Version: 8.0.0
Date: Tue Jan 28 2025
14 results
Allele/Variant Genes: CPLX3 (Hsa)

(GRCh38)15:74830131A>G

(Homo sapiens)
Allele/Variant
Source: rs372883520
Genes: CPLX3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant
Diseases: Not Available
Variant Name: (GRCh38)15:74830131A>G

(GRCh38)15:74830171C>A

(Homo sapiens)
Allele/Variant
Source: rs143709534
Genes: CPLX3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)15:74830171C>A

(GRCh38)15:74830152T>C

(Homo sapiens)
Allele/Variant
Source: rs1209596277
Genes: CPLX3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)15:74830152T>C

(GRCh38)15:74830181C>A

(Homo sapiens)
Allele/Variant
Source: rs147232026
Genes: CPLX3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)15:74830181C>A

(GRCh38)15:74826734G>A

(Homo sapiens)
Allele/Variant
Source: rs750321038
Genes: CPLX3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)15:74826734G>A

(GRCh38)15:74830263T>G

(Homo sapiens)
Allele/Variant
Source: NC_000015.10:g.74830263T>G
Genes: CPLX3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)15:74830263T>G

(GRCh38)15:74828074C>T

(Homo sapiens)
Allele/Variant
Source: rs750876615
Genes: CPLX3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)15:74828074C>T

(GRCh38)15:74828080A>G

(Homo sapiens)
Allele/Variant
Source: rs889466758
Genes: CPLX3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)15:74828080A>G

(GRCh38)15:74828108A>G

(Homo sapiens)
Allele/Variant
Source: rs770689700
Genes: CPLX3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)15:74828108A>G

(GRCh38)15:74830172G>A

(Homo sapiens)
Allele/Variant
Source: rs199684945
Genes: CPLX3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)15:74830172G>A

(GRCh38)15:74826818A>G

(Homo sapiens)
Allele/Variant
Source: rs761543817
Genes: CPLX3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)15:74826818A>G

(GRCh38)15:74828045A>G

(Homo sapiens)
Allele/Variant
Source: rs763267758
Genes: CPLX3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)15:74828045A>G

(GRCh38)15:74828099G>A

(Homo sapiens)
Allele/Variant
Source: rs746835545
Genes: CPLX3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)15:74828099G>A

(GRCh38)15:74830169G>A

(Homo sapiens)
Allele/Variant
Source: rs775522144
Genes: CPLX3 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)15:74830169G>A