SNP Links for Protein (Select 49619228) - SNP

Links from Protein

Items: 1 to 20 of 154

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Select item 14907856981.

rs1490785698 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 17:81922712 (GRCh38)
17:79880588 (GRCh37)
Canonical SPDI:: NC_000017.11:81922711:G:T
Gene:: MAFG (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
HGVS:: NC_000017.11:g.81922712G>T, NC_000017.10:g.79880588G>T, NM_002359.4:c.382C>A, NM_002359.3:c.382C>A, NM_032711.4:c.382C>A, NM_032711.3:c.382C>A, XM_047436069.1:c.382C>A, XM_047436071.1:c.382C>A, XM_047436068.1:c.382C>A, XM_047436072.1:c.382C>A, XM_047436070.1:c.382C>A, NP_002350.1:p.Pro128Thr, NP_116100.2:p.Pro128Thr, XP_047292025.1:p.Pro128Thr, XP_047292027.1:p.Pro128Thr, XP_047292024.1:p.Pro128Thr, XP_047292028.1:p.Pro128Thr, XP_047292026.1:p.Pro128Thr

Select item 14842416842.

rs1484241684 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 17:81922696 (GRCh38)
17:79880572 (GRCh37)
Canonical SPDI:: NC_000017.11:81922695:A:G
Gene:: MAFG (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
HGVS:: NC_000017.11:g.81922696A>G, NC_000017.10:g.79880572A>G, NM_002359.4:c.398T>C, NM_002359.3:c.398T>C, NM_032711.4:c.398T>C, NM_032711.3:c.398T>C, XM_047436069.1:c.398T>C, XM_047436071.1:c.398T>C, XM_047436068.1:c.398T>C, XM_047436072.1:c.398T>C, XM_047436070.1:c.398T>C, NP_002350.1:p.Leu133Pro, NP_116100.2:p.Leu133Pro, XP_047292025.1:p.Leu133Pro, XP_047292027.1:p.Leu133Pro, XP_047292024.1:p.Leu133Pro, XP_047292028.1:p.Leu133Pro, XP_047292026.1:p.Leu133Pro

Select item 14842270773.

rs1484227077 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 17:81922756 (GRCh38)
17:79880632 (GRCh37)
Canonical SPDI:: NC_000017.11:81922755:G:A,NC_000017.11:81922755:G:T
Gene:: MAFG (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)
HGVS:: NC_000017.11:g.81922756G>A, NC_000017.11:g.81922756G>T, NC_000017.10:g.79880632G>A, NC_000017.10:g.79880632G>T, NM_002359.4:c.338C>T, NM_002359.4:c.338C>A, NM_002359.3:c.338C>T, NM_002359.3:c.338C>A, NM_032711.4:c.338C>T, NM_032711.4:c.338C>A, NM_032711.3:c.338C>T, NM_032711.3:c.338C>A, XM_047436069.1:c.338C>T, XM_047436069.1:c.338C>A, XM_047436071.1:c.338C>T, XM_047436071.1:c.338C>A, XM_047436068.1:c.338C>T, XM_047436068.1:c.338C>A, XM_047436072.1:c.338C>T, XM_047436072.1:c.338C>A, XM_047436070.1:c.338C>T, XM_047436070.1:c.338C>A, NP_002350.1:p.Ala113Val, NP_002350.1:p.Ala113Glu, NP_116100.2:p.Ala113Val, NP_116100.2:p.Ala113Glu, XP_047292025.1:p.Ala113Val, XP_047292025.1:p.Ala113Glu, XP_047292027.1:p.Ala113Val, XP_047292027.1:p.Ala113Glu, XP_047292024.1:p.Ala113Val, XP_047292024.1:p.Ala113Glu, XP_047292028.1:p.Ala113Val, XP_047292028.1:p.Ala113Glu, XP_047292026.1:p.Ala113Val, XP_047292026.1:p.Ala113Glu

Select item 14785652004.

