SNP Links for Protein (Select 332634911) - SNP

Links from Protein

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Select item 14870930721.

rs1487093072 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 6:29440307 (GRCh38)
6:29408084 (GRCh37)
Canonical SPDI:: NC_000006.12:29440306:C:T
Gene:: OR11A1 (Varview), OR10C1 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,coding_sequence_variant,missense_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (GnomAD_exomes)
T=0.000004/1 (TOPMED)
HGVS:: NC_000006.12:g.29440307C>T, NC_000006.11:g.29408084C>T, NT_113891.3:g.926756C>T, NT_113891.2:g.926862C>T, NT_167248.2:g.705776C>T, NT_167248.1:g.711372C>T, NT_167245.2:g.705829C>T, NT_167245.1:g.711414C>T, NT_167249.2:g.749318C>T, NT_167249.1:g.748616C>T, NT_167246.2:g.705442C>T, NT_167246.1:g.711062C>T, NT_167247.2:g.705676C>T, NT_167247.1:g.711261C>T, NT_167244.2:g.705971C>T, NT_167244.1:g.711565C>T, NM_013941.4:c.292C>T, NM_013941.3:c.292C>T, NP_039229.3:p.Leu98Phe

Select item 14859418372.

rs1485941837 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 6:29440318 (GRCh38)
6:29408095 (GRCh37)
Canonical SPDI:: NC_000006.12:29440317:C:T
Gene:: OR11A1 (Varview), OR10C1 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,coding_sequence_variant,synonymous_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000006.12:g.29440318C>T, NC_000006.11:g.29408095C>T, NT_113891.3:g.926767C>T, NT_113891.2:g.926873C>T, NT_167248.2:g.705787C>T, NT_167248.1:g.711383C>T, NT_167245.2:g.705840C>T, NT_167245.1:g.711425C>T, NT_167249.2:g.749329C>T, NT_167249.1:g.748627C>T, NT_167246.2:g.705453C>T, NT_167246.1:g.711073C>T, NT_167247.2:g.705687C>T, NT_167247.1:g.711272C>T, NT_167244.2:g.705982C>T, NT_167244.1:g.711576C>T, NM_013941.4:c.303C>T, NM_013941.3:c.303C>T

Select item 14816930833.

rs1481693083 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 6:29440654 (GRCh38)
6:29408431 (GRCh37)
Canonical SPDI:: NC_000006.12:29440653:C:A,NC_000006.12:29440653:C:T
Gene:: OR11A1 (Varview), OR10C1 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,coding_sequence_variant,synonymous_variant,intron_variant
HGVS:: NC_000006.12:g.29440654C>A, NC_000006.12:g.29440654C>T, NC_000006.11:g.29408431C>A, NC_000006.11:g.29408431C>T, NT_113891.3:g.927103C>A, NT_113891.3:g.927103C>T, NT_113891.2:g.927209C>A, NT_113891.2:g.927209C>T, NT_167248.2:g.706123C>A, NT_167248.2:g.706123C>T, NT_167248.1:g.711719C>A, NT_167248.1:g.711719C>T, NT_167245.2:g.706176C>A, NT_167245.2:g.706176C>T, NT_167245.1:g.711761C>A, NT_167245.1:g.711761C>T, NT_167249.2:g.749665C>A, NT_167249.2:g.749665C>T, NT_167249.1:g.748963C>A, NT_167249.1:g.748963C>T, NT_167246.2:g.705789C>A, NT_167246.2:g.705789C>T, NT_167246.1:g.711409C>A, NT_167246.1:g.711409C>T, NT_167247.2:g.706023C>A, NT_167247.2:g.706023C>T, NT_167247.1:g.711608C>A, NT_167247.1:g.711608C>T, NT_167244.2:g.706318C>A, NT_167244.2:g.706318C>T, NT_167244.1:g.711912C>A, NT_167244.1:g.711912C>T, NM_013941.4:c.639C>A, NM_013941.4:c.639C>T, NM_013941.3:c.639C>A, NM_013941.3:c.639C>T

Select item 14761114324.

