SNP Links for Protein (Select 52317255) - SNP

Warning: The NCBI web site requires JavaScript to function. more...

Links from Protein

Items: 1 to 20 of 356

<< First< Prev

Page of 18

Next >Last >>

Select item 14907115251.

rs1490711525 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 14:20034662 (GRCh38)
14:20502821 (GRCh37)
Canonical SPDI:: NC_000014.9:20034661:C:T
Gene:: OR4K13 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000014.9:g.20034662C>T, NW_025791796.1:g.237343C>T, NC_000014.8:g.20502821C>T, NM_001004714.2:c.97G>A, NM_001004714.1:c.97G>A, NM_001386029.1:c.97G>A, NP_001004714.1:p.Val33Met, NP_001372958.1:p.Val33Met

Select item 14900627332.

rs1490062733 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 14:20034691 (GRCh38)
14:20502850 (GRCh37)
Canonical SPDI:: NC_000014.9:20034690:A:T
Gene:: OR4K13 (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_000014.9:g.20034691A>T, NW_025791796.1:g.237372A>T, NC_000014.8:g.20502850A>T, NM_001004714.2:c.68T>A, NM_001004714.1:c.68T>A, NM_001386029.1:c.68T>A, NP_001004714.1:p.Leu23His, NP_001372958.1:p.Leu23His

Select item 14898956303.

rs1489895630 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 14:20034231 (GRCh38)
14:20502390 (GRCh37)
Canonical SPDI:: NC_000014.9:20034230:G:A
Gene:: OR4K13 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000014.9:g.20034231G>A, NW_025791796.1:g.236912G>A, NC_000014.8:g.20502390G>A, NM_001004714.2:c.528C>T, NM_001004714.1:c.528C>T, NM_001386029.1:c.528C>T

Select item 14880769844.

rs1488076984 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 14:20033908 (GRCh38)
14:20502067 (GRCh37)
Canonical SPDI:: NC_000014.9:20033907:G:C
Gene:: OR4K13 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000014.9:g.20033908G>C, NW_025791796.1:g.236589G>C, NC_000014.8:g.20502067G>C, NM_001004714.2:c.851C>G, NM_001004714.1:c.851C>G, NM_001386029.1:c.851C>G, NP_001004714.1:p.Pro284Arg, NP_001372958.1:p.Pro284Arg

Select item 14795216595.

rs1479521659 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 14:20034416 (GRCh38)
14:20502575 (GRCh37)
Canonical SPDI:: NC_000014.9:20034415:G:T
Gene:: OR4K13 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000014.9:g.20034416G>T, NW_025791796.1:g.237097G>T, NC_000014.8:g.20502575G>T, NM_001004714.2:c.343C>A, NM_001004714.1:c.343C>A, NM_001386029.1:c.343C>A, NP_001004714.1:p.Leu115Ile, NP_001372958.1:p.Leu115Ile

Select item 14794662566.

rs1479466256 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 14:20034675 (GRCh38)
14:20502834 (GRCh37)
Canonical SPDI:: NC_000014.9:20034674:G:A,NC_000014.9:20034674:G:T
Gene:: OR4K13 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.00014/3 (ALFA)
A=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000014.9:g.20034675G>A, NC_000014.9:g.20034675G>T, NW_025791796.1:g.237356G>A, NW_025791796.1:g.237356G>T, NC_000014.8:g.20502834G>A, NC_000014.8:g.20502834G>T, NM_001004714.2:c.84C>T, NM_001004714.2:c.84C>A, NM_001004714.1:c.84C>T, NM_001004714.1:c.84C>A, NM_001386029.1:c.84C>T, NM_001386029.1:c.84C>A, NP_001004714.1:p.Phe28Leu, NP_001372958.1:p.Phe28Leu

Select item 14790489957.

rs1479048995 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 14:20034701 (GRCh38)
14:20502860 (GRCh37)
Canonical SPDI:: NC_000014.9:20034700:A:G
Gene:: OR4K13 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000014.9:g.20034701A>G, NW_025791796.1:g.237382A>G, NC_000014.8:g.20502860A>G, NM_001004714.2:c.58T>C, NM_001004714.1:c.58T>C, NM_001386029.1:c.58T>C, NP_001004714.1:p.Ser20Pro, NP_001372958.1:p.Ser20Pro

Select item 14775589408.

