Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: RADIL (Hsa) Molecular Consequence: non coding transcript variant
(GRCh38)7:4860352T>C
(Homo sapiens)Allele/Variant
Source: rs17857123
Genes: RADIL (Hsa), PAPOLB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:4860352T>C
(GRCh38)7:4860529T>C
(Homo sapiens)Allele/Variant
Source: rs1334706700
Genes: RADIL (Hsa), PAPOLB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:4860529T>C
(GRCh38)7:4860873A>C
(Homo sapiens)Allele/Variant
Source: rs369419952
Genes: RADIL (Hsa), PAPOLB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:4860873A>C
(GRCh38)7:4861253T>A
(Homo sapiens)Allele/Variant
Source: NC_000007.14:g.4861253T>A
Genes: RADIL (Hsa), PAPOLB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:4861253T>A
(GRCh38)7:4861377T>C
(Homo sapiens)Allele/Variant
Source: rs1403283915
Genes: RADIL (Hsa), PAPOLB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:4861377T>C
(GRCh38)7:4860131C>A
(Homo sapiens)Allele/Variant
Source: rs747545626
Genes: RADIL (Hsa), PAPOLB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:4860131C>A
(GRCh38)7:4860037C>T
(Homo sapiens)Allele/Variant
Source: rs867228239
Genes: RADIL (Hsa), PAPOLB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:4860037C>T
(GRCh38)7:4860148T>C
(Homo sapiens)Allele/Variant
Source: rs1562453759
Genes: RADIL (Hsa), PAPOLB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:4860148T>C
(GRCh38)7:4861665G>T
(Homo sapiens)Allele/Variant
Source: rs1784003576
Genes: RADIL (Hsa), PAPOLB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:4861665G>T
(GRCh38)7:4860519A>G
(Homo sapiens)Allele/Variant
Source: rs563953783
Genes: RADIL (Hsa), PAPOLB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:4860519A>G
(GRCh38)7:4861803G>A
(Homo sapiens)Allele/Variant
Source: rs752931444
Genes: RADIL (Hsa), PAPOLB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:4861803G>A
(GRCh38)7:4860943C>G
(Homo sapiens)Allele/Variant
Source: NC_000007.14:g.4860943C>G
Genes: RADIL (Hsa), PAPOLB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:4860943C>G
(GRCh38)7:4860925G>T
(Homo sapiens)Allele/Variant
Source: rs566900862
Genes: RADIL (Hsa), PAPOLB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:4860925G>T
(GRCh38)7:4860096G>A
(Homo sapiens)Allele/Variant
Source: rs1783942283
Genes: RADIL (Hsa), PAPOLB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:4860096G>A
(GRCh38)7:4860882C>T
(Homo sapiens)Allele/Variant
Source: rs548603183
Genes: RADIL (Hsa), PAPOLB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:4860882C>T
(GRCh38)7:4861186C>T
(Homo sapiens)Allele/Variant
Source: rs376031779
Genes: RADIL (Hsa), PAPOLB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:4861186C>T
(GRCh38)7:4861208G>C
(Homo sapiens)Allele/Variant
Source: NC_000007.14:g.4861208G>C
Genes: RADIL (Hsa), PAPOLB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:4861208G>C
(GRCh38)7:4861732T>C
(Homo sapiens)Allele/Variant
Source: rs1294688105
Genes: RADIL (Hsa), PAPOLB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:4861732T>C
(GRCh38)7:4861804G>A
(Homo sapiens)Allele/Variant
Source: rs376936354
Genes: RADIL (Hsa), PAPOLB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:4861804G>A
(GRCh38)7:4860502T>A
(Homo sapiens)Allele/Variant
Source: rs755584689
Genes: RADIL (Hsa), PAPOLB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:4860502T>A
(GRCh38)7:4859959T>C
(Homo sapiens)Allele/Variant
Source: rs751136080
Genes: RADIL (Hsa), PAPOLB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:4859959T>C
(GRCh38)7:4859968C>T
(Homo sapiens)Allele/Variant
Source: rs375132133
