Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: FUCA1 (Hsa)
(GRCh38)1:23848684C>T
(Homo sapiens)Allele/Variant
Source: rs794727774
Genes: FUCA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: (GRCh38)1:23848684C>T
(GRCh38)1:23854412T>C
(Homo sapiens)Allele/Variant
Source: rs749790121
Genes: FUCA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:23854412T>C
(GRCh38)1:23865497C>T
(Homo sapiens)Allele/Variant
Source: rs148194937
Genes: FUCA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:23865497C>T
(GRCh38)1:23865498G>A
(Homo sapiens)Allele/Variant
Source: rs768069468
Genes: FUCA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:23865498G>A
(GRCh38)1:23865551G>A
(Homo sapiens)Allele/Variant
Source: rs587779398
Genes: FUCA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:23865551G>A
(GRCh38)1:23865577C>T
(Homo sapiens)Allele/Variant
Source: rs766878135
Genes: FUCA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:23865577C>T
(GRCh38)1:23867960C>T
(Homo sapiens)Allele/Variant
Source: rs61996281
Genes: FUCA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:23867960C>T
(GRCh38)1:23867971A>G
(Homo sapiens)Allele/Variant
Source: NC_000001.11:g.23867971A>G
Genes: FUCA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:23867971A>G
(GRCh38)1:23868027G>A
(Homo sapiens)Allele/Variant
Source: rs138378067
Genes: FUCA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:23868027G>A
(GRCh38)1:23845835T>C
(Homo sapiens)Allele/Variant
Source: NC_000001.11:g.23845835T>C
Genes: FUCA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:23845835T>C
(GRCh38)1:23845171A>T
(Homo sapiens)Allele/Variant
Source: rs886046321
Genes: FUCA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)1:23845171A>T
(GRCh38)1:23845445A>G
(Homo sapiens)Allele/Variant
Source: rs143441916
Genes: FUCA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)1:23845445A>G
(GRCh38)1:23845757G>A
(Homo sapiens)Allele/Variant
Source: rs147866670
Genes: FUCA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:23845757G>A
(GRCh38)1:23845790G>A
(Homo sapiens)Allele/Variant
Source: rs924511473
Genes: FUCA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:23845790G>A
(GRCh38)1:23846142T>C
(Homo sapiens)Allele/Variant
Source: rs548070711
Genes: FUCA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:23846142T>C
(GRCh38)1:23846151C>T
(Homo sapiens)Allele/Variant
Source: rs1570670906
Genes: FUCA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:23846151C>T
(GRCh38)1:23846178G>A
(Homo sapiens)Allele/Variant
Source: rs1324596939
Genes: FUCA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:23846178G>A
(GRCh38)1:23846190A>G
(Homo sapiens)Allele/Variant
Source: rs1438011380
Genes: FUCA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:23846190A>G
(GRCh38)1:23846392C>T
(Homo sapiens)Allele/Variant
Source: rs145900261
Genes: FUCA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:23846392C>T
(GRCh38)1:23848660T>A
(Homo sapiens)Allele/Variant
Source: rs1474078454
Genes: FUCA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:23848660T>A
(GRCh38)1:23845724T>A
(Homo sapiens)Allele/Variant
Source: rs2148436869
Genes: FUCA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:23845724T>A
(GRCh38)1:23845738T>C
(Homo sapiens)Allele/Variant
Source: rs774128532
Genes: FUCA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:23845738T>C
(GRCh38)1:23845756C>T
(Homo sapiens)Allele/Variant
Source: rs377360830
Genes: FUCA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:23845756C>T
(GRCh38)1:23845856C>T
(Homo sapiens)Allele/Variant
Source: NC_000001.11:g.23845856C>T
Genes: FUCA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_acceptor_variant
Diseases: Not Available
Variant Name: (GRCh38)1:23845856C>T
(GRCh38)1:23848733C>T
(Homo sapiens)Allele/Variant
Source: rs1393793214
Genes: FUCA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:23848733C>T
