Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: BMP4 (Hsa)
(GRCh38)14:53950654G>A
(Homo sapiens)Allele/Variant
Source: rs770008356
Genes: BMP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)14:53950654G>A
(GRCh38)14:53950809G>C
(Homo sapiens)Allele/Variant
Source: rs767216159
Genes: BMP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)14:53950809G>C
(GRCh38)14:53952104C>T
(Homo sapiens)Allele/Variant
Source: rs777606324
Genes: BMP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)14:53952104C>T
(GRCh38)14:53952160C>T
(Homo sapiens)Allele/Variant
Source: NC_000014.9:g.53952160C>T
Genes: BMP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)14:53952160C>T
(GRCh38)14:53951935T>C
(Homo sapiens)Allele/Variant
Source: rs886050541
Genes: BMP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)14:53951935T>C
(GRCh38)14:53951943C>T
(Homo sapiens)Allele/Variant
Source: NC_000014.9:g.53951943C>T
Genes: BMP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)14:53951943C>T
(GRCh38)14:53951983C>A
(Homo sapiens)Allele/Variant
Source: rs747861439
Genes: BMP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)14:53951983C>A
(GRCh38)14:53952180G>C
(Homo sapiens)Allele/Variant
Source: rs1236268255
Genes: BMP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)14:53952180G>C
(GRCh38)14:53949883C>T
(Homo sapiens)Allele/Variant
Source: rs74495140
Genes: BMP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)14:53949883C>T
(GRCh38)14:53950227T>C
(Homo sapiens)Allele/Variant
Source: rs1191198347
Genes: BMP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)14:53950227T>C
(GRCh38)14:53950088T>C
(Homo sapiens)Allele/Variant
Source: rs781343227
Genes: BMP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)14:53950088T>C
(GRCh38)14:53950778A>G
(Homo sapiens)Allele/Variant
Source: rs749431429
Genes: BMP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)14:53950778A>G
(GRCh38)14:53950798G>A
(Homo sapiens)Allele/Variant
Source: rs935421961
Genes: BMP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)14:53950798G>A
(GRCh38)14:53951866G>A
(Homo sapiens)Allele/Variant
Source: rs757681410
Genes: BMP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)14:53951866G>A
(GRCh38)14:53950666C>T
(Homo sapiens)Allele/Variant
Source: rs773506129
Genes: BMP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)14:53950666C>T
(GRCh38)14:53950763C>T
(Homo sapiens)Allele/Variant
Source: rs372637689
Genes: BMP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)14:53950763C>T
(GRCh38)14:53952172C>G
(Homo sapiens)Allele/Variant
Source: rs758335370
Genes: BMP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)14:53952172C>G
(GRCh38)14:53952219T>A
(Homo sapiens)Allele/Variant
Source: rs760019960
Genes: BMP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)14:53952219T>A
(GRCh38)14:53950446G>A
(Homo sapiens)Allele/Variant
Source: rs373162816
Genes: BMP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)14:53950446G>A
(GRCh38)14:53950141C>T
(Homo sapiens)Allele/Variant
Source: NC_000014.9:g.53950141C>T
Genes: BMP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)14:53950141C>T
(GRCh38)14:53956572C>T
(Homo sapiens)Allele/Variant
Source: rs540859284
Genes: BMP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)14:53956572C>T
(GRCh38)14:53956668G>C
(Homo sapiens)Allele/Variant
Source: rs1023300708
Genes: BMP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)14:53956668G>C
(GRCh38)14:53950525C>T
(Homo sapiens)Allele/Variant
Source: rs149883007
Genes: BMP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)14:53950525C>T
(GRCh38)14:53952115G>A
(Homo sapiens)Allele/Variant
Source: rs371023244
Genes: BMP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)14:53952115G>A
(GRCh38)14:53952130C>G
(Homo sapiens)Allele/Variant
Source: rs375563326
Genes: BMP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)14:53952130C>G
