SNP Links for Protein (Select 154707916) - SNP

Select item 14908826901.

rs1490882690 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 4:105845540 (GRCh38)
4:106766697 (GRCh37)
Canonical SPDI:: NC_000004.12:105845539:C:T
Gene:: GSTCD (Varview)
Functional Consequence:: genic_downstream_transcript_variant,missense_variant,coding_sequence_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (GnomAD_exomes)
T=0.000007/1 (GnomAD)
T=0.000008/2 (TOPMED)
HGVS:: NC_000004.12:g.105845540C>T, NC_000004.11:g.106766697C>T, XM_011532252.4:c.1865C>T, XM_011532252.3:c.1865C>T, XM_011532252.2:c.1865C>T, XM_011532252.1:c.1865C>T, XM_011532248.4:c.1865C>T, XM_011532248.3:c.1865C>T, XM_011532248.2:c.1865C>T, XM_011532248.1:c.1865C>T, XM_011532249.4:c.1865C>T, XM_011532249.3:c.1865C>T, XM_011532249.2:c.1865C>T, XM_011532249.1:c.1865C>T, NM_001031720.3:c.1865C>T, NM_024751.3:c.1604C>T, NM_001370181.1:c.1865C>T, XM_047416179.1:c.1604C>T, XP_011530554.1:p.Ser622Phe, XP_011530550.1:p.Ser622Phe, XP_011530551.1:p.Ser622Phe, NP_001026890.2:p.Ser622Phe, NP_079027.2:p.Ser535Phe, NP_001357110.1:p.Ser622Phe, XP_047272135.1:p.Ser535Phe

Select item 14906065622.

rs1490606562 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 4:105726675 (GRCh38)
4:106647832 (GRCh37)
Canonical SPDI:: NC_000004.12:105726674:G:A
Gene:: GSTCD (Varview)
Functional Consequence:: missense_variant,non_coding_transcript_variant,coding_sequence_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000015/4 (TOPMED)
HGVS:: NC_000004.12:g.105726675G>A, NC_000004.11:g.106647832G>A, XM_011532252.4:c.991G>A, XM_011532252.3:c.991G>A, XM_011532252.2:c.991G>A, XM_011532252.1:c.991G>A, XM_011532248.4:c.991G>A, XM_011532248.3:c.991G>A, XM_011532248.2:c.991G>A, XM_011532248.1:c.991G>A, XM_011532249.4:c.991G>A, XM_011532249.3:c.991G>A, XM_011532249.2:c.991G>A, XM_011532249.1:c.991G>A, NM_001031720.3:c.991G>A, NM_024751.3:c.730G>A, XR_938771.2:n.1245G>A, XR_938771.1:n.1251G>A, NM_001370181.1:c.991G>A, XM_047416179.1:c.730G>A, XP_011530554.1:p.Ala331Thr, XP_011530550.1:p.Ala331Thr, XP_011530551.1:p.Ala331Thr, NP_001026890.2:p.Ala331Thr, NP_079027.2:p.Ala244Thr, NP_001357110.1:p.Ala331Thr, XP_047272135.1:p.Ala244Thr

Select item 14891433063.

rs1489143306 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 4:105729460 (GRCh38)
4:106650617 (GRCh37)
Canonical SPDI:: NC_000004.12:105729459:G:A
Gene:: GSTCD (Varview)
Functional Consequence:: missense_variant,non_coding_transcript_variant,coding_sequence_variant
Validated:: by frequency,by cluster
MAF:: A=0.000008/2 (GnomAD_exomes)
A=0.000071/1 (TOMMO)
HGVS:: NC_000004.12:g.105729460G>A, NC_000004.11:g.106650617G>A, XM_011532252.4:c.1201G>A, XM_011532252.3:c.1201G>A, XM_011532252.2:c.1201G>A, XM_011532252.1:c.1201G>A, XM_011532248.4:c.1201G>A, XM_011532248.3:c.1201G>A, XM_011532248.2:c.1201G>A, XM_011532248.1:c.1201G>A, XM_011532249.4:c.1201G>A, XM_011532249.3:c.1201G>A, XM_011532249.2:c.1201G>A, XM_011532249.1:c.1201G>A, NM_001031720.3:c.1201G>A, NM_024751.3:c.940G>A, XR_938771.2:n.1455G>A, XR_938771.1:n.1461G>A, NM_001370181.1:c.1201G>A, XM_047416179.1:c.940G>A, XP_011530554.1:p.Asp401Asn, XP_011530550.1:p.Asp401Asn, XP_011530551.1:p.Asp401Asn, NP_001026890.2:p.Asp401Asn, NP_079027.2:p.Asp314Asn, NP_001357110.1:p.Asp401Asn, XP_047272135.1:p.Asp314Asn

