Version: 8.0.0
Date: Tue Jan 28 2025

Allele/Variant

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6 results
Allele/Variant Genes: SAP30 (Hsa) Molecular Consequence: intron variant

(GRCh38)4:173374006G>A

(Homo sapiens)
Allele/Variant
Source: rs1334996759
Genes: SAP30 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)4:173374006G>A

(GRCh38)4:173377260A>G

(Homo sapiens)
Allele/Variant
Source: rs766319460
Genes: SAP30 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)4:173377260A>G

(GRCh38)4:173373997T>C

(Homo sapiens)
Allele/Variant
Source: NC_000004.12:g.173373997T>C
Genes: SAP30 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)4:173373997T>C

(GRCh38)4:173373504G>C

(Homo sapiens)
Allele/Variant
Source: rs760157384
Genes: SAP30 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)4:173373504G>C

(GRCh38)4:173377313A>G

(Homo sapiens)
Allele/Variant
Source: rs372261909
Genes: SAP30 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)4:173377313A>G

(GRCh38)4:173377251C>T

(Homo sapiens)
Allele/Variant
Source: rs985898074
Genes: SAP30 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)4:173377251C>T