Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: E2F8 (Hsa)
(GRCh38)11:19224788C>T
(Homo sapiens)Allele/Variant
Source: rs370899212
Genes: E2F8 (Hsa), CSRP3-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:19224788C>T
(GRCh38)11:19225459T>A
(Homo sapiens)Allele/Variant
Source: rs200045087
Genes: E2F8 (Hsa), CSRP3-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:19225459T>A
(GRCh38)11:19225738T>C
(Homo sapiens)Allele/Variant
Source: rs793274
Genes: E2F8 (Hsa), CSRP3-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:19225738T>C
(GRCh38)11:19237873T>G
(Homo sapiens)Allele/Variant
Source: NC_000011.10:g.19237873T>G
Genes: E2F8 (Hsa), CSRP3-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:19237873T>G
(GRCh38)11:19238015G>A
(Homo sapiens)Allele/Variant
Source: rs769970471
Genes: E2F8 (Hsa), CSRP3-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:19238015G>A
(GRCh38)11:19232237T>C
(Homo sapiens)Allele/Variant
Source: NC_000011.10:g.19232237T>C
Genes: E2F8 (Hsa), CSRP3-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:19232237T>C
(GRCh38)11:19225336T>C
(Homo sapiens)Allele/Variant
Source: rs780624931
Genes: E2F8 (Hsa), CSRP3-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, stop_retained_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:19225336T>C
(GRCh38)11:19238070G>A
(Homo sapiens)Allele/Variant
Source: rs73416784
Genes: E2F8 (Hsa), CSRP3-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:19238070G>A
(GRCh38)11:19229705G>A
(Homo sapiens)Allele/Variant
Source: rs1350612574
Genes: E2F8 (Hsa), CSRP3-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:19229705G>A
(GRCh38)11:19224728T>C
(Homo sapiens)Allele/Variant
Source: rs137938238
Genes: E2F8 (Hsa), CSRP3-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:19224728T>C
(GRCh38)11:19234752A>C
(Homo sapiens)Allele/Variant
Source: rs569729834
Genes: E2F8 (Hsa), CSRP3-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:19234752A>C
(GRCh38)11:19225402T>C
(Homo sapiens)Allele/Variant
Source: rs747630290
Genes: E2F8 (Hsa), CSRP3-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:19225402T>C
(GRCh38)11:19225795A>G
(Homo sapiens)Allele/Variant
Source: rs574624357
Genes: E2F8 (Hsa), CSRP3-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:19225795A>G
(GRCh38)11:19225830G>A
(Homo sapiens)Allele/Variant
Source: rs764017564
Genes: E2F8 (Hsa), CSRP3-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:19225830G>A
(GRCh38)11:19229972C>T
(Homo sapiens)Allele/Variant
Source: rs201330589
Genes: E2F8 (Hsa), CSRP3-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:19229972C>T
(GRCh38)11:19234818A>G
(Homo sapiens)Allele/Variant
Source: rs201855427
Genes: E2F8 (Hsa), CSRP3-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:19234818A>G
(GRCh38)11:19229656T>G
(Homo sapiens)Allele/Variant
Source: rs147228502
Genes: E2F8 (Hsa), CSRP3-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:19229656T>G
(GRCh38)11:19225361C>T
(Homo sapiens)Allele/Variant
Source: rs367819993
Genes: E2F8 (Hsa), CSRP3-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:19225361C>T
(GRCh38)11:19234392T>G
(Homo sapiens)Allele/Variant
Source: rs371037224
Genes: E2F8 (Hsa), CSRP3-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:19234392T>G
(GRCh38)11:19237944A>G
(Homo sapiens)Allele/Variant
Source: rs12291291
Genes: E2F8 (Hsa), CSRP3-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:19237944A>G
(GRCh38)11:19225551C>T
(Homo sapiens)Allele/Variant
Source: rs3740965
Genes: E2F8 (Hsa), CSRP3-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:19225551C>T
(GRCh38)11:19234900C>T
(Homo sapiens)Allele/Variant
Source: rs757747922
Genes: E2F8 (Hsa), CSRP3-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:19234900C>T
(GRCh38)11:19237863G>C
(Homo sapiens)Allele/Variant
Source: rs775677981
Genes: E2F8 (Hsa), CSRP3-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:19237863G>C
(GRCh38)11:19230699A>G
(Homo sapiens)Allele/Variant
Source: rs1374848080
Genes: E2F8 (Hsa), CSRP3-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:19230699A>G
(GRCh38)11:19230786C>T
(Homo sapiens)Allele/Variant
Source: rs375962806