Select item 14879615264.

rs1487961526 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 4:105837882 (GRCh38)
4:106759039 (GRCh37)
Canonical SPDI:: NC_000004.12:105837881:C:A
Gene:: GSTCD (Varview), LOC124900749 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,non_coding_transcript_variant,coding_sequence_variant,stop_gained
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000008/2 (TOPMED)
HGVS:: NC_000004.12:g.105837882C>A, NC_000004.11:g.106759039C>A, XM_011532252.4:c.1688C>A, XM_011532252.3:c.1688C>A, XM_011532252.2:c.1688C>A, XM_011532252.1:c.1688C>A, XM_011532248.4:c.1688C>A, XM_011532248.3:c.1688C>A, XM_011532248.2:c.1688C>A, XM_011532248.1:c.1688C>A, XM_011532249.4:c.1688C>A, XM_011532249.3:c.1688C>A, XM_011532249.2:c.1688C>A, XM_011532249.1:c.1688C>A, NM_001031720.3:c.1688C>A, NM_024751.3:c.1427C>A, XR_007058216.1:n.3739G>T, NM_001370181.1:c.1688C>A, XM_047416179.1:c.1427C>A, XP_011530554.1:p.Ser563Ter, XP_011530550.1:p.Ser563Ter, XP_011530551.1:p.Ser563Ter, NP_001026890.2:p.Ser563Ter, NP_079027.2:p.Ser476Ter, NP_001357110.1:p.Ser563Ter, XP_047272135.1:p.Ser476Ter

Select item 14857393425.

rs1485739342 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 4:105729413 (GRCh38)
4:106650570 (GRCh37)
Canonical SPDI:: NC_000004.12:105729412:G:A
Gene:: GSTCD (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000004.12:g.105729413G>A, NC_000004.11:g.106650570G>A, XM_011532252.4:c.1154G>A, XM_011532252.3:c.1154G>A, XM_011532252.2:c.1154G>A, XM_011532252.1:c.1154G>A, XM_011532248.4:c.1154G>A, XM_011532248.3:c.1154G>A, XM_011532248.2:c.1154G>A, XM_011532248.1:c.1154G>A, XM_011532249.4:c.1154G>A, XM_011532249.3:c.1154G>A, XM_011532249.2:c.1154G>A, XM_011532249.1:c.1154G>A, NM_001031720.3:c.1154G>A, NM_024751.3:c.893G>A, XR_938771.2:n.1408G>A, XR_938771.1:n.1414G>A, NM_001370181.1:c.1154G>A, XM_047416179.1:c.893G>A, XP_011530554.1:p.Gly385Asp, XP_011530550.1:p.Gly385Asp, XP_011530551.1:p.Gly385Asp, NP_001026890.2:p.Gly385Asp, NP_079027.2:p.Gly298Asp, NP_001357110.1:p.Gly385Asp, XP_047272135.1:p.Gly298Asp

Select item 14851919086.

rs1485191908 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 4:105717635 (GRCh38)
4:106638792 (GRCh37)
Canonical SPDI:: NC_000004.12:105717634:C:T
Gene:: GSTCD (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,non_coding_transcript_variant
Validated:: by frequency
MAF:: T=0.000005/1 (GnomAD_exomes)
HGVS:: NC_000004.12:g.105717635C>T, NC_000004.11:g.106638792C>T, XM_011532252.4:c.22C>T, XM_011532252.3:c.22C>T, XM_011532252.2:c.22C>T, XM_011532252.1:c.22C>T, XM_011532248.4:c.22C>T, XM_011532248.3:c.22C>T, XM_011532248.2:c.22C>T, XM_011532248.1:c.22C>T, XM_011532249.4:c.22C>T, XM_011532249.3:c.22C>T, XM_011532249.2:c.22C>T, XM_011532249.1:c.22C>T, NM_001031720.3:c.22C>T, NM_024751.3:c.22C>T, XR_938771.2:n.276C>T, XR_938771.1:n.282C>T, NM_001370181.1:c.22C>T, XM_047416179.1:c.22C>T, XP_011530554.1:p.Leu8Phe, XP_011530550.1:p.Leu8Phe, XP_011530551.1:p.Leu8Phe, NP_001026890.2:p.Leu8Phe, NP_079027.2:p.Leu8Phe, NP_001357110.1:p.Leu8Phe, XP_047272135.1:p.Leu8Phe

