 (GRCh38)
14:20248761 (GRCh37)
Canonical SPDI:: NC_000014.9:19780601:TTT:TT
Gene:: OR4M1 (Varview)
Functional Consequence:: coding_sequence_variant,frameshift_variant
HGVS:: NC_000014.9:g.19780604del, NC_000014.8:g.20248763del, NM_001005500.2:c.282del, NM_001005500.1:c.282del, NP_001005500.1:p.Phe94fs

Select item 14791417216.

rs1479141721 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 14:19781063 (GRCh38)
14:20249222 (GRCh37)
Canonical SPDI:: NC_000014.9:19781062:C:T
Gene:: OR4M1 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (GnomAD_exomes)
T=0.000014/2 (GnomAD)
T=0.000015/4 (TOPMED)
HGVS:: NC_000014.9:g.19781063C>T, NC_000014.8:g.20249222C>T, NM_001005500.2:c.741C>T, NM_001005500.1:c.741C>T

Select item 14779630777.

rs1477963077 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 14:19780422 (GRCh38)
14:20248581 (GRCh37)
Canonical SPDI:: NC_000014.9:19780421:T:C
Gene:: OR4M1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: C=0.000016/4 (GnomAD_exomes)
HGVS:: NC_000014.9:g.19780422T>C, NC_000014.8:g.20248581T>C, NM_001005500.2:c.100T>C, NM_001005500.1:c.100T>C, NP_001005500.1:p.Phe34Leu

Select item 14779315388.

rs1477931538 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 14:19780905 (GRCh38)
14:20249064 (GRCh37)
Canonical SPDI:: NC_000014.9:19780904:G:A
Gene:: OR4M1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000014.9:g.19780905G>A, NC_000014.8:g.20249064G>A, NM_001005500.2:c.583G>A, NM_001005500.1:c.583G>A, NP_001005500.1:p.Glu195Lys

Select item 14750490169.

rs1475049016 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 14:19781131 (GRCh38)
14:20249290 (GRCh37)
Canonical SPDI:: NC_000014.9:19781130:A:T
Gene:: OR4M1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
HGVS:: NC_000014.9:g.19781131A>T, NC_000014.8:g.20249290A>T, NM_001005500.2:c.809A>T, NM_001005500.1:c.809A>T, NP_001005500.1:p.Asp270Val

Select item 147148477710.

rs1471484777 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 14:19780523 (GRCh38)
14:20248682 (GRCh37)
Canonical SPDI:: NC_000014.9:19780522:C:A,NC_000014.9:19780522:C:T
Gene:: OR4M1 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000014.9:g.19780523C>A, NC_000014.9:g.19780523C>T, NC_000014.8:g.20248682C>A, NC_000014.8:g.20248682C>T, NM_001005500.2:c.201C>A, NM_001005500.2:c.201C>T, NM_001005500.1:c.201C>A, NM_001005500.1:c.201C>T

Select item 147075537711.

rs1470755377 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 14:19781015 (GRCh38)
14:20249174 (GRCh37)
Canonical SPDI:: NC_000014.9:19781014:A:C
Gene:: OR4M1 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000014.9:g.19781015A>C, NC_000014.8:g.20249174A>C, NM_001005500.2:c.693A>C, NM_001005500.1:c.693A>C

Select item 146893388412.

rs1468933884 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 14:19780804 (GRCh38)
14:20248963 (GRCh37)
Canonical SPDI:: NC_000014.9:19780803:C:A,NC_000014.9:19780803:C:T
Gene:: OR4M1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000014.9:g.19780804C>A, NC_000014.9:g.19780804C>T, NC_000014.8:g.20248963C>A, NC_000014.8:g.20248963C>T, NM_001005500.2:c.482C>A, NM_001005500.2:c.482C>T, NM_001005500.1:c.482C>A, NM_001005500.1:c.482C>T, NP_001005500.1:p.Ala161Asp, NP_001005500.1:p.Ala161Val

Select item 146836222513.

rs1468362225 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 14:19781069 (GRCh38)
14:20249228 (GRCh37)
Canonical SPDI:: NC_000014.9:19781068:G:A
Gene:: OR4M1 (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=0.000106/2 (TOMMO)
HGVS:: NC_000014.9:g.19781069G>A, NC_000014.8:g.20249228G>A, NM_001005500.2:c.747G>A, NM_001005500.1:c.747G>A

Select item 146172866114.

