Version: 8.0.0
Date: Tue Jan 28 2025
553 results for noxred1
Allele/Variant

Noxred1em2Gpt

(Mus musculus)
Allele/Variant
Source: MGI:7303143
Genes: Noxred1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Noxred1 (Mmu)
Genes: Noxred1 (Mmu)
Symbol: Noxred1em2Gpt

Noxred1em1(IMPC)J

(Mus musculus)
Allele/Variant
Source: MGI:6294782
Genes: Noxred1 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Noxred1 (Mmu)
Genes: Noxred1 (Mmu)
Symbol: Noxred1em1(IMPC)J

sa15278

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-130530-464
Genes: noxred1 (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: 5_prime_UTR_variant, stop_gained
Diseases: Not Available
Variant Name: Not Available
Genes: noxred1 (Dre)

sa42997

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-160601-8638
Genes: noxred1 (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: 5_prime_UTR_variant, stop_gained
Diseases: Not Available
Variant Name: Not Available
Genes: noxred1 (Dre)

(GRCh38)14:77422828C>T

(Homo sapiens)
Allele/Variant
Source: rs780712348
Genes: NOXRED1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)14:77422828C>T

(GRCh38)14:77407609T>C

(Homo sapiens)
Allele/Variant
Source: rs371595572
Genes: NOXRED1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)14:77407609T>C

(GRCh38)14:77413954G>C

(Homo sapiens)
Allele/Variant
Source: rs757173995
Genes: NOXRED1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)14:77413954G>C

(GRCh38)14:77413969C>T

(Homo sapiens)
Allele/Variant
Source: NC_000014.9:g.77413969C>T
Genes: NOXRED1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)14:77413969C>T

(GRCh38)14:77407518G>C

(Homo sapiens)
Allele/Variant
Source: rs188778580
Genes: NOXRED1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)14:77407518G>C

(GRCh38)14:77406864A>G

(Homo sapiens)
Allele/Variant
Source: rs1566708952
Genes: NOXRED1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)14:77406864A>G

(GRCh38)14:77406865G>C

(Homo sapiens)
Allele/Variant
Source: rs538185220
Genes: NOXRED1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)14:77406865G>C

(GRCh38)14:77394699A>T

(Homo sapiens)
Allele/Variant
Source: NC_000014.9:g.77394699A>T
Genes: NOXRED1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)14:77394699A>T

(GRCh38)14:77405937T>C

(Homo sapiens)
Allele/Variant
Source: rs779010896
Genes: NOXRED1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)14:77405937T>C

(GRCh38)14:77406090G>A

(Homo sapiens)
Allele/Variant
Source: rs775895152
Genes: NOXRED1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)14:77406090G>A

(GRCh38)14:77414086A>G

(Homo sapiens)
Allele/Variant
Source: rs369533855
Genes: NOXRED1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)14:77414086A>G

(GRCh38)14:77407574A>G

(Homo sapiens)
Allele/Variant
Source: rs778838625
Genes: NOXRED1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)14:77407574A>G

(GRCh38)14:77407577T>G

(Homo sapiens)
Allele/Variant
Source: rs147504601
Genes: NOXRED1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)14:77407577T>G

(GRCh38)14:77407601C>T

(Homo sapiens)
Allele/Variant
Source: rs375791518
Genes: NOXRED1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)14:77407601C>T

(GRCh38)14:77407487C>T

(Homo sapiens)
Allele/Variant
Source: rs747599930
Genes: NOXRED1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)14:77407487C>T

(GRCh38)14:77394732G>A

(Homo sapiens)
Allele/Variant
Source: rs375720829
Genes: NOXRED1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)14:77394732G>A

(GRCh38)14:77405934C>T

(Homo sapiens)
Allele/Variant
Source: rs1392499215
Genes: NOXRED1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)14:77405934C>T

(GRCh38)14:77413993T>C

(Homo sapiens)
Allele/Variant
Source: rs1413923932
Genes: NOXRED1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)14:77413993T>C

(GRCh38)14:77422798C>T

(Homo sapiens)
Allele/Variant
Source: rs761422368
Genes: NOXRED1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)14:77422798C>T