rs1476111432 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 6:29440832 (GRCh38)
6:29408609 (GRCh37)
Canonical SPDI:: NC_000006.12:29440831:G:A
Gene:: OR11A1 (Varview), OR10C1 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,missense_variant,coding_sequence_variant,intron_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_000006.12:g.29440832G>A, NC_000006.11:g.29408609G>A, NT_113891.3:g.927281G>A, NT_113891.2:g.927387G>A, NT_167248.2:g.706301G>A, NT_167248.1:g.711897G>A, NT_167245.2:g.706354G>A, NT_167245.1:g.711939G>A, NT_167249.2:g.749843G>A, NT_167249.1:g.749141G>A, NT_167246.2:g.705967G>A, NT_167246.1:g.711587G>A, NT_167247.2:g.706201G>A, NT_167247.1:g.711786G>A, NT_167244.2:g.706496G>A, NT_167244.1:g.712090G>A, NM_013941.4:c.817G>A, NM_013941.3:c.817G>A, NP_039229.3:p.Val273Met

Select item 14722611245.

rs1472261124 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 6:29440412 (GRCh38)
6:29408189 (GRCh37)
Canonical SPDI:: NC_000006.12:29440411:C:T
Gene:: OR11A1 (Varview), OR10C1 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,synonymous_variant,coding_sequence_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.29440412C>T, NC_000006.11:g.29408189C>T, NT_113891.3:g.926861C>T, NT_113891.2:g.926967C>T, NT_167248.2:g.705881C>T, NT_167248.1:g.711477C>T, NT_167245.2:g.705934C>T, NT_167245.1:g.711519C>T, NT_167249.2:g.749423C>T, NT_167249.1:g.748721C>T, NT_167246.2:g.705547C>T, NT_167246.1:g.711167C>T, NT_167247.2:g.705781C>T, NT_167247.1:g.711366C>T, NT_167244.2:g.706076C>T, NT_167244.1:g.711670C>T, NM_013941.4:c.397C>T, NM_013941.3:c.397C>T

Select item 14682031076.

rs1468203107 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 6:29440844 (GRCh38)
6:29408621 (GRCh37)
Canonical SPDI:: NC_000006.12:29440843:T:C
Gene:: OR11A1 (Varview), OR10C1 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,missense_variant,coding_sequence_variant,intron_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000006.12:g.29440844T>C, NC_000006.11:g.29408621T>C, NT_113891.3:g.927293T>C, NT_113891.2:g.927399T>C, NT_167248.2:g.706313T>C, NT_167248.1:g.711909T>C, NT_167245.2:g.706366T>C, NT_167245.1:g.711951T>C, NT_167249.2:g.749855T>C, NT_167249.1:g.749153T>C, NT_167246.2:g.705979T>C, NT_167246.1:g.711599T>C, NT_167247.2:g.706213T>C, NT_167247.1:g.711798T>C, NT_167244.2:g.706508T>C, NT_167244.1:g.712102T>C, NM_013941.4:c.829T>C, NM_013941.3:c.829T>C, NP_039229.3:p.Tyr277His

Select item 14645936617.

rs1464593661 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 6:29440576 (GRCh38)
6:29408353 (GRCh37)
Canonical SPDI:: NC_000006.12:29440575:A:G
Gene:: OR11A1 (Varview), OR10C1 (Varview)
Functional Consequence:: synonymous_variant,genic_upstream_transcript_variant,coding_sequence_variant,intron_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000006.12:g.29440576A>G, NC_000006.11:g.29408353A>G, NT_113891.3:g.927025A>G, NT_113891.2:g.927131A>G, NT_167248.2:g.706045A>G, NT_167248.1:g.711641A>G, NT_167245.2:g.706098A>G, NT_167245.1:g.711683A>G, NT_167249.2:g.749587A>G, NT_167249.1:g.748885A>G, NT_167246.2:g.705711A>G, NT_167246.1:g.711331A>G, NT_167247.2:g.705945A>G, NT_167247.1:g.711530A>G, NT_167244.2:g.706240A>G, NT_167244.1:g.711834A>G, NM_013941.4:c.561A>G, NM_013941.3:c.561A>G