Select item 14833384557.

rs1483338455 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 4:105719182 (GRCh38)
4:106640339 (GRCh37)
Canonical SPDI:: NC_000004.12:105719181:T:C
Gene:: GSTCD (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant,non_coding_transcript_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_000004.12:g.105719182T>C, NC_000004.11:g.106640339T>C, XM_011532252.4:c.549T>C, XM_011532252.3:c.549T>C, XM_011532252.2:c.549T>C, XM_011532252.1:c.549T>C, XM_011532248.4:c.549T>C, XM_011532248.3:c.549T>C, XM_011532248.2:c.549T>C, XM_011532248.1:c.549T>C, XM_011532249.4:c.549T>C, XM_011532249.3:c.549T>C, XM_011532249.2:c.549T>C, XM_011532249.1:c.549T>C, NM_001031720.3:c.549T>C, NM_024751.3:c.288T>C, XR_938771.2:n.803T>C, XR_938771.1:n.809T>C, NM_001370181.1:c.549T>C, XM_047416179.1:c.288T>C

Select item 14830241478.

rs1483024147 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 4:105825755 (GRCh38)
4:106746912 (GRCh37)
Canonical SPDI:: NC_000004.12:105825754:C:A
Gene:: GSTCD (Varview), GSTCD-AS1 (Varview)
Functional Consequence:: intron_variant,coding_sequence_variant,non_coding_transcript_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000029/4 (GnomAD)
A=0.000049/13 (TOPMED)
A=0.000156/1 (1000Genomes)
HGVS:: NC_000004.12:g.105825755C>A, NC_000004.11:g.106746912C>A, XM_011532252.4:c.1485C>A, XM_011532252.3:c.1485C>A, XM_011532252.2:c.1485C>A, XM_011532252.1:c.1485C>A, XM_011532248.4:c.1485C>A, XM_011532248.3:c.1485C>A, XM_011532248.2:c.1485C>A, XM_011532248.1:c.1485C>A, XM_011532249.4:c.1485C>A, XM_011532249.3:c.1485C>A, XM_011532249.2:c.1485C>A, XM_011532249.1:c.1485C>A, NM_001031720.3:c.1485C>A, NM_024751.3:c.1224C>A, XR_938771.2:n.1739C>A, XR_938771.1:n.1745C>A, NM_001370181.1:c.1485C>A, XM_047416179.1:c.1224C>A, XP_011530554.1:p.Phe495Leu, XP_011530550.1:p.Phe495Leu, XP_011530551.1:p.Phe495Leu, NP_001026890.2:p.Phe495Leu, NP_079027.2:p.Phe408Leu, NP_001357110.1:p.Phe495Leu, XP_047272135.1:p.Phe408Leu

Select item 14797611939.

rs1479761193 [Homo sapiens]

