SNP Links for Protein (Select 1034639898) - SNP

Select item 14850717801.

rs1485071780 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 4:139704045 (GRCh38)
4:140625199 (GRCh37)
Canonical SPDI:: NC_000004.12:139704044:T:C
Gene:: MGST2 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (GnomAD_exomes)
C=0.000007/1 (GnomAD)
C=0.000008/2 (TOPMED)
HGVS:: NC_000004.12:g.139704045T>C, NC_000004.11:g.140625199T>C, NM_002413.5:c.341T>C, NM_002413.4:c.341T>C, XM_017008212.3:c.341T>C, XM_017008212.2:c.341T>C, XM_017008212.1:c.341T>C, XM_017008211.3:c.341T>C, XM_017008211.2:c.341T>C, XM_017008211.1:c.341T>C, NM_001204366.2:c.341T>C, NM_001204366.1:c.341T>C, NM_001204367.2:c.137T>C, NM_001204367.1:c.137T>C, XM_017008213.2:c.341T>C, XM_017008213.1:c.341T>C, NM_001204368.2:c.*36T>C, NM_001204368.1:c.*36T>C, XM_047415701.1:c.341T>C, NP_002404.1:p.Ile114Thr, XP_016863701.1:p.Ile114Thr, XP_016863700.1:p.Ile114Thr, NP_001191295.1:p.Ile114Thr, NP_001191296.1:p.Ile46Thr, XP_016863702.1:p.Ile114Thr, XP_047271657.1:p.Ile114Thr

Select item 14849685752.

rs1484968575 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 4:139666052 (GRCh38)
4:140587206 (GRCh37)
Canonical SPDI:: NC_000004.12:139666051:C:G
Gene:: MGST2 (Varview)
Functional Consequence:: 5_prime_UTR_variant,coding_sequence_variant,synonymous_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000004.12:g.139666052C>G, NC_000004.11:g.140587206C>G, NG_083488.1:g.775C>G, NM_002413.5:c.33C>G, NM_002413.4:c.33C>G, XM_017008212.3:c.33C>G, XM_017008212.2:c.33C>G, XM_017008212.1:c.33C>G, XM_017008211.3:c.33C>G, XM_017008211.2:c.33C>G, XM_017008211.1:c.33C>G, NM_001204366.2:c.33C>G, NM_001204366.1:c.33C>G, NM_001204367.2:c.-72C>G, NM_001204367.1:c.-72C>G, XM_017008213.2:c.33C>G, XM_017008213.1:c.33C>G, NM_001204368.2:c.33C>G, NM_001204368.1:c.33C>G, XM_047415701.1:c.33C>G

Select item 14644557603.

rs1464455760 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->T [Show Flanks]
Chromosome:: 4:139678619 (GRCh38)
4:140599774 (GRCh37)
Canonical SPDI:: NC_000004.12:139678619:TTT:TTTT
Gene:: MGST2 (Varview)
Functional Consequence:: stop_gained,intron_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: TTTT=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000004.12:g.139678622dup, NC_000004.11:g.140599776dup, NM_002413.5:c.138dup, NM_002413.4:c.138dup, XM_017008212.3:c.138dup, XM_017008212.2:c.138dup, XM_017008212.1:c.138dup, XM_017008211.3:c.138dup, XM_017008211.2:c.138dup, XM_017008211.1:c.138dup, NM_001204366.2:c.138dup, NM_001204366.1:c.138dup, XM_017008213.2:c.138dup, XM_017008213.1:c.138dup, NM_001204368.2:c.138dup, NM_001204368.1:c.138dup, XM_047415701.1:c.138dup, NP_002404.1:p.Glu47Ter, XP_016863701.1:p.Glu47Ter, XP_016863700.1:p.Glu47Ter, NP_001191295.1:p.Glu47Ter, XP_016863702.1:p.Glu47Ter, NP_001191297.1:p.Glu47Ter, XP_047271657.1:p.Glu47Ter

Select item 14606512224.

