SNP Links for Protein (Select 153791202) - SNP

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Links from Protein

Items: 1 to 20 of 305

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Select item 14893380461.

rs1489338046 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 17:3398369 (GRCh38)
17:3301663 (GRCh37)
Canonical SPDI:: NC_000017.11:3398368:G:A
Gene:: OR1E1 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_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_000017.11:g.3398369G>A, NC_000017.10:g.3301663G>A, NM_003553.3:c.42C>T, NM_003553.2:c.42C>T

Select item 14857667682.

rs1485766768 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 17:3398399 (GRCh38)
17:3301693 (GRCh37)
Canonical SPDI:: NC_000017.11:3398398:T:C
Gene:: OR1E1 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000017.11:g.3398399T>C, NC_000017.10:g.3301693T>C, NM_003553.3:c.12A>G, NM_003553.2:c.12A>G

Select item 14788710343.

rs1478871034 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 17:3397553 (GRCh38)
17:3300847 (GRCh37)
Canonical SPDI:: NC_000017.11:3397552:G:T
Gene:: OR1E1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000017.11:g.3397553G>T, NC_000017.10:g.3300847G>T, NM_003553.3:c.858C>A, NM_003553.2:c.858C>A, NP_003544.2:p.Asn286Lys

Select item 14784875224.

rs1478487522 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 17:3397529 (GRCh38)
17:3300823 (GRCh37)
Canonical SPDI:: NC_000017.11:3397528:G:C
Gene:: OR1E1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000017.11:g.3397529G>C, NC_000017.10:g.3300823G>C, NM_003553.3:c.882C>G, NM_003553.2:c.882C>G, NP_003544.2:p.Asn294Lys

Select item 14772359165.

rs1477235916 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 17:3397971 (GRCh38)
17:3301265 (GRCh37)
Canonical SPDI:: NC_000017.11:3397970:A:G
Gene:: OR1E1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000017.11:g.3397971A>G, NC_000017.10:g.3301265A>G, NM_003553.3:c.440T>C, NM_003553.2:c.440T>C, NP_003544.2:p.Leu147Pro

Select item 14724952616.

rs1472495261 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 17:3397507 (GRCh38)
17:3300801 (GRCh37)
Canonical SPDI:: NC_000017.11:3397506:T:C
Gene:: OR1E1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
HGVS:: NC_000017.11:g.3397507T>C, NC_000017.10:g.3300801T>C, NM_003553.3:c.904A>G, NM_003553.2:c.904A>G, NP_003544.2:p.Ser302Gly

Select item 14706019047.

rs1470601904 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 17:3398060 (GRCh38)
17:3301354 (GRCh37)
Canonical SPDI:: NC_000017.11:3398059:G:T
Gene:: OR1E1 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000011/3 (TOPMED)
T=0.000014/2 (GnomAD)
HGVS:: NC_000017.11:g.3398060G>T, NC_000017.10:g.3301354G>T, NM_003553.3:c.351C>A, NM_003553.2:c.351C>A

Select item 14682929618.

rs1468292961 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 17:3398184 (GRCh38)
17:3301478 (GRCh37)
Canonical SPDI:: NC_000017.11:3398183:A:C
Gene:: OR1E1 (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=0.000007/1 (GnomAD)
HGVS:: NC_000017.11:g.3398184A>C, NC_000017.10:g.3301478A>C, NM_003553.3:c.227T>G, NM_003553.2:c.227T>G, NP_003544.2:p.Val76Gly

Select item 14675190739.

rs1467519073 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 17:3398174 (GRCh38)
17:3301468 (GRCh37)
Canonical SPDI:: NC_000017.11:3398173:G:A
Gene:: OR1E1 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: A=0.000111/1 (ALFA)
A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000017.11:g.3398174G>A, NC_000017.10:g.3301468G>A, NM_003553.3:c.237C>T, NM_003553.2:c.237C>T

Select item 146245191010.

rs1462451910 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 17:3397502 (GRCh38)
17:3300796 (GRCh37)
Canonical SPDI:: NC_000017.11:3397501:T:C
Gene:: OR1E1 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000008/2 (TOPMED)
HGVS:: NC_000017.11:g.3397502T>C, NC_000017.10:g.3300796T>C, NM_003553.3:c.909A>G, NM_003553.2:c.909A>G

Select item 145889373111.

