Version: 8.1.0Date: Fri Apr 18 2025
Allele/Variant Molecular Consequence: non coding transcript exon variant
(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)14:77407487C>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)14:77406090G>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, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)14:77406090G>A
(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, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)14:77406096A>G
(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)14:77422828C>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)14:77407518G>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)14:77407574A>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)14:77407601C>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)14:77394732G>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)14:77405937T>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, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)14:77405937T>C
(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, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)14:77406784C>T
(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)14:77406865G>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, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)14:77406865G>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)14:77406774G>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, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)14:77406774G>T
(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, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)14:77406864A>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)14:77422876T>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
(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, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)14:77406759G>A
(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)14:77405934C>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, intron_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)14:77414086A>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