rs1460651222 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 4:139703528 (GRCh38)
4:140624682 (GRCh37)
Canonical SPDI:: NC_000004.12:139703527:T:C
Gene:: MGST2 (Varview)
Functional Consequence:: stop_lost,terminator_codon_variant,synonymous_variant,coding_sequence_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000004.12:g.139703528T>C, NC_000004.11:g.140624682T>C, NM_002413.5:c.303T>C, NM_002413.4:c.303T>C, XM_017008212.3:c.303T>C, XM_017008212.2:c.303T>C, XM_017008212.1:c.303T>C, XM_017008211.3:c.303T>C, XM_017008211.2:c.303T>C, XM_017008211.1:c.303T>C, NM_001204366.2:c.303T>C, NM_001204366.1:c.303T>C, NM_001204367.2:c.99T>C, NM_001204367.1:c.99T>C, XM_017008213.2:c.303T>C, XM_017008213.1:c.303T>C, NM_001204368.2:c.232T>C, NM_001204368.1:c.232T>C, XM_047415701.1:c.303T>C, NP_001191297.1:p.Ter78Gln

Select item 14540185785.

rs1454018578 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 4:139704064 (GRCh38)
4:140625218 (GRCh37)
Canonical SPDI:: NC_000004.12:139704063:C:G
Gene:: MGST2 (Varview)
Functional Consequence:: 3_prime_UTR_variant,synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000004.12:g.139704064C>G, NC_000004.11:g.140625218C>G, NM_002413.5:c.360C>G, NM_002413.4:c.360C>G, XM_017008212.3:c.360C>G, XM_017008212.2:c.360C>G, XM_017008212.1:c.360C>G, XM_017008211.3:c.360C>G, XM_017008211.2:c.360C>G, XM_017008211.1:c.360C>G, NM_001204366.2:c.360C>G, NM_001204366.1:c.360C>G, NM_001204367.2:c.156C>G, NM_001204367.1:c.156C>G, XM_017008213.2:c.360C>G, XM_017008213.1:c.360C>G, NM_001204368.2:c.*55C>G, NM_001204368.1:c.*55C>G, XM_047415701.1:c.360C>G

Select item 14438397986.

rs1443839798 [Homo sapiens]

Variant type:: DELINS
Alleles:: G>- [Show Flanks]
Chromosome:: 4:139695249 (GRCh38)
4:140616403 (GRCh37)
Canonical SPDI:: NC_000004.12:139695248:GGG:GG
Gene:: MGST2 (Varview)
Functional Consequence:: intron_variant,frameshift_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: GG=0./0 (ALFA)
-=0.000004/1 (TOPMED)
-=0.000007/1 (GnomAD)
HGVS:: NC_000004.12:g.139695251del, NC_000004.11:g.140616405del, NM_002413.5:c.213del, NM_002413.4:c.213del, XM_017008212.3:c.213del, XM_017008212.2:c.213del, XM_017008212.1:c.213del, XM_017008211.3:c.213del, XM_017008211.2:c.213del, XM_017008211.1:c.213del, NM_001204366.2:c.213del, NM_001204366.1:c.213del, NM_001204367.2:c.9del, NM_001204367.1:c.9del, XM_017008213.2:c.213del, XM_017008213.1:c.213del, XM_047415701.1:c.213del, NP_002404.1:p.Trp72fs, XP_016863701.1:p.Trp72fs, XP_016863700.1:p.Trp72fs, NP_001191295.1:p.Trp72fs, NP_001191296.1:p.Trp4fs, XP_016863702.1:p.Trp72fs, XP_047271657.1:p.Trp72fs

Select item 14417795177.