rs1477558940 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 14:20033853 (GRCh38)
14:20502012 (GRCh37)
Canonical SPDI:: NC_000014.9:20033852:G:A
Gene:: OR4K13 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: A=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000014.9:g.20033853G>A, NW_025791796.1:g.236534G>A, NC_000014.8:g.20502012G>A, NM_001004714.2:c.906C>T, NM_001004714.1:c.906C>T, NM_001386029.1:c.906C>T

Select item 14753388009.

rs1475338800 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 14:20034225 (GRCh38)
14:20502384 (GRCh37)
Canonical SPDI:: NC_000014.9:20034224:G:A
Gene:: OR4K13 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000014.9:g.20034225G>A, NW_025791796.1:g.236906G>A, NC_000014.8:g.20502384G>A, NM_001004714.2:c.534C>T, NM_001004714.1:c.534C>T, NM_001386029.1:c.534C>T

Select item 147500341910.

rs1475003419 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 14:20034421 (GRCh38)
14:20502580 (GRCh37)
Canonical SPDI:: NC_000014.9:20034420:A:G
Gene:: OR4K13 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000031/1 (ALFA)
G=0.000004/1 (GnomAD_exomes)
G=0.000008/2 (TOPMED)
HGVS:: NC_000014.9:g.20034421A>G, NW_025791796.1:g.237102A>G, NC_000014.8:g.20502580A>G, NM_001004714.2:c.338T>C, NM_001004714.1:c.338T>C, NM_001386029.1:c.338T>C, NP_001004714.1:p.Met113Thr, NP_001372958.1:p.Met113Thr

Select item 147305028311.

rs1473050283 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 14:20033863 (GRCh38)
14:20502022 (GRCh37)
Canonical SPDI:: NC_000014.9:20033862:T:C,NC_000014.9:20033862:T:G
Gene:: OR4K13 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (GnomAD_exomes)
G=0.000004/1 (TOPMED)
HGVS:: NC_000014.9:g.20033863T>C, NC_000014.9:g.20033863T>G, NW_025791796.1:g.236544T>C, NW_025791796.1:g.236544T>G, NC_000014.8:g.20502022T>C, NC_000014.8:g.20502022T>G, NM_001004714.2:c.896A>G, NM_001004714.2:c.896A>C, NM_001004714.1:c.896A>G, NM_001004714.1:c.896A>C, NM_001386029.1:c.896A>G, NM_001386029.1:c.896A>C, NP_001004714.1:p.Lys299Arg, NP_001004714.1:p.Lys299Thr, NP_001372958.1:p.Lys299Arg, NP_001372958.1:p.Lys299Thr

Select item 147304058812.

rs1473040588 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 14:20034480 (GRCh38)
14:20502639 (GRCh37)
Canonical SPDI:: NC_000014.9:20034479:T:C
Gene:: OR4K13 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000011/3 (TOPMED)
C=0.000016/4 (GnomAD_exomes)
HGVS:: NC_000014.9:g.20034480T>C, NW_025791796.1:g.237161T>C, NC_000014.8:g.20502639T>C, NM_001004714.2:c.279A>G, NM_001004714.1:c.279A>G, NM_001386029.1:c.279A>G

Select item 147289691013.

rs1472896910 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 14:20033964 (GRCh38)
14:20502123 (GRCh37)
Canonical SPDI:: NC_000014.9:20033963:G:A
Gene:: OR4K13 (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_000014.9:g.20033964G>A, NW_025791796.1:g.236645G>A, NC_000014.8:g.20502123G>A, NM_001004714.2:c.795C>T, NM_001004714.1:c.795C>T, NM_001386029.1:c.795C>T

Select item 146756325414.

rs1467563254 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 14:20034630 (GRCh38)
14:20502789 (GRCh37)
Canonical SPDI:: NC_000014.9:20034629:C:A
Gene:: OR4K13 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
HGVS:: NC_000014.9:g.20034630C>A, NW_025791796.1:g.237311C>A, NC_000014.8:g.20502789C>A, NM_001004714.2:c.129G>T, NM_001004714.1:c.129G>T, NM_001386029.1:c.129G>T

Select item 146744573115.

