Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Molecular Consequence: intron variant
(GRCh38)9:136367620G>A
(Homo sapiens)Allele/Variant
Source: rs371771167
Genes: CARD9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:136367620G>A
(GRCh38)9:136364362C>T
(Homo sapiens)Allele/Variant
Source: rs77469895
Genes: CARD9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:136364362C>T
(GRCh38)9:136370448C>A
(Homo sapiens)Allele/Variant
Source: rs528166226
Genes: CARD9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:136370448C>A
(GRCh38)9:136369735C>A
(Homo sapiens)Allele/Variant
Source: NC_000009.12:g.136369735C>A
Genes: CARD9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:136369735C>A
(GRCh38)9:136370279C>T
(Homo sapiens)Allele/Variant
Source: rs555867171
Genes: CARD9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:136370279C>T
(GRCh38)9:136370274C>T
(Homo sapiens)Allele/Variant
Source: rs569579324
Genes: CARD9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:136370274C>T
(GRCh38)9:136370279C>G
(Homo sapiens)Allele/Variant
Source: rs555867171
Genes: CARD9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:136370279C>G
(GRCh38)9:136370290C>T
(Homo sapiens)Allele/Variant
Source: rs757527643
Genes: CARD9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:136370290C>T
(GRCh38)9:136370510C>T
(Homo sapiens)Allele/Variant
Source: rs74954029
Genes: CARD9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:136370510C>T
(GRCh38)9:136365182A>G
(Homo sapiens)Allele/Variant
Source: rs373635926
Genes: CARD9 (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)9:136365182A>G
(GRCh38)9:136364172C>T
(Homo sapiens)Allele/Variant
Source: rs545913331
Genes: CARD9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:136364172C>T
(GRCh38)9:136370445G>A
(Homo sapiens)Allele/Variant
Source: rs542391727
Genes: CARD9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:136370445G>A
(GRCh38)9:136370515G>A
(Homo sapiens)Allele/Variant
Source: rs377757780
Genes: CARD9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:136370515G>A
(GRCh38)9:136369886C>T
(Homo sapiens)Allele/Variant
Source: rs747130473
Genes: CARD9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:136369886C>T
(GRCh38)9:136365186C>T
(Homo sapiens)Allele/Variant
Source: rs770178187
Genes: CARD9 (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)9:136365186C>T
(GRCh38)9:136365206C>T
(Homo sapiens)Allele/Variant
Source: rs756953515
Genes: CARD9 (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)9:136365206C>T
(GRCh38)9:136364410A>G
(Homo sapiens)Allele/Variant
Source: rs1201296952
Genes: CARD9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:136364410A>G
(GRCh38)9:136372011G>A
(Homo sapiens)Allele/Variant
Source: rs775267971
Genes: CARD9 (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)9:136372011G>A
(GRCh38)9:136372044C>T
(Homo sapiens)Allele/Variant
Source: rs4077515
Genes: CARD9 (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)9:136372044C>T
(GRCh38)9:136372064C>T
(Homo sapiens)Allele/Variant
Source: rs1462985722
Genes: CARD9 (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)9:136372064C>T
(GRCh38)9:136369733C>A
(Homo sapiens)Allele/Variant
Source: NC_000009.12:g.136369733C>A
Genes: CARD9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:136369733C>A
(GRCh38)9:136370285C>T
(Homo sapiens)Allele/Variant
Source: rs924360777
Genes: CARD9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:136370285C>T
(GRCh38)9:136364502T>C
(Homo sapiens)Allele/Variant
Source: NC_000009.12:g.136364502T>C
Genes: CARD9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:136364502T>C
(GRCh38)9:136364540C>G
(Homo sapiens)Allele/Variant
Source: NC_000009.12:g.136364540C>G
Genes: CARD9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:136364540C>G
(GRCh38)9:136364304A>G
(Homo sapiens)Allele/Variant
Source: rs1405807688
