SNP Links for Protein (Select 95113651) - SNP

Links from Protein

Items: 1 to 20 of 321

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Select item 14883420811.

rs1488342081 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 10:130160015 (GRCh38)
10:131958279 (GRCh37)
Canonical SPDI:: NC_000010.11:130160014:T:C
Gene:: GLRX3 (Varview)
Functional Consequence:: synonymous_variant,coding_sequence_variant,5_prime_UTR_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000010.11:g.130160015T>C, NC_000010.10:g.131958279T>C, NG_029886.1:g.28641T>C, NM_006541.5:c.222T>C, NM_006541.4:c.222T>C, NM_001321980.2:c.-217T>C, NM_001321980.1:c.-217T>C, NM_001199868.2:c.222T>C, NM_001199868.1:c.222T>C

Select item 14820983102.

rs1482098310 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 10:130166635 (GRCh38)
10:131964899 (GRCh37)
Canonical SPDI:: NC_000010.11:130166634:C:G
Gene:: GLRX3 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000010.11:g.130166635C>G, NC_000010.10:g.131964899C>G, NG_029886.1:g.35261C>G, NM_006541.5:c.607C>G, NM_006541.4:c.607C>G, NM_001321980.2:c.169C>G, NM_001321980.1:c.169C>G, NM_001199868.2:c.607C>G, NM_001199868.1:c.607C>G, NP_006532.2:p.Leu203Val, NP_001308909.1:p.Leu57Val, NP_001186797.1:p.Leu203Val

Select item 14803106503.

rs1480310650 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 10:130160894 (GRCh38)
10:131959158 (GRCh37)
Canonical SPDI:: NC_000010.11:130160893:T:C
Gene:: GLRX3 (Varview)
Functional Consequence:: coding_sequence_variant,5_prime_UTR_variant,synonymous_variant
Validated:: by frequency
MAF:: C=0.000008/2 (GnomAD_exomes)
HGVS:: NC_000010.11:g.130160894T>C, NC_000010.10:g.131959158T>C, NG_029886.1:g.29520T>C, NM_006541.5:c.375T>C, NM_006541.4:c.375T>C, NM_001321980.2:c.-64T>C, NM_001321980.1:c.-64T>C, NM_001199868.2:c.375T>C, NM_001199868.1:c.375T>C

Select item 14781329244.

rs1478132924 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 10:130145281 (GRCh38)
10:131943545 (GRCh37)
Canonical SPDI:: NC_000010.11:130145280:G:C
Gene:: GLRX3 (Varview)
Functional Consequence:: coding_sequence_variant,5_prime_UTR_variant,missense_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000010.11:g.130145281G>C, NC_000010.10:g.131943545G>C, NG_029886.1:g.13907G>C, NM_006541.5:c.163G>C, NM_006541.4:c.163G>C, NM_001321980.2:c.-365G>C, NM_001321980.1:c.-365G>C, NM_001199868.2:c.163G>C, NM_001199868.1:c.163G>C, NP_006532.2:p.Glu55Gln, NP_001186797.1:p.Glu55Gln

Select item 14780216835.

rs1478021683 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 10:130166668 (GRCh38)
10:131964932 (GRCh37)
Canonical SPDI:: NC_000010.11:130166667:G:C
Gene:: GLRX3 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa
MAF:: C=0.000047/1 (ALFA)
C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000010.11:g.130166668G>C, NC_000010.10:g.131964932G>C, NG_029886.1:g.35294G>C, NM_006541.5:c.640G>C, NM_006541.4:c.640G>C, NM_001321980.2:c.202G>C, NM_001321980.1:c.202G>C, NM_001199868.2:c.640G>C, NM_001199868.1:c.640G>C, NP_006532.2:p.Asp214His, NP_001308909.1:p.Asp68His, NP_001186797.1:p.Asp214His

Select item 14773535906.

rs1477353590 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 10:130175032 (GRCh38)
10:131973296 (GRCh37)
Canonical SPDI:: NC_000010.11:130175031:A:G
Gene:: GLRX3 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (GnomAD_exomes)
G=0.000004/1 (TOPMED)
HGVS:: NC_000010.11:g.130175032A>G, NC_000010.10:g.131973296A>G, NG_029886.1:g.43658A>G, NM_006541.5:c.900A>G, NM_006541.4:c.900A>G, NM_001321980.2:c.462A>G, NM_001321980.1:c.462A>G, NM_001199868.2:c.900A>G, NM_001199868.1:c.900A>G

