Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: RADIL (Hsa)
(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)7:4877775G>A
(Homo sapiens)Allele/Variant
Source: rs758052894
Genes: RADIL (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:4877775G>A
(GRCh38)7:4877795C>G
(Homo sapiens)Allele/Variant
Source: NC_000007.14:g.4877795C>G
Genes: RADIL (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)7:4877795C>G
(GRCh38)7:4877997G>A
(Homo sapiens)Allele/Variant
Source: rs373342102
Genes: RADIL (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:4877997G>A
(GRCh38)7:4835044C>T
(Homo sapiens)Allele/Variant
Source: rs1203516800
Genes: RADIL (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:4835044C>T
(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)7:4860519A>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)7:4878117A>C
(Homo sapiens)Allele/Variant
Source: NC_000007.14:g.4878117A>C
Genes: RADIL (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:4878117A>C
(GRCh38)7:4835067G>A
(Homo sapiens)Allele/Variant
Source: rs1783257349
Genes: RADIL (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:4835067G>A
(GRCh38)7:4835118C>A
(Homo sapiens)Allele/Variant
Source: rs778925992
Genes: RADIL (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:4835118C>A
(GRCh38)7:4835126G>A
(Homo sapiens)Allele/Variant
Source: rs184696145
Genes: RADIL (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)7:4835126G>A
(GRCh38)7:4836459C>T
(Homo sapiens)Allele/Variant
Source: rs1420430280
Genes: RADIL (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:4836459C>T
(GRCh38)7:4836521G>T
(Homo sapiens)Allele/Variant
Source: rs778563888
Genes: RADIL (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:4836521G>T
(GRCh38)7:4801836G>A
(Homo sapiens)Allele/Variant
Source: rs766194793
Genes: RADIL (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:4801836G>A
(GRCh38)7:4803596C>T
(Homo sapiens)Allele/Variant
Source: rs763195339
Genes: RADIL (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:4803596C>T
(GRCh38)7:4803560G>C
(Homo sapiens)Allele/Variant
Source: NC_000007.14:g.4803560G>C
Genes: RADIL (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:4803560G>C
(GRCh38)7:4834688C>A
(Homo sapiens)Allele/Variant
Source: rs2115001507
Genes: RADIL (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:4834688C>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)7:4799645C>T
(Homo sapiens)Allele/Variant
Source: rs780676358
Genes: RADIL (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:4799645C>T
(GRCh38)7:4801784G>A
(Homo sapiens)Allele/Variant
Source: rs183793391
Genes: RADIL (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:4801784G>A
(GRCh38)7:4801814G>A
(Homo sapiens)Allele/Variant
Source: NC_000007.14:g.4801814G>A
Genes: RADIL (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:4801814G>A
(GRCh38)7:4799416T>C
(Homo sapiens)Allele/Variant
Source: rs547399191
Genes: RADIL (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:4799416T>C
(GRCh38)7:4836453C>A
(Homo sapiens)Allele/Variant
Source: rs376852518
Genes: RADIL (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:4836453C>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)7:4801913C>T
(Homo sapiens)Allele/Variant
Source: rs966309842
Genes: RADIL (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:4801913C>T
(GRCh38)7:4816257G>A
(Homo sapiens)Allele/Variant
Source: rs762828531
Genes: RADIL (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:4816257G>A
(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)7:4801895C>T
(Homo sapiens)Allele/Variant
Source: rs199920495
Genes: RADIL (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:4801895C>T
(GRCh38)7:4803613C>T
(Homo sapiens)Allele/Variant
Source: rs535008712
Genes: RADIL (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:4803613C>T
(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)7:4835062G>C
(Homo sapiens)Allele/Variant
Source: rs754936589
Genes: RADIL (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:4835062G>C
(GRCh38)7:4799389G>A
(Homo sapiens)Allele/Variant
Source: rs770434987
Genes: RADIL (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:4799389G>A
(GRCh38)7:4801697C>G
(Homo sapiens)Allele/Variant
Source: rs766597809
Genes: RADIL (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:4801697C>G
(GRCh38)7:4799386G>A
(Homo sapiens)Allele/Variant
Source: rs945819113
Genes: RADIL (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:4799386G>A
(GRCh38)7:4801853G>T
(Homo sapiens)Allele/Variant
Source: NC_000007.14:g.4801853G>T
Genes: RADIL (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:4801853G>T
(GRCh38)7:4801890G>C
(Homo sapiens)Allele/Variant
Source: rs140056635
Genes: RADIL (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:4801890G>C
(GRCh38)7:4803635G>A
(Homo sapiens)Allele/Variant
Source: rs545184177
Genes: RADIL (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:4803635G>A
(GRCh38)7:4805659G>C
(Homo sapiens)Allele/Variant
Source: rs368100702
Genes: RADIL (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:4805659G>C
(GRCh38)7:4805704C>T
(Homo sapiens)Allele/Variant
Source: rs944310651
Genes: RADIL (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:4805704C>T
(GRCh38)7:4815399C>T
(Homo sapiens)Allele/Variant
Source: rs774115748
Genes: RADIL (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:4815399C>T
(GRCh38)7:4816392G>A
(Homo sapiens)Allele/Variant
Source: rs778018782
Genes: RADIL (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:4816392G>A