Select item 14611091228.

rs1461109122 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 6:29440816 (GRCh38)
6:29408593 (GRCh37)
Canonical SPDI:: NC_000006.12:29440815:G:A
Gene:: OR11A1 (Varview), OR10C1 (Varview)
Functional Consequence:: synonymous_variant,genic_upstream_transcript_variant,coding_sequence_variant,intron_variant
HGVS:: NC_000006.12:g.29440816G>A, NC_000006.11:g.29408593G>A, NT_113891.3:g.927265G>A, NT_113891.2:g.927371G>A, NT_167248.2:g.706285G>A, NT_167248.1:g.711881G>A, NT_167245.2:g.706338G>A, NT_167245.1:g.711923G>A, NT_167249.2:g.749827G>A, NT_167249.1:g.749125G>A, NT_167246.2:g.705951G>A, NT_167246.1:g.711571G>A, NT_167247.2:g.706185G>A, NT_167247.1:g.711770G>A, NT_167244.2:g.706480G>A, NT_167244.1:g.712074G>A, NM_013941.4:c.801G>A, NM_013941.3:c.801G>A

Select item 14600763779.

rs1460076377 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 6:29440892 (GRCh38)
6:29408669 (GRCh37)
Canonical SPDI:: NC_000006.12:29440891:A:C
Gene:: OR11A1 (Varview), OR10C1 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,coding_sequence_variant,missense_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000006.12:g.29440892A>C, NC_000006.11:g.29408669A>C, NT_113891.3:g.927341A>C, NT_113891.2:g.927447A>C, NT_167248.2:g.706361A>C, NT_167248.1:g.711957A>C, NT_167245.2:g.706414A>C, NT_167245.1:g.711999A>C, NT_167249.2:g.749903A>C, NT_167249.1:g.749201A>C, NT_167246.2:g.706027A>C, NT_167246.1:g.711647A>C, NT_167247.2:g.706261A>C, NT_167247.1:g.711846A>C, NT_167244.2:g.706556A>C, NT_167244.1:g.712150A>C, NM_013941.4:c.877A>C, NM_013941.3:c.877A>C, NP_039229.3:p.Asn293His

Select item 145646932610.

rs1456469326 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 6:29440272 (GRCh38)
6:29408049 (GRCh37)
Canonical SPDI:: NC_000006.12:29440271:C:T
Gene:: OR11A1 (Varview), OR10C1 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,coding_sequence_variant,missense_variant,intron_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000006.12:g.29440272C>T, NC_000006.11:g.29408049C>T, NT_113891.3:g.926721C>T, NT_113891.2:g.926827C>T, NT_167248.2:g.705741C>T, NT_167248.1:g.711337C>T, NT_167245.2:g.705794C>T, NT_167245.1:g.711379C>T, NT_167249.2:g.749283C>T, NT_167249.1:g.748581C>T, NT_167246.2:g.705407C>T, NT_167246.1:g.711027C>T, NT_167247.2:g.705641C>T, NT_167247.1:g.711226C>T, NT_167244.2:g.705936C>T, NT_167244.1:g.711530C>T, NM_013941.4:c.257C>T, NM_013941.3:c.257C>T, NP_039229.3:p.Thr86Ile

Select item 145596701811.

rs1455967018 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 6:29440215 (GRCh38)
6:29407992 (GRCh37)
Canonical SPDI:: NC_000006.12:29440214:C:T
Gene:: OR11A1 (Varview), OR10C1 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,coding_sequence_variant,missense_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000006.12:g.29440215C>T, NC_000006.11:g.29407992C>T, NT_113891.3:g.926664C>T, NT_113891.2:g.926770C>T, NT_167248.2:g.705684C>T, NT_167248.1:g.711280C>T, NT_167245.2:g.705737C>T, NT_167245.1:g.711322C>T, NT_167249.2:g.749226C>T, NT_167249.1:g.748524C>T, NT_167246.2:g.705350C>T, NT_167246.1:g.710970C>T, NT_167247.2:g.705584C>T, NT_167247.1:g.711169C>T, NT_167244.2:g.705879C>T, NT_167244.1:g.711473C>T, NM_013941.4:c.200C>T, NM_013941.3:c.200C>T, NP_039229.3:p.Ala67Val

