Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Species: Homo sapiens
(GRCh38)3:57757801G>A
(Homo sapiens)Allele/Variant
Source: rs781119976
Genes: SLMAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)3:57757801G>A
(GRCh38)3:57831464C>G
(Homo sapiens)Allele/Variant
Source: rs1295613390
Genes: SLMAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:57831464C>G
(GRCh38)3:57757693G>T
(Homo sapiens)Allele/Variant
Source: rs760264345
Genes: SLMAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)3:57757693G>T
(GRCh38)3:57841360G>T
(Homo sapiens)Allele/Variant
Source: rs145924069
Genes: SLMAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)3:57841360G>T
(GRCh38)3:57841364C>T
(Homo sapiens)Allele/Variant
Source: rs748820617
Genes: SLMAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:57841364C>T
(GRCh38)3:57841538A>G
(Homo sapiens)Allele/Variant
Source: rs116002844
Genes: SLMAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:57841538A>G
(GRCh38)3:57847180T>A
(Homo sapiens)Allele/Variant
Source: rs536292946
Genes: SLMAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:57847180T>A
(GRCh38)3:57847181A>T
(Homo sapiens)Allele/Variant
Source: rs2153574252
Genes: SLMAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:57847181A>T
(GRCh38)3:57847211C>A
(Homo sapiens)Allele/Variant
Source: rs1159969169
Genes: SLMAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:57847211C>A
(GRCh38)3:57909163C>T
(Homo sapiens)Allele/Variant
Source: rs1009843149
Genes: SLMAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:57909163C>T
(GRCh38)3:57860820G>C
(Homo sapiens)Allele/Variant
Source: rs1211281068
Genes: SLMAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:57860820G>C
(GRCh38)3:57860837G>A
(Homo sapiens)Allele/Variant
Source: rs146606397
Genes: SLMAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:57860837G>A
(GRCh38)3:57862048G>A
(Homo sapiens)Allele/Variant
Source: rs754387957
Genes: SLMAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:57862048G>A
(GRCh38)3:57862057G>A
(Homo sapiens)Allele/Variant
Source: rs1424987573
Genes: SLMAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:57862057G>A
(GRCh38)3:57864644G>A
(Homo sapiens)Allele/Variant
Source: rs149548827
Genes: SLMAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:57864644G>A
(GRCh38)3:57871616G>A
(Homo sapiens)Allele/Variant
Source: rs775405372
Genes: SLMAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:57871616G>A
(GRCh38)3:57890077T>C
(Homo sapiens)Allele/Variant
Source: rs547267872
Genes: SLMAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:57890077T>C
(GRCh38)3:57896893G>T
(Homo sapiens)Allele/Variant
Source: NC_000003.12:g.57896893G>T
Genes: SLMAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:57896893G>T
(GRCh38)3:57907933G>A
(Homo sapiens)Allele/Variant
Source: NC_000003.12:g.57907933G>A
Genes: SLMAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:57907933G>A
(GRCh38)3:57907954C>G
(Homo sapiens)Allele/Variant
Source: rs775234969
Genes: SLMAP (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)3:57907954C>G
(GRCh38)3:57871687T>C
(Homo sapiens)Allele/Variant
Source: rs375841302
Genes: SLMAP (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)3:57871687T>C
(GRCh38)3:57896936C>T
(Homo sapiens)Allele/Variant
Source: rs539985706
Genes: SLMAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:57896936C>T
(GRCh38)3:57907962A>C
(Homo sapiens)Allele/Variant
Source: rs2096607956
Genes: SLMAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:57907962A>C
(GRCh38)3:57912479G>A
(Homo sapiens)Allele/Variant
Source: rs753780730
Genes: SLMAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, stop_retained_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:57912479G>A
(GRCh38)3:57912524C>T
(Homo sapiens)Allele/Variant
Source: rs1379169914
Genes: SLMAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:57912524C>T
(GRCh38)3:57927370G>A