rs1441779517 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 4:139704101 (GRCh38)
4:140625255 (GRCh37)
Canonical SPDI:: NC_000004.12:139704100:G:A
Gene:: MGST2 (Varview)
Functional Consequence:: 3_prime_UTR_variant,missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000011/3 (TOPMED)
HGVS:: NC_000004.12:g.139704101G>A, NC_000004.11:g.140625255G>A, NM_002413.5:c.397G>A, NM_002413.4:c.397G>A, XM_017008212.3:c.397G>A, XM_017008212.2:c.397G>A, XM_017008212.1:c.397G>A, XM_017008211.3:c.397G>A, XM_017008211.2:c.397G>A, XM_017008211.1:c.397G>A, NM_001204366.2:c.397G>A, NM_001204366.1:c.397G>A, NM_001204367.2:c.193G>A, NM_001204367.1:c.193G>A, XM_017008213.2:c.397G>A, XM_017008213.1:c.397G>A, NM_001204368.2:c.*92G>A, NM_001204368.1:c.*92G>A, XM_047415701.1:c.397G>A, NP_002404.1:p.Glu133Lys, XP_016863701.1:p.Glu133Lys, XP_016863700.1:p.Glu133Lys, NP_001191295.1:p.Glu133Lys, NP_001191296.1:p.Glu65Lys, XP_016863702.1:p.Glu133Lys, XP_047271657.1:p.Glu133Lys

Select item 14412946558.

rs1441294655 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 4:139704146 (GRCh38)
4:140625300 (GRCh37)
Canonical SPDI:: NC_000004.12:139704145:T:C
Gene:: MGST2 (Varview)
Functional Consequence:: 3_prime_UTR_variant,terminator_codon_variant,stop_lost
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000011/3 (TOPMED)
C=0.000014/2 (GnomAD)
C=0.000036/9 (GnomAD_exomes)
HGVS:: NC_000004.12:g.139704146T>C, NC_000004.11:g.140625300T>C, NM_002413.5:c.442T>C, NM_002413.4:c.442T>C, XM_017008212.3:c.442T>C, XM_017008212.2:c.442T>C, XM_017008212.1:c.442T>C, XM_017008211.3:c.442T>C, XM_017008211.2:c.442T>C, XM_017008211.1:c.442T>C, NM_001204366.2:c.442T>C, NM_001204366.1:c.442T>C, NM_001204367.2:c.238T>C, NM_001204367.1:c.238T>C, XM_017008213.2:c.442T>C, XM_017008213.1:c.442T>C, NM_001204368.2:c.*137T>C, NM_001204368.1:c.*137T>C, XM_047415701.1:c.442T>C, NP_002404.1:p.Ter148Gln, XP_016863701.1:p.Ter148Gln, XP_016863700.1:p.Ter148Gln, NP_001191295.1:p.Ter148Gln, NP_001191296.1:p.Ter80Gln, XP_016863702.1:p.Ter148Gln, XP_047271657.1:p.Ter148Gln

Select item 14291919179.

rs1429191917 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 4:139678615 (GRCh38)
4:140599769 (GRCh37)
Canonical SPDI:: NC_000004.12:139678614:C:T
Gene:: MGST2 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,intron_variant
Validated:: by frequency
MAF:: T=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000004.12:g.139678615C>T, NC_000004.11:g.140599769C>T, NM_002413.5:c.131C>T, NM_002413.4:c.131C>T, XM_017008212.3:c.131C>T, XM_017008212.2:c.131C>T, XM_017008212.1:c.131C>T, XM_017008211.3:c.131C>T, XM_017008211.2:c.131C>T, XM_017008211.1:c.131C>T, NM_001204366.2:c.131C>T, NM_001204366.1:c.131C>T, XM_017008213.2:c.131C>T, XM_017008213.1:c.131C>T, NM_001204368.2:c.131C>T, NM_001204368.1:c.131C>T, XM_047415701.1:c.131C>T, NP_002404.1:p.Pro44Leu, XP_016863701.1:p.Pro44Leu, XP_016863700.1:p.Pro44Leu, NP_001191295.1:p.Pro44Leu, XP_016863702.1:p.Pro44Leu, NP_001191297.1:p.Pro44Leu, XP_047271657.1:p.Pro44Leu

Select item 142770198110.