rs1478565200 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G,T [Show Flanks]
Chromosome:: 17:81922702 (GRCh38)
17:79880578 (GRCh37)
Canonical SPDI:: NC_000017.11:81922701:C:G,NC_000017.11:81922701:C:T
Gene:: MAFG (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
G=0.0017/48 (TOMMO)
HGVS:: NC_000017.11:g.81922702C>G, NC_000017.11:g.81922702C>T, NC_000017.10:g.79880578C>G, NC_000017.10:g.79880578C>T, NM_002359.4:c.392G>C, NM_002359.4:c.392G>A, NM_002359.3:c.392G>C, NM_002359.3:c.392G>A, NM_032711.4:c.392G>C, NM_032711.4:c.392G>A, NM_032711.3:c.392G>C, NM_032711.3:c.392G>A, XM_047436069.1:c.392G>C, XM_047436069.1:c.392G>A, XM_047436071.1:c.392G>C, XM_047436071.1:c.392G>A, XM_047436068.1:c.392G>C, XM_047436068.1:c.392G>A, XM_047436072.1:c.392G>C, XM_047436072.1:c.392G>A, XM_047436070.1:c.392G>C, XM_047436070.1:c.392G>A, NP_002350.1:p.Gly131Ala, NP_002350.1:p.Gly131Asp, NP_116100.2:p.Gly131Ala, NP_116100.2:p.Gly131Asp, XP_047292025.1:p.Gly131Ala, XP_047292025.1:p.Gly131Asp, XP_047292027.1:p.Gly131Ala, XP_047292027.1:p.Gly131Asp, XP_047292024.1:p.Gly131Ala, XP_047292024.1:p.Gly131Asp, XP_047292028.1:p.Gly131Ala, XP_047292028.1:p.Gly131Asp, XP_047292026.1:p.Gly131Ala, XP_047292026.1:p.Gly131Asp

Select item 14673423315.

rs1467342331 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 17:81922962 (GRCh38)
17:79880838 (GRCh37)
Canonical SPDI:: NC_000017.11:81922961:C:A
Gene:: MAFG (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000017.11:g.81922962C>A, NC_000017.10:g.79880838C>A, NM_002359.4:c.132G>T, NM_002359.3:c.132G>T, NM_032711.4:c.132G>T, NM_032711.3:c.132G>T, XM_047436069.1:c.132G>T, XM_047436071.1:c.132G>T, XM_047436068.1:c.132G>T, XM_047436072.1:c.132G>T, XM_047436070.1:c.132G>T

Select item 14649451506.

rs1464945150 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 17:81922968 (GRCh38)
17:79880844 (GRCh37)
Canonical SPDI:: NC_000017.11:81922967:C:A,NC_000017.11:81922967:C:T
Gene:: MAFG (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)
T=0.000035/1 (TOMMO)
HGVS:: NC_000017.11:g.81922968C>A, NC_000017.11:g.81922968C>T, NC_000017.10:g.79880844C>A, NC_000017.10:g.79880844C>T, NM_002359.4:c.126G>T, NM_002359.4:c.126G>A, NM_002359.3:c.126G>T, NM_002359.3:c.126G>A, NM_032711.4:c.126G>T, NM_032711.4:c.126G>A, NM_032711.3:c.126G>T, NM_032711.3:c.126G>A, XM_047436069.1:c.126G>T, XM_047436069.1:c.126G>A, XM_047436071.1:c.126G>T, XM_047436071.1:c.126G>A, XM_047436068.1:c.126G>T, XM_047436068.1:c.126G>A, XM_047436072.1:c.126G>T, XM_047436072.1:c.126G>A, XM_047436070.1:c.126G>T, XM_047436070.1:c.126G>A

Select item 14640555657.

