Version: 8.0.0
Date: Tue Jan 28 2025
5 results
Allele/Variant Genes: RTCB (Hsa) Molecular Consequence: missense variant

(GRCh38)22:32407123T>C

(Homo sapiens)
Allele/Variant
Source: rs207477955
Genes: RTCB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)22:32407123T>C

(GRCh38)22:32398100A>G

(Homo sapiens)
Allele/Variant
Source: rs750059803
Genes: RTCB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)22:32398100A>G

(GRCh38)22:32399645G>A

(Homo sapiens)
Allele/Variant
Source: rs267606232
Genes: RTCB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)22:32399645G>A

(GRCh38)22:32395164C>G

(Homo sapiens)
Allele/Variant
Source: rs41310258
Genes: RTCB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)22:32395164C>G

(GRCh38)22:32396236A>G

(Homo sapiens)
Allele/Variant
Source: rs10222228
Genes: RTCB (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)22:32396236A>G