Select item 145473132812.

rs1454731328 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 6:29440715 (GRCh38)
6:29408492 (GRCh37)
Canonical SPDI:: NC_000006.12:29440714:C:A,NC_000006.12:29440714:C:T
Gene:: OR11A1 (Varview), OR10C1 (Varview)
Functional Consequence:: genic_upstream_transcript_variant,coding_sequence_variant,missense_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: T=0.000028/1 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000006.12:g.29440715C>A, NC_000006.12:g.29440715C>T, NC_000006.11:g.29408492C>A, NC_000006.11:g.29408492C>T, NT_113891.3:g.927164C>A, NT_113891.3:g.927164C>T, NT_113891.2:g.927270C>A, NT_113891.2:g.927270C>T, NT_167248.2:g.706184C>A, NT_167248.2:g.706184C>T, NT_167248.1:g.711780C>A, NT_167248.1:g.711780C>T, NT_167245.2:g.706237C>A, NT_167245.2:g.706237C>T, NT_167245.1:g.711822C>A, NT_167245.1:g.711822C>T, NT_167249.2:g.749726C>A, NT_167249.2:g.749726C>T, NT_167249.1:g.749024C>A, NT_167249.1:g.749024C>T, NT_167246.2:g.705850C>A, NT_167246.2:g.705850C>T, NT_167246.1:g.711470C>A, NT_167246.1:g.711470C>T, NT_167247.2:g.706084C>A, NT_167247.2:g.706084C>T, NT_167247.1:g.711669C>A, NT_167247.1:g.711669C>T, NT_167244.2:g.706379C>A, NT_167244.2:g.706379C>T, NT_167244.1:g.711973C>A, NT_167244.1:g.711973C>T, NM_013941.4:c.700C>A, NM_013941.4:c.700C>T, NM_013941.3:c.700C>A, NM_013941.3:c.700C>T, NP_039229.3:p.Arg234Ser, NP_039229.3:p.Arg234Cys

Select item 145412775113.

rs1454127751 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 6:29440336 (GRCh38)
6:29408113 (GRCh37)
Canonical SPDI:: NC_000006.12:29440335:C:T
Gene:: OR11A1 (Varview), OR10C1 (Varview)
Functional Consequence:: intron_variant,coding_sequence_variant,synonymous_variant,genic_upstream_transcript_variant
HGVS:: NC_000006.12:g.29440336C>T, NC_000006.11:g.29408113C>T, NT_113891.3:g.926785C>T, NT_113891.2:g.926891C>T, NT_167248.2:g.705805C>T, NT_167248.1:g.711401C>T, NT_167245.2:g.705858C>T, NT_167245.1:g.711443C>T, NT_167249.2:g.749347C>T, NT_167249.1:g.748645C>T, NT_167246.2:g.705471C>T, NT_167246.1:g.711091C>T, NT_167247.2:g.705705C>T, NT_167247.1:g.711290C>T, NT_167244.2:g.706000C>T, NT_167244.1:g.711594C>T, NM_013941.4:c.321C>T, NM_013941.3:c.321C>T

Select item 145365073714.

rs1453650737 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 6:29440850 (GRCh38)
6:29408627 (GRCh37)
Canonical SPDI:: NC_000006.12:29440849:G:A
Gene:: OR11A1 (Varview), OR10C1 (Varview)
Functional Consequence:: intron_variant,coding_sequence_variant,missense_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000028/1 (ALFA)
A=0.000004/1 (GnomAD_exomes)
A=0.000007/1 (GnomAD)
A=0.000008/2 (TOPMED)
HGVS:: NC_000006.12:g.29440850G>A, NC_000006.11:g.29408627G>A, NT_113891.3:g.927299G>A, NT_113891.2:g.927405G>A, NT_167248.2:g.706319G>A, NT_167248.1:g.711915G>A, NT_167245.2:g.706372G>A, NT_167245.1:g.711957G>A, NT_167249.2:g.749861G>A, NT_167249.1:g.749159G>A, NT_167246.2:g.705985G>A, NT_167246.1:g.711605G>A, NT_167247.2:g.706219G>A, NT_167247.1:g.711804G>A, NT_167244.2:g.706514G>A, NT_167244.1:g.712108G>A, NM_013941.4:c.835G>A, NM_013941.3:c.835G>A, NP_039229.3:p.Val279Met