rs1464055565 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 17:81922924 (GRCh38)
17:79880800 (GRCh37)
Canonical SPDI:: NC_000017.11:81922923:C:T
Gene:: MAFG (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
HGVS:: NC_000017.11:g.81922924C>T, NC_000017.10:g.79880800C>T, NM_002359.4:c.170G>A, NM_002359.3:c.170G>A, NM_032711.4:c.170G>A, NM_032711.3:c.170G>A, XM_047436069.1:c.170G>A, XM_047436071.1:c.170G>A, XM_047436068.1:c.170G>A, XM_047436072.1:c.170G>A, XM_047436070.1:c.170G>A, NP_002350.1:p.Arg57His, NP_116100.2:p.Arg57His, XP_047292025.1:p.Arg57His, XP_047292027.1:p.Arg57His, XP_047292024.1:p.Arg57His, XP_047292028.1:p.Arg57His, XP_047292026.1:p.Arg57His

Select item 14567888048.

rs1456788804 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 17:81922967 (GRCh38)
17:79880843 (GRCh37)
Canonical SPDI:: NC_000017.11:81922966:C:T
Gene:: MAFG (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000017.11:g.81922967C>T, NC_000017.10:g.79880843C>T, NM_002359.4:c.127G>A, NM_002359.3:c.127G>A, NM_032711.4:c.127G>A, NM_032711.3:c.127G>A, XM_047436069.1:c.127G>A, XM_047436071.1:c.127G>A, XM_047436068.1:c.127G>A, XM_047436072.1:c.127G>A, XM_047436070.1:c.127G>A, NP_002350.1:p.Gly43Ser, NP_116100.2:p.Gly43Ser, XP_047292025.1:p.Gly43Ser, XP_047292027.1:p.Gly43Ser, XP_047292024.1:p.Gly43Ser, XP_047292028.1:p.Gly43Ser, XP_047292026.1:p.Gly43Ser

Select item 14527495019.

rs1452749501 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 17:81922751 (GRCh38)
17:79880627 (GRCh37)
Canonical SPDI:: NC_000017.11:81922750:G:T
Gene:: MAFG (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
HGVS:: NC_000017.11:g.81922751G>T, NC_000017.10:g.79880627G>T, NM_002359.4:c.343C>A, NM_002359.3:c.343C>A, NM_032711.4:c.343C>A, NM_032711.3:c.343C>A, XM_047436069.1:c.343C>A, XM_047436071.1:c.343C>A, XM_047436068.1:c.343C>A, XM_047436072.1:c.343C>A, XM_047436070.1:c.343C>A, NP_002350.1:p.Gln115Lys, NP_116100.2:p.Gln115Lys, XP_047292025.1:p.Gln115Lys, XP_047292027.1:p.Gln115Lys, XP_047292024.1:p.Gln115Lys, XP_047292028.1:p.Gln115Lys, XP_047292026.1:p.Gln115Lys

Select item 144122457210.

rs1441224572 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 17:81922726 (GRCh38)
17:79880602 (GRCh37)
Canonical SPDI:: NC_000017.11:81922725:C:T
Gene:: MAFG (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
HGVS:: NC_000017.11:g.81922726C>T, NC_000017.10:g.79880602C>T, NM_002359.4:c.368G>A, NM_002359.3:c.368G>A, NM_032711.4:c.368G>A, NM_032711.3:c.368G>A, XM_047436069.1:c.368G>A, XM_047436071.1:c.368G>A, XM_047436068.1:c.368G>A, XM_047436072.1:c.368G>A, XM_047436070.1:c.368G>A, NP_002350.1:p.Arg123His, NP_116100.2:p.Arg123His, XP_047292025.1:p.Arg123His, XP_047292027.1:p.Arg123His, XP_047292024.1:p.Arg123His, XP_047292028.1:p.Arg123His, XP_047292026.1:p.Arg123His

Select item 143468985911.

rs1434689859 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 17:81923026 (GRCh38)
17:79880902 (GRCh37)
Canonical SPDI:: NC_000017.11:81923025:C:T
Gene:: MAFG (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
HGVS:: NC_000017.11:g.81923026C>T, NC_000017.10:g.79880902C>T, NM_002359.4:c.68G>A, NM_002359.3:c.68G>A, NM_032711.4:c.68G>A, NM_032711.3:c.68G>A, XM_047436069.1:c.68G>A, XM_047436071.1:c.68G>A, XM_047436068.1:c.68G>A, XM_047436072.1:c.68G>A, XM_047436070.1:c.68G>A, NP_002350.1:p.Ser23Asn, NP_116100.2:p.Ser23Asn, XP_047292025.1:p.Ser23Asn, XP_047292027.1:p.Ser23Asn, XP_047292024.1:p.Ser23Asn, XP_047292028.1:p.Ser23Asn, XP_047292026.1:p.Ser23Asn

