Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: HRAS (Hsa)
(GRCh38)11:532668C>T
(Homo sapiens)Allele/Variant
Source: rs772602067
Genes: HRAS (Hsa), LRRC56 (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)11:532668C>T
(GRCh38)11:532639G>C
(Homo sapiens)Allele/Variant
Source: rs1324657141
Genes: HRAS (Hsa), LRRC56 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:532639G>C
(GRCh38)11:532775A>C
(Homo sapiens)Allele/Variant
Source: NC_000011.10:g.532775A>C
Genes: HRAS (Hsa), LRRC56 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:532775A>C
(GRCh38)11:533308C>T
(Homo sapiens)Allele/Variant
Source: rs764211685
Genes: HRAS (Hsa), LRRC56 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:533308C>T
(GRCh38)11:533623G>A
(Homo sapiens)Allele/Variant
Source: rs750444909
Genes: HRAS (Hsa), LRRC56 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:533623G>A
(GRCh38)11:533765C>G
(Homo sapiens)Allele/Variant
Source: rs1851270546
Genes: HRAS (Hsa), LRRC56 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, splice_donor_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:533765C>G
(GRCh38)11:533777G>A
(Homo sapiens)Allele/Variant
Source: rs2133989886
Genes: HRAS (Hsa), LRRC56 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:533777G>A
(GRCh38)11:533545G>A
(Homo sapiens)Allele/Variant
Source: rs397517139
Genes: HRAS (Hsa), LRRC56 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:533545G>A
(GRCh38)11:533585C>T
(Homo sapiens)Allele/Variant
Source: rs1053376922
Genes: HRAS (Hsa), LRRC56 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:533585C>T
(GRCh38)11:533586G>C
(Homo sapiens)Allele/Variant
Source: rs730880462
Genes: HRAS (Hsa), LRRC56 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:533586G>C
(GRCh38)11:532685G>T
(Homo sapiens)Allele/Variant
Source: rs2133982181
Genes: HRAS (Hsa), LRRC56 (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)11:532685G>T
(GRCh38)11:532639G>A
(Homo sapiens)Allele/Variant
Source: rs1324657141
Genes: HRAS (Hsa), LRRC56 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:532639G>A
(GRCh38)11:532642G>C
(Homo sapiens)Allele/Variant
Source: rs2133981970
Genes: HRAS (Hsa), LRRC56 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:532642G>C
(GRCh38)11:532655C>G
(Homo sapiens)Allele/Variant
Source: rs2133982018
Genes: HRAS (Hsa), LRRC56 (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)11:532655C>G
(GRCh38)11:532660C>T
(Homo sapiens)Allele/Variant
Source: rs748639813
Genes: HRAS (Hsa), LRRC56 (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)11:532660C>T
(GRCh38)11:532743C>T
(Homo sapiens)Allele/Variant
Source: rs1171537215
Genes: HRAS (Hsa), LRRC56 (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)11:532743C>T
(GRCh38)11:532722C>G
(Homo sapiens)Allele/Variant
Source: rs1564787942
Genes: HRAS (Hsa), LRRC56 (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)11:532722C>G
(GRCh38)11:533037G>A
(Homo sapiens)Allele/Variant
Source: rs45626636
Genes: HRAS (Hsa), LRRC56 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:533037G>A
(GRCh38)11:533433G>A
(Homo sapiens)Allele/Variant
Source: rs201524241
Genes: HRAS (Hsa), LRRC56 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:533433G>A
(GRCh38)11:533435G>A
(Homo sapiens)Allele/Variant
Source: rs1057522255
Genes: HRAS (Hsa), LRRC56 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:533435G>A
(GRCh38)11:532803G>A
(Homo sapiens)Allele/Variant
Source: rs45607337
Genes: HRAS (Hsa), LRRC56 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:532803G>A
(GRCh38)11:533311G>C
(Homo sapiens)Allele/Variant
Source: rs377676071
Genes: HRAS (Hsa), LRRC56 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:533311G>C
(GRCh38)11:533329G>A
(Homo sapiens)Allele/Variant
Source: rs1057522069
Genes: HRAS (Hsa), LRRC56 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:533329G>A
(GRCh38)11:533539C>T
(Homo sapiens)Allele/Variant
Source: rs1851244921
Genes: HRAS (Hsa), LRRC56 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:533539C>T
(GRCh38)11:533543C>G
(Homo sapiens)Allele/Variant
Source: rs1851245565
Genes: HRAS (Hsa), LRRC56 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:533543C>G