Variant type:: INS
Alleles:: ->A [Show Flanks]
Chromosome:: 4:105842111 (GRCh38)
4:106763269 (GRCh37)
Canonical SPDI:: NC_000004.12:105842111::A
Gene:: GSTCD (Varview), LOC124900749 (Varview)
Functional Consequence:: coding_sequence_variant,upstream_transcript_variant,genic_downstream_transcript_variant,frameshift_variant,2KB_upstream_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_000004.12:g.105842111_105842112insA, NC_000004.11:g.106763268_106763269insA, XM_011532252.4:c.1742_1743insA, XM_011532252.3:c.1742_1743insA, XM_011532252.2:c.1742_1743insA, XM_011532252.1:c.1742_1743insA, XM_011532248.4:c.1742_1743insA, XM_011532248.3:c.1742_1743insA, XM_011532248.2:c.1742_1743insA, XM_011532248.1:c.1742_1743insA, XM_011532249.4:c.1742_1743insA, XM_011532249.3:c.1742_1743insA, XM_011532249.2:c.1742_1743insA, XM_011532249.1:c.1742_1743insA, NM_001031720.3:c.1742_1743insA, NM_024751.3:c.1481_1482insA, NM_001370181.1:c.1742_1743insA, XM_047416179.1:c.1481_1482insA, XP_011530554.1:p.Pro583fs, XP_011530550.1:p.Pro583fs, XP_011530551.1:p.Pro583fs, NP_001026890.2:p.Pro583fs, NP_079027.2:p.Pro496fs, NP_001357110.1:p.Pro583fs, XP_047272135.1:p.Pro496fs

Select item 147909838910.

rs1479098389 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 4:105834505 (GRCh38)
4:106755662 (GRCh37)
Canonical SPDI:: NC_000004.12:105834504:G:A
Gene:: GSTCD (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant,non_coding_transcript_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_000004.12:g.105834505G>A, NC_000004.11:g.106755662G>A, XM_011532252.4:c.1575G>A, XM_011532252.3:c.1575G>A, XM_011532252.2:c.1575G>A, XM_011532252.1:c.1575G>A, XM_011532248.4:c.1575G>A, XM_011532248.3:c.1575G>A, XM_011532248.2:c.1575G>A, XM_011532248.1:c.1575G>A, XM_011532249.4:c.1575G>A, XM_011532249.3:c.1575G>A, XM_011532249.2:c.1575G>A, XM_011532249.1:c.1575G>A, NM_001031720.3:c.1575G>A, NM_024751.3:c.1314G>A, XR_938771.2:n.1936G>A, XR_938771.1:n.1942G>A, NM_001370181.1:c.1575G>A, XM_047416179.1:c.1314G>A

Select item 147541038611.

rs1475410386 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 4:105719297 (GRCh38)
4:106640454 (GRCh37)
Canonical SPDI:: NC_000004.12:105719296:C:T
Gene:: GSTCD (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,non_coding_transcript_variant
Validated:: by frequency,by cluster
MAF:: T=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000004.12:g.105719297C>T, NC_000004.11:g.106640454C>T, XM_011532252.4:c.664C>T, XM_011532252.3:c.664C>T, XM_011532252.2:c.664C>T, XM_011532252.1:c.664C>T, XM_011532248.4:c.664C>T, XM_011532248.3:c.664C>T, XM_011532248.2:c.664C>T, XM_011532248.1:c.664C>T, XM_011532249.4:c.664C>T, XM_011532249.3:c.664C>T, XM_011532249.2:c.664C>T, XM_011532249.1:c.664C>T, NM_001031720.3:c.664C>T, NM_024751.3:c.403C>T, XR_938771.2:n.918C>T, XR_938771.1:n.924C>T, NM_001370181.1:c.664C>T, XM_047416179.1:c.403C>T, XP_011530554.1:p.His222Tyr, XP_011530550.1:p.His222Tyr, XP_011530551.1:p.His222Tyr, NP_001026890.2:p.His222Tyr, NP_079027.2:p.His135Tyr, NP_001357110.1:p.His222Tyr, XP_047272135.1:p.His135Tyr

Select item 147342383512.

rs1473423835 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 4:105845457 (GRCh38)
4:106766614 (GRCh37)
Canonical SPDI:: NC_000004.12:105845456:C:A
Gene:: GSTCD (Varview)
Functional Consequence:: stop_gained,coding_sequence_variant,genic_downstream_transcript_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
HGVS:: NC_000004.12:g.105845457C>A, NC_000004.11:g.106766614C>A, XM_011532252.4:c.1782C>A, XM_011532252.3:c.1782C>A, XM_011532252.2:c.1782C>A, XM_011532252.1:c.1782C>A, XM_011532248.4:c.1782C>A, XM_011532248.3:c.1782C>A, XM_011532248.2:c.1782C>A, XM_011532248.1:c.1782C>A, XM_011532249.4:c.1782C>A, XM_011532249.3:c.1782C>A, XM_011532249.2:c.1782C>A, XM_011532249.1:c.1782C>A, NM_001031720.3:c.1782C>A, NM_024751.3:c.1521C>A, NM_001370181.1:c.1782C>A, XM_047416179.1:c.1521C>A, XP_011530554.1:p.Cys594Ter, XP_011530550.1:p.Cys594Ter, XP_011530551.1:p.Cys594Ter, NP_001026890.2:p.Cys594Ter, NP_079027.2:p.Cys507Ter, NP_001357110.1:p.Cys594Ter, XP_047272135.1:p.Cys507Ter

