SNP Links for Protein (Select 7330337) - SNP

Links from Protein

Items: 1 to 20 of 385

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Select item 14899148351.

rs1489914835 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 19:15728507 (GRCh38)
19:15839317 (GRCh37)
Canonical SPDI:: NC_000019.10:15728506:T:A
Gene:: OR10H2 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000224/1 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000019.10:g.15728507T>A, NC_000019.9:g.15839317T>A, NM_013939.2:c.464T>A, NP_039227.1:p.Met155Lys

Select item 14895929172.

rs1489592917 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 19:15728199 (GRCh38)
19:15839009 (GRCh37)
Canonical SPDI:: NC_000019.10:15728198:G:A
Gene:: OR10H2 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000019.10:g.15728199G>A, NC_000019.9:g.15839009G>A, NM_013939.2:c.156G>A

Select item 14895421673.

rs1489542167 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 19:15728739 (GRCh38)
19:15839549 (GRCh37)
Canonical SPDI:: NC_000019.10:15728738:T:C
Gene:: OR10H2 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: C=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000019.10:g.15728739T>C, NC_000019.9:g.15839549T>C, NM_013939.2:c.696T>C

Select item 14838685904.

rs1483868590 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 19:15728608 (GRCh38)
19:15839418 (GRCh37)
Canonical SPDI:: NC_000019.10:15728607:T:G
Gene:: OR10H2 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
HGVS:: NC_000019.10:g.15728608T>G, NC_000019.9:g.15839418T>G, NM_013939.2:c.565T>G, NP_039227.1:p.Cys189Gly

Select item 14822992995.

rs1482299299 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 19:15728190 (GRCh38)
19:15839000 (GRCh37)
Canonical SPDI:: NC_000019.10:15728189:C:T
Gene:: OR10H2 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_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_000019.10:g.15728190C>T, NC_000019.9:g.15839000C>T, NM_013939.2:c.147C>T

Select item 14821293486.

rs1482129348 [Homo sapiens]

Variant type:: DEL
Alleles:: CGCCCT>- [Show Flanks]
Chromosome:: 19:15728891 (GRCh38)
19:15839701 (GRCh37)
Canonical SPDI:: NC_000019.10:15728890:CGCCCT:
Gene:: OR10H2 (Varview)
Functional Consequence:: inframe_indel,coding_sequence_variant
HGVS:: NC_000019.10:g.15728891_15728896del, NC_000019.9:g.15839701_15839706del, NM_013939.2:c.848_853del, NP_039227.1:p.Thr283_Phe285delinsIle

Select item 14805119307.

rs1480511930 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,T [Show Flanks]
Chromosome:: 19:15728375 (GRCh38)
19:15839185 (GRCh37)
Canonical SPDI:: NC_000019.10:15728374:A:C,NC_000019.10:15728374:A:T
Gene:: OR10H2 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000014/2 (GnomAD)
C=0.001638/3 (Korea1K)
HGVS:: NC_000019.10:g.15728375A>C, NC_000019.10:g.15728375A>T, NC_000019.9:g.15839185A>C, NC_000019.9:g.15839185A>T, NM_013939.2:c.332A>C, NM_013939.2:c.332A>T, NP_039227.1:p.His111Pro, NP_039227.1:p.His111Leu

Select item 14793225538.

rs1479322553 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 19:15728829 (GRCh38)
19:15839639 (GRCh37)
Canonical SPDI:: NC_000019.10:15728828:G:A,NC_000019.10:15728828:G:T
Gene:: OR10H2 (Varview)
Functional Consequence:: synonymous_variant,missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000028/1 (ALFA)
A=0.000014/2 (GnomAD)
HGVS:: NC_000019.10:g.15728829G>A, NC_000019.10:g.15728829G>T, NC_000019.9:g.15839639G>A, NC_000019.9:g.15839639G>T, NM_013939.2:c.786G>A, NM_013939.2:c.786G>T, NP_039227.1:p.Lys262Asn

Select item 14773849289.

rs1477384928 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,G,T [Show Flanks]
Chromosome:: 19:15728430 (GRCh38)
19:15839240 (GRCh37)
Canonical SPDI:: NC_000019.10:15728429:C:A,NC_000019.10:15728429:C:G,NC_000019.10:15728429:C:T
Gene:: OR10H2 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
A=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000019.10:g.15728430C>A, NC_000019.10:g.15728430C>G, NC_000019.10:g.15728430C>T, NC_000019.9:g.15839240C>A, NC_000019.9:g.15839240C>G, NC_000019.9:g.15839240C>T, NM_013939.2:c.387C>A, NM_013939.2:c.387C>G, NM_013939.2:c.387C>T