Genes: RADIL (Hsa), PAPOLB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:4859968C>T
(GRCh38)7:4860041T>G
(Homo sapiens)Allele/Variant
Source: rs767038059
Genes: RADIL (Hsa), PAPOLB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:4860041T>G
(GRCh38)7:4861216T>C
(Homo sapiens)Allele/Variant
Source: rs754213353
Genes: RADIL (Hsa), PAPOLB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:4861216T>C
(GRCh38)7:4861474C>T
(Homo sapiens)Allele/Variant
Source: rs374812651
Genes: RADIL (Hsa), PAPOLB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:4861474C>T
(GRCh38)7:4861511C>G
(Homo sapiens)Allele/Variant
Source: rs142317142
Genes: RADIL (Hsa), PAPOLB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:4861511C>G
(GRCh38)7:4861539A>G
(Homo sapiens)Allele/Variant
Source: rs1783996439
Genes: RADIL (Hsa), PAPOLB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:4861539A>G
(GRCh38)7:4861688C>A
(Homo sapiens)Allele/Variant
Source: rs773789412
Genes: RADIL (Hsa), PAPOLB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:4861688C>A
(GRCh38)7:4860811T>C
(Homo sapiens)Allele/Variant
Source: rs764719157
Genes: RADIL (Hsa), PAPOLB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:4860811T>C
(GRCh38)7:4861404G>C
(Homo sapiens)Allele/Variant
Source: rs1783990359
Genes: RADIL (Hsa), PAPOLB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:4861404G>C
(GRCh38)7:4860316G>A
(Homo sapiens)Allele/Variant
Source: rs774276156
Genes: RADIL (Hsa), PAPOLB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:4860316G>A
(GRCh38)7:4860726A>C
(Homo sapiens)Allele/Variant
Source: NC_000007.14:g.4860726A>C
Genes: RADIL (Hsa), PAPOLB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:4860726A>C
(GRCh38)7:4861125T>C
(Homo sapiens)Allele/Variant
Source: rs199530978
Genes: RADIL (Hsa), PAPOLB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:4861125T>C
(GRCh38)7:4861287G>A
(Homo sapiens)Allele/Variant
Source: rs920429798
Genes: RADIL (Hsa), PAPOLB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:4861287G>A
(GRCh38)7:4859964G>T
(Homo sapiens)Allele/Variant
Source: rs1783934948
Genes: RADIL (Hsa), PAPOLB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:4859964G>T
(GRCh38)7:4860214T>G
(Homo sapiens)Allele/Variant
Source: rs759344020
Genes: RADIL (Hsa), PAPOLB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:4860214T>G
(GRCh38)7:4861195G>A
(Homo sapiens)Allele/Variant
Source: rs780392920
Genes: RADIL (Hsa), PAPOLB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:4861195G>A
(GRCh38)7:4861652G>C
(Homo sapiens)Allele/Variant
Source: rs368004972
Genes: RADIL (Hsa), PAPOLB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:4861652G>C
(GRCh38)7:4860865T>C
(Homo sapiens)Allele/Variant
Source: rs750372901
Genes: RADIL (Hsa), PAPOLB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:4860865T>C
(GRCh38)7:4860249T>C
(Homo sapiens)Allele/Variant
Source: NC_000007.14:g.4860249T>C
Genes: RADIL (Hsa), PAPOLB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:4860249T>C
(GRCh38)7:4861500T>G
(Homo sapiens)Allele/Variant
Source: NC_000007.14:g.4861500T>G
Genes: RADIL (Hsa), PAPOLB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:4861500T>G
(GRCh38)7:4860427G>T
(Homo sapiens)Allele/Variant
Source: NC_000007.14:g.4860427G>T
Genes: RADIL (Hsa), PAPOLB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:4860427G>T
(GRCh38)7:4860552T>C
(Homo sapiens)Allele/Variant
Source: rs764458419
Genes: RADIL (Hsa), PAPOLB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:4860552T>C
(GRCh38)7:4861504A>T
(Homo sapiens)Allele/Variant
Source: rs746563809
Genes: RADIL (Hsa), PAPOLB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:4861504A>T