rs1458893731 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 17:3397943 (GRCh38)
17:3301237 (GRCh37)
Canonical SPDI:: NC_000017.11:3397942:G:C
Gene:: OR1E1 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000011/3 (TOPMED)
C=0.000012/3 (GnomAD_exomes)
HGVS:: NC_000017.11:g.3397943G>C, NC_000017.10:g.3301237G>C, NM_003553.3:c.468C>G, NM_003553.2:c.468C>G

Select item 145668699812.

rs1456686998 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 17:3398192 (GRCh38)
17:3301486 (GRCh37)
Canonical SPDI:: NC_000017.11:3398191:G:A
Gene:: OR1E1 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
HGVS:: NC_000017.11:g.3398192G>A, NC_000017.10:g.3301486G>A, NM_003553.3:c.219C>T, NM_003553.2:c.219C>T

Select item 145551490913.

rs1455514909 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 17:3398154 (GRCh38)
17:3301448 (GRCh37)
Canonical SPDI:: NC_000017.11:3398153:T:G
Gene:: OR1E1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000017.11:g.3398154T>G, NC_000017.10:g.3301448T>G, NM_003553.3:c.257A>C, NM_003553.2:c.257A>C, NP_003544.2:p.Gln86Pro

Select item 144823435014.

rs1448234350 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 17:3398347 (GRCh38)
17:3301641 (GRCh37)
Canonical SPDI:: NC_000017.11:3398346:C:G
Gene:: OR1E1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000017.11:g.3398347C>G, NC_000017.10:g.3301641C>G, NM_003553.3:c.64G>C, NM_003553.2:c.64G>C, NP_003544.2:p.Glu22Gln

Select item 144433937615.

rs1444339376 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 17:3398180 (GRCh38)
17:3301474 (GRCh37)
Canonical SPDI:: NC_000017.11:3398179:G:T
Gene:: OR1E1 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
HGVS:: NC_000017.11:g.3398180G>T, NC_000017.10:g.3301474G>T, NM_003553.3:c.231C>A, NM_003553.2:c.231C>A

Select item 144374577816.

rs1443745778 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 17:3397897 (GRCh38)
17:3301191 (GRCh37)
Canonical SPDI:: NC_000017.11:3397896:T:C
Gene:: OR1E1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000017.11:g.3397897T>C, NC_000017.10:g.3301191T>C, NM_003553.3:c.514A>G, NM_003553.2:c.514A>G, NP_003544.2:p.Asn172Asp

Select item 144178335217.

rs1441783352 [Homo sapiens]

Variant type:: DELINS
Alleles:: ACTA>- [Show Flanks]
Chromosome:: 17:3397613 (GRCh38)
17:3300907 (GRCh37)
Canonical SPDI:: NC_000017.11:3397611:AACTA:A
Gene:: OR1E1 (Varview)
Functional Consequence:: coding_sequence_variant,frameshift_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
-=0.000004/1 (TOPMED)
HGVS:: NC_000017.11:g.3397613_3397616del, NC_000017.10:g.3300907_3300910del, NM_003553.3:c.796_799del, NM_003553.2:c.796_799del, NP_003544.2:p.Ser266fs

Select item 143612546818.

rs1436125468 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 17:3397787 (GRCh38)
17:3301081 (GRCh37)
Canonical SPDI:: NC_000017.11:3397786:G:A
Gene:: OR1E1 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000008/2 (TOPMED)
HGVS:: NC_000017.11:g.3397787G>A, NC_000017.10:g.3301081G>A, NM_003553.3:c.624C>T, NM_003553.2:c.624C>T

Select item 143284003519.

rs1432840035 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 17:3398256 (GRCh38)
17:3301550 (GRCh37)
Canonical SPDI:: NC_000017.11:3398255:T:C
Gene:: OR1E1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_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_000017.11:g.3398256T>C, NC_000017.10:g.3301550T>C, NM_003553.3:c.155A>G, NM_003553.2:c.155A>G, NP_003544.2:p.Asp52Gly

Select item 143259599620.

rs1432595996 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 17:3398165 (GRCh38)
17:3301459 (GRCh37)
Canonical SPDI:: NC_000017.11:3398164:T:C
Gene:: OR1E1 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000017.11:g.3398165T>C, NC_000017.10:g.3301459T>C, NM_003553.3:c.246A>G, NM_003553.2:c.246A>G

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