Select item 14746928177.

rs1474692817 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 10:130145220 (GRCh38)
10:131943484 (GRCh37)
Canonical SPDI:: NC_000010.11:130145219:T:C
Gene:: GLRX3 (Varview)
Functional Consequence:: coding_sequence_variant,5_prime_UTR_variant,synonymous_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
C=0.000011/3 (TOPMED)
HGVS:: NC_000010.11:g.130145220T>C, NC_000010.10:g.131943484T>C, NG_029886.1:g.13846T>C, NM_006541.5:c.102T>C, NM_006541.4:c.102T>C, NM_001321980.2:c.-426T>C, NM_001321980.1:c.-426T>C, NM_001199868.2:c.102T>C, NM_001199868.1:c.102T>C

Select item 14689055448.

rs1468905544 [Homo sapiens]

Variant type:: SNV
Alleles:: A>C [Show Flanks]
Chromosome:: 10:130160839 (GRCh38)
10:131959103 (GRCh37)
Canonical SPDI:: NC_000010.11:130160838:A:C
Gene:: GLRX3 (Varview)
Functional Consequence:: coding_sequence_variant,5_prime_UTR_variant,missense_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000010.11:g.130160839A>C, NC_000010.10:g.131959103A>C, NG_029886.1:g.29465A>C, NM_006541.5:c.320A>C, NM_006541.4:c.320A>C, NM_001321980.2:c.-119A>C, NM_001321980.1:c.-119A>C, NM_001199868.2:c.320A>C, NM_001199868.1:c.320A>C, NP_006532.2:p.Glu107Ala, NP_001186797.1:p.Glu107Ala

Select item 14683708479.

rs1468370847 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 10:130145290 (GRCh38)
10:131943554 (GRCh37)
Canonical SPDI:: NC_000010.11:130145289:A:G
Gene:: GLRX3 (Varview)
Functional Consequence:: coding_sequence_variant,5_prime_UTR_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000071/1 (ALFA)
G=0.000015/4 (TOPMED)
HGVS:: NC_000010.11:g.130145290A>G, NC_000010.10:g.131943554A>G, NG_029886.1:g.13916A>G, NM_006541.5:c.172A>G, NM_006541.4:c.172A>G, NM_001321980.2:c.-356A>G, NM_001321980.1:c.-356A>G, NM_001199868.2:c.172A>G, NM_001199868.1:c.172A>G, NP_006532.2:p.Lys58Glu, NP_001186797.1:p.Lys58Glu

Select item 146656271310.

rs1466562713 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A,T [Show Flanks]
Chromosome:: 10:130171594 (GRCh38)
10:131969858 (GRCh37)
Canonical SPDI:: NC_000010.11:130171593:G:A,NC_000010.11:130171593:G:T
Gene:: GLRX3 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000010.11:g.130171594G>A, NC_000010.11:g.130171594G>T, NC_000010.10:g.131969858G>A, NC_000010.10:g.131969858G>T, NG_029886.1:g.40220G>A, NG_029886.1:g.40220G>T, NM_006541.5:c.782G>A, NM_006541.5:c.782G>T, NM_006541.4:c.782G>A, NM_006541.4:c.782G>T, NM_001321980.2:c.344G>A, NM_001321980.2:c.344G>T, NM_001321980.1:c.344G>A, NM_001321980.1:c.344G>T, NM_001199868.2:c.782G>A, NM_001199868.2:c.782G>T, NM_001199868.1:c.782G>A, NM_001199868.1:c.782G>T, NP_006532.2:p.Cys261Tyr, NP_006532.2:p.Cys261Phe, NP_001308909.1:p.Cys115Tyr, NP_001308909.1:p.Cys115Phe, NP_001186797.1:p.Cys261Tyr, NP_001186797.1:p.Cys261Phe

Select item 146136103211.

rs1461361032 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 10:130145213 (GRCh38)
10:131943477 (GRCh37)
Canonical SPDI:: NC_000010.11:130145212:C:G
Gene:: GLRX3 (Varview)
Functional Consequence:: coding_sequence_variant,5_prime_UTR_variant,missense_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000010.11:g.130145213C>G, NC_000010.10:g.131943477C>G, NG_029886.1:g.13839C>G, NM_006541.5:c.95C>G, NM_006541.4:c.95C>G, NM_001321980.2:c.-433C>G, NM_001321980.1:c.-433C>G, NM_001199868.2:c.95C>G, NM_001199868.1:c.95C>G, NP_006532.2:p.Ser32Cys, NP_001186797.1:p.Ser32Cys