Select item 147195515413.

rs1471955154 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 4:105719309 (GRCh38)
4:106640466 (GRCh37)
Canonical SPDI:: NC_000004.12:105719308:A:G
Gene:: GSTCD (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,non_coding_transcript_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000004.12:g.105719309A>G, NC_000004.11:g.106640466A>G, XM_011532252.4:c.676A>G, XM_011532252.3:c.676A>G, XM_011532252.2:c.676A>G, XM_011532252.1:c.676A>G, XM_011532248.4:c.676A>G, XM_011532248.3:c.676A>G, XM_011532248.2:c.676A>G, XM_011532248.1:c.676A>G, XM_011532249.4:c.676A>G, XM_011532249.3:c.676A>G, XM_011532249.2:c.676A>G, XM_011532249.1:c.676A>G, NM_001031720.3:c.676A>G, NM_024751.3:c.415A>G, XR_938771.2:n.930A>G, XR_938771.1:n.936A>G, NM_001370181.1:c.676A>G, XM_047416179.1:c.415A>G, XP_011530554.1:p.Thr226Ala, XP_011530550.1:p.Thr226Ala, XP_011530551.1:p.Thr226Ala, NP_001026890.2:p.Thr226Ala, NP_079027.2:p.Thr139Ala, NP_001357110.1:p.Thr226Ala, XP_047272135.1:p.Thr139Ala

Select item 146987399914.

rs1469873999 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 4:105719216 (GRCh38)
4:106640373 (GRCh37)
Canonical SPDI:: NC_000004.12:105719215:C:T
Gene:: GSTCD (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
HGVS:: NC_000004.12:g.105719216C>T, NC_000004.11:g.106640373C>T, XM_011532252.4:c.583C>T, XM_011532252.3:c.583C>T, XM_011532252.2:c.583C>T, XM_011532252.1:c.583C>T, XM_011532248.4:c.583C>T, XM_011532248.3:c.583C>T, XM_011532248.2:c.583C>T, XM_011532248.1:c.583C>T, XM_011532249.4:c.583C>T, XM_011532249.3:c.583C>T, XM_011532249.2:c.583C>T, XM_011532249.1:c.583C>T, NM_001031720.3:c.583C>T, NM_024751.3:c.322C>T, XR_938771.2:n.837C>T, XR_938771.1:n.843C>T, NM_001370181.1:c.583C>T, XM_047416179.1:c.322C>T, XP_011530554.1:p.Leu195Phe, XP_011530550.1:p.Leu195Phe, XP_011530551.1:p.Leu195Phe, NP_001026890.2:p.Leu195Phe, NP_079027.2:p.Leu108Phe, NP_001357110.1:p.Leu195Phe, XP_047272135.1:p.Leu108Phe

Select item 146958879015.

rs1469588790 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 4:105825747 (GRCh38)
4:106746904 (GRCh37)
Canonical SPDI:: NC_000004.12:105825746:A:G
Gene:: GSTCD (Varview), GSTCD-AS1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,non_coding_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (GnomAD_exomes)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000004.12:g.105825747A>G, NC_000004.11:g.106746904A>G, XM_011532252.4:c.1477A>G, XM_011532252.3:c.1477A>G, XM_011532252.2:c.1477A>G, XM_011532252.1:c.1477A>G, XM_011532248.4:c.1477A>G, XM_011532248.3:c.1477A>G, XM_011532248.2:c.1477A>G, XM_011532248.1:c.1477A>G, XM_011532249.4:c.1477A>G, XM_011532249.3:c.1477A>G, XM_011532249.2:c.1477A>G, XM_011532249.1:c.1477A>G, NM_001031720.3:c.1477A>G, NM_024751.3:c.1216A>G, XR_938771.2:n.1731A>G, XR_938771.1:n.1737A>G, NM_001370181.1:c.1477A>G, XM_047416179.1:c.1216A>G, XP_011530554.1:p.Ile493Val, XP_011530550.1:p.Ile493Val, XP_011530551.1:p.Ile493Val, NP_001026890.2:p.Ile493Val, NP_079027.2:p.Ile406Val, NP_001357110.1:p.Ile493Val, XP_047272135.1:p.Ile406Val