rs1427701981 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 4:139703525 (GRCh38)
4:140624679 (GRCh37)
Canonical SPDI:: NC_000004.12:139703524:T:A
Gene:: MGST2 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000004.12:g.139703525T>A, NC_000004.11:g.140624679T>A, NM_002413.5:c.300T>A, NM_002413.4:c.300T>A, XM_017008212.3:c.300T>A, XM_017008212.2:c.300T>A, XM_017008212.1:c.300T>A, XM_017008211.3:c.300T>A, XM_017008211.2:c.300T>A, XM_017008211.1:c.300T>A, NM_001204366.2:c.300T>A, NM_001204366.1:c.300T>A, NM_001204367.2:c.96T>A, NM_001204367.1:c.96T>A, XM_017008213.2:c.300T>A, XM_017008213.1:c.300T>A, NM_001204368.2:c.229T>A, NM_001204368.1:c.229T>A, XM_047415701.1:c.300T>A, NP_001191297.1:p.Cys77Ser

Select item 139882249211.

rs1398822492 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 4:139704043 (GRCh38)
4:140625197 (GRCh37)
Canonical SPDI:: NC_000004.12:139704042:G:A
Gene:: MGST2 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000004.12:g.139704043G>A, NC_000004.11:g.140625197G>A, NM_002413.5:c.339G>A, NM_002413.4:c.339G>A, XM_017008212.3:c.339G>A, XM_017008212.2:c.339G>A, XM_017008212.1:c.339G>A, XM_017008211.3:c.339G>A, XM_017008211.2:c.339G>A, XM_017008211.1:c.339G>A, NM_001204366.2:c.339G>A, NM_001204366.1:c.339G>A, NM_001204367.2:c.135G>A, NM_001204367.1:c.135G>A, XM_017008213.2:c.339G>A, XM_017008213.1:c.339G>A, NM_001204368.2:c.*34G>A, NM_001204368.1:c.*34G>A, XM_047415701.1:c.339G>A

Select item 139724476412.

rs1397244764 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 4:139695250 (GRCh38)
4:140616404 (GRCh37)
Canonical SPDI:: NC_000004.12:139695249:G:A
Gene:: MGST2 (Varview)
Functional Consequence:: intron_variant,coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: A=0.000047/1 (ALFA)
A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000004.12:g.139695250G>A, NC_000004.11:g.140616404G>A, NM_002413.5:c.212G>A, NM_002413.4:c.212G>A, XM_017008212.3:c.212G>A, XM_017008212.2:c.212G>A, XM_017008212.1:c.212G>A, XM_017008211.3:c.212G>A, XM_017008211.2:c.212G>A, XM_017008211.1:c.212G>A, NM_001204366.2:c.212G>A, NM_001204366.1:c.212G>A, NM_001204367.2:c.8G>A, NM_001204367.1:c.8G>A, XM_017008213.2:c.212G>A, XM_017008213.1:c.212G>A, XM_047415701.1:c.212G>A, NP_002404.1:p.Gly71Glu, XP_016863701.1:p.Gly71Glu, XP_016863700.1:p.Gly71Glu, NP_001191295.1:p.Gly71Glu, NP_001191296.1:p.Gly3Glu, XP_016863702.1:p.Gly71Glu, XP_047271657.1:p.Gly71Glu

Select item 139581179413.

rs1395811794 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 4:139695251 (GRCh38)
4:140616405 (GRCh37)
Canonical SPDI:: NC_000004.12:139695250:G:A
Gene:: MGST2 (Varview)
Functional Consequence:: intron_variant,synonymous_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000004.12:g.139695251G>A, NC_000004.11:g.140616405G>A, NM_002413.5:c.213G>A, NM_002413.4:c.213G>A, XM_017008212.3:c.213G>A, XM_017008212.2:c.213G>A, XM_017008212.1:c.213G>A, XM_017008211.3:c.213G>A, XM_017008211.2:c.213G>A, XM_017008211.1:c.213G>A, NM_001204366.2:c.213G>A, NM_001204366.1:c.213G>A, NM_001204367.2:c.9G>A, NM_001204367.1:c.9G>A, XM_017008213.2:c.213G>A, XM_017008213.1:c.213G>A, XM_047415701.1:c.213G>A

Select item 138014650614.

