Version: 8.2.0Date: Wed Aug 27 2025
Allele/Variant Genes: KIF5A (Hsa)
(GRCh38)12:57581073G>T
(Homo sapiens)Allele/Variant
Source: rs1017745641
Genes: KIF5A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:57581073G>T
(GRCh38)12:57581084C>T
(Homo sapiens)Allele/Variant
Source: rs771819798
Genes: KIF5A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)12:57581084C>T
(GRCh38)12:57581175G>C
(Homo sapiens)Allele/Variant
Source: rs1416076720
Genes: KIF5A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:57581175G>C
(GRCh38)12:57581441C>T
(Homo sapiens)Allele/Variant
Source: rs1163611256
Genes: KIF5A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:57581441C>T
(GRCh38)12:57582582C>T
(Homo sapiens)Allele/Variant
Source: rs375827219
Genes: KIF5A (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)12:57582582C>T
(GRCh38)12:57583113G>A
(Homo sapiens)Allele/Variant
Source: rs148434838
Genes: KIF5A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:57583113G>A
(GRCh38)12:57583119C>G
(Homo sapiens)Allele/Variant
Source: NC_000012.12:g.57583119C>G
Genes: KIF5A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:57583119C>G
(GRCh38)12:57564094C>A
(Homo sapiens)Allele/Variant
Source: rs778921032
Genes: KIF5A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:57564094C>A
(GRCh38)12:57568990G>T
(Homo sapiens)Allele/Variant
Source: NC_000012.12:g.57568990G>T
Genes: KIF5A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)12:57568990G>T
(GRCh38)12:57564198G>A
(Homo sapiens)Allele/Variant
Source: rs2140159178
Genes: KIF5A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:57564198G>A
(GRCh38)12:57550294G>T
(Homo sapiens)Allele/Variant
Source: NC_000012.12:g.57550294G>T
Genes: KIF5A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:57550294G>T
(GRCh38)12:57550409C>T
(Homo sapiens)Allele/Variant
Source: rs372131378
Genes: KIF5A (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)12:57550409C>T
(GRCh38)12:57563662A>G
(Homo sapiens)Allele/Variant
Source: NC_000012.12:g.57563662A>G
Genes: KIF5A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:57563662A>G
(GRCh38)12:57563699G>C
(Homo sapiens)Allele/Variant
Source: rs761034249
Genes: KIF5A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:57563699G>C
(GRCh38)12:57564119C>T
(Homo sapiens)Allele/Variant
Source: rs769191561
Genes: KIF5A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:57564119C>T
(GRCh38)12:57564993A>G
(Homo sapiens)Allele/Variant
Source: rs2140159724
Genes: KIF5A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:57564993A>G
(GRCh38)12:57565280G>A
(Homo sapiens)Allele/Variant
Source: rs140470142
Genes: KIF5A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:57565280G>A
(GRCh38)12:57569012T>C
(Homo sapiens)Allele/Variant
Source: rs2140162579
Genes: KIF5A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)12:57569012T>C
(GRCh38)12:57569049C>T
(Homo sapiens)Allele/Variant
Source: rs368628303
Genes: KIF5A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)12:57569049C>T
(GRCh38)12:57569646T>C
(Homo sapiens)Allele/Variant
Source: rs1376993995
Genes: KIF5A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)12:57569646T>C
(GRCh38)12:57584602C>T
(Homo sapiens)Allele/Variant
Source: rs1005821727
Genes: KIF5A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:57584602C>T
(GRCh38)12:57584673A>T
(Homo sapiens)Allele/Variant
Source: rs886049705
Genes: KIF5A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:57584673A>T
(GRCh38)12:57572562C>T
(Homo sapiens)Allele/Variant
Source: NC_000012.12:g.57572562C>T
Genes: KIF5A (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)12:57572562C>T
(GRCh38)12:57572711C>T
(Homo sapiens)Allele/Variant
Source: rs2140165659
Genes: KIF5A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:57572711C>T
(GRCh38)12:57572720T>G
(Homo sapiens)Allele/Variant
Source: rs1882294516
Genes: KIF5A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:57572720T>G
