Version: 8.0.0
Date: Tue Jan 28 2025
10 results
Allele/Variant Genes: SAP30L (Hsa)

(GRCh38)5:154456003C>T

(Homo sapiens)
Allele/Variant
Source: rs201712433
Genes: SAP30L (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:154456003C>T

(GRCh38)5:154446704G>A

(Homo sapiens)
Allele/Variant
Source: rs763733486
Genes: SAP30L (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:154446704G>A

(GRCh38)5:154451208C>A

(Homo sapiens)
Allele/Variant
Source: rs1464617195
Genes: SAP30L (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:154451208C>A

(GRCh38)5:154446644C>A

(Homo sapiens)
Allele/Variant
Source: rs763566646
Genes: SAP30L (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:154446644C>A

(GRCh38)5:154446640A>C

(Homo sapiens)
Allele/Variant
Source: rs755763544
Genes: SAP30L (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:154446640A>C

(GRCh38)5:154455960A>G

(Homo sapiens)
Allele/Variant
Source: rs916419432
Genes: SAP30L (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:154455960A>G

(GRCh38)5:154453456A>C

(Homo sapiens)
Allele/Variant
Source: rs367725958
Genes: SAP30L (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:154453456A>C

(GRCh38)5:154451166A>G

(Homo sapiens)
Allele/Variant
Source: rs200193163
Genes: SAP30L (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:154451166A>G

(GRCh38)5:154451208C>G

(Homo sapiens)
Allele/Variant
Source: rs1464617195
Genes: SAP30L (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:154451208C>G

(GRCh38)5:154446660C>T

(Homo sapiens)
Allele/Variant
Source: rs774022587
Genes: SAP30L (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)5:154446660C>T