Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: PRKCE (Hsa)
(GRCh38)2:46086231A>T
(Homo sapiens)Allele/Variant
Source: NC_000002.12:g.46086231A>T
Genes: PRKCE (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)2:46086231A>T
(GRCh38)2:46007602C>T
(Homo sapiens)Allele/Variant
Source: rs772347149
Genes: PRKCE (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:46007602C>T
(GRCh38)2:46086289C>A
(Homo sapiens)Allele/Variant
Source: rs773271544
Genes: PRKCE (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)2:46086289C>A
(GRCh38)2:46159645G>A
(Homo sapiens)Allele/Variant
Source: rs35777875
Genes: PRKCE (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)2:46159645G>A
(GRCh38)2:46007564C>G
(Homo sapiens)Allele/Variant
Source: rs55767130
Genes: PRKCE (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)2:46007564C>G
(GRCh38)2:46010391G>A
(Homo sapiens)Allele/Variant
Source: rs56005919
Genes: PRKCE (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 3_prime_UTR_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)2:46010391G>A
(GRCh38)2:45976482C>A
(Homo sapiens)Allele/Variant
Source: rs1470650959
Genes: PRKCE (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)2:45976482C>A
(GRCh38)2:46151202C>A
(Homo sapiens)Allele/Variant
Source: NC_000002.12:g.46151202C>A
Genes: PRKCE (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)2:46151202C>A
(GRCh38)2:45652107G>C
(Homo sapiens)Allele/Variant
Source: NC_000002.12:g.45652107G>C
Genes: PRKCE (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:45652107G>C
(GRCh38)2:46007502A>G
(Homo sapiens)Allele/Variant
Source: rs41281465
Genes: PRKCE (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)2:46007502A>G
(GRCh38)2:46007504T>A
(Homo sapiens)Allele/Variant
Source: rs1301202682
Genes: PRKCE (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)2:46007504T>A
(GRCh38)2:45976465G>A
(Homo sapiens)Allele/Variant
Source: rs752964225
Genes: PRKCE (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)2:45976465G>A
(GRCh38)2:46086305A>G
(Homo sapiens)Allele/Variant
Source: rs1669634029
Genes: PRKCE (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)2:46086305A>G
(GRCh38)2:46007549G>C
(Homo sapiens)Allele/Variant
Source: rs919285181
Genes: PRKCE (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:46007549G>C
(GRCh38)2:46151104G>A
(Homo sapiens)Allele/Variant
Source: rs1553363925
Genes: PRKCE (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)2:46151104G>A
(GRCh38)2:46007492A>C
(Homo sapiens)Allele/Variant
Source: NC_000002.12:g.46007492A>C
Genes: PRKCE (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:46007492A>C
(GRCh38)2:45692171C>T
(Homo sapiens)Allele/Variant
Source: rs207461693
Genes: PRKCE (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:45692171C>T
(GRCh38)2:46001554G>A
(Homo sapiens)Allele/Variant
Source: rs41305977
Genes: PRKCE (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:46001554G>A
(GRCh38)2:45762113A>G
(Homo sapiens)Allele/Variant
Source: rs207461694
Genes: PRKCE (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:45762113A>G
(GRCh38)2:46086303C>G
(Homo sapiens)Allele/Variant
Source: rs765421914
Genes: PRKCE (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)2:46086303C>G
(GRCh38)2:46086299G>A
(Homo sapiens)Allele/Variant
Source: rs74990336
Genes: PRKCE (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)2:46086299G>A
(GRCh38)2:45984593G>A
(Homo sapiens)Allele/Variant
Source: rs746022435
Genes: PRKCE (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)2:45984593G>A
(GRCh38)2:46007479A>G
(Homo sapiens)Allele/Variant
Source: rs770831489
Genes: PRKCE (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)2:46007479A>G
(GRCh38)2:46010445A>G
(Homo sapiens)Allele/Variant
Source: rs61730655
Genes: PRKCE (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 3_prime_UTR_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)2:46010445A>G