SNP Links for Nucleotide (Select 116875818) - SNP

Links from Nucleotide

Items: 1 to 20 of 333

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Select item 14891600391.

rs1489160039 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 7:143183610 (GRCh38)
7:142880703 (GRCh37)
Canonical SPDI:: NC_000007.14:143183609:T:A
Gene:: TAS2R39 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000007.14:g.143183610T>A, NC_000007.13:g.142880703T>A, NM_176881.2:c.192T>A

Select item 14868308582.

rs1486830858 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 7:143183781 (GRCh38)
7:142880874 (GRCh37)
Canonical SPDI:: NC_000007.14:143183780:T:C,NC_000007.14:143183780:T:G
Gene:: TAS2R39 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
G=0./0 (Korea1K)
C=0.000008/2 (TOPMED)
HGVS:: NC_000007.14:g.143183781T>C, NC_000007.14:g.143183781T>G, NC_000007.13:g.142880874T>C, NC_000007.13:g.142880874T>G, NM_176881.2:c.363T>C, NM_176881.2:c.363T>G, NP_795362.2:p.Asn121Lys

Select item 14835830103.

rs1483583010 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 7:143184366 (GRCh38)
7:142881459 (GRCh37)
Canonical SPDI:: NC_000007.14:143184365:T:C
Gene:: TAS2R39 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
HGVS:: NC_000007.14:g.143184366T>C, NC_000007.13:g.142881459T>C, NM_176881.2:c.948T>C

Select item 14809026994.

rs1480902699 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 7:143183437 (GRCh38)
7:142880530 (GRCh37)
Canonical SPDI:: NC_000007.14:143183436:C:A
Gene:: TAS2R39 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by cluster
MAF:: A=0.000007/1 (GnomAD)
HGVS:: NC_000007.14:g.143183437C>A, NC_000007.13:g.142880530C>A, NM_176881.2:c.19C>A, NP_795362.2:p.Pro7Thr

Select item 14807087305.

rs1480708730 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 7:143184132 (GRCh38)
7:142881225 (GRCh37)
Canonical SPDI:: NC_000007.14:143184131:C:T
Gene:: TAS2R39 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000008/2 (TOPMED)
HGVS:: NC_000007.14:g.143184132C>T, NC_000007.13:g.142881225C>T, NM_176881.2:c.714C>T

Select item 14801742696.

rs1480174269 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 7:143183721 (GRCh38)
7:142880814 (GRCh37)
Canonical SPDI:: NC_000007.14:143183720:A:G
Gene:: TAS2R39 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000007.14:g.143183721A>G, NC_000007.13:g.142880814A>G, NM_176881.2:c.303A>G

Select item 14792746067.

rs1479274606 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 7:143183620 (GRCh38)
7:142880713 (GRCh37)
Canonical SPDI:: NC_000007.14:143183619:G:A
Gene:: TAS2R39 (Varview)
Functional Consequence:: missense_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_000007.14:g.143183620G>A, NC_000007.13:g.142880713G>A, NM_176881.2:c.202G>A, NP_795362.2:p.Ala68Thr

Select item 14788877908.

rs1478887790 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 7:143183491 (GRCh38)
7:142880584 (GRCh37)
Canonical SPDI:: NC_000007.14:143183490:G:A
Gene:: TAS2R39 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000007.14:g.143183491G>A, NC_000007.13:g.142880584G>A, NM_176881.2:c.73G>A, NP_795362.2:p.Ala25Thr

Select item 14765411049.

rs1476541104 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 7:143183484 (GRCh38)
7:142880577 (GRCh37)
Canonical SPDI:: NC_000007.14:143183483:C:A,NC_000007.14:143183483:C:T
Gene:: TAS2R39 (Varview)
Functional Consequence:: stop_gained,coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000014/2 (GnomAD)
T=0.000019/5 (TOPMED)
HGVS:: NC_000007.14:g.143183484C>A, NC_000007.14:g.143183484C>T, NC_000007.13:g.142880577C>A, NC_000007.13:g.142880577C>T, NM_176881.2:c.66C>A, NM_176881.2:c.66C>T, NP_795362.2:p.Cys22Ter

Select item 147431067110.

rs1474310671 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 7:143184141 (GRCh38)
7:142881234 (GRCh37)
Canonical SPDI:: NC_000007.14:143184140:C:T
Gene:: TAS2R39 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000007.14:g.143184141C>T, NC_000007.13:g.142881234C>T, NM_176881.2:c.723C>T

Select item 146965267911.

