Version: 8.0.0
Date: Tue Jan 28 2025
679 results for card9
Allele/Variant

Card9em1Gpt

(Mus musculus)
Allele/Variant
Source: MGI:7296244
Genes: Card9 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Card9 (Mmu)
Genes: Card9 (Mmu)
Symbol: Card9em1Gpt

Card9tm1Tks

(Mus musculus)
Allele/Variant
Source: MGI:3715521
Genes: Card9 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Card9 (Mmu)
Genes: Card9 (Mmu)
Symbol: Card9tm1Tks

Card9tm1Xlin

(Mus musculus)
Allele/Variant
Source: MGI:3698412
Genes: Card9 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Card9 (Mmu)
Genes: Card9 (Mmu)
Symbol: Card9tm1Xlin

Card9tm1a(EUCOMM)Hmgu

(Mus musculus)
Allele/Variant
Source: MGI:4841496
Genes: Card9 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Card9 (Mmu)
Genes: Card9 (Mmu)
Symbol: Card9tm1a(EUCOMM)Hmgu

Card9tm1c(EUCOMM)Hmgu

(Mus musculus)
Allele/Variant
Source: MGI:5806258
Genes: Card9 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Card9 (Mmu)
Genes: Card9 (Mmu)
Symbol: Card9tm1c(EUCOMM)Hmgu

Card9em1Yiw

(Mus musculus)
Allele/Variant
Source: MGI:7385038
Genes: Card9 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Card9 (Mmu)
Genes: Card9 (Mmu)
Symbol: Card9em1Yiw

Card9tm1Jrld

(Mus musculus)
Allele/Variant
Source: MGI:3663486
Genes: Card9 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Card9 (Mmu)
Genes: Card9 (Mmu)
Symbol: Card9tm1Jrld

Card9em1Cya

(Mus musculus)
Allele/Variant
Source: MGI:7582714
Genes: Card9 (Mmu)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Symbol: Card9 (Mmu)
Genes: Card9 (Mmu)
Symbol: Card9em1Cya

xt31

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-240213-3
Genes: card9 (Dre)
Synonyms: Not Available
Variant Type: unreported
Molecular Consequence: Not Available
Diseases: Not Available
Variant Name: Not Available
Genes: card9 (Dre)

sa11441

(Danio rerio)
Allele/Variant
Source: ZFIN:ZDB-ALT-130411-1276
Genes: card9 (Dre)
Synonyms: Not Available
Variant Type: point_mutation
Molecular Consequence: stop_gained, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: Not Available
Genes: card9 (Dre)

(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)9:136367643G>A

(Homo sapiens)
Allele/Variant
Source: rs559114246
Genes: CARD9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:136367643G>A

(GRCh38)9:136367647G>A

(Homo sapiens)
Allele/Variant
Source: rs767880614
Genes: CARD9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)9:136367647G>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)9:136367801C>T

(Homo sapiens)
Allele/Variant
Source: rs141270365
Genes: CARD9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)9:136367801C>T

(GRCh38)9:136367805C>T

(Homo sapiens)
Allele/Variant
Source: rs566481759
Genes: CARD9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:136367805C>T

(GRCh38)9:136370375C>T

(Homo sapiens)
Allele/Variant
Source: rs115057256
Genes: CARD9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:136370375C>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)9:136370543C>T

(Homo sapiens)
Allele/Variant
Source: rs202143480
Genes: CARD9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:136370543C>T

(GRCh38)9:136370377C>A

(Homo sapiens)
Allele/Variant
Source: rs964199466
Genes: CARD9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)9:136370377C>A

(GRCh38)9:136370528G>A

(Homo sapiens)
Allele/Variant
Source: rs143884319
Genes: CARD9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:136370528G>A

(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)9:136370374G>A

(Homo sapiens)
Allele/Variant
Source: rs1204500437
Genes: CARD9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:136370374G>A

(GRCh38)9:136370387G>A

(Homo sapiens)
Allele/Variant
Source: rs745509934
Genes: CARD9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:136370387G>A

(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)9:136370351G>C

(Homo sapiens)
Allele/Variant
Source: rs757648134
Genes: CARD9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:136370351G>C

(GRCh38)9:136370362G>A

(Homo sapiens)
Allele/Variant
Source: rs121918338
Genes: CARD9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)9:136370362G>A

(GRCh38)9:136370996G>A

(Homo sapiens)
Allele/Variant
Source: rs1342330215
Genes: CARD9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)9:136370996G>A

(GRCh38)9:136369858C>T

(Homo sapiens)
Allele/Variant
Source: rs374601657
Genes: CARD9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:136369858C>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)9:136369827T>A

(Homo sapiens)
Allele/Variant
Source: NC_000009.12:g.136369827T>A
Genes: CARD9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)9:136369827T>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)9:136367250T>C

(Homo sapiens)
Allele/Variant
Source: rs760553828
Genes: CARD9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)9:136367250T>C

(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)9:136367749C>T

(Homo sapiens)
Allele/Variant
Source: rs752913001
Genes: CARD9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)9:136367749C>T

(GRCh38)9:136364010A>G

(Homo sapiens)
Allele/Variant
Source: rs1135314
Genes: CARD9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)9:136364010A>G

(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)9:136367649C>T

(Homo sapiens)
Allele/Variant
Source: rs1291912498
Genes: CARD9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)9:136367649C>T

(GRCh38)9:136367669G>A

(Homo sapiens)
Allele/Variant
Source: rs752685448
Genes: CARD9 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)9:136367669G>A

(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