SNP Links for Protein (Select 156119607) - SNP

Links from Protein

Items: 1 to 20 of 433

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Select item 14863148951.

rs1486314895 [Homo sapiens]

Variant type:: DELINS
Alleles:: C>- [Show Flanks]
Chromosome:: 11:48489577 (GRCh38)
11:48511129 (GRCh37)
Canonical SPDI:: NC_000011.10:48489576:CC:C
Gene:: OR4A47 (Varview)
Functional Consequence:: frameshift_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: CC=0./0 (ALFA)
-=0.000011/3 (TOPMED)
HGVS:: NC_000011.10:g.48489578del, NC_000011.9:g.48511130del, NM_001005512.2:c.786del, NP_001005512.2:p.Phe263fs

Select item 14845836692.

rs1484583669 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:48488972 (GRCh38)
11:48510524 (GRCh37)
Canonical SPDI:: NC_000011.10:48488971:T:C
Gene:: OR4A47 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.48488972T>C, NC_000011.9:g.48510524T>C, NM_001005512.2:c.180T>C

Select item 14845624343.

rs1484562434 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:48489521 (GRCh38)
11:48511073 (GRCh37)
Canonical SPDI:: NC_000011.10:48489520:T:C
Gene:: OR4A47 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.00008/20 (GnomAD_exomes)
C=0.000228/32 (GnomAD)
C=0.000249/66 (TOPMED)
HGVS:: NC_000011.10:g.48489521T>C, NC_000011.9:g.48511073T>C, NM_001005512.2:c.729T>C

Select item 14839664074.

rs1483966407 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,C [Show Flanks]
Chromosome:: 11:48489402 (GRCh38)
11:48510954 (GRCh37)
Canonical SPDI:: NC_000011.10:48489401:G:A,NC_000011.10:48489401:G:C
Gene:: OR4A47 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000011.10:g.48489402G>A, NC_000011.10:g.48489402G>C, NC_000011.9:g.48510954G>A, NC_000011.9:g.48510954G>C, NM_001005512.2:c.610G>A, NM_001005512.2:c.610G>C, NP_001005512.2:p.Ala204Thr, NP_001005512.2:p.Ala204Pro

Select item 14835497405.

rs1483549740 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:48489252 (GRCh38)
11:48510804 (GRCh37)
Canonical SPDI:: NC_000011.10:48489251:T:C
Gene:: OR4A47 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.48489252T>C, NC_000011.9:g.48510804T>C, NM_001005512.2:c.460T>C, NP_001005512.2:p.Ser154Pro

Select item 14831458196.

rs1483145819 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:48489198 (GRCh38)
11:48510750 (GRCh37)
Canonical SPDI:: NC_000011.10:48489197:C:T
Gene:: OR4A47 (Varview)
Functional Consequence:: coding_sequence_variant,stop_gained
Validated:: by frequency,by alfa
MAF:: T=0.000047/1 (ALFA)
T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.48489198C>T, NC_000011.9:g.48510750C>T, NM_001005512.2:c.406C>T, NP_001005512.2:p.Gln136Ter

Select item 14777796497.

rs1477779649 [Homo sapiens]

Variant type:: DELINS
Alleles:: GT>- [Show Flanks]
Chromosome:: 11:48489605 (GRCh38)
11:48511157 (GRCh37)
Canonical SPDI:: NC_000011.10:48489600:GTGTGT:GTGT
Gene:: OR4A47 (Varview)
Functional Consequence:: frameshift_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: GTGT=0./0 (ALFA)
-=0.000008/2 (TOPMED)
HGVS:: NC_000011.10:g.48489601GT[2], NC_000011.9:g.48511153GT[2], NM_001005512.2:c.813_814del, NP_001005512.2:p.Phe272fs

Select item 14770977818.

rs1477097781 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 11:48488797 (GRCh38)
11:48510349 (GRCh37)
Canonical SPDI:: NC_000011.10:48488796:A:T
Gene:: OR4A47 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (GnomAD_exomes)
T=0.000007/1 (GnomAD)
T=0.000008/2 (TOPMED)
T=0.000035/1 (TOMMO)
HGVS:: NC_000011.10:g.48488797A>T, NC_000011.9:g.48510349A>T, NM_001005512.2:c.5A>T, NP_001005512.2:p.Glu2Val

Select item 14757195059.

rs1475719505 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 11:48489438 (GRCh38)
11:48510990 (GRCh37)
Canonical SPDI:: NC_000011.10:48489437:T:G
Gene:: OR4A47 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by cluster
MAF:: G=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.48489438T>G, NC_000011.9:g.48510990T>G, NM_001005512.2:c.646T>G, NP_001005512.2:p.Tyr216Asp

Select item 147500710610.

rs1475007106 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G,T [Show Flanks]
Chromosome:: 11:48489682 (GRCh38)
11:48511234 (GRCh37)
Canonical SPDI:: NC_000011.10:48489681:A:G,NC_000011.10:48489681:A:T
Gene:: OR4A47 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.48489682A>G, NC_000011.10:g.48489682A>T, NC_000011.9:g.48511234A>G, NC_000011.9:g.48511234A>T, NM_001005512.2:c.890A>G, NM_001005512.2:c.890A>T, NP_001005512.2:p.Lys297Arg, NP_001005512.2:p.Lys297Met