Select item 145280112615.

rs1452801126 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,G [Show Flanks]
Chromosome:: 6:29440909 (GRCh38)
6:29408686 (GRCh37)
Canonical SPDI:: NC_000006.12:29440908:T:A,NC_000006.12:29440908:T:G
Gene:: OR11A1 (Varview), OR10C1 (Varview)
Functional Consequence:: intron_variant,coding_sequence_variant,synonymous_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000008/2 (TOPMED)
G=0.000014/2 (GnomAD)
A=0.000684/2 (KOREAN)
HGVS:: NC_000006.12:g.29440909T>A, NC_000006.12:g.29440909T>G, NC_000006.11:g.29408686T>A, NC_000006.11:g.29408686T>G, NT_113891.3:g.927358T>A, NT_113891.3:g.927358T>G, NT_113891.2:g.927464T>A, NT_113891.2:g.927464T>G, NT_167248.2:g.706378T>A, NT_167248.2:g.706378T>G, NT_167248.1:g.711974T>A, NT_167248.1:g.711974T>G, NT_167245.2:g.706431T>A, NT_167245.2:g.706431T>G, NT_167245.1:g.712016T>A, NT_167245.1:g.712016T>G, NT_167249.2:g.749920T>A, NT_167249.2:g.749920T>G, NT_167249.1:g.749218T>A, NT_167249.1:g.749218T>G, NT_167246.2:g.706044T>A, NT_167246.2:g.706044T>G, NT_167246.1:g.711664T>A, NT_167246.1:g.711664T>G, NT_167247.2:g.706278T>A, NT_167247.2:g.706278T>G, NT_167247.1:g.711863T>A, NT_167247.1:g.711863T>G, NT_167244.2:g.706573T>A, NT_167244.2:g.706573T>G, NT_167244.1:g.712167T>A, NT_167244.1:g.712167T>G, NM_013941.4:c.894T>A, NM_013941.4:c.894T>G, NM_013941.3:c.894T>A, NM_013941.3:c.894T>G

Select item 145251966916.

rs1452519669 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 6:29440641 (GRCh38)
6:29408418 (GRCh37)
Canonical SPDI:: NC_000006.12:29440640:C:G
Gene:: OR11A1 (Varview), OR10C1 (Varview)
Functional Consequence:: intron_variant,coding_sequence_variant,missense_variant,genic_upstream_transcript_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_000006.12:g.29440641C>G, NC_000006.11:g.29408418C>G, NT_113891.3:g.927090C>G, NT_113891.2:g.927196C>G, NT_167248.2:g.706110C>G, NT_167248.1:g.711706C>G, NT_167245.2:g.706163C>G, NT_167245.1:g.711748C>G, NT_167249.2:g.749652C>G, NT_167249.1:g.748950C>G, NT_167246.2:g.705776C>G, NT_167246.1:g.711396C>G, NT_167247.2:g.706010C>G, NT_167247.1:g.711595C>G, NT_167244.2:g.706305C>G, NT_167244.1:g.711899C>G, NM_013941.4:c.626C>G, NM_013941.3:c.626C>G, NP_039229.3:p.Pro209Arg

Select item 144231376417.

