Version: 8.0.0
Date: Tue Jan 28 2025
11 results for calc1
Allele/Variant

(GRCh38)11:14967805G>A

(Homo sapiens)
Allele/Variant
Source: rs782816793
Genes: CALCA (Hsa), CALCB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:14967805G>A
Gene Synonyms: CALC1

(GRCh38)11:14970040G>A

(Homo sapiens)
Allele/Variant
Source: rs147263808
Genes: CALCA (Hsa), CALCB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:14970040G>A
Gene Synonyms: CALC1

(GRCh38)11:14968891C>A

(Homo sapiens)
Allele/Variant
Source: rs34670162
Genes: CALCA (Hsa), CALCB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:14968891C>A
Gene Synonyms: CALC1

(GRCh38)11:14967804C>T

(Homo sapiens)
Allele/Variant
Source: rs782028430
Genes: CALCA (Hsa), CALCB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:14967804C>T
Gene Synonyms: CALC1

(GRCh38)11:14968847C>T

(Homo sapiens)
Allele/Variant
Source: rs35425520
Genes: CALCA (Hsa), CALCB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:14968847C>T
Gene Synonyms: CALC1

(GRCh38)11:14967707G>T

(Homo sapiens)
Allele/Variant
Source: rs781977175
Genes: CALCA (Hsa), CALCB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:14967707G>T
Gene Synonyms: CALC1

(GRCh38)11:14968907G>A

(Homo sapiens)
Allele/Variant
Source: rs142242325
Genes: CALCA (Hsa), CALCB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:14968907G>A
Gene Synonyms: CALC1

(GRCh38)11:14967715G>A

(Homo sapiens)
Allele/Variant
Source: rs782436716
Genes: CALCA (Hsa), CALCB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:14967715G>A
Gene Synonyms: CALC1

(GRCh38)11:14967810G>T

(Homo sapiens)
Allele/Variant
Source: rs1376969693
Genes: CALCA (Hsa), CALCB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:14967810G>T
Gene Synonyms: CALC1

(GRCh38)11:14971141A>T

(Homo sapiens)
Allele/Variant
Source: rs144571175
Genes: CALCA (Hsa), CALCB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:14971141A>T
Gene Synonyms: CALC1

(GRCh38)11:14971162C>T

(Homo sapiens)
Allele/Variant
Source: rs1555026441
Genes: CALCA (Hsa), CALCB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)11:14971162C>T
Gene Synonyms: CALC1