Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: XPO1 (Hsa) Molecular Consequence: intron variant
(GRCh38)2:61490712T>A
(Homo sapiens)Allele/Variant
Source: NC_000002.12:g.61490712T>A
Genes: XPO1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:61490712T>A
(GRCh38)2:61481268G>C
(Homo sapiens)Allele/Variant
Source: NC_000002.12:g.61481268G>C
Genes: USP34-DT (Hsa), XPO1 (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)2:61481268G>C
(GRCh38)2:61488207C>T
(Homo sapiens)Allele/Variant
Source: rs373800890
Genes: XPO1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:61488207C>T
(GRCh38)2:61488631G>A
(Homo sapiens)Allele/Variant
Source: rs184305497
Genes: XPO1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, stop_gained, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:61488631G>A
(GRCh38)2:61526477A>C
(Homo sapiens)Allele/Variant
Source: NC_000002.12:g.61526477A>C
Genes: XPO1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:61526477A>C
(GRCh38)2:61488243A>C
(Homo sapiens)Allele/Variant
Source: rs762581181
Genes: XPO1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, stop_lost, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:61488243A>C
(GRCh38)2:61492047A>C
(Homo sapiens)Allele/Variant
Source: rs143005485
Genes: XPO1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:61492047A>C
(GRCh38)2:61530673T>G
(Homo sapiens)Allele/Variant
Source: rs181420109
Genes: XPO1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:61530673T>G
(GRCh38)2:61526437G>C
(Homo sapiens)Allele/Variant
Source: NC_000002.12:g.61526437G>C
Genes: XPO1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:61526437G>C
(GRCh38)2:61502304T>A
(Homo sapiens)Allele/Variant
Source: rs1697567637
Genes: XPO1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:61502304T>A
(GRCh38)2:61484076C>T
(Homo sapiens)Allele/Variant
Source: rs13385575
Genes: XPO1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:61484076C>T
(GRCh38)2:61482950T>A
(Homo sapiens)Allele/Variant
Source: rs769202956
Genes: USP34-DT (Hsa), XPO1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:61482950T>A
(GRCh38)2:61492425T>C
(Homo sapiens)Allele/Variant
Source: rs1281320213
Genes: XPO1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:61492425T>C
(GRCh38)2:61496870T>C
(Homo sapiens)Allele/Variant
Source: rs140857799
Genes: XPO1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:61496870T>C
(GRCh38)2:61492336T>A
(Homo sapiens)Allele/Variant
Source: rs1057520010
Genes: XPO1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:61492336T>A
(GRCh38)2:61492797T>C
(Homo sapiens)Allele/Variant
Source: rs587778011
Genes: XPO1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:61492797T>C
(GRCh38)2:61498765G>A
(Homo sapiens)Allele/Variant
Source: rs2104491349
Genes: XPO1 (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)2:61498765G>A
(GRCh38)2:61502014T>C
(Homo sapiens)Allele/Variant
Source: rs146254944
Genes: XPO1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:61502014T>C
(GRCh38)2:61492336T>G
(Homo sapiens)Allele/Variant
Source: rs1057520010
Genes: XPO1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:61492336T>G
(GRCh38)2:61478944G>A
(Homo sapiens)Allele/Variant
Source: NC_000002.12:g.61478944G>A
Genes: USP34-DT (Hsa), XPO1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:61478944G>A
(GRCh38)2:61492337C>T
(Homo sapiens)Allele/Variant
Source: rs1057520009
Genes: XPO1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:61492337C>T