Genes: E2F8 (Hsa), CSRP3-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:19230786C>T
(GRCh38)11:19230828C>G
(Homo sapiens)Allele/Variant
Source: rs77599073
Genes: E2F8 (Hsa), CSRP3-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:19230828C>G
(GRCh38)11:19230817G>C
(Homo sapiens)Allele/Variant
Source: rs138078778
Genes: E2F8 (Hsa), CSRP3-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:19230817G>C
(GRCh38)11:19234831C>T
(Homo sapiens)Allele/Variant
Source: rs200081576
Genes: E2F8 (Hsa), CSRP3-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:19234831C>T
(GRCh38)11:19225279G>T
(Homo sapiens)Allele/Variant
Source: rs770128838
Genes: E2F8 (Hsa), CSRP3-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:19225279G>T
(GRCh38)11:19225514C>T
(Homo sapiens)Allele/Variant
Source: rs780401976
Genes: E2F8 (Hsa), CSRP3-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:19225514C>T
(GRCh38)11:19229504A>G
(Homo sapiens)Allele/Variant
Source: rs529723766
Genes: E2F8 (Hsa), CSRP3-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:19229504A>G
(GRCh38)11:19229827G>T
(Homo sapiens)Allele/Variant
Source: rs145509272
Genes: E2F8 (Hsa), CSRP3-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:19229827G>T
(GRCh38)11:19232329C>T
(Homo sapiens)Allele/Variant
Source: rs1029877491
Genes: E2F8 (Hsa), CSRP3-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:19232329C>T
(GRCh38)11:19225552G>A
(Homo sapiens)Allele/Variant
Source: rs760381605
Genes: E2F8 (Hsa), CSRP3-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:19225552G>A
(GRCh38)11:19229857A>T
(Homo sapiens)Allele/Variant
Source: rs148418534
Genes: E2F8 (Hsa), CSRP3-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:19229857A>T
(GRCh38)11:19225759G>C
(Homo sapiens)Allele/Variant
Source: rs776118364
Genes: E2F8 (Hsa), CSRP3-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:19225759G>C
(GRCh38)11:19237906C>A
(Homo sapiens)Allele/Variant
Source: rs762902793
Genes: E2F8 (Hsa), CSRP3-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:19237906C>A
(GRCh38)11:19230679G>A
(Homo sapiens)Allele/Variant
Source: rs754611426
Genes: E2F8 (Hsa), CSRP3-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:19230679G>A
(GRCh38)11:19225770A>G
(Homo sapiens)Allele/Variant
Source: rs574772592
Genes: E2F8 (Hsa), CSRP3-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:19225770A>G
(GRCh38)11:19230723C>T
(Homo sapiens)Allele/Variant
Source: rs1382432966
Genes: E2F8 (Hsa), CSRP3-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:19230723C>T
(GRCh38)11:19225344C>G
(Homo sapiens)Allele/Variant
Source: rs770286107
Genes: E2F8 (Hsa), CSRP3-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:19225344C>G
(GRCh38)11:19225495G>A
(Homo sapiens)Allele/Variant
Source: rs755593331
Genes: E2F8 (Hsa), CSRP3-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:19225495G>A
(GRCh38)11:19234437A>G
(Homo sapiens)Allele/Variant
Source: rs529296056
Genes: E2F8 (Hsa), CSRP3-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:19234437A>G
(GRCh38)11:19234761C>T
(Homo sapiens)Allele/Variant
Source: rs369864278
Genes: E2F8 (Hsa), CSRP3-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:19234761C>T
(GRCh38)11:19238002T>C
(Homo sapiens)Allele/Variant
Source: rs111756396
Genes: E2F8 (Hsa), CSRP3-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:19238002T>C
(GRCh38)11:19229578C>T
(Homo sapiens)Allele/Variant
Source: rs1318640582
Genes: E2F8 (Hsa), CSRP3-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:19229578C>T
(GRCh38)11:19234404A>G
(Homo sapiens)Allele/Variant
Source: rs749926881
Genes: E2F8 (Hsa), CSRP3-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:19234404A>G
(GRCh38)11:19234759C>T
(Homo sapiens)Allele/Variant
Source: rs199935572
Genes: E2F8 (Hsa), CSRP3-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:19234759C>T
(GRCh38)11:19234875T>C
(Homo sapiens)Allele/Variant
Source: rs769519617
Genes: E2F8 (Hsa), CSRP3-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:19234875T>C
(GRCh38)11:19229887G>A
(Homo sapiens)Allele/Variant
Source: rs745914893
Genes: E2F8 (Hsa), CSRP3-AS1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:19229887G>A