Genes: CARD9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, stop_lost, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:136364304A>G
(GRCh38)9:136365151C>A
(Homo sapiens)Allele/Variant
Source: rs374115294
Genes: CARD9 (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)9:136365151C>A
(GRCh38)9:136365165C>T
(Homo sapiens)Allele/Variant
Source: rs199617524
Genes: CARD9 (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)9:136365165C>T
(GRCh38)9:136369730C>G
(Homo sapiens)Allele/Variant
Source: rs558323305
Genes: CARD9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:136369730C>G
(GRCh38)9:136369739C>T
(Homo sapiens)Allele/Variant
Source: rs763912665
Genes: CARD9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:136369739C>T
(GRCh38)9:136365142T>C
(Homo sapiens)Allele/Variant
Source: rs1588719771
Genes: CARD9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:136365142T>C
(GRCh38)9:136364520G>T
(Homo sapiens)Allele/Variant
Source: rs1339311526
Genes: CARD9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:136364520G>T
(GRCh38)9:136365128G>A
(Homo sapiens)Allele/Variant
Source: rs764189894
Genes: CARD9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:136365128G>A
(GRCh38)9:136365141A>G
(Homo sapiens)Allele/Variant
Source: rs150480370
Genes: CARD9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:136365141A>G
(GRCh38)9:136365168G>T
(Homo sapiens)Allele/Variant
Source: rs1588719803
Genes: CARD9 (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)9:136365168G>T
(GRCh38)9:136365170G>A
(Homo sapiens)Allele/Variant
Source: rs770567400
Genes: CARD9 (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)9:136365170G>A
(GRCh38)9:136365202C>G
(Homo sapiens)Allele/Variant
Source: rs144348041
Genes: CARD9 (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)9:136365202C>G
(GRCh38)9:136367196C>T
(Homo sapiens)Allele/Variant
Source: NC_000009.12:g.136367196C>T
Genes: CARD9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:136367196C>T
(GRCh38)9:136367198G>A
(Homo sapiens)Allele/Variant
Source: rs200873988
Genes: CARD9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:136367198G>A
(GRCh38)9:136371466G>A
(Homo sapiens)Allele/Variant
Source: rs760533705
Genes: CARD9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:136371466G>A
(GRCh38)9:136371881G>A
(Homo sapiens)Allele/Variant
Source: rs1446416155
Genes: CARD9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)9:136371881G>A
(GRCm39)2:26248483C>A
(Mus musculus)Allele/Variant
Source: rs219593700
Genes: Card9 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)2:26248483C>A
(GRCm39)2:26249902C>T
(Mus musculus)Allele/Variant
Source: rs236288973
Genes: Card9 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)2:26249902C>T
(GRCm39)2:26250250C>T
(Mus musculus)Allele/Variant
Source: rs245620342
Genes: Card9 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)2:26250250C>T
(GRCm39)2:26250549T>C
(Mus musculus)Allele/Variant
Source: rs263419826
Genes: Card9 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)2:26250549T>C
(GRCm39)2:26244092G>A
(Mus musculus)Allele/Variant
Source: rs27215920
Genes: Card9 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)2:26244092G>A
(GRCm39)2:26245759G>A
(Mus musculus)Allele/Variant
Source: rs247888416
Genes: Card9 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)2:26245759G>A
(GRCm39)2:26245802A>G
(Mus musculus)Allele/Variant
Source: rs238277346
Genes: Card9 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)2:26245802A>G
(GRCm39)2:26243121G>A
(Mus musculus)Allele/Variant
Source: rs263106450
Genes: Card9 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)2:26243121G>A
(GRCm39)2:26246448C>A
(Mus musculus)Allele/Variant
Source: rs231188544
Genes: Card9 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)2:26246448C>A
(GRCm39)2:26245221G>C
(Mus musculus)Allele/Variant
Source: rs27215918
Genes: Card9 (Mmu)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCm39)2:26245221G>C