Select item 147632663310.

rs1476326633 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 19:15728054 (GRCh38)
19:15838864 (GRCh37)
Canonical SPDI:: NC_000019.10:15728053:T:C
Gene:: OR10H2 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
HGVS:: NC_000019.10:g.15728054T>C, NC_000019.9:g.15838864T>C, NM_013939.2:c.11T>C, NP_039227.1:p.Leu4Pro

Select item 147232050911.

rs1472320509 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 19:15728198 (GRCh38)
19:15839008 (GRCh37)
Canonical SPDI:: NC_000019.10:15728197:A:C
Gene:: OR10H2 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
HGVS:: NC_000019.10:g.15728198A>C, NC_000019.9:g.15839008A>C, NM_013939.2:c.155A>C, NP_039227.1:p.Glu52Ala

Select item 147097101412.

rs1470971014 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 19:15728076 (GRCh38)
19:15838886 (GRCh37)
Canonical SPDI:: NC_000019.10:15728075:A:G
Gene:: OR10H2 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000019.10:g.15728076A>G, NC_000019.9:g.15838886A>G, NM_013939.2:c.33A>G

Select item 146720113013.

rs1467201130 [Homo sapiens]

Variant type:: DELINS
Alleles:: ACCGTCTGGAGCGAGCGCAGCC>- [Show Flanks]
Chromosome:: 19:15728185 (GRCh38)
19:15838995 (GRCh37)
Canonical SPDI:: NC_000019.10:15728181:GCCACCGTCTGGAGCGAGCGCAGCC:GCC
Gene:: OR10H2 (Varview)
Functional Consequence:: frameshift_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: GCC=0./0 (ALFA)
HGVS:: NC_000019.10:g.15728185_15728206del, NC_000019.9:g.15838995_15839016del, NM_013939.2:c.142_163del, NP_039227.1:p.Thr48fs

Select item 146445844314.

rs1464458443 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 19:15728298 (GRCh38)
19:15839108 (GRCh37)
Canonical SPDI:: NC_000019.10:15728297:G:A
Gene:: OR10H2 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: A=0.000012/3 (GnomAD_exomes)
HGVS:: NC_000019.10:g.15728298G>A, NC_000019.9:g.15839108G>A, NM_013939.2:c.255G>A

Select item 146313400915.

rs1463134009 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 19:15728543 (GRCh38)
19:15839353 (GRCh37)
Canonical SPDI:: NC_000019.10:15728542:C:G
Gene:: OR10H2 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000008/2 (GnomAD_exomes)
G=0.000008/2 (TOPMED)
HGVS:: NC_000019.10:g.15728543C>G, NC_000019.9:g.15839353C>G, NM_013939.2:c.500C>G, NP_039227.1:p.Thr167Ser

Select item 146243653916.

rs1462436539 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 19:15728139 (GRCh38)
19:15838949 (GRCh37)
Canonical SPDI:: NC_000019.10:15728138:G:A
Gene:: OR10H2 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_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_000019.10:g.15728139G>A, NC_000019.9:g.15838949G>A, NM_013939.2:c.96G>A

Select item 146223580217.

rs1462235802 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 19:15728051 (GRCh38)
19:15838861 (GRCh37)
Canonical SPDI:: NC_000019.10:15728050:G:C
Gene:: OR10H2 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000019.10:g.15728051G>C, NC_000019.9:g.15838861G>C, NM_013939.2:c.8G>C, NP_039227.1:p.Gly3Ala

Select item 145982367218.

rs1459823672 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 19:15728281 (GRCh38)
19:15839091 (GRCh37)
Canonical SPDI:: NC_000019.10:15728280:C:T
Gene:: OR10H2 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: T=0.000028/1 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000019.10:g.15728281C>T, NC_000019.9:g.15839091C>T, NM_013939.2:c.238C>T, NP_039227.1:p.Arg80Cys

Select item 145834107119.

rs1458341071 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 19:15728850 (GRCh38)
19:15839660 (GRCh37)
Canonical SPDI:: NC_000019.10:15728849:G:A
Gene:: OR10H2 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_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_000019.10:g.15728850G>A, NC_000019.9:g.15839660G>A, NM_013939.2:c.807G>A

Select item 145340385220.

rs1453403852 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 19:15728725 (GRCh38)
19:15839535 (GRCh37)
Canonical SPDI:: NC_000019.10:15728724:A:C
Gene:: OR10H2 (Varview)
Functional Consequence:: coding_sequence_variant,missense_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_000019.10:g.15728725A>C, NC_000019.9:g.15839535A>C, NM_013939.2:c.682A>C, NP_039227.1:p.Lys228Gln

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