Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: KMT2C (Hsa)
(GRCh38)7:152194426G>A
(Homo sapiens)Allele/Variant
Source: rs1355253914
Genes: KMT2C (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)7:152194426G>A
(GRCh38)7:152252106T>C
(Homo sapiens)Allele/Variant
Source: rs762988552
Genes: KMT2C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:152252106T>C
(GRCh38)7:152136909T>G
(Homo sapiens)Allele/Variant
Source: rs779818288
Genes: KMT2C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, 3_prime_UTR_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)7:152136909T>G
(GRCh38)7:152139713C>T
(Homo sapiens)Allele/Variant
Source: rs1179701584
Genes: KMT2C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)7:152139713C>T
(GRCh38)7:152139731C>T
(Homo sapiens)Allele/Variant
Source: rs2129089876
Genes: KMT2C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)7:152139731C>T
(GRCh38)7:152148810G>A
(Homo sapiens)Allele/Variant
Source: rs1057522023
Genes: KMT2C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)7:152148810G>A
(GRCh38)7:152148720A>C
(Homo sapiens)Allele/Variant
Source: NC_000007.14:g.152148720A>C
Genes: KMT2C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)7:152148720A>C
(GRCh38)7:152162428C>G
(Homo sapiens)Allele/Variant
Source: rs587778506
Genes: KMT2C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:152162428C>G
(GRCh38)7:152152788G>A
(Homo sapiens)Allele/Variant
Source: rs141718495
Genes: KMT2C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:152152788G>A
(GRCh38)7:152152804G>C
(Homo sapiens)Allele/Variant
Source: rs530766982
Genes: KMT2C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, stop_gained, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:152152804G>C
(GRCh38)7:152163217A>G
(Homo sapiens)Allele/Variant
Source: NC_000007.14:g.152163217A>G
Genes: KMT2C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)7:152163217A>G
(GRCh38)7:152163590C>T
(Homo sapiens)Allele/Variant
Source: rs200804156
Genes: KMT2C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:152163590C>T
(GRCh38)7:152167336G>C
(Homo sapiens)Allele/Variant
Source: rs1179763290
Genes: KMT2C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:152167336G>C
(GRCh38)7:152177061C>G
(Homo sapiens)Allele/Variant
Source: rs2129114146
Genes: KMT2C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:152177061C>G
(GRCh38)7:152177420G>A
(Homo sapiens)Allele/Variant
Source: rs749652990
Genes: KMT2C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)7:152177420G>A
(GRCh38)7:152176566G>A
(Homo sapiens)Allele/Variant
Source: rs187761353
Genes: KMT2C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)7:152176566G>A
(GRCh38)7:152176862T>A
(Homo sapiens)Allele/Variant
Source: rs1175330866
Genes: KMT2C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, stop_lost
Diseases: Not Available
Variant Name: (GRCh38)7:152176862T>A
(GRCh38)7:152176928T>C
(Homo sapiens)Allele/Variant
Source: NC_000007.14:g.152176928T>C
Genes: KMT2C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)7:152176928T>C
(GRCh38)7:152177817A>G
(Homo sapiens)Allele/Variant
Source: rs2129115447
Genes: KMT2C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)7:152177817A>G
(GRCh38)7:152177822T>C
(Homo sapiens)Allele/Variant
Source: rs752687658
Genes: KMT2C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)7:152177822T>C
(GRCh38)7:152162242G>C
(Homo sapiens)Allele/Variant
Source: rs375641244
Genes: KMT2C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:152162242G>C
(GRCh38)7:152162252T>A
(Homo sapiens)Allele/Variant
Source: rs2129103632
Genes: KMT2C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:152162252T>A
(GRCh38)7:152163329C>T
(Homo sapiens)Allele/Variant
Source: rs1014894801
Genes: KMT2C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:152163329C>T
(GRCh38)7:152163403T>C
(Homo sapiens)Allele/Variant
Source: NC_000007.14:g.152163403T>C
Genes: KMT2C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)7:152163403T>C
(GRCh38)7:152163241T>A
(Homo sapiens)Allele/Variant