(Homo sapiens)Allele/Variant
Source: rs557921655
Genes: SLMAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)3:57927370G>A
(GRCh38)3:57927406G>A
(Homo sapiens)Allele/Variant
Source: rs149054976
Genes: SLMAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)3:57927406G>A
(GRCh38)3:57757802C>G
(Homo sapiens)Allele/Variant
Source: NC_000003.12:g.57757802C>G
Genes: SLMAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:57757802C>G
(GRCh38)3:57849762T>C
(Homo sapiens)Allele/Variant
Source: NC_000003.12:g.57849762T>C
Genes: SLMAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)3:57849762T>C
(GRCh38)3:57849777G>C
(Homo sapiens)Allele/Variant
Source: rs770086716
Genes: SLMAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:57849777G>C
(GRCh38)3:57857780T>C
(Homo sapiens)Allele/Variant
Source: rs2094864988
Genes: SLMAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)3:57857780T>C
(GRCh38)3:57841389C>T
(Homo sapiens)Allele/Variant
Source: rs372203871
Genes: SLMAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:57841389C>T
(GRCh38)3:57847250T>A
(Homo sapiens)Allele/Variant
Source: rs1041435648
Genes: SLMAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:57847250T>A
(GRCh38)3:57860798C>G
(Homo sapiens)Allele/Variant
Source: rs765000724
Genes: SLMAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:57860798C>G
(GRCh38)3:57861981C>T
(Homo sapiens)Allele/Variant
Source: rs770395051
Genes: SLMAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)3:57861981C>T
(GRCh38)3:57862101T>A
(Homo sapiens)Allele/Variant
Source: rs368708547
Genes: SLMAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:57862101T>A
(GRCh38)3:57871659G>A
(Homo sapiens)Allele/Variant
Source: rs1203771969
Genes: SLMAP (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)3:57871659G>A
(GRCh38)3:57871668A>G
(Homo sapiens)Allele/Variant
Source: rs746146243
Genes: SLMAP (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)3:57871668A>G
(GRCh38)3:57890054C>T
(Homo sapiens)Allele/Variant
Source: rs139832644
Genes: SLMAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:57890054C>T
(GRCh38)3:57864690C>G
(Homo sapiens)Allele/Variant
Source: rs766605023
Genes: SLMAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:57864690C>G
(GRCh38)3:57916890A>G
(Homo sapiens)Allele/Variant
Source: rs752677684
Genes: SLMAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:57916890A>G
(GRCh38)3:57861998A>G
(Homo sapiens)Allele/Variant
Source: rs1352585607
Genes: SLMAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:57861998A>G
(GRCh38)3:57862093A>G
(Homo sapiens)Allele/Variant
Source: rs769226967
Genes: SLMAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:57862093A>G
(GRCh38)3:57890022C>T
(Homo sapiens)Allele/Variant
Source: rs777178496
Genes: SLMAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:57890022C>T
(GRCh38)3:57864647C>T
(Homo sapiens)Allele/Variant
Source: rs1470689481
Genes: SLMAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:57864647C>T
(GRCh38)3:57912597C>T
(Homo sapiens)Allele/Variant
Source: rs1420792918
Genes: SLMAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:57912597C>T
(GRCh38)3:57912369A>G
(Homo sapiens)Allele/Variant
Source: rs2096721496
Genes: SLMAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:57912369A>G
(GRCh38)3:57896585A>C
(Homo sapiens)Allele/Variant
Source: NC_000003.12:g.57896585A>C
Genes: SLMAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:57896585A>C
(GRCh38)3:57896588A>G
(Homo sapiens)Allele/Variant
Source: rs773600560
Genes: SLMAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant, non_coding_transcript_exon_variant
Diseases: Not Available
Variant Name: (GRCh38)3:57896588A>G
(GRCh38)3:57912702G>A
(Homo sapiens)Allele/Variant
Source: rs869025527
Genes: SLMAP (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, splice_donor_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)3:57912702G>A