(GRCh38)14:77406096A>G

(Homo sapiens)
Allele/Variant
Source: rs1468300976
Genes: NOXRED1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)14:77406096A>G

(GRCh38)14:77406774G>T

(Homo sapiens)
Allele/Variant
Source: rs150616937
Genes: NOXRED1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)14:77406774G>T

(GRCh38)14:77406784C>T

(Homo sapiens)
Allele/Variant
Source: NC_000014.9:g.77406784C>T
Genes: NOXRED1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)14:77406784C>T

(GRCh38)14:77406759G>A

(Homo sapiens)
Allele/Variant
Source: rs141814619
Genes: NOXRED1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)14:77406759G>A

(GRCh38)14:77422876T>C

(Homo sapiens)
Allele/Variant
Source: rs1275154256
Genes: NOXRED1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)14:77422876T>C

(mRatBN7.2)6:106882979G>T

(Rattus norvegicus)
Allele/Variant
Source: rs3320909920
Genes: Noxred1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)6:106882979G>T

(mRatBN7.2)6:106869711C>G

(Rattus norvegicus)
Allele/Variant
Source: rs3320854426
Genes: Noxred1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)6:106869711C>G

(mRatBN7.2)6:106873568C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3320909812
Genes: Noxred1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)6:106873568C>T

(mRatBN7.2)6:106876251A>C

(Rattus norvegicus)
Allele/Variant
Source: rs3320854461
Genes: Noxred1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)6:106876251A>C

(mRatBN7.2)6:106868956G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3320891646
Genes: Noxred1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)6:106868956G>A

(mRatBN7.2)6:106883369T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3320830200
Genes: Noxred1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)6:106883369T>C

(mRatBN7.2)6:106884177C>T

(Rattus norvegicus)
Allele/Variant
Source: NC_051341.1:g.106884177C>T
Genes: Noxred1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)6:106884177C>T

(mRatBN7.2)6:106869877G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3320923068
Genes: Noxred1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)6:106869877G>A

(mRatBN7.2)6:106872088T>A

(Rattus norvegicus)
Allele/Variant
Source: rs3320923057
Genes: Noxred1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)6:106872088T>A

(mRatBN7.2)6:106872553C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3320937243
Genes: Noxred1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)6:106872553C>T

(mRatBN7.2)6:106884125T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3320940238
Genes: Noxred1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)6:106884125T>C

(mRatBN7.2)6:106886672T>G

(Rattus norvegicus)
Allele/Variant
Source: rs3320830122
Genes: Noxred1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)6:106886672T>G

(mRatBN7.2)6:106872494C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3320891798
Genes: Noxred1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)6:106872494C>T

(mRatBN7.2)6:106873066A>G

(Rattus norvegicus)
Allele/Variant
Source: rs3320910685
Genes: Noxred1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)6:106873066A>G

(mRatBN7.2)6:106875033C>A

(Rattus norvegicus)
Allele/Variant
Source: rs3320733429
Genes: Noxred1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)6:106875033C>A

(mRatBN7.2)6:106865815T>A

(Rattus norvegicus)
Allele/Variant
Source: rs3320911860
Genes: Noxred1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)6:106865815T>A

(mRatBN7.2)6:106887724C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3320733432
Genes: Noxred1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)6:106887724C>T

(mRatBN7.2)6:106888067T>C

(Rattus norvegicus)
Allele/Variant
Source: rs3320960982
Genes: Noxred1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)6:106888067T>C

(mRatBN7.2)6:106877621C>G

(Rattus norvegicus)
Allele/Variant
Source: rs3320830171
Genes: Noxred1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)6:106877621C>G

(mRatBN7.2)6:106866682G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3320937208
Genes: Noxred1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)6:106866682G>A

(mRatBN7.2)6:106865944G>A

(Rattus norvegicus)
Allele/Variant
Source: rs3320854384
Genes: Noxred1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)6:106865944G>A

(mRatBN7.2)6:106884060C>T

(Rattus norvegicus)
Allele/Variant
Source: rs3320937183
Genes: Noxred1 (Rno)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (mRatBN7.2)6:106884060C>T