Version: 8.0.0
Date: Tue Jan 28 2025
5 results
Allele/Variant Genes: SAP30-DT (Hsa)

(GRCh38)4:173371244C>T

(Homo sapiens)
Allele/Variant
Source: rs1216814236
Genes: SAP30-DT (Hsa), SAP30 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:173371244C>T

(GRCh38)4:173371346C>T

(Homo sapiens)
Allele/Variant
Source: rs761794960
Genes: SAP30-DT (Hsa), SAP30 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:173371346C>T

(GRCh38)4:173371354G>A

(Homo sapiens)
Allele/Variant
Source: rs773166192
Genes: SAP30-DT (Hsa), SAP30 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:173371354G>A

(GRCh38)4:173371378C>G

(Homo sapiens)
Allele/Variant
Source: rs201052655
Genes: SAP30-DT (Hsa), SAP30 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:173371378C>G

(GRCh38)4:173371198C>T

(Homo sapiens)
Allele/Variant
Source: rs755058022
Genes: SAP30-DT (Hsa), SAP30 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)4:173371198C>T