Select item 145968037412.

rs1459680374 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 10:130166955 (GRCh38)
10:131965219 (GRCh37)
Canonical SPDI:: NC_000010.11:130166954:C:T
Gene:: GLRX3 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
T=0.000014/2 (GnomAD)
HGVS:: NC_000010.11:g.130166955C>T, NC_000010.10:g.131965219C>T, NG_029886.1:g.35581C>T, NM_006541.5:c.688C>T, NM_006541.4:c.688C>T, NM_001321980.2:c.250C>T, NM_001321980.1:c.250C>T, NM_001199868.2:c.688C>T, NM_001199868.1:c.688C>T, NP_006532.2:p.Pro230Ser, NP_001308909.1:p.Pro84Ser, NP_001186797.1:p.Pro230Ser

Select item 145668021313.

rs1456680213 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 10:130160059 (GRCh38)
10:131958323 (GRCh37)
Canonical SPDI:: NC_000010.11:130160058:T:G
Gene:: GLRX3 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant,5_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000010.11:g.130160059T>G, NC_000010.10:g.131958323T>G, NG_029886.1:g.28685T>G, NM_006541.5:c.266T>G, NM_006541.4:c.266T>G, NM_001321980.2:c.-173T>G, NM_001321980.1:c.-173T>G, NM_001199868.2:c.266T>G, NM_001199868.1:c.266T>G, NP_006532.2:p.Leu89Arg, NP_001186797.1:p.Leu89Arg

Select item 145273023814.

rs1452730238 [Homo sapiens]

Variant type:: DELINS
Alleles:: G>-,GG [Show Flanks]
Chromosome:: 10:130136429 (GRCh38)
10:131934693 (GRCh37)
Canonical SPDI:: NC_000010.11:130136428:GGGGG:GGGG,NC_000010.11:130136428:GGGGG:GGGGGG
Gene:: GLRX3 (Varview), LOC105378561 (Varview)
Functional Consequence:: 5_prime_UTR_variant,frameshift_variant,upstream_transcript_variant,coding_sequence_variant,2KB_upstream_variant
Validated:: by frequency,by cluster
MAF:: -=0.0255/108 (GoESP)
HGVS:: NC_000010.11:g.130136433del, NC_000010.11:g.130136433dup, NC_000010.10:g.131934697del, NC_000010.10:g.131934697dup, NG_029886.1:g.5059del, NG_029886.1:g.5059dup, NM_006541.5:c.13del, NM_006541.5:c.13dup, NM_006541.4:c.13del, NM_006541.4:c.13dup, NM_001321980.2:c.-515del, NM_001321980.2:c.-515dup, NM_001321980.1:c.-515del, NM_001321980.1:c.-515dup, NM_001199868.2:c.13del, NM_001199868.2:c.13dup, NM_001199868.1:c.13del, NM_001199868.1:c.13dup, NP_006532.2:p.Ala5fs, NP_006532.2:p.Ala5fs, NP_001186797.1:p.Ala5fs, NP_001186797.1:p.Ala5fs

Select item 144763089015.

rs1447630890 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 10:130166946 (GRCh38)
10:131965210 (GRCh37)
Canonical SPDI:: NC_000010.11:130166945:A:G
Gene:: GLRX3 (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.130166946A>G, NC_000010.10:g.131965210A>G, NG_029886.1:g.35572A>G, NM_006541.5:c.679A>G, NM_006541.4:c.679A>G, NM_001321980.2:c.241A>G, NM_001321980.1:c.241A>G, NM_001199868.2:c.679A>G, NM_001199868.1:c.679A>G, NP_006532.2:p.Thr227Ala, NP_001308909.1:p.Thr81Ala, NP_001186797.1:p.Thr227Ala

Select item 144709206216.