rs1469652679 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 7:143184291 (GRCh38)
7:142881384 (GRCh37)
Canonical SPDI:: NC_000007.14:143184290:G:A,NC_000007.14:143184290:G:T
Gene:: TAS2R39 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
A=0.000004/1 (GnomAD_exomes)
A=0.000004/1 (TOPMED)
HGVS:: NC_000007.14:g.143184291G>A, NC_000007.14:g.143184291G>T, NC_000007.13:g.142881384G>A, NC_000007.13:g.142881384G>T, NM_176881.2:c.873G>A, NM_176881.2:c.873G>T

Select item 146760399012.

rs1467603990 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 7:143183743 (GRCh38)
7:142880836 (GRCh37)
Canonical SPDI:: NC_000007.14:143183742:G:A
Gene:: TAS2R39 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000007.14:g.143183743G>A, NC_000007.13:g.142880836G>A, NM_176881.2:c.325G>A, NP_795362.2:p.Val109Ile

Select item 146139404613.

rs1461394046 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G [Show Flanks]
Chromosome:: 7:143184422 (GRCh38)
7:142881515 (GRCh37)
Canonical SPDI:: NC_000007.14:143184421:A:C,NC_000007.14:143184421:A:G
Gene:: TAS2R39 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000007/1 (GnomAD)
HGVS:: NC_000007.14:g.143184422A>C, NC_000007.14:g.143184422A>G, NC_000007.13:g.142881515A>C, NC_000007.13:g.142881515A>G, NM_176881.2:c.1004A>C, NM_176881.2:c.1004A>G, NP_795362.2:p.Glu335Ala, NP_795362.2:p.Glu335Gly

Select item 145409620414.

rs1454096204 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 7:143183878 (GRCh38)
7:142880971 (GRCh37)
Canonical SPDI:: NC_000007.14:143183877:A:G
Gene:: TAS2R39 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000007.14:g.143183878A>G, NC_000007.13:g.142880971A>G, NM_176881.2:c.460A>G, NP_795362.2:p.Ile154Val

Select item 145374845015.

rs1453748450 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 7:143183482 (GRCh38)
7:142880575 (GRCh37)
Canonical SPDI:: NC_000007.14:143183481:T:C
Gene:: TAS2R39 (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_000007.14:g.143183482T>C, NC_000007.13:g.142880575T>C, NM_176881.2:c.64T>C, NP_795362.2:p.Cys22Arg

Select item 145030745816.

rs1450307458 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 7:143183875 (GRCh38)
7:142880968 (GRCh37)
Canonical SPDI:: NC_000007.14:143183874:A:G
Gene:: TAS2R39 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000007.14:g.143183875A>G, NC_000007.13:g.142880968A>G, NM_176881.2:c.457A>G, NP_795362.2:p.Arg153Gly

Select item 144787068517.

rs1447870685 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 7:143183638 (GRCh38)
7:142880731 (GRCh37)
Canonical SPDI:: NC_000007.14:143183637:A:G
Gene:: TAS2R39 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000007.14:g.143183638A>G, NC_000007.13:g.142880731A>G, NM_176881.2:c.220A>G, NP_795362.2:p.Arg74Gly

Select item 144506804118.

rs1445068041 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 7:143184259 (GRCh38)
7:142881352 (GRCh37)
Canonical SPDI:: NC_000007.14:143184258:T:C
Gene:: TAS2R39 (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_000007.14:g.143184259T>C, NC_000007.13:g.142881352T>C, NM_176881.2:c.841T>C, NP_795362.2:p.Tyr281His

Select item 143915532819.

rs1439155328 [Homo sapiens]

Variant type:: DELINS
Alleles:: CT>- [Show Flanks]
Chromosome:: 7:143184250 (GRCh38)
7:142881343 (GRCh37)
Canonical SPDI:: NC_000007.14:143184247:CTCT:CT
Gene:: TAS2R39 (Varview)
Functional Consequence:: frameshift_variant,coding_sequence_variant
Validated:: by frequency
MAF:: -=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000007.14:g.143184248CT[1], NC_000007.13:g.142881341CT[1], NM_176881.2:c.832_833del, NP_795362.2:p.Leu278fs

Select item 143685586820.

rs1436855868 [Homo sapiens]

Variant type:: DELINS
Alleles:: AATGC>- [Show Flanks]
Chromosome:: 7:143184151 (GRCh38)
7:142881244 (GRCh37)
Canonical SPDI:: NC_000007.14:143184148:GCAATGC:GC
Gene:: TAS2R39 (Varview)
Functional Consequence:: frameshift_variant,coding_sequence_variant
Validated:: by frequency
MAF:: -=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000007.14:g.143184151_143184155del, NC_000007.13:g.142881244_142881248del, NM_176881.2:c.733_737del, NP_795362.2:p.Asn245fs

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