rs1467445731 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 14:20033960 (GRCh38)
14:20502119 (GRCh37)
Canonical SPDI:: NC_000014.9:20033959:C:T
Gene:: OR4K13 (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)
HGVS:: NC_000014.9:g.20033960C>T, NW_025791796.1:g.236641C>T, NC_000014.8:g.20502119C>T, NM_001004714.2:c.799G>A, NM_001004714.1:c.799G>A, NM_001386029.1:c.799G>A, NP_001004714.1:p.Val267Ile, NP_001372958.1:p.Val267Ile

Select item 146516499416.

rs1465164994 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 14:20033995 (GRCh38)
14:20502154 (GRCh37)
Canonical SPDI:: NC_000014.9:20033994:A:G
Gene:: OR4K13 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: G=0.0001/1 (ALFA)
HGVS:: NC_000014.9:g.20033995A>G, NW_025791796.1:g.236676A>G, NC_000014.8:g.20502154A>G, NM_001004714.2:c.764T>C, NM_001004714.1:c.764T>C, NM_001386029.1:c.764T>C, NP_001004714.1:p.Val255Ala, NP_001372958.1:p.Val255Ala

Select item 146496990917.

rs1464969909 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 14:20034385 (GRCh38)
14:20502544 (GRCh37)
Canonical SPDI:: NC_000014.9:20034384:G:A
Gene:: OR4K13 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000043/1 (ALFA)
A=0.000004/1 (GnomAD_exomes)
A=0.000004/1 (TOPMED)
A=0.000021/3 (GnomAD)
HGVS:: NC_000014.9:g.20034385G>A, NW_025791796.1:g.237066G>A, NC_000014.8:g.20502544G>A, NM_001004714.2:c.374C>T, NM_001004714.1:c.374C>T, NM_001386029.1:c.374C>T, NP_001004714.1:p.Ala125Val, NP_001372958.1:p.Ala125Val

Select item 146077088818.

rs1460770888 [Homo sapiens]

Variant type:: SNV
Alleles:: A>T [Show Flanks]
Chromosome:: 14:20034718 (GRCh38)
14:20502877 (GRCh37)
Canonical SPDI:: NC_000014.9:20034717:A:T
Gene:: OR4K13 (Varview)
Functional Consequence:: stop_gained,coding_sequence_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000014.9:g.20034718A>T, NW_025791796.1:g.237399A>T, NC_000014.8:g.20502877A>T, NM_001004714.2:c.41T>A, NM_001004714.1:c.41T>A, NM_001386029.1:c.41T>A, NP_001004714.1:p.Leu14Ter, NP_001372958.1:p.Leu14Ter

Select item 145842012419.

rs1458420124 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 14:20033935 (GRCh38)
14:20502094 (GRCh37)
Canonical SPDI:: NC_000014.9:20033934:T:C
Gene:: OR4K13 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
HGVS:: NC_000014.9:g.20033935T>C, NW_025791796.1:g.236616T>C, NC_000014.8:g.20502094T>C, NM_001004714.2:c.824A>G, NM_001004714.1:c.824A>G, NM_001386029.1:c.824A>G, NP_001004714.1:p.Tyr275Cys, NP_001372958.1:p.Tyr275Cys

Select item 145729804920.

rs1457298049 [Homo sapiens]

Variant type:: DELINS
Alleles:: AACAAAATAAATTCCGATAC>- [Show Flanks]
Chromosome:: 14:20034715 (GRCh38)
14:20502874 (GRCh37)
Canonical SPDI:: NC_000014.9:20034713:CAACAAAATAAATTCCGATAC:C
Gene:: OR4K13 (Varview)
Functional Consequence:: frameshift_variant,coding_sequence_variant
Validated:: by frequency,by cluster
MAF:: -=0.000007/1 (GnomAD)
HGVS:: NC_000014.9:g.20034715_20034734del, NW_025791796.1:g.237396_237415del, NC_000014.8:g.20502874_20502893del, NM_001004714.2:c.26_45del, NM_001004714.1:c.26_45del, NM_001386029.1:c.26_45del, NP_001004714.1:p.Val9fs, NP_001372958.1:p.Val9fs

<< First< Prev

Page of 18

Next >Last >>

Supplemental Content

Filters: Manage Filters

Find related data

Recent activity

Clear Turn Off Turn On

SNP Links for Protein (Select 52317255) (356)
SNP

Your browsing activity is empty.

Activity recording is turned off.

Turn recording back on

dbSNP

Result Filters

Validation Status

Function Class

Variation Class

Annotation

Global MAF

Custom range

Additional filters

Display Settings:

Send to: