Version: 8.0.0
Date: Tue Jan 28 2025
15 results
Allele/Variant Genes: PRKCE (Hsa) Molecular Consequence: synonymous variant

(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)2:46151202C>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)2:46007549G>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)2:45984593G>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