(GRCh38)11:533528C>G
(Homo sapiens)Allele/Variant
Source: rs1851243465
Genes: HRAS (Hsa), LRRC56 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:533528C>G
(GRCh38)11:533534G>A
(Homo sapiens)Allele/Variant
Source: rs200945755
Genes: HRAS (Hsa), LRRC56 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:533534G>A
(GRCh38)11:533586G>A
(Homo sapiens)Allele/Variant
Source: rs730880462
Genes: HRAS (Hsa), LRRC56 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:533586G>A
(GRCh38)11:533796G>T
(Homo sapiens)Allele/Variant
Source: rs1851272986
Genes: HRAS (Hsa), LRRC56 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:533796G>T
(GRCh38)11:533922A>T
(Homo sapiens)Allele/Variant
Source: rs1028352031
Genes: HRAS (Hsa), LRRC56 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:533922A>T
(GRCh38)11:535413C>T
(Homo sapiens)Allele/Variant
Source: NC_000011.10:g.535413C>T
Genes: HRAS (Hsa), LRRC56 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:535413C>T
(GRCh38)11:535596C>T
(Homo sapiens)Allele/Variant
Source: rs8176335
Genes: HRAS (Hsa), LRRC56 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:535596C>T
(GRCh38)11:533455G>A
(Homo sapiens)Allele/Variant
Source: rs1064796999
Genes: HRAS (Hsa), LRRC56 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, stop_gained, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:533455G>A
(GRCh38)11:533756C>T
(Homo sapiens)Allele/Variant
Source: rs769212136
Genes: HRAS (Hsa), LRRC56 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:533756C>T
(GRCh38)11:533757G>C
(Homo sapiens)Allele/Variant
Source: rs747854581
Genes: HRAS (Hsa), LRRC56 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:533757G>C
(GRCh38)11:533828C>T
(Homo sapiens)Allele/Variant
Source: rs1057522598
Genes: HRAS (Hsa), LRRC56 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:533828C>T
(GRCh38)11:533541G>T
(Homo sapiens)Allele/Variant
Source: rs376667492
Genes: HRAS (Hsa), LRRC56 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:533541G>T
(GRCh38)11:533846C>T
(Homo sapiens)Allele/Variant
Source: rs1371974169
Genes: HRAS (Hsa), LRRC56 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:533846C>T
(GRCh38)11:533571A>G
(Homo sapiens)Allele/Variant
Source: rs1564789063
Genes: HRAS (Hsa), LRRC56 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:533571A>G
(GRCh38)11:533855C>T
(Homo sapiens)Allele/Variant
Source: NC_000011.10:g.533855C>T
Genes: HRAS (Hsa), LRRC56 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:533855C>T
(GRCh38)11:533861G>A
(Homo sapiens)Allele/Variant
Source: rs898057728
Genes: HRAS (Hsa), LRRC56 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:533861G>A
(GRCh38)11:533512G>A
(Homo sapiens)Allele/Variant
Source: rs376688893
Genes: HRAS (Hsa), LRRC56 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:533512G>A
(GRCh38)11:533512G>C
(Homo sapiens)Allele/Variant
Source: rs376688893
Genes: HRAS (Hsa), LRRC56 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:533512G>C
(GRCh38)11:535369G>A
(Homo sapiens)Allele/Variant
Source: rs111720508
Genes: HRAS (Hsa), LRRC56 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:535369G>A
(GRCh38)11:532666G>A
(Homo sapiens)Allele/Variant
Source: rs976055009
Genes: HRAS (Hsa), LRRC56 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:532666G>A
(GRCh38)11:532607G>A
(Homo sapiens)Allele/Variant
Source: rs375219797
Genes: HRAS (Hsa), LRRC56 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:532607G>A
(GRCh38)11:532661A>G
(Homo sapiens)Allele/Variant
Source: rs1851174858
Genes: HRAS (Hsa), LRRC56 (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)11:532661A>G
(GRCh38)11:532765G>A
(Homo sapiens)Allele/Variant
Source: rs1589789759
Genes: HRAS (Hsa), LRRC56 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:532765G>A
(GRCh38)11:533617G>C
(Homo sapiens)Allele/Variant
Source: rs1851252077
Genes: HRAS (Hsa), LRRC56 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:533617G>C
(GRCh38)11:533763C>A
(Homo sapiens)Allele/Variant
Source: rs771562113
Genes: HRAS (Hsa), LRRC56 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:533763C>A