rs1447092062 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 10:130145301 (GRCh38)
10:131943565 (GRCh37)
Canonical SPDI:: NC_000010.11:130145300:T:C
Gene:: GLRX3 (Varview)
Functional Consequence:: coding_sequence_variant,synonymous_variant,5_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000010.11:g.130145301T>C, NC_000010.10:g.131943565T>C, NG_029886.1:g.13927T>C, NM_006541.5:c.183T>C, NM_006541.4:c.183T>C, NM_001321980.2:c.-345T>C, NM_001321980.1:c.-345T>C, NM_001199868.2:c.183T>C, NM_001199868.1:c.183T>C

Select item 144634847217.

rs1446348472 [Homo sapiens]

Variant type:: DEL
Alleles:: GA>- [Show Flanks]
Chromosome:: 10:130174871 (GRCh38)
10:131973135 (GRCh37)
Canonical SPDI:: NC_000010.11:130174870:GA:
Gene:: GLRX3 (Varview)
Functional Consequence:: coding_sequence_variant,frameshift_variant
Validated:: by frequency,by alfa
MAF:: -=0.0002/2 (ALFA)
HGVS:: NC_000010.11:g.130174871_130174872del, NC_000010.10:g.131973135_131973136del, NG_029886.1:g.43497_43498del, NM_006541.5:c.829_830del, NM_006541.4:c.829_830del, NM_001321980.2:c.391_392del, NM_001321980.1:c.391_392del, NM_001199868.2:c.829_830del, NM_001199868.1:c.829_830del, NP_006532.2:p.Glu277fs, NP_001308909.1:p.Glu131fs, NP_001186797.1:p.Glu277fs

Select item 144628737618.

rs1446287376 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 10:130166656 (GRCh38)
10:131964920 (GRCh37)
Canonical SPDI:: NC_000010.11:130166655:A:G
Gene:: GLRX3 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000010.11:g.130166656A>G, NC_000010.10:g.131964920A>G, NG_029886.1:g.35282A>G, NM_006541.5:c.628A>G, NM_006541.4:c.628A>G, NM_001321980.2:c.190A>G, NM_001321980.1:c.190A>G, NM_001199868.2:c.628A>G, NM_001199868.1:c.628A>G, NP_006532.2:p.Ile210Val, NP_001308909.1:p.Ile64Val, NP_001186797.1:p.Ile210Val

Select item 144547325419.

rs1445473254 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 10:130166570 (GRCh38)
10:131964834 (GRCh37)
Canonical SPDI:: NC_000010.11:130166569:T:C
Gene:: GLRX3 (Varview)
Functional Consequence:: coding_sequence_variant,missense_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000007/1 (GnomAD)
HGVS:: NC_000010.11:g.130166570T>C, NC_000010.10:g.131964834T>C, NG_029886.1:g.35196T>C, NM_006541.5:c.542T>C, NM_006541.4:c.542T>C, NM_001321980.2:c.104T>C, NM_001321980.1:c.104T>C, NM_001199868.2:c.542T>C, NM_001199868.1:c.542T>C, NP_006532.2:p.Ile181Thr, NP_001308909.1:p.Ile35Thr, NP_001186797.1:p.Ile181Thr

Select item 144456010920.

rs1444560109 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,T [Show Flanks]
Chromosome:: 10:130136473 (GRCh38)
10:131934737 (GRCh37)
Canonical SPDI:: NC_000010.11:130136472:C:A,NC_000010.11:130136472:C:T
Gene:: GLRX3 (Varview), LOC105378561 (Varview)
Functional Consequence:: 2KB_upstream_variant,upstream_transcript_variant,stop_gained,5_prime_UTR_variant,coding_sequence_variant,missense_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_000010.11:g.130136473C>A, NC_000010.11:g.130136473C>T, NC_000010.10:g.131934737C>A, NC_000010.10:g.131934737C>T, NG_029886.1:g.5099C>A, NG_029886.1:g.5099C>T, NM_006541.5:c.53C>A, NM_006541.5:c.53C>T, NM_006541.4:c.53C>A, NM_006541.4:c.53C>T, NM_001321980.2:c.-475C>A, NM_001321980.2:c.-475C>T, NM_001321980.1:c.-475C>A, NM_001321980.1:c.-475C>T, NM_001199868.2:c.53C>A, NM_001199868.2:c.53C>T, NM_001199868.1:c.53C>A, NM_001199868.1:c.53C>T, NP_006532.2:p.Ser18Ter, NP_006532.2:p.Ser18Leu, NP_001186797.1:p.Ser18Ter, NP_001186797.1:p.Ser18Leu

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