rs1442313764 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 6:29440180 (GRCh38)
6:29407957 (GRCh37)
Canonical SPDI:: NC_000006.12:29440179:G:A
Gene:: OR11A1 (Varview), OR10C1 (Varview)
Functional Consequence:: intron_variant,coding_sequence_variant,synonymous_variant,genic_upstream_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
A=0.000004/1 (TOPMED)
HGVS:: NC_000006.12:g.29440180G>A, NC_000006.11:g.29407957G>A, NT_113891.3:g.926629G>A, NT_113891.2:g.926735G>A, NT_167248.2:g.705649G>A, NT_167248.1:g.711245G>A, NT_167245.2:g.705702G>A, NT_167245.1:g.711287G>A, NT_167249.2:g.749191G>A, NT_167249.1:g.748489G>A, NT_167246.2:g.705315G>A, NT_167246.1:g.710935G>A, NT_167247.2:g.705549G>A, NT_167247.1:g.711134G>A, NT_167244.2:g.705844G>A, NT_167244.1:g.711438G>A, NM_013941.4:c.165G>A, NM_013941.3:c.165G>A

Select item 144150001918.

rs1441500019 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 6:29440300 (GRCh38)
6:29408077 (GRCh37)
Canonical SPDI:: NC_000006.12:29440299:A:G
Gene:: OR11A1 (Varview), OR10C1 (Varview)
Functional Consequence:: coding_sequence_variant,intron_variant,genic_upstream_transcript_variant,synonymous_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_000006.12:g.29440300A>G, NC_000006.11:g.29408077A>G, NT_113891.3:g.926749A>G, NT_113891.2:g.926855A>G, NT_167248.2:g.705769A>G, NT_167248.1:g.711365A>G, NT_167245.2:g.705822A>G, NT_167245.1:g.711407A>G, NT_167249.2:g.749311A>G, NT_167249.1:g.748609A>G, NT_167246.2:g.705435A>G, NT_167246.1:g.711055A>G, NT_167247.2:g.705669A>G, NT_167247.1:g.711254A>G, NT_167244.2:g.705964A>G, NT_167244.1:g.711558A>G, NM_013941.4:c.285A>G, NM_013941.3:c.285A>G

Select item 143571204019.

rs1435712040 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 6:29440225 (GRCh38)
6:29408002 (GRCh37)
Canonical SPDI:: NC_000006.12:29440224:T:C
Gene:: OR11A1 (Varview), OR10C1 (Varview)
Functional Consequence:: coding_sequence_variant,intron_variant,genic_upstream_transcript_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.29440225T>C, NC_000006.11:g.29408002T>C, NT_113891.3:g.926674T>C, NT_113891.2:g.926780T>C, NT_167248.2:g.705694T>C, NT_167248.1:g.711290T>C, NT_167245.2:g.705747T>C, NT_167245.1:g.711332T>C, NT_167249.2:g.749236T>C, NT_167249.1:g.748534T>C, NT_167246.2:g.705360T>C, NT_167246.1:g.710980T>C, NT_167247.2:g.705594T>C, NT_167247.1:g.711179T>C, NT_167244.2:g.705889T>C, NT_167244.1:g.711483T>C, NM_013941.4:c.210T>C, NM_013941.3:c.210T>C

Select item 143111110620.

rs1431111106 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 6:29440141 (GRCh38)
6:29407918 (GRCh37)
Canonical SPDI:: NC_000006.12:29440140:C:T
Gene:: OR11A1 (Varview), OR10C1 (Varview)
Functional Consequence:: coding_sequence_variant,intron_variant,genic_upstream_transcript_variant,synonymous_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=0.000019/5 (TOPMED)
HGVS:: NC_000006.12:g.29440141C>T, NC_000006.11:g.29407918C>T, NT_113891.3:g.926590C>T, NT_113891.2:g.926696C>T, NT_167248.2:g.705610C>T, NT_167248.1:g.711206C>T, NT_167245.2:g.705663C>T, NT_167245.1:g.711248C>T, NT_167249.2:g.749152C>T, NT_167249.1:g.748450C>T, NT_167246.2:g.705276C>T, NT_167246.1:g.710896C>T, NT_167247.2:g.705510C>T, NT_167247.1:g.711095C>T, NT_167244.2:g.705805C>T, NT_167244.1:g.711399C>T, NM_013941.4:c.126C>T, NM_013941.3:c.126C>T

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