rs1461728661 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 14:19781241 (GRCh38)
14:20249400 (GRCh37)
Canonical SPDI:: NC_000014.9:19781240:T:C
Gene:: OR4M1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
HGVS:: NC_000014.9:g.19781241T>C, NC_000014.8:g.20249400T>C, NM_001005500.2:c.919T>C, NM_001005500.1:c.919T>C, NP_001005500.1:p.Tyr307His

Select item 145968637015.

rs1459686370 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 14:19780583 (GRCh38)
14:20248742 (GRCh37)
Canonical SPDI:: NC_000014.9:19780582:G:A
Gene:: OR4M1 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000014.9:g.19780583G>A, NC_000014.8:g.20248742G>A, NM_001005500.2:c.261G>A, NM_001005500.1:c.261G>A

Select item 145965161516.

rs1459651615 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 14:19780375 (GRCh38)
14:20248534 (GRCh37)
Canonical SPDI:: NC_000014.9:19780374:C:G,NC_000014.9:19780374:C:T
Gene:: OR4M1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000029/4 (GnomAD)
HGVS:: NC_000014.9:g.19780375C>G, NC_000014.9:g.19780375C>T, NC_000014.8:g.20248534C>G, NC_000014.8:g.20248534C>T, NM_001005500.2:c.53C>G, NM_001005500.2:c.53C>T, NM_001005500.1:c.53C>G, NM_001005500.1:c.53C>T, NP_001005500.1:p.Ser18Cys, NP_001005500.1:p.Ser18Phe

Select item 145862972017.

rs1458629720 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 14:19780592 (GRCh38)
14:20248751 (GRCh37)
Canonical SPDI:: NC_000014.9:19780591:G:T
Gene:: OR4M1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000014.9:g.19780592G>T, NC_000014.8:g.20248751G>T, NM_001005500.2:c.270G>T, NM_001005500.1:c.270G>T, NP_001005500.1:p.Lys90Asn

Select item 145603241018.

rs1456032410 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,G,T [Show Flanks]
Chromosome:: 14:19781026 (GRCh38)
14:20249185 (GRCh37)
Canonical SPDI:: NC_000014.9:19781025:C:A,NC_000014.9:19781025:C:G,NC_000014.9:19781025:C:T
Gene:: OR4M1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
G=0.000004/1 (TOPMED)
HGVS:: NC_000014.9:g.19781026C>A, NC_000014.9:g.19781026C>G, NC_000014.9:g.19781026C>T, NC_000014.8:g.20249185C>A, NC_000014.8:g.20249185C>G, NC_000014.8:g.20249185C>T, NM_001005500.2:c.704C>A, NM_001005500.2:c.704C>G, NM_001005500.2:c.704C>T, NM_001005500.1:c.704C>A, NM_001005500.1:c.704C>G, NM_001005500.1:c.704C>T, NP_001005500.1:p.Thr235Asn, NP_001005500.1:p.Thr235Ser, NP_001005500.1:p.Thr235Ile

Select item 145382083719.

rs1453820837 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C,G [Show Flanks]
Chromosome:: 14:19780638 (GRCh38)
14:20248797 (GRCh37)
Canonical SPDI:: NC_000014.9:19780637:T:A,NC_000014.9:19780637:T:C,NC_000014.9:19780637:T:G
Gene:: OR4M1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000014.9:g.19780638T>A, NC_000014.9:g.19780638T>C, NC_000014.9:g.19780638T>G, NC_000014.8:g.20248797T>A, NC_000014.8:g.20248797T>C, NC_000014.8:g.20248797T>G, NM_001005500.2:c.316T>A, NM_001005500.2:c.316T>C, NM_001005500.2:c.316T>G, NM_001005500.1:c.316T>A, NM_001005500.1:c.316T>C, NM_001005500.1:c.316T>G, NP_001005500.1:p.Phe106Ile, NP_001005500.1:p.Phe106Leu, NP_001005500.1:p.Phe106Val

Select item 145042532020.

rs1450425320 [Homo sapiens]

Variant type:: DELINS
Alleles:: CCT>- [Show Flanks]
Chromosome:: 14:19780494 (GRCh38)
14:20248653 (GRCh37)
Canonical SPDI:: NC_000014.9:19780491:CTCCT:CT
Gene:: OR4M1 (Varview)
Functional Consequence:: coding_sequence_variant,inframe_deletion
HGVS:: NC_000014.9:g.19780494_19780496del, NC_000014.8:g.20248653_20248655del, NM_001005500.2:c.172_174del, NM_001005500.1:c.172_174del, NP_001005500.1:p.Pro58del

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