Select item 143441158312.

rs1434411583 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 17:81922889 (GRCh38)
17:79880765 (GRCh37)
Canonical SPDI:: NC_000017.11:81922888:G:A
Gene:: MAFG (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
HGVS:: NC_000017.11:g.81922889G>A, NC_000017.10:g.79880765G>A, NM_002359.4:c.205C>T, NM_002359.3:c.205C>T, NM_032711.4:c.205C>T, NM_032711.3:c.205C>T, XM_047436069.1:c.205C>T, XM_047436071.1:c.205C>T, XM_047436068.1:c.205C>T, XM_047436072.1:c.205C>T, XM_047436070.1:c.205C>T, NP_002350.1:p.Arg69Cys, NP_116100.2:p.Arg69Cys, XP_047292025.1:p.Arg69Cys, XP_047292027.1:p.Arg69Cys, XP_047292024.1:p.Arg69Cys, XP_047292028.1:p.Arg69Cys, XP_047292026.1:p.Arg69Cys

Select item 142907571713.

rs1429075717 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 17:81922770 (GRCh38)
17:79880646 (GRCh37)
Canonical SPDI:: NC_000017.11:81922769:G:A
Gene:: MAFG (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000071/1 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000014/2 (GnomAD)
HGVS:: NC_000017.11:g.81922770G>A, NC_000017.10:g.79880646G>A, NM_002359.4:c.324C>T, NM_002359.3:c.324C>T, NM_032711.4:c.324C>T, NM_032711.3:c.324C>T, XM_047436069.1:c.324C>T, XM_047436071.1:c.324C>T, XM_047436068.1:c.324C>T, XM_047436072.1:c.324C>T, XM_047436070.1:c.324C>T

Select item 142153874414.

rs1421538744 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 17:81922925 (GRCh38)
17:79880801 (GRCh37)
Canonical SPDI:: NC_000017.11:81922924:G:C
Gene:: MAFG (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
HGVS:: NC_000017.11:g.81922925G>C, NC_000017.10:g.79880801G>C, NM_002359.4:c.169C>G, NM_002359.3:c.169C>G, NM_032711.4:c.169C>G, NM_032711.3:c.169C>G, XM_047436069.1:c.169C>G, XM_047436071.1:c.169C>G, XM_047436068.1:c.169C>G, XM_047436072.1:c.169C>G, XM_047436070.1:c.169C>G, NP_002350.1:p.Arg57Gly, NP_116100.2:p.Arg57Gly, XP_047292025.1:p.Arg57Gly, XP_047292027.1:p.Arg57Gly, XP_047292024.1:p.Arg57Gly, XP_047292028.1:p.Arg57Gly, XP_047292026.1:p.Arg57Gly

Select item 142072674515.

rs1420726745 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 17:81922650 (GRCh38)
17:79880526 (GRCh37)
Canonical SPDI:: NC_000017.11:81922649:G:A,NC_000017.11:81922649:G:T
Gene:: MAFG (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0.000071/1 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
A=0.000035/1 (TOMMO)
HGVS:: NC_000017.11:g.81922650G>A, NC_000017.11:g.81922650G>T, NC_000017.10:g.79880526G>A, NC_000017.10:g.79880526G>T, NM_002359.4:c.444C>T, NM_002359.4:c.444C>A, NM_002359.3:c.444C>T, NM_002359.3:c.444C>A, NM_032711.4:c.444C>T, NM_032711.4:c.444C>A, NM_032711.3:c.444C>T, NM_032711.3:c.444C>A, XM_047436069.1:c.444C>T, XM_047436069.1:c.444C>A, XM_047436071.1:c.444C>T, XM_047436071.1:c.444C>A, XM_047436068.1:c.444C>T, XM_047436068.1:c.444C>A, XM_047436072.1:c.444C>T, XM_047436072.1:c.444C>A, XM_047436070.1:c.444C>T, XM_047436070.1:c.444C>A