rs1380146506 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 4:139704104 (GRCh38)
4:140625258 (GRCh37)
Canonical SPDI:: NC_000004.12:139704103:T:A
Gene:: MGST2 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,3_prime_UTR_variant
Validated:: by frequency
MAF:: A=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000004.12:g.139704104T>A, NC_000004.11:g.140625258T>A, NM_002413.5:c.400T>A, NM_002413.4:c.400T>A, XM_017008212.3:c.400T>A, XM_017008212.2:c.400T>A, XM_017008212.1:c.400T>A, XM_017008211.3:c.400T>A, XM_017008211.2:c.400T>A, XM_017008211.1:c.400T>A, NM_001204366.2:c.400T>A, NM_001204366.1:c.400T>A, NM_001204367.2:c.196T>A, NM_001204367.1:c.196T>A, XM_017008213.2:c.400T>A, XM_017008213.1:c.400T>A, NM_001204368.2:c.*95T>A, NM_001204368.1:c.*95T>A, XM_047415701.1:c.400T>A, NP_002404.1:p.Tyr134Asn, XP_016863701.1:p.Tyr134Asn, XP_016863700.1:p.Tyr134Asn, NP_001191295.1:p.Tyr134Asn, NP_001191296.1:p.Tyr66Asn, XP_016863702.1:p.Tyr134Asn, XP_047271657.1:p.Tyr134Asn

Select item 137378415115.

rs1373784151 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 4:139695225 (GRCh38)
4:140616379 (GRCh37)
Canonical SPDI:: NC_000004.12:139695224:T:C
Gene:: MGST2 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,5_prime_UTR_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000011/3 (TOPMED)
C=0.000021/3 (GnomAD)
HGVS:: NC_000004.12:g.139695225T>C, NC_000004.11:g.140616379T>C, NM_002413.5:c.187T>C, NM_002413.4:c.187T>C, XM_017008212.3:c.187T>C, XM_017008212.2:c.187T>C, XM_017008212.1:c.187T>C, XM_017008211.3:c.187T>C, XM_017008211.2:c.187T>C, XM_017008211.1:c.187T>C, NM_001204366.2:c.187T>C, NM_001204366.1:c.187T>C, NM_001204367.2:c.-18T>C, NM_001204367.1:c.-18T>C, XM_017008213.2:c.187T>C, XM_017008213.1:c.187T>C, XM_047415701.1:c.187T>C, NP_002404.1:p.Phe63Leu, XP_016863701.1:p.Phe63Leu, XP_016863700.1:p.Phe63Leu, NP_001191295.1:p.Phe63Leu, XP_016863702.1:p.Phe63Leu, XP_047271657.1:p.Phe63Leu

Select item 133374153716.

rs1333741537 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 4:139695198 (GRCh38)
4:140616352 (GRCh37)
Canonical SPDI:: NC_000004.12:139695197:C:A
Gene:: MGST2 (Varview)
Functional Consequence:: intron_variant,missense_variant,coding_sequence_variant,5_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000071/1 (ALFA)
A=0.000008/1 (ExAC)
A=0.000008/2 (GnomAD_exomes)
A=0.000029/4 (GnomAD)
A=0.000079/21 (TOPMED)
HGVS:: NC_000004.12:g.139695198C>A, NC_000004.11:g.140616352C>A, NM_002413.5:c.160C>A, NM_002413.4:c.160C>A, XM_017008212.3:c.160C>A, XM_017008212.2:c.160C>A, XM_017008212.1:c.160C>A, XM_017008211.3:c.160C>A, XM_017008211.2:c.160C>A, XM_017008211.1:c.160C>A, NM_001204366.2:c.160C>A, NM_001204366.1:c.160C>A, NM_001204367.2:c.-45C>A, NM_001204367.1:c.-45C>A, XM_017008213.2:c.160C>A, XM_017008213.1:c.160C>A, XM_047415701.1:c.160C>A, NP_002404.1:p.Gln54Lys, XP_016863701.1:p.Gln54Lys, XP_016863700.1:p.Gln54Lys, NP_001191295.1:p.Gln54Lys, XP_016863702.1:p.Gln54Lys, XP_047271657.1:p.Gln54Lys