(GRCh38)12:57575071T>C
(Homo sapiens)Allele/Variant
Source: rs2140167357
Genes: KIF5A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:57575071T>C
(GRCh38)12:57575281C>G
(Homo sapiens)Allele/Variant
Source: rs2140167541
Genes: KIF5A (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)12:57575281C>G
(GRCh38)12:57575628T>C
(Homo sapiens)Allele/Variant
Source: NC_000012.12:g.57575628T>C
Genes: KIF5A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:57575628T>C
(GRCh38)12:57575687G>C
(Homo sapiens)Allele/Variant
Source: rs775994678
Genes: KIF5A (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)12:57575687G>C
(GRCh38)12:57576753C>T
(Homo sapiens)Allele/Variant
Source: rs762234885
Genes: KIF5A (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)12:57576753C>T
(GRCh38)12:57563665C>T
(Homo sapiens)Allele/Variant
Source: NC_000012.12:g.57563665C>T
Genes: KIF5A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:57563665C>T
(GRCh38)12:57564922C>A
(Homo sapiens)Allele/Variant
Source: rs369182603
Genes: KIF5A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)12:57564922C>A
(GRCh38)12:57564937C>G
(Homo sapiens)Allele/Variant
Source: NC_000012.12:g.57564937C>G
Genes: KIF5A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)12:57564937C>G
(GRCh38)12:57564946G>T
(Homo sapiens)Allele/Variant
Source: NC_000012.12:g.57564946G>T
Genes: KIF5A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)12:57564946G>T
(GRCh38)12:57564143T>G
(Homo sapiens)Allele/Variant
Source: rs777103564
Genes: KIF5A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:57564143T>G
(GRCh38)12:57570084C>A
(Homo sapiens)Allele/Variant
Source: NC_000012.12:g.57570084C>A
Genes: KIF5A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)12:57570084C>A
(GRCh38)12:57570087G>C
(Homo sapiens)Allele/Variant
Source: rs758977709
Genes: KIF5A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)12:57570087G>C
(GRCh38)12:57569612A>G
(Homo sapiens)Allele/Variant
Source: NC_000012.12:g.57569612A>G
Genes: KIF5A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:57569612A>G
(GRCh38)12:57569993A>G
(Homo sapiens)Allele/Variant
Source: NC_000012.12:g.57569993A>G
Genes: KIF5A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:57569993A>G
(GRCh38)12:57570022G>A
(Homo sapiens)Allele/Variant
Source: rs753854351
Genes: KIF5A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:57570022G>A
(GRCh38)12:57570036G>A
(Homo sapiens)Allele/Variant
Source: rs758700375
Genes: KIF5A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)12:57570036G>A
(GRCh38)12:57570042C>T
(Homo sapiens)Allele/Variant
Source: rs780381269
Genes: KIF5A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)12:57570042C>T
(GRCh38)12:57570084C>T
(Homo sapiens)Allele/Variant
Source: rs267603611
Genes: KIF5A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)12:57570084C>T
(GRCh38)12:57570124G>A
(Homo sapiens)Allele/Variant
Source: rs755243063
Genes: KIF5A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:57570124G>A
(GRCh38)12:57570143A>G
(Homo sapiens)Allele/Variant
Source: rs1565699454
Genes: KIF5A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:57570143A>G
(GRCh38)12:57571332C>G
(Homo sapiens)Allele/Variant
Source: rs1267848296
Genes: KIF5A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:57571332C>G
(GRCh38)12:57571334A>C
(Homo sapiens)Allele/Variant
Source: rs776102034
Genes: KIF5A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:57571334A>C
(GRCh38)12:57572056T>C
(Homo sapiens)Allele/Variant
Source: rs747818828
Genes: KIF5A (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)12:57572056T>C
(GRCh38)12:57575066C>T
(Homo sapiens)Allele/Variant
Source: rs1882379859
Genes: KIF5A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:57575066C>T
(GRCh38)12:57576337C>T
(Homo sapiens)Allele/Variant
Source: rs773330335
Genes: KIF5A (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)12:57576337C>T