Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: PHOX2B-AS1 (Hsa)
(GRCh38)4:41748539C>T
(Homo sapiens)Allele/Variant
Source: rs910430385
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748539C>T
(GRCh38)4:41748452G>C
(Homo sapiens)Allele/Variant
Source: rs1733982727
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748452G>C
(GRCh38)4:41748875C>T
(Homo sapiens)Allele/Variant
Source: rs886059415
Genes: PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748875C>T
(GRCh38)4:41748373C>A
(Homo sapiens)Allele/Variant
Source: rs550472167
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748373C>A
(GRCh38)4:41748380C>T
(Homo sapiens)Allele/Variant
Source: rs376060053
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748380C>T
(GRCh38)4:41748540G>C
(Homo sapiens)Allele/Variant
Source: rs1577561345
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748540G>C
(GRCh38)4:41748473C>T
(Homo sapiens)Allele/Variant
Source: rs1486629336
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748473C>T
(GRCh38)4:41748358G>A
(Homo sapiens)Allele/Variant
Source: rs1369090763
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748358G>A
(GRCh38)4:41748389C>A
(Homo sapiens)Allele/Variant
Source: rs1577561176
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748389C>A
(GRCh38)4:41748395G>C
(Homo sapiens)Allele/Variant
Source: rs1733980273
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748395G>C
(GRCh38)4:41748423C>A
(Homo sapiens)Allele/Variant
Source: rs2153113046
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748423C>A
(GRCh38)4:41748515G>T
(Homo sapiens)Allele/Variant
Source: NC_000004.12:g.41748515G>T
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748515G>T
(GRCh38)4:41748456C>T
(Homo sapiens)Allele/Variant
Source: NC_000004.12:g.41748456C>T
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748456C>T
(GRCh38)4:41748468C>G
(Homo sapiens)Allele/Variant
Source: NC_000004.12:g.41748468C>G
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748468C>G
(GRCh38)4:41748527T>C
(Homo sapiens)Allele/Variant
Source: rs2153113066
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748527T>C
(GRCh38)4:41748440G>A
(Homo sapiens)Allele/Variant
Source: NC_000004.12:g.41748440G>A
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748440G>A
(GRCh38)4:41833841G>T
(Homo sapiens)Allele/Variant
Source: rs207464561
Genes: PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41833841G>T
(GRCh38)4:41748468C>T
(Homo sapiens)Allele/Variant
Source: rs1733983472
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748468C>T
(GRCh38)4:41748470T>C
(Homo sapiens)Allele/Variant
Source: rs1577561264
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748470T>C
(GRCh38)4:41748520C>T
(Homo sapiens)Allele/Variant
Source: rs2153113064
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748520C>T
(GRCh38)4:41748526C>A
(Homo sapiens)Allele/Variant
Source: NC_000004.12:g.41748526C>A
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748526C>A
(GRCh38)4:41748373C>G
(Homo sapiens)Allele/Variant
Source: NC_000004.12:g.41748373C>G
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748373C>G
(GRCh38)4:41748453G>A
(Homo sapiens)Allele/Variant
Source: rs1488529123
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748453G>A
(GRCh38)4:41748543G>C
(Homo sapiens)Allele/Variant
Source: rs1389889634
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748543G>C
(GRCh38)4:41748474G>C
(Homo sapiens)Allele/Variant
Source: rs1381435898
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748474G>C
(GRCh38)4:41748492C>G
(Homo sapiens)Allele/Variant
Source: NC_000004.12:g.41748492C>G
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748492C>G
(GRCh38)4:41748511T>C
(Homo sapiens)Allele/Variant
Source: rs1733985253
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748511T>C
(GRCh38)4:41748381G>C
(Homo sapiens)Allele/Variant
Source: rs1733979767
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748381G>C
(GRCh38)4:41748555G>T
(Homo sapiens)Allele/Variant
Source: rs1353983410
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748555G>T
(GRCh38)4:41748376C>G
(Homo sapiens)Allele/Variant
Source: NC_000004.12:g.41748376C>G
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748376C>G
(GRCh38)4:41748560A>G
(Homo sapiens)Allele/Variant
Source: rs1577561406
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748560A>G
(GRCh38)4:41748377G>T
(Homo sapiens)Allele/Variant
Source: NC_000004.12:g.41748377G>T
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748377G>T
(GRCh38)4:41748377G>C
(Homo sapiens)Allele/Variant
Source: rs73810366
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748377G>C
(GRCh38)4:41748480T>C
(Homo sapiens)Allele/Variant
Source: NC_000004.12:g.41748480T>C
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748480T>C
(GRCh38)4:41748376C>T
(Homo sapiens)Allele/Variant
Source: rs1733979302
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748376C>T
(GRCh38)4:41748391G>A
(Homo sapiens)Allele/Variant
Source: rs1297909281
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748391G>A
(GRCh38)4:41748805C>T
(Homo sapiens)Allele/Variant
Source: rs775569375
Genes: PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748805C>T
(GRCh38)4:41748444C>A
(Homo sapiens)Allele/Variant
Source: rs1733982125
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748444C>A
(GRCh38)4:41748380C>A
(Homo sapiens)Allele/Variant
Source: rs376060053
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748380C>A
(GRCh38)4:41748383A>G
(Homo sapiens)Allele/Variant
Source: NC_000004.12:g.41748383A>G
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748383A>G
(GRCh38)4:41748450G>C
(Homo sapiens)Allele/Variant
Source: rs1733982603
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748450G>C
(GRCh38)4:41748374G>T
(Homo sapiens)Allele/Variant
Source: NC_000004.12:g.41748374G>T
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748374G>T
(GRCh38)4:41748490C>A
(Homo sapiens)Allele/Variant
Source: NC_000004.12:g.41748490C>A
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748490C>A
(GRCh38)4:41748514A>T
(Homo sapiens)Allele/Variant
Source: rs1043632230
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748514A>T
(GRCh38)4:41748523A>C
(Homo sapiens)Allele/Variant
Source: rs1060501122
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748523A>C
(GRCh38)4:41748610T>C
(Homo sapiens)Allele/Variant
Source: NC_000004.12:g.41748610T>C
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, start_lost, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748610T>C
(GRCh38)4:41748545G>T
(Homo sapiens)Allele/Variant
Source: rs2153113068
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748545G>T
(GRCh38)4:41748548C>T
(Homo sapiens)Allele/Variant
Source: NC_000004.12:g.41748548C>T
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748548C>T
(GRCh38)4:41748472T>C
(Homo sapiens)Allele/Variant
Source: NC_000004.12:g.41748472T>C
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748472T>C
(GRCh38)4:41748504C>T
(Homo sapiens)Allele/Variant
Source: NC_000004.12:g.41748504C>T
Genes: PHOX2B (Hsa), PHOX2B-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)4:41748504C>T