Select item 133263107517.

rs1332631075 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 4:139666054 (GRCh38)
4:140587208 (GRCh37)
Canonical SPDI:: NC_000004.12:139666053:C:G
Gene:: MGST2 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,5_prime_UTR_variant
Validated:: by frequency,by cluster
MAF:: G=0.000007/1 (GnomAD)
HGVS:: NC_000004.12:g.139666054C>G, NC_000004.11:g.140587208C>G, NG_083488.1:g.777C>G, NM_002413.5:c.35C>G, NM_002413.4:c.35C>G, XM_017008212.3:c.35C>G, XM_017008212.2:c.35C>G, XM_017008212.1:c.35C>G, XM_017008211.3:c.35C>G, XM_017008211.2:c.35C>G, XM_017008211.1:c.35C>G, NM_001204366.2:c.35C>G, NM_001204366.1:c.35C>G, NM_001204367.2:c.-70C>G, NM_001204367.1:c.-70C>G, XM_017008213.2:c.35C>G, XM_017008213.1:c.35C>G, NM_001204368.2:c.35C>G, NM_001204368.1:c.35C>G, XM_047415701.1:c.35C>G, NP_002404.1:p.Ser12Cys, XP_016863701.1:p.Ser12Cys, XP_016863700.1:p.Ser12Cys, NP_001191295.1:p.Ser12Cys, XP_016863702.1:p.Ser12Cys, NP_001191297.1:p.Ser12Cys, XP_047271657.1:p.Ser12Cys

Select item 133153302618.

rs1331533026 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 4:139703526 (GRCh38)
4:140624680 (GRCh37)
Canonical SPDI:: NC_000004.12:139703525:G:A
Gene:: MGST2 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000071/1 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000004.12:g.139703526G>A, NC_000004.11:g.140624680G>A, NM_002413.5:c.301G>A, NM_002413.4:c.301G>A, XM_017008212.3:c.301G>A, XM_017008212.2:c.301G>A, XM_017008212.1:c.301G>A, XM_017008211.3:c.301G>A, XM_017008211.2:c.301G>A, XM_017008211.1:c.301G>A, NM_001204366.2:c.301G>A, NM_001204366.1:c.301G>A, NM_001204367.2:c.97G>A, NM_001204367.1:c.97G>A, XM_017008213.2:c.301G>A, XM_017008213.1:c.301G>A, NM_001204368.2:c.230G>A, NM_001204368.1:c.230G>A, XM_047415701.1:c.301G>A, NP_002404.1:p.Ala101Thr, XP_016863701.1:p.Ala101Thr, XP_016863700.1:p.Ala101Thr, NP_001191295.1:p.Ala101Thr, NP_001191296.1:p.Ala33Thr, XP_016863702.1:p.Ala101Thr, NP_001191297.1:p.Cys77Tyr, XP_047271657.1:p.Ala101Thr

Select item 132542952019.