Select item 146749663916.

rs1467496639 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C,G [Show Flanks]
Chromosome:: 4:105719174 (GRCh38)
4:106640331 (GRCh37)
Canonical SPDI:: NC_000004.12:105719173:A:C,NC_000004.12:105719173:A:G
Gene:: GSTCD (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
HGVS:: NC_000004.12:g.105719174A>C, NC_000004.12:g.105719174A>G, NC_000004.11:g.106640331A>C, NC_000004.11:g.106640331A>G, XM_011532252.4:c.541A>C, XM_011532252.4:c.541A>G, XM_011532252.3:c.541A>C, XM_011532252.3:c.541A>G, XM_011532252.2:c.541A>C, XM_011532252.2:c.541A>G, XM_011532252.1:c.541A>C, XM_011532252.1:c.541A>G, XM_011532248.4:c.541A>C, XM_011532248.4:c.541A>G, XM_011532248.3:c.541A>C, XM_011532248.3:c.541A>G, XM_011532248.2:c.541A>C, XM_011532248.2:c.541A>G, XM_011532248.1:c.541A>C, XM_011532248.1:c.541A>G, XM_011532249.4:c.541A>C, XM_011532249.4:c.541A>G, XM_011532249.3:c.541A>C, XM_011532249.3:c.541A>G, XM_011532249.2:c.541A>C, XM_011532249.2:c.541A>G, XM_011532249.1:c.541A>C, XM_011532249.1:c.541A>G, NM_001031720.3:c.541A>C, NM_001031720.3:c.541A>G, NM_024751.3:c.280A>C, NM_024751.3:c.280A>G, XR_938771.2:n.795A>C, XR_938771.2:n.795A>G, XR_938771.1:n.801A>C, XR_938771.1:n.801A>G, NM_001370181.1:c.541A>C, NM_001370181.1:c.541A>G, XM_047416179.1:c.280A>C, XM_047416179.1:c.280A>G, XP_011530554.1:p.Lys181Gln, XP_011530554.1:p.Lys181Glu, XP_011530550.1:p.Lys181Gln, XP_011530550.1:p.Lys181Glu, XP_011530551.1:p.Lys181Gln, XP_011530551.1:p.Lys181Glu, NP_001026890.2:p.Lys181Gln, NP_001026890.2:p.Lys181Glu, NP_079027.2:p.Lys94Gln, NP_079027.2:p.Lys94Glu, NP_001357110.1:p.Lys181Gln, NP_001357110.1:p.Lys181Glu, XP_047272135.1:p.Lys94Gln, XP_047272135.1:p.Lys94Glu

Select item 146636061817.

rs1466360618 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 4:105726815 (GRCh38)
4:106647972 (GRCh37)
Canonical SPDI:: NC_000004.12:105726814:C:A
Gene:: GSTCD (Varview)
Functional Consequence:: coding_sequence_variant,non_coding_transcript_variant,synonymous_variant
Validated:: by frequency
MAF:: A=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000004.12:g.105726815C>A, NC_000004.11:g.106647972C>A, XM_011532252.4:c.1131C>A, XM_011532252.3:c.1131C>A, XM_011532252.2:c.1131C>A, XM_011532252.1:c.1131C>A, XM_011532248.4:c.1131C>A, XM_011532248.3:c.1131C>A, XM_011532248.2:c.1131C>A, XM_011532248.1:c.1131C>A, XM_011532249.4:c.1131C>A, XM_011532249.3:c.1131C>A, XM_011532249.2:c.1131C>A, XM_011532249.1:c.1131C>A, NM_001031720.3:c.1131C>A, NM_024751.3:c.870C>A, XR_938771.2:n.1385C>A, XR_938771.1:n.1391C>A, NM_001370181.1:c.1131C>A, XM_047416179.1:c.870C>A