Source: rs902827242
Genes: KMT2C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)7:152163241T>A
(GRCh38)7:152167296T>C
(Homo sapiens)Allele/Variant
Source: rs2092772366
Genes: KMT2C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)7:152167296T>C
(GRCh38)7:152177612C>A
(Homo sapiens)Allele/Variant
Source: rs767634921
Genes: KMT2C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)7:152177612C>A
(GRCh38)7:152163799C>T
(Homo sapiens)Allele/Variant
Source: NC_000007.14:g.152163799C>T
Genes: KMT2C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)7:152163799C>T
(GRCh38)7:152177272G>A
(Homo sapiens)Allele/Variant
Source: rs1322390862
Genes: KMT2C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, stop_gained, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)7:152177272G>A
(GRCh38)7:152177724G>A
(Homo sapiens)Allele/Variant
Source: rs758721377
Genes: KMT2C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)7:152177724G>A
(GRCh38)7:152247896C>A
(Homo sapiens)Allele/Variant
Source: rs3888468
Genes: KMT2C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:152247896C>A
(GRCh38)7:152247920A>G
(Homo sapiens)Allele/Variant
Source: rs1316899199
Genes: KMT2C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)7:152247920A>G
(GRCh38)7:152185650G>A
(Homo sapiens)Allele/Variant
Source: rs62481492
Genes: KMT2C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:152185650G>A
(GRCh38)7:152148784T>C
(Homo sapiens)Allele/Variant
Source: rs763456325
Genes: KMT2C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)7:152148784T>C
(GRCh38)7:152144698A>G
(Homo sapiens)Allele/Variant
Source: rs764549868
Genes: KMT2C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:152144698A>G
(GRCh38)7:152151444T>C
(Homo sapiens)Allele/Variant
Source: rs1339162677
Genes: KMT2C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)7:152151444T>C
(GRCh38)7:152146689C>A
(Homo sapiens)Allele/Variant
Source: rs745406929
Genes: KMT2C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:152146689C>A
(GRCh38)7:152150924T>C
(Homo sapiens)Allele/Variant
Source: rs1199326789
Genes: KMT2C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)7:152150924T>C
(GRCh38)7:152148393G>T
(Homo sapiens)Allele/Variant
Source: rs375361560
Genes: KMT2C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:152148393G>T
(GRCh38)7:152151538G>A
(Homo sapiens)Allele/Variant
Source: rs149872298
Genes: KMT2C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)7:152151538G>A
(GRCh38)7:152154463C>T
(Homo sapiens)Allele/Variant
Source: rs2129098891
Genes: KMT2C (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)7:152154463C>T
(GRCh38)7:152146675T>C
(Homo sapiens)Allele/Variant
Source: rs1367775137
Genes: KMT2C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:152146675T>C
(GRCh38)7:152162123T>C
(Homo sapiens)Allele/Variant
Source: rs886250600
Genes: KMT2C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)7:152162123T>C
(GRCh38)7:152162666G>A
(Homo sapiens)Allele/Variant
Source: rs138353962
Genes: KMT2C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)7:152162666G>A
(GRCh38)7:152162191C>T
(Homo sapiens)Allele/Variant
Source: rs2092491509
Genes: KMT2C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)7:152162191C>T
(GRCh38)7:152156227G>A
(Homo sapiens)Allele/Variant
Source: rs767946417
Genes: KMT2C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)7:152156227G>A
(GRCh38)7:152162214G>A
(Homo sapiens)Allele/Variant
Source: rs770450253
Genes: KMT2C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:152162214G>A
(GRCh38)7:152162243T>G
(Homo sapiens)Allele/Variant
Source: NC_000007.14:g.152162243T>G
Genes: KMT2C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)7:152162243T>G
(GRCh38)7:152158920G>A
(Homo sapiens)Allele/Variant
Source: rs369567780
Genes: KMT2C (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)7:152158920G>A
(GRCh38)7:152154278G>A
(Homo sapiens)Allele/Variant
Source: rs367748947
Genes: KMT2C (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)7:152154278G>A