(GRCh38)14:53953365C>A
(Homo sapiens)Allele/Variant
Source: NC_000014.9:g.53953365C>A
Genes: BMP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)14:53953365C>A
(GRCh38)14:53951878G>A
(Homo sapiens)Allele/Variant
Source: rs143687498
Genes: BMP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)14:53951878G>A
(GRCh38)14:53951897C>T
(Homo sapiens)Allele/Variant
Source: rs773235106
Genes: BMP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)14:53951897C>T
(GRCh38)14:53950171G>A
(Homo sapiens)Allele/Variant
Source: NC_000014.9:g.53950171G>A
Genes: BMP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)14:53950171G>A
(GRCh38)14:53950402C>T
(Homo sapiens)Allele/Variant
Source: rs550226363
Genes: BMP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)14:53950402C>T
(GRCh38)14:53950396C>T
(Homo sapiens)Allele/Variant
Source: rs370847935
Genes: BMP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)14:53950396C>T
(GRCh38)14:53950400G>A
(Homo sapiens)Allele/Variant
Source: rs1435675398
Genes: BMP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)14:53950400G>A
(GRCh38)14:53950441A>G
(Homo sapiens)Allele/Variant
Source: rs2140234580
Genes: BMP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)14:53950441A>G
(GRCh38)14:53950582C>T
(Homo sapiens)Allele/Variant
Source: rs538330477
Genes: BMP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)14:53950582C>T
(GRCh38)14:53952043T>C
(Homo sapiens)Allele/Variant
Source: NC_000014.9:g.53952043T>C
Genes: BMP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)14:53952043T>C
(GRCh38)14:53951930T>C
(Homo sapiens)Allele/Variant
Source: rs1376487986
Genes: BMP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)14:53951930T>C
(GRCh38)14:53952008T>C
(Homo sapiens)Allele/Variant
Source: rs771047931
Genes: BMP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)14:53952008T>C
(GRCh38)14:53950865T>A
(Homo sapiens)Allele/Variant
Source: rs199935719
Genes: BMP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)14:53950865T>A
(GRCh38)14:53951834A>G
(Homo sapiens)Allele/Variant
Source: rs1466355881
Genes: BMP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)14:53951834A>G
(GRCh38)14:53950635A>G
(Homo sapiens)Allele/Variant
Source: rs770637496
Genes: BMP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)14:53950635A>G
(GRCh38)14:53949997G>C
(Homo sapiens)Allele/Variant
Source: rs886050540
Genes: BMP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)14:53949997G>C
(GRCh38)14:53952362C>G
(Homo sapiens)Allele/Variant
Source: rs79762003
Genes: BMP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)14:53952362C>G
(GRCh38)14:53952392G>C
(Homo sapiens)Allele/Variant
Source: rs10130587
Genes: BMP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)14:53952392G>C
(GRCh38)14:53956782G>C
(Homo sapiens)Allele/Variant
Source: NC_000014.9:g.53956782G>C
Genes: BMP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)14:53956782G>C
(GRCh38)14:53956563A>G
(Homo sapiens)Allele/Variant
Source: rs73267467
Genes: BMP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)14:53956563A>G
(GRCh38)14:53956752C>G
(Homo sapiens)Allele/Variant
Source: rs988140396
Genes: BMP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)14:53956752C>G
(GRCh38)14:53956759C>T
(Homo sapiens)Allele/Variant
Source: rs778139957
Genes: BMP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)14:53956759C>T
(GRCh38)14:53950912G>A
(Homo sapiens)Allele/Variant
Source: rs34984774
Genes: BMP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)14:53950912G>A
(GRCh38)14:53950222G>A
(Homo sapiens)Allele/Variant
Source: rs121912766
Genes: BMP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)14:53950222G>A
(GRCh38)14:53950331G>A
(Homo sapiens)Allele/Variant
Source: rs770777693
Genes: BMP4 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)14:53950331G>A