Select item 146618116718.

rs1466181167 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 4:105825792 (GRCh38)
4:106746949 (GRCh37)
Canonical SPDI:: NC_000004.12:105825791:A:G
Gene:: GSTCD (Varview), GSTCD-AS1 (Varview)
Functional Consequence:: missense_variant,coding_sequence_variant,non_coding_transcript_variant,intron_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000004.12:g.105825792A>G, NC_000004.11:g.106746949A>G, XM_011532252.4:c.1522A>G, XM_011532252.3:c.1522A>G, XM_011532252.2:c.1522A>G, XM_011532252.1:c.1522A>G, XM_011532248.4:c.1522A>G, XM_011532248.3:c.1522A>G, XM_011532248.2:c.1522A>G, XM_011532248.1:c.1522A>G, XM_011532249.4:c.1522A>G, XM_011532249.3:c.1522A>G, XM_011532249.2:c.1522A>G, XM_011532249.1:c.1522A>G, NM_001031720.3:c.1522A>G, NM_024751.3:c.1261A>G, XR_938771.2:n.1776A>G, XR_938771.1:n.1782A>G, NM_001370181.1:c.1522A>G, XM_047416179.1:c.1261A>G, XP_011530554.1:p.Asn508Asp, XP_011530550.1:p.Asn508Asp, XP_011530551.1:p.Asn508Asp, NP_001026890.2:p.Asn508Asp, NP_079027.2:p.Asn421Asp, NP_001357110.1:p.Asn508Asp, XP_047272135.1:p.Asn421Asp

Select item 146524538819.

rs1465245388 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 4:105719233 (GRCh38)
4:106640390 (GRCh37)
Canonical SPDI:: NC_000004.12:105719232:C:T
Gene:: GSTCD (Varview)
Functional Consequence:: coding_sequence_variant,non_coding_transcript_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (GnomAD_exomes)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000004.12:g.105719233C>T, NC_000004.11:g.106640390C>T, XM_011532252.4:c.600C>T, XM_011532252.3:c.600C>T, XM_011532252.2:c.600C>T, XM_011532252.1:c.600C>T, XM_011532248.4:c.600C>T, XM_011532248.3:c.600C>T, XM_011532248.2:c.600C>T, XM_011532248.1:c.600C>T, XM_011532249.4:c.600C>T, XM_011532249.3:c.600C>T, XM_011532249.2:c.600C>T, XM_011532249.1:c.600C>T, NM_001031720.3:c.600C>T, NM_024751.3:c.339C>T, XR_938771.2:n.854C>T, XR_938771.1:n.860C>T, NM_001370181.1:c.600C>T, XM_047416179.1:c.339C>T

Select item 146258379320.

rs1462583793 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 4:105834502 (GRCh38)
4:106755659 (GRCh37)
Canonical SPDI:: NC_000004.12:105834501:T:G
Gene:: GSTCD (Varview)
Functional Consequence:: non_coding_transcript_variant,coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000071/1 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000004.12:g.105834502T>G, NC_000004.11:g.106755659T>G, XM_011532252.4:c.1572T>G, XM_011532252.3:c.1572T>G, XM_011532252.2:c.1572T>G, XM_011532252.1:c.1572T>G, XM_011532248.4:c.1572T>G, XM_011532248.3:c.1572T>G, XM_011532248.2:c.1572T>G, XM_011532248.1:c.1572T>G, XM_011532249.4:c.1572T>G, XM_011532249.3:c.1572T>G, XM_011532249.2:c.1572T>G, XM_011532249.1:c.1572T>G, NM_001031720.3:c.1572T>G, NM_024751.3:c.1311T>G, XR_938771.2:n.1933T>G, XR_938771.1:n.1939T>G, NM_001370181.1:c.1572T>G, XM_047416179.1:c.1311T>G, XP_011530554.1:p.Ile524Met, XP_011530550.1:p.Ile524Met, XP_011530551.1:p.Ile524Met, NP_001026890.2:p.Ile524Met, NP_079027.2:p.Ile437Met, NP_001357110.1:p.Ile524Met, XP_047272135.1:p.Ile437Met

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Result Filters

Validation Status

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Custom range

Additional filters

Display Settings:

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Items: 1 to 20 of 513

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