SNP Links for Protein (Select 4557265) - SNP

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Links from Protein

Items: 1 to 20 of 541

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Select item 14908986881.

rs1490898688 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 10:114044594 (GRCh38)
10:115804353 (GRCh37)
Canonical SPDI:: NC_000010.11:114044593:G:A
Gene:: ADRB1 (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=0.000007/1 (GnomAD)
HGVS:: NC_000010.11:g.114044594G>A, NC_000010.10:g.115804353G>A, NG_012187.1:g.5548G>A, NM_000684.3:c.462G>A, NM_000684.2:c.462G>A

Select item 14908251542.

rs1490825154 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 10:114045055 (GRCh38)
10:115804814 (GRCh37)
Canonical SPDI:: NC_000010.11:114045054:A:G
Gene:: ADRB1 (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)
G=0.000015/2 (GnomAD)
HGVS:: NC_000010.11:g.114045055A>G, NC_000010.10:g.115804814A>G, NG_012187.1:g.6009A>G, NM_000684.3:c.923A>G, NM_000684.2:c.923A>G, NP_000675.1:p.Lys308Arg

Select item 14904102363.

rs1490410236 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 10:114044259 (GRCh38)
10:115804018 (GRCh37)
Canonical SPDI:: NC_000010.11:114044258:C:T
Gene:: ADRB1 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
HGVS:: NC_000010.11:g.114044259C>T, NC_000010.10:g.115804018C>T, NG_012187.1:g.5213C>T, NM_000684.3:c.127C>T, NM_000684.2:c.127C>T

Select item 14889043204.

rs1488904320 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 10:114044166 (GRCh38)
10:115803925 (GRCh37)
Canonical SPDI:: NC_000010.11:114044165:G:A
Gene:: ADRB1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000010.11:g.114044166G>A, NC_000010.10:g.115803925G>A, NG_012187.1:g.5120G>A, NM_000684.3:c.34G>A, NM_000684.2:c.34G>A, NP_000675.1:p.Glu12Lys

Select item 14887750115.

rs1488775011 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 10:114045428 (GRCh38)
10:115805187 (GRCh37)
Canonical SPDI:: NC_000010.11:114045427:C:T
Gene:: ADRB1 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
C=0.5/1 (SGDP_PRJ)
HGVS:: NC_000010.11:g.114045428C>T, NC_000010.10:g.115805187C>T, NG_012187.1:g.6382C>T, NM_000684.3:c.1296C>T, NM_000684.2:c.1296C>T

Select item 14882596576.

rs1488259657 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 10:114045049 (GRCh38)
10:115804808 (GRCh37)
Canonical SPDI:: NC_000010.11:114045048:C:G,NC_000010.11:114045048:C:T
Gene:: ADRB1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
G=0.000004/1 (TOPMED)
T=0.000015/2 (GnomAD)
HGVS:: NC_000010.11:g.114045049C>G, NC_000010.11:g.114045049C>T, NC_000010.10:g.115804808C>G, NC_000010.10:g.115804808C>T, NG_012187.1:g.6003C>G, NG_012187.1:g.6003C>T, NM_000684.3:c.917C>G, NM_000684.3:c.917C>T, NM_000684.2:c.917C>G, NM_000684.2:c.917C>T, NP_000675.1:p.Ala306Gly, NP_000675.1:p.Ala306Val

Select item 14878976327.

rs1487897632 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 10:114044193 (GRCh38)
10:115803952 (GRCh37)
Canonical SPDI:: NC_000010.11:114044192:C:A,NC_000010.11:114044192:C:T
Gene:: ADRB1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000007/1 (GnomAD)
A=0.00016/2 (GnomAD_exomes)
HGVS:: NC_000010.11:g.114044193C>A, NC_000010.11:g.114044193C>T, NC_000010.10:g.115803952C>A, NC_000010.10:g.115803952C>T, NG_012187.1:g.5147C>A, NG_012187.1:g.5147C>T, NM_000684.3:c.61C>A, NM_000684.3:c.61C>T, NM_000684.2:c.61C>A, NM_000684.2:c.61C>T, NP_000675.1:p.Pro21Thr, NP_000675.1:p.Pro21Ser

Select item 14821031698.

rs1482103169 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 10:114045518 (GRCh38)
10:115805277 (GRCh37)
Canonical SPDI:: NC_000010.11:114045517:C:A
Gene:: ADRB1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000011/3 (TOPMED)
A=0.000022/3 (GnomAD)
HGVS:: NC_000010.11:g.114045518C>A, NC_000010.10:g.115805277C>A, NG_012187.1:g.6472C>A, NM_000684.3:c.1386C>A, NM_000684.2:c.1386C>A, NP_000675.1:p.Ser462Arg

Select item 14809847759.

rs1480984775 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 10:114044907 (GRCh38)
10:115804666 (GRCh37)
Canonical SPDI:: NC_000010.11:114044906:G:A
Gene:: ADRB1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000010.11:g.114044907G>A, NC_000010.10:g.115804666G>A, NG_012187.1:g.5861G>A, NM_000684.3:c.775G>A, NM_000684.2:c.775G>A, NP_000675.1:p.Asp259Asn

Select item 148093299910.

rs1480932999 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 10:114044212 (GRCh38)
10:115803971 (GRCh37)
Canonical SPDI:: NC_000010.11:114044211:C:T
Gene:: ADRB1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
HGVS:: NC_000010.11:g.114044212C>T, NC_000010.10:g.115803971C>T, NG_012187.1:g.5166C>T, NM_000684.3:c.80C>T, NM_000684.2:c.80C>T, NP_000675.1:p.Ala27Val