Select item 141939513416.

rs1419395134 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 17:81923159 (GRCh38)
17:79881035 (GRCh37)
Canonical SPDI:: NC_000017.11:81923158:C:T
Gene:: MAFG (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)
T=0.000008/2 (TOPMED)
C=0.5/1 (SGDP_PRJ)
HGVS:: NC_000017.11:g.81923159C>T, NC_000017.10:g.79881035C>T, NM_002359.4:c.27G>A, NM_002359.3:c.27G>A, NM_032711.4:c.27G>A, NM_032711.3:c.27G>A, XM_047436069.1:c.27G>A, XM_047436071.1:c.27G>A, XM_047436068.1:c.27G>A, XM_047436072.1:c.27G>A, XM_047436070.1:c.27G>A

Select item 141093541217.

rs1410935412 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 17:81923030 (GRCh38)
17:79880906 (GRCh37)
Canonical SPDI:: NC_000017.11:81923029:T:C
Gene:: MAFG (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
HGVS:: NC_000017.11:g.81923030T>C, NC_000017.10:g.79880906T>C, NM_002359.4:c.64A>G, NM_002359.3:c.64A>G, NM_032711.4:c.64A>G, NM_032711.3:c.64A>G, XM_047436069.1:c.64A>G, XM_047436071.1:c.64A>G, XM_047436068.1:c.64A>G, XM_047436072.1:c.64A>G, XM_047436070.1:c.64A>G, NP_002350.1:p.Thr22Ala, NP_116100.2:p.Thr22Ala, XP_047292025.1:p.Thr22Ala, XP_047292027.1:p.Thr22Ala, XP_047292024.1:p.Thr22Ala, XP_047292028.1:p.Thr22Ala, XP_047292026.1:p.Thr22Ala

Select item 141019228418.

rs1410192284 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 17:81922710 (GRCh38)
17:79880586 (GRCh37)
Canonical SPDI:: NC_000017.11:81922709:T:C
Gene:: MAFG (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000021/3 (GnomAD)
HGVS:: NC_000017.11:g.81922710T>C, NC_000017.10:g.79880586T>C, NM_002359.4:c.384A>G, NM_002359.3:c.384A>G, NM_032711.4:c.384A>G, NM_032711.3:c.384A>G, XM_047436069.1:c.384A>G, XM_047436071.1:c.384A>G, XM_047436068.1:c.384A>G, XM_047436072.1:c.384A>G, XM_047436070.1:c.384A>G

Select item 139454593619.

rs1394545936 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 17:81922880 (GRCh38)
17:79880756 (GRCh37)
Canonical SPDI:: NC_000017.11:81922879:G:T
Gene:: MAFG (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000017.11:g.81922880G>T, NC_000017.10:g.79880756G>T, NM_002359.4:c.214C>A, NM_002359.3:c.214C>A, NM_032711.4:c.214C>A, NM_032711.3:c.214C>A, XM_047436069.1:c.214C>A, XM_047436071.1:c.214C>A, XM_047436068.1:c.214C>A, XM_047436072.1:c.214C>A, XM_047436070.1:c.214C>A

Select item 139002456620.

rs1390024566 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 17:81923162 (GRCh38)
17:79881038 (GRCh37)
Canonical SPDI:: NC_000017.11:81923161:G:A
Gene:: MAFG (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000017.11:g.81923162G>A, NC_000017.10:g.79881038G>A, NM_002359.4:c.24C>T, NM_002359.3:c.24C>T, NM_032711.4:c.24C>T, NM_032711.3:c.24C>T, XM_047436069.1:c.24C>T, XM_047436071.1:c.24C>T, XM_047436068.1:c.24C>T, XM_047436072.1:c.24C>T, XM_047436070.1:c.24C>T

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