Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: SAP30L-AS1 (Hsa)
(GRCh38)5:154412971G>C
(Homo sapiens)Allele/Variant
Source: rs754240894
Genes: SAP30L-AS1 (Hsa), GALNT10 (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)5:154412971G>C
(GRCh38)5:154415905G>A
(Homo sapiens)Allele/Variant
Source: rs35405339
Genes: SAP30L-AS1 (Hsa), GALNT10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)5:154415905G>A
(GRCh38)5:154412977G>A
(Homo sapiens)Allele/Variant
Source: rs779123658
Genes: SAP30L-AS1 (Hsa), GALNT10 (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)5:154412977G>A
(GRCh38)5:154329585C>T
(Homo sapiens)Allele/Variant
Source: rs150192577
Genes: SAP30L-AS1 (Hsa), GALNT10 (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)5:154329585C>T
(GRCh38)5:154329693G>C
(Homo sapiens)Allele/Variant
Source: rs1754813589
Genes: SAP30L-AS1 (Hsa), GALNT10 (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)5:154329693G>C
(GRCh38)5:154380499T>C
(Homo sapiens)Allele/Variant
Source: rs1327489320
Genes: SAP30L-AS1 (Hsa), GALNT10 (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)5:154380499T>C
(GRCh38)5:154380547G>A
(Homo sapiens)Allele/Variant
Source: rs1310370303
Genes: SAP30L-AS1 (Hsa), GALNT10 (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)5:154380547G>A
(GRCh38)5:154380592C>T
(Homo sapiens)Allele/Variant
Source: rs1263772085
Genes: SAP30L-AS1 (Hsa), GALNT10 (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)5:154380592C>T
(GRCh38)5:154409607G>A
(Homo sapiens)Allele/Variant
Source: rs267600504
Genes: SAP30L-AS1 (Hsa), GALNT10 (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)5:154409607G>A
(GRCh38)5:154329663G>A
(Homo sapiens)Allele/Variant
Source: rs780422451
Genes: SAP30L-AS1 (Hsa), GALNT10 (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)5:154329663G>A
(GRCh38)5:154365612C>G
(Homo sapiens)Allele/Variant
Source: rs207466473
Genes: SAP30L-AS1 (Hsa), GALNT10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)5:154365612C>G
(GRCh38)5:154376348C>T
(Homo sapiens)Allele/Variant
Source: rs760733045
Genes: SAP30L-AS1 (Hsa), GALNT10 (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)5:154376348C>T
(GRCh38)5:154416829C>T
(Homo sapiens)Allele/Variant
Source: rs1162720679
Genes: SAP30L-AS1 (Hsa), GALNT10 (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)5:154416829C>T
(GRCh38)5:154329699G>C
(Homo sapiens)Allele/Variant
Source: rs760251759
Genes: SAP30L-AS1 (Hsa), GALNT10 (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)5:154329699G>C
(GRCh38)5:154409733G>A
(Homo sapiens)Allele/Variant
Source: rs117925322
Genes: SAP30L-AS1 (Hsa), GALNT10 (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)5:154409733G>A
(GRCh38)5:154380516C>T
(Homo sapiens)Allele/Variant
Source: rs1182774029
Genes: SAP30L-AS1 (Hsa), GALNT10 (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)5:154380516C>T
(GRCh38)5:154329679A>G
(Homo sapiens)Allele/Variant
Source: rs143021082
Genes: SAP30L-AS1 (Hsa), GALNT10 (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)5:154329679A>G
(GRCh38)5:154380579C>T
(Homo sapiens)Allele/Variant
Source: rs2161344
Genes: SAP30L-AS1 (Hsa), GALNT10 (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)5:154380579C>T
(GRCh38)5:154415855G>A
(Homo sapiens)Allele/Variant
Source: rs745580007
Genes: SAP30L-AS1 (Hsa), GALNT10 (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)5:154415855G>A
(GRCh38)5:154329721A>C
(Homo sapiens)Allele/Variant
Source: NC_000005.10:g.154329721A>C
Genes: SAP30L-AS1 (Hsa), GALNT10 (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)5:154329721A>C
(GRCh38)5:154329665C>T
(Homo sapiens)Allele/Variant
Source: rs267600503
Genes: SAP30L-AS1 (Hsa), GALNT10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)5:154329665C>T
(GRCh38)5:154404123G>A
(Homo sapiens)Allele/Variant
Source: rs745659437
Genes: SAP30L-AS1 (Hsa), GALNT10 (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)5:154404123G>A
(GRCh38)5:154416934A>G
(Homo sapiens)Allele/Variant
Source: rs765242816
Genes: SAP30L-AS1 (Hsa), GALNT10 (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)5:154416934A>G
(GRCh38)5:154376312C>T
(Homo sapiens)Allele/Variant
Source: rs781081604
Genes: SAP30L-AS1 (Hsa), GALNT10 (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)5:154376312C>T
(GRCh38)5:154415814G>A
(Homo sapiens)Allele/Variant
Source: rs777623511
Genes: SAP30L-AS1 (Hsa), GALNT10 (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)5:154415814G>A
(GRCh38)5:154329658G>T
(Homo sapiens)Allele/Variant
Source: rs1395963489
Genes: SAP30L-AS1 (Hsa), GALNT10 (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)5:154329658G>T
(GRCh38)5:154409732C>T
(Homo sapiens)Allele/Variant
Source: rs142666444
Genes: SAP30L-AS1 (Hsa), GALNT10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)5:154409732C>T
(GRCh38)5:154412893G>A
(Homo sapiens)Allele/Variant
Source: rs142635658
Genes: SAP30L-AS1 (Hsa), GALNT10 (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)5:154412893G>A
(GRCh38)5:154416913C>G
(Homo sapiens)Allele/Variant
Source: NC_000005.10:g.154416913C>G
Genes: SAP30L-AS1 (Hsa), GALNT10 (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)5:154416913C>G
(GRCh38)5:154376390G>T
(Homo sapiens)Allele/Variant
Source: rs775888631
Genes: SAP30L-AS1 (Hsa), GALNT10 (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)5:154376390G>T
(GRCh38)5:154329719C>T
(Homo sapiens)Allele/Variant
Source: rs138007001
Genes: SAP30L-AS1 (Hsa), GALNT10 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)5:154329719C>T
(GRCh38)5:154376306A>G
(Homo sapiens)Allele/Variant
Source: rs751467853
Genes: SAP30L-AS1 (Hsa), GALNT10 (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)5:154376306A>G
(GRCh38)5:154416962A>G
(Homo sapiens)Allele/Variant
Source: rs1756525852
Genes: SAP30L-AS1 (Hsa), GALNT10 (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)5:154416962A>G