Version: 8.0.0
Date: Tue Jan 28 2025
16 results
Allele/Variant Genes: GLTP (Hsa)

(GRCh38)12:109855756T>C

(Homo sapiens)
Allele/Variant
Source: rs751532192
Genes: GLTP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:109855756T>C

(GRCh38)12:109852643C>T

(Homo sapiens)
Allele/Variant
Source: rs150208595
Genes: GLTP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)12:109852643C>T

(GRCh38)12:109857580T>C

(Homo sapiens)
Allele/Variant
Source: rs140842833
Genes: GLTP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:109857580T>C

(GRCh38)12:109855685G>A

(Homo sapiens)
Allele/Variant
Source: rs76870414
Genes: GLTP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)12:109855685G>A

(GRCh38)12:109855692C>T

(Homo sapiens)
Allele/Variant
Source: rs201283523
Genes: GLTP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)12:109855692C>T

(GRCh38)12:109880322A>G

(Homo sapiens)
Allele/Variant
Source: rs1869036028
Genes: GLTP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:109880322A>G

(GRCh38)12:109855686T>C

(Homo sapiens)
Allele/Variant
Source: rs749464539
Genes: GLTP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)12:109855686T>C

(GRCh38)12:109852629T>C

(Homo sapiens)
Allele/Variant
Source: rs752001793
Genes: GLTP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:109852629T>C

(GRCh38)12:109857644A>G

(Homo sapiens)
Allele/Variant
Source: rs767629735
Genes: GLTP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)12:109857644A>G

(GRCh38)12:109880370G>A

(Homo sapiens)
Allele/Variant
Source: rs866777297
Genes: GLTP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:109880370G>A

(GRCh38)12:109855752T>C

(Homo sapiens)
Allele/Variant
Source: rs1183364715
Genes: GLTP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:109855752T>C

(GRCh38)12:109855729C>T

(Homo sapiens)
Allele/Variant
Source: rs749955260
Genes: GLTP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:109855729C>T

(GRCh38)12:109857620G>A

(Homo sapiens)
Allele/Variant
Source: rs772754913
Genes: GLTP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)12:109857620G>A

(GRCh38)12:109855760G>T

(Homo sapiens)
Allele/Variant
Source: rs139982828
Genes: GLTP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)12:109855760G>T

(GRCh38)12:109858712T>C

(Homo sapiens)
Allele/Variant
Source: rs145689737
Genes: GLTP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)12:109858712T>C

(GRCh38)12:109855720G>A

(Homo sapiens)
Allele/Variant
Source: rs199522267
Genes: GLTP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)12:109855720G>A