(GRCh38)1:23848792A>G
(Homo sapiens)Allele/Variant
Source: rs560947454
Genes: FUCA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:23848792A>G
(GRCh38)1:23846170A>C
(Homo sapiens)Allele/Variant
Source: NC_000001.11:g.23846170A>C
Genes: FUCA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: (GRCh38)1:23846170A>C
(GRCh38)1:23848661G>A
(Homo sapiens)Allele/Variant
Source: rs114490852
Genes: FUCA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:23848661G>A
(GRCh38)1:23854538C>A
(Homo sapiens)Allele/Variant
Source: NC_000001.11:g.23854538C>A
Genes: FUCA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:23854538C>A
(GRCh38)1:23859868C>T
(Homo sapiens)Allele/Variant
Source: rs1441298926
Genes: FUCA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: (GRCh38)1:23859868C>T
(GRCh38)1:23846105A>C
(Homo sapiens)Allele/Variant
Source: rs80358199
Genes: FUCA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:23846105A>C
(GRCh38)1:23848811C>T
(Homo sapiens)Allele/Variant
Source: rs1013512148
Genes: FUCA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:23848811C>T
(GRCh38)1:23867993C>G
(Homo sapiens)Allele/Variant
Source: rs773469453
Genes: FUCA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:23867993C>G
(GRCh38)1:23868257C>T
(Homo sapiens)Allele/Variant
Source: rs886046326
Genes: FUCA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:23868257C>T
(GRCh38)1:23846098G>A
(Homo sapiens)Allele/Variant
Source: rs1310643655
Genes: FUCA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:23846098G>A
(GRCh38)1:23848707C>T
(Homo sapiens)Allele/Variant
Source: rs374427540
Genes: FUCA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:23848707C>T
(GRCh38)1:23848716T>C
(Homo sapiens)Allele/Variant
Source: rs1639194544
Genes: FUCA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:23848716T>C
(GRCh38)1:23848732C>T
(Homo sapiens)Allele/Variant
Source: rs777813005
Genes: FUCA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:23848732C>T
(GRCh38)1:23865582A>G
(Homo sapiens)Allele/Variant
Source: rs150062050
Genes: FUCA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:23865582A>G
(GRCh38)1:23867942G>A
(Homo sapiens)Allele/Variant
Source: NC_000001.11:g.23867942G>A
Genes: FUCA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:23867942G>A
(GRCh38)1:23845842C>T
(Homo sapiens)Allele/Variant
Source: rs150422575
Genes: FUCA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:23845842C>T
(GRCh38)1:23854380C>T
(Homo sapiens)Allele/Variant
Source: rs779512930
Genes: FUCA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:23854380C>T
(GRCh38)1:23854386C>T
(Homo sapiens)Allele/Variant
Source: rs746590345
Genes: FUCA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)1:23854386C>T
(GRCh38)1:23868286T>C
(Homo sapiens)Allele/Variant
Source: rs558338123
Genes: FUCA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: start_lost
Diseases: Not Available
Variant Name: (GRCh38)1:23868286T>C
(GRCh38)1:23845373G>T
(Homo sapiens)Allele/Variant
Source: rs1023386054
Genes: FUCA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)1:23845373G>T
(GRCh38)1:23845781G>C
(Homo sapiens)Allele/Variant
Source: rs372223382
Genes: FUCA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:23845781G>C
(GRCh38)1:23848720G>A
(Homo sapiens)Allele/Variant
Source: rs1443768545
Genes: FUCA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:23848720G>A
(GRCh38)1:23848629C>T
(Homo sapiens)Allele/Variant
Source: rs1326350955
Genes: FUCA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:23848629C>T
(GRCh38)1:23854546T>C
(Homo sapiens)Allele/Variant
Source: NC_000001.11:g.23854546T>C
Genes: FUCA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)1:23854546T>C
(GRCh38)1:23854687C>T
(Homo sapiens)Allele/Variant
Source: rs12748109
Genes: FUCA1 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)1:23854687C>T