rs1325429520 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A,C [Show Flanks]
Chromosome:: 4:139703514 (GRCh38)
4:140624668 (GRCh37)
Canonical SPDI:: NC_000004.12:139703513:T:A,NC_000004.12:139703513:T:C
Gene:: MGST2 (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)
C=0.000007/1 (GnomAD)
HGVS:: NC_000004.12:g.139703514T>A, NC_000004.12:g.139703514T>C, NC_000004.11:g.140624668T>A, NC_000004.11:g.140624668T>C, NM_002413.5:c.289T>A, NM_002413.5:c.289T>C, NM_002413.4:c.289T>A, NM_002413.4:c.289T>C, XM_017008212.3:c.289T>A, XM_017008212.3:c.289T>C, XM_017008212.2:c.289T>A, XM_017008212.2:c.289T>C, XM_017008212.1:c.289T>A, XM_017008212.1:c.289T>C, XM_017008211.3:c.289T>A, XM_017008211.3:c.289T>C, XM_017008211.2:c.289T>A, XM_017008211.2:c.289T>C, XM_017008211.1:c.289T>A, XM_017008211.1:c.289T>C, NM_001204366.2:c.289T>A, NM_001204366.2:c.289T>C, NM_001204366.1:c.289T>A, NM_001204366.1:c.289T>C, NM_001204367.2:c.85T>A, NM_001204367.2:c.85T>C, NM_001204367.1:c.85T>A, NM_001204367.1:c.85T>C, XM_017008213.2:c.289T>A, XM_017008213.2:c.289T>C, XM_017008213.1:c.289T>A, XM_017008213.1:c.289T>C, NM_001204368.2:c.218T>A, NM_001204368.2:c.218T>C, NM_001204368.1:c.218T>A, NM_001204368.1:c.218T>C, XM_047415701.1:c.289T>A, XM_047415701.1:c.289T>C, NP_002404.1:p.Tyr97Asn, NP_002404.1:p.Tyr97His, XP_016863701.1:p.Tyr97Asn, XP_016863701.1:p.Tyr97His, XP_016863700.1:p.Tyr97Asn, XP_016863700.1:p.Tyr97His, NP_001191295.1:p.Tyr97Asn, NP_001191295.1:p.Tyr97His, NP_001191296.1:p.Tyr29Asn, NP_001191296.1:p.Tyr29His, XP_016863702.1:p.Tyr97Asn, XP_016863702.1:p.Tyr97His, NP_001191297.1:p.Ile73Lys, NP_001191297.1:p.Ile73Thr, XP_047271657.1:p.Tyr97Asn, XP_047271657.1:p.Tyr97His

Select item 131084287120.

rs1310842871 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 4:139678614 (GRCh38)
4:140599768 (GRCh37)
Canonical SPDI:: NC_000004.12:139678613:C:A,NC_000004.12:139678613:C:T
Gene:: MGST2 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0./0 (KOREAN)
T=0.000004/1 (TOPMED)
A=0.000035/1 (TOMMO)
HGVS:: NC_000004.12:g.139678614C>A, NC_000004.12:g.139678614C>T, NC_000004.11:g.140599768C>A, NC_000004.11:g.140599768C>T, NM_002413.5:c.130C>A, NM_002413.5:c.130C>T, NM_002413.4:c.130C>A, NM_002413.4:c.130C>T, XM_017008212.3:c.130C>A, XM_017008212.3:c.130C>T, XM_017008212.2:c.130C>A, XM_017008212.2:c.130C>T, XM_017008212.1:c.130C>A, XM_017008212.1:c.130C>T, XM_017008211.3:c.130C>A, XM_017008211.3:c.130C>T, XM_017008211.2:c.130C>A, XM_017008211.2:c.130C>T, XM_017008211.1:c.130C>A, XM_017008211.1:c.130C>T, NM_001204366.2:c.130C>A, NM_001204366.2:c.130C>T, NM_001204366.1:c.130C>A, NM_001204366.1:c.130C>T, XM_017008213.2:c.130C>A, XM_017008213.2:c.130C>T, XM_017008213.1:c.130C>A, XM_017008213.1:c.130C>T, NM_001204368.2:c.130C>A, NM_001204368.2:c.130C>T, NM_001204368.1:c.130C>A, NM_001204368.1:c.130C>T, XM_047415701.1:c.130C>A, XM_047415701.1:c.130C>T, NP_002404.1:p.Pro44Thr, NP_002404.1:p.Pro44Ser, XP_016863701.1:p.Pro44Thr, XP_016863701.1:p.Pro44Ser, XP_016863700.1:p.Pro44Thr, XP_016863700.1:p.Pro44Ser, NP_001191295.1:p.Pro44Thr, NP_001191295.1:p.Pro44Ser, XP_016863702.1:p.Pro44Thr, XP_016863702.1:p.Pro44Ser, NP_001191297.1:p.Pro44Thr, NP_001191297.1:p.Pro44Ser, XP_047271657.1:p.Pro44Thr, XP_047271657.1:p.Pro44Ser

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Result Filters

Clinical Significance

Validation Status

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Global MAF

Custom range

Additional filters

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Items: 1 to 20 of 146

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