Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: CPVL (Hsa) Molecular Consequence: non coding transcript exon variant
(GRCh38)7:29146646C>T
(Homo sapiens)Allele/Variant
Source: rs1173270890
Genes: CPVL (Hsa), CHN2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:29146646C>T
(GRCh38)7:29092666C>T
(Homo sapiens)Allele/Variant
Source: rs751543732
Genes: CPVL (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)7:29092666C>T
(GRCh38)7:29066049T>G
(Homo sapiens)Allele/Variant
Source: rs139506136
Genes: CPVL (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:29066049T>G
(GRCh38)7:29072332G>A
(Homo sapiens)Allele/Variant
Source: rs191349364
Genes: CPVL (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)7:29072332G>A
(GRCh38)7:28995780C>A
(Homo sapiens)Allele/Variant
Source: rs201613280
Genes: CPVL-AS2 (Hsa), CPVL (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:28995780C>A
(GRCh38)7:28995812C>T
(Homo sapiens)Allele/Variant
Source: rs147771477
Genes: CPVL-AS2 (Hsa), CPVL (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:28995812C>T
(GRCh38)7:29030680T>C
(Homo sapiens)Allele/Variant
Source: rs561008600
Genes: CPVL (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)7:29030680T>C
(GRCh38)7:29146908T>C
(Homo sapiens)Allele/Variant
Source: rs1157919216
Genes: CPVL (Hsa), CHN2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:29146908T>C
(GRCh38)7:29030638T>G
(Homo sapiens)Allele/Variant
Source: rs1459503620
Genes: CPVL (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)7:29030638T>G
(GRCh38)7:29086486C>G
(Homo sapiens)Allele/Variant
Source: rs376816938
Genes: CPVL (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant
Diseases: Not Available
Variant Name: (GRCh38)7:29086486C>G
(GRCh38)7:29095139C>T
(Homo sapiens)Allele/Variant
Source: rs376539416
Genes: CPVL (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)7:29095139C>T
(GRCh38)7:29064231G>A
(Homo sapiens)Allele/Variant
Source: rs1200521846
Genes: CPVL (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:29064231G>A
(GRCh38)7:29146841C>T
(Homo sapiens)Allele/Variant
Source: rs151181647
Genes: CPVL (Hsa), CHN2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:29146841C>T
(GRCh38)7:29064135C>G
(Homo sapiens)Allele/Variant
Source: rs1782913333
Genes: CPVL (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:29064135C>G
(GRCh38)7:29095102C>T
(Homo sapiens)Allele/Variant
Source: rs374510304
Genes: CPVL (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)7:29095102C>T
(GRCh38)7:29146601G>A
(Homo sapiens)Allele/Variant
Source: rs187292682
Genes: CPVL (Hsa), CHN2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:29146601G>A
(GRCh38)7:29064111T>C
(Homo sapiens)Allele/Variant
Source: NC_000007.14:g.29064111T>C
Genes: CPVL (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:29064111T>C
(GRCh38)7:29146736T>G
(Homo sapiens)Allele/Variant
Source: rs763980926
Genes: CPVL (Hsa), CHN2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:29146736T>G
(GRCh38)7:29194936G>A
(Homo sapiens)Allele/Variant
Source: rs368239468
Genes: CPVL (Hsa), CHN2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:29194936G>A
(GRCh38)7:29030651T>C
(Homo sapiens)Allele/Variant
Source: rs949471035
Genes: CPVL (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)7:29030651T>C
(GRCh38)7:29194958A>C
(Homo sapiens)Allele/Variant
Source: rs201909711
Genes: CPVL (Hsa), CHN2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:29194958A>C
(GRCh38)7:29030726C>T
(Homo sapiens)Allele/Variant
Source: rs776719397
Genes: CPVL (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)7:29030726C>T
(GRCh38)7:29092653T>G
(Homo sapiens)Allele/Variant
Source: rs775653828
Genes: CPVL (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)7:29092653T>G
(GRCh38)7:29064087A>C
(Homo sapiens)Allele/Variant
Source: NC_000007.14:g.29064087A>C
Genes: CPVL (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)7:29064087A>C