Select item 148085734611.

rs1480857346 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 10:114044749 (GRCh38)
10:115804508 (GRCh37)
Canonical SPDI:: NC_000010.11:114044748:C:A
Gene:: ADRB1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
HGVS:: NC_000010.11:g.114044749C>A, NC_000010.10:g.115804508C>A, NG_012187.1:g.5703C>A, NM_000684.3:c.617C>A, NM_000684.2:c.617C>A, NP_000675.1:p.Ala206Glu

Select item 148020723012.

rs1480207230 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,G [Show Flanks]
Chromosome:: 10:114045309 (GRCh38)
10:115805068 (GRCh37)
Canonical SPDI:: NC_000010.11:114045308:T:A,NC_000010.11:114045308:T:G
Gene:: ADRB1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
A=0.000005/1 (GnomAD_exomes)
G=0.000008/2 (TOPMED)
HGVS:: NC_000010.11:g.114045309T>A, NC_000010.11:g.114045309T>G, NC_000010.10:g.115805068T>A, NC_000010.10:g.115805068T>G, NG_012187.1:g.6263T>A, NG_012187.1:g.6263T>G, NM_000684.3:c.1177T>A, NM_000684.3:c.1177T>G, NM_000684.2:c.1177T>A, NM_000684.2:c.1177T>G, NP_000675.1:p.Cys393Ser, NP_000675.1:p.Cys393Gly

Select item 148015573813.

rs1480155738 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 10:114044664 (GRCh38)
10:115804423 (GRCh37)
Canonical SPDI:: NC_000010.11:114044663:C:T
Gene:: ADRB1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000142/2 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000011/3 (TOPMED)
HGVS:: NC_000010.11:g.114044664C>T, NC_000010.10:g.115804423C>T, NG_012187.1:g.5618C>T, NM_000684.3:c.532C>T, NM_000684.2:c.532C>T, NP_000675.1:p.Leu178Phe

Select item 147934718014.

rs1479347180 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 10:114045201 (GRCh38)
10:115804960 (GRCh37)
Canonical SPDI:: NC_000010.11:114045200:C:G
Gene:: ADRB1 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000010.11:g.114045201C>G, NC_000010.10:g.115804960C>G, NG_012187.1:g.6155C>G, NM_000684.3:c.1069C>G, NM_000684.2:c.1069C>G, NP_000675.1:p.Arg357Gly

Select item 147843647215.

rs1478436472 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 10:114045281 (GRCh38)
10:115805040 (GRCh37)
Canonical SPDI:: NC_000010.11:114045280:C:G
Gene:: ADRB1 (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_000010.11:g.114045281C>G, NC_000010.10:g.115805040C>G, NG_012187.1:g.6235C>G, NM_000684.3:c.1149C>G, NM_000684.2:c.1149C>G, NP_000675.1:p.Phe383Leu

Select item 147623090516.

rs1476230905 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 10:114045137 (GRCh38)
10:115804896 (GRCh37)
Canonical SPDI:: NC_000010.11:114045136:C:T
Gene:: ADRB1 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
HGVS:: NC_000010.11:g.114045137C>T, NC_000010.10:g.115804896C>T, NG_012187.1:g.6091C>T, NM_000684.3:c.1005C>T, NM_000684.2:c.1005C>T

Select item 147585464517.

rs1475854645 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 10:114044429 (GRCh38)
10:115804188 (GRCh37)
Canonical SPDI:: NC_000010.11:114044428:C:G
Gene:: ADRB1 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000010.11:g.114044429C>G, NC_000010.10:g.115804188C>G, NG_012187.1:g.5383C>G, NM_000684.3:c.297C>G, NM_000684.2:c.297C>G

Select item 147144646018.

rs1471446460 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,G [Show Flanks]
Chromosome:: 10:114045536 (GRCh38)
10:115805295 (GRCh37)
Canonical SPDI:: NC_000010.11:114045535:C:A,NC_000010.11:114045535:C:G
Gene:: ADRB1 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
A=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000010.11:g.114045536C>A, NC_000010.11:g.114045536C>G, NC_000010.10:g.115805295C>A, NC_000010.10:g.115805295C>G, NG_012187.1:g.6490C>A, NG_012187.1:g.6490C>G, NM_000684.3:c.1404C>A, NM_000684.3:c.1404C>G, NM_000684.2:c.1404C>A, NM_000684.2:c.1404C>G

Select item 146814720719.

rs1468147207 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 10:114045146 (GRCh38)
10:115804905 (GRCh37)
Canonical SPDI:: NC_000010.11:114045145:G:A
Gene:: ADRB1 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000010.11:g.114045146G>A, NC_000010.10:g.115804905G>A, NG_012187.1:g.6100G>A, NM_000684.3:c.1014G>A, NM_000684.2:c.1014G>A

Select item 146806568220.

rs1468065682 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 10:114044445 (GRCh38)
10:115804204 (GRCh37)
Canonical SPDI:: NC_000010.11:114044444:C:T
Gene:: ADRB1 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000010.11:g.114044445C>T, NC_000010.10:g.115804204C>T, NG_012187.1:g.5399C>T, NM_000684.3:c.313C>T, NM_000684.2:c.313C>T

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