Select item 147209146511.

rs1472091465 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 11:48488980 (GRCh38)
11:48510532 (GRCh37)
Canonical SPDI:: NC_000011.10:48488979:G:A,NC_000011.10:48488979:G:T
Gene:: OR4A47 (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=0.000007/1 (GnomAD)
HGVS:: NC_000011.10:g.48488980G>A, NC_000011.10:g.48488980G>T, NC_000011.9:g.48510532G>A, NC_000011.9:g.48510532G>T, NM_001005512.2:c.188G>A, NM_001005512.2:c.188G>T, NP_001005512.2:p.Gly63Asp, NP_001005512.2:p.Gly63Val

Select item 147158421412.

rs1471584214 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C [Show Flanks]
Chromosome:: 11:48488810 (GRCh38)
11:48510362 (GRCh37)
Canonical SPDI:: NC_000011.10:48488809:T:A,NC_000011.10:48488809:T:C
Gene:: OR4A47 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
HGVS:: NC_000011.10:g.48488810T>A, NC_000011.10:g.48488810T>C, NC_000011.9:g.48510362T>A, NC_000011.9:g.48510362T>C, NM_001005512.2:c.18T>A, NM_001005512.2:c.18T>C, NP_001005512.2:p.Asn6Lys

Select item 146852821713.

rs1468528217 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 11:48489582 (GRCh38)
11:48511134 (GRCh37)
Canonical SPDI:: NC_000011.10:48489581:C:T
Gene:: OR4A47 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.48489582C>T, NC_000011.9:g.48511134C>T, NM_001005512.2:c.790C>T, NP_001005512.2:p.Pro264Ser

Select item 146721930114.

rs1467219301 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 11:48489388 (GRCh38)
11:48510940 (GRCh37)
Canonical SPDI:: NC_000011.10:48489387:C:A
Gene:: OR4A47 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.48489388C>A, NC_000011.9:g.48510940C>A, NM_001005512.2:c.596C>A, NP_001005512.2:p.Ala199Asp

Select item 146702959115.

rs1467029591 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:48489265 (GRCh38)
11:48510817 (GRCh37)
Canonical SPDI:: NC_000011.10:48489264:T:C
Gene:: OR4A47 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
C=0.000014/2 (GnomAD)
HGVS:: NC_000011.10:g.48489265T>C, NC_000011.9:g.48510817T>C, NM_001005512.2:c.473T>C, NP_001005512.2:p.Leu158Pro

Select item 146686041316.

rs1466860413 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 11:48489196 (GRCh38)
11:48510748 (GRCh37)
Canonical SPDI:: NC_000011.10:48489195:G:A,NC_000011.10:48489195:G:T
Gene:: OR4A47 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
T=0.000071/2 (TOMMO)
HGVS:: NC_000011.10:g.48489196G>A, NC_000011.10:g.48489196G>T, NC_000011.9:g.48510748G>A, NC_000011.9:g.48510748G>T, NM_001005512.2:c.404G>A, NM_001005512.2:c.404G>T, NP_001005512.2:p.Arg135Lys, NP_001005512.2:p.Arg135Ile

Select item 146605172817.

rs1466051728 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 11:48488984 (GRCh38)
11:48510536 (GRCh37)
Canonical SPDI:: NC_000011.10:48488983:A:T
Gene:: OR4A47 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.48488984A>T, NC_000011.9:g.48510536A>T, NM_001005512.2:c.192A>T, NP_001005512.2:p.Leu64Phe

Select item 146107592618.

rs1461075926 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 11:48489640 (GRCh38)
11:48511192 (GRCh37)
Canonical SPDI:: NC_000011.10:48489639:T:A
Gene:: OR4A47 (Varview)
Functional Consequence:: coding_sequence_variant,stop_gained
Validated:: by cluster
HGVS:: NC_000011.10:g.48489640T>A, NC_000011.9:g.48511192T>A, NM_001005512.2:c.848T>A, NP_001005512.2:p.Leu283Ter

Select item 145529496519.

rs1455294965 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 11:48488936 (GRCh38)
11:48510488 (GRCh37)
Canonical SPDI:: NC_000011.10:48488935:T:C
Gene:: OR4A47 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
HGVS:: NC_000011.10:g.48488936T>C, NC_000011.9:g.48510488T>C, NM_001005512.2:c.144T>C

Select item 145259231220.

rs1452592312 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 11:48489345 (GRCh38)
11:48510897 (GRCh37)
Canonical SPDI:: NC_000011.10:48489344:C:A,NC_000011.10:48489344:C:T
Gene:: OR4A47 (Varview)
Functional Consequence:: missense_variant,synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000011.10:g.48489345C>A, NC_000011.10:g.48489345C>T, NC_000011.9:g.48510897C>A, NC_000011.9:g.48510897C>T, NM_001005512.2:c.553C>A, NM_001005512.2:c.553C>T, NP_001005512.2:p.Leu185Met

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Items: 1 to 20 of 433

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