Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: MMP2 (Hsa)
(GRCh38)16:55485437G>A
(Homo sapiens)Allele/Variant
Source: rs201653184
Genes: MMP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:55485437G>A
(GRCh38)16:55488565C>T
(Homo sapiens)Allele/Variant
Source: rs760006274
Genes: MMP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)16:55488565C>T
(GRCh38)16:55491958T>G
(Homo sapiens)Allele/Variant
Source: rs746668134
Genes: MMP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_donor_variant
Diseases: Not Available
Variant Name: (GRCh38)16:55491958T>G
(GRCh38)16:55485755G>C
(Homo sapiens)Allele/Variant
Source: rs895002709
Genes: MMP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:55485755G>C
(GRCh38)16:55505535C>T
(Homo sapiens)Allele/Variant
Source: rs112159982
Genes: MMP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)16:55505535C>T
(GRCh38)16:55498313C>T
(Homo sapiens)Allele/Variant
Source: rs143247099
Genes: MMP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:55498313C>T
(GRCh38)16:55506454T>A
(Homo sapiens)Allele/Variant
Source: rs1447267044
Genes: MMP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)16:55506454T>A
(GRCh38)16:55464509A>G
(Homo sapiens)Allele/Variant
Source: rs207475962
Genes: MMP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:55464509A>G
(GRCh38)16:55479279C>G
(Homo sapiens)Allele/Variant
Source: rs886052124
Genes: MMP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:55479279C>G
(GRCh38)16:55479419G>C
(Homo sapiens)Allele/Variant
Source: rs2287073
Genes: MMP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:55479419G>C
(GRCh38)16:55481709T>C
(Homo sapiens)Allele/Variant
Source: rs1030869
Genes: MMP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:55481709T>C
(GRCh38)16:55484092G>A
(Homo sapiens)Allele/Variant
Source: rs144334568
Genes: MMP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:55484092G>A
(GRCh38)16:55485734C>A
(Homo sapiens)Allele/Variant
Source: rs2142349089
Genes: MMP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: stop_gained
Diseases: Not Available
Variant Name: (GRCh38)16:55485734C>A
(GRCh38)16:55493292C>T
(Homo sapiens)Allele/Variant
Source: rs771097911
Genes: MMP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:55493292C>T
(GRCh38)16:55496974G>A
(Homo sapiens)Allele/Variant
Source: rs2142365800
Genes: MMP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)16:55496974G>A
(GRCh38)16:55496994C>T
(Homo sapiens)Allele/Variant
Source: rs1443486268
Genes: MMP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:55496994C>T
(GRCh38)16:55493166C>T
(Homo sapiens)Allele/Variant
Source: NC_000016.10:g.55493166C>T
Genes: MMP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:55493166C>T
(GRCh38)16:55493181G>T
(Homo sapiens)Allele/Variant
Source: rs2142361148
Genes: MMP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:55493181G>T
(GRCh38)16:55505895C>G
(Homo sapiens)Allele/Variant
Source: rs562314074
Genes: MMP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:55505895C>G
(GRCh38)16:55506490C>T
(Homo sapiens)Allele/Variant
Source: rs776889997
Genes: MMP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)16:55506490C>T
(GRCh38)16:55485324C>T
(Homo sapiens)Allele/Variant
Source: rs753761872
Genes: MMP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)16:55485324C>T
(GRCh38)16:55493274A>T
(Homo sapiens)Allele/Variant
Source: rs141440582
Genes: MMP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:55493274A>T
(GRCh38)16:55496860T>G
(Homo sapiens)Allele/Variant
Source: rs243838
Genes: MMP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:55496860T>G
(GRCh38)16:55492001G>C
(Homo sapiens)Allele/Variant
Source: rs243846
Genes: MMP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:55492001G>C
(GRCh38)16:55493216T>G
(Homo sapiens)Allele/Variant
Source: rs2142361266
Genes: MMP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)16:55493216T>G
(GRCh38)16:55505625A>G
(Homo sapiens)Allele/Variant
Source: rs111371964
Genes: MMP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:55505625A>G
(GRCh38)16:55506314C>T
(Homo sapiens)Allele/Variant
Source: rs140455191
Genes: MMP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)16:55506314C>T
(GRCh38)16:55506372C>T
(Homo sapiens)Allele/Variant
Source: rs886052130
Genes: MMP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)16:55506372C>T
(GRCh38)16:55479480A>T
(Homo sapiens)Allele/Variant
Source: rs1451803374
Genes: MMP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: start_lost, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:55479480A>T
(GRCh38)16:55479473C>A
(Homo sapiens)Allele/Variant
Source: rs765195089
Genes: MMP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:55479473C>A
(GRCh38)16:55485354C>T
(Homo sapiens)Allele/Variant
Source: rs199814532
Genes: MMP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)16:55485354C>T
(GRCh38)16:55488566G>A
(Homo sapiens)Allele/Variant
Source: rs753867656
Genes: MMP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:55488566G>A
(GRCh38)16:55488618A>T
(Homo sapiens)Allele/Variant
Source: rs1567376093
Genes: MMP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:55488618A>T
(GRCh38)16:55505400C>T
(Homo sapiens)Allele/Variant
Source: rs112831239
Genes: MMP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_exon_variant, synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)16:55505400C>T
(GRCh38)16:55505601T>C
(Homo sapiens)Allele/Variant
Source: rs17860019
Genes: MMP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, 3_prime_UTR_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:55505601T>C
(GRCh38)16:55498301G>T
(Homo sapiens)Allele/Variant
Source: rs2142367615
Genes: MMP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:55498301G>T
(GRCh38)16:55498338C>G
(Homo sapiens)Allele/Variant
Source: rs747523622
Genes: MMP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant
Diseases: Not Available
Variant Name: (GRCh38)16:55498338C>G
(GRCh38)16:55498390G>A
(Homo sapiens)Allele/Variant
Source: rs752981351
Genes: MMP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant
Diseases: Not Available
Variant Name: (GRCh38)16:55498390G>A
(GRCh38)16:55479516C>T
(Homo sapiens)Allele/Variant
Source: rs780763772
Genes: MMP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:55479516C>T
(GRCh38)16:55479592C>T
(Homo sapiens)Allele/Variant
Source: rs1192301679
Genes: MMP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:55479592C>T
(GRCh38)16:55506646A>G
(Homo sapiens)Allele/Variant
Source: rs758075499
Genes: MMP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 3_prime_UTR_variant
Diseases: Not Available
Variant Name: (GRCh38)16:55506646A>G
(GRCh38)16:55479495G>A
(Homo sapiens)Allele/Variant
Source: rs1287389935
Genes: MMP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:55479495G>A
(GRCh38)16:55479517C>G
(Homo sapiens)Allele/Variant
Source: rs1183157128
Genes: MMP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:55479517C>G
(GRCh38)16:55479594G>A
(Homo sapiens)Allele/Variant
Source: rs1392610505
Genes: MMP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:55479594G>A
(GRCh38)16:55479575G>T
(Homo sapiens)Allele/Variant
Source: rs146220690
Genes: MMP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:55479575G>T
(GRCh38)16:55479603G>T
(Homo sapiens)Allele/Variant
Source: rs1016960822
Genes: MMP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:55479603G>T
(GRCh38)16:55477894C>T
(Homo sapiens)Allele/Variant
Source: rs243865
Genes: MMP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:55477894C>T
(GRCh38)16:55479032G>T
(Homo sapiens)Allele/Variant
Source: rs17859829
Genes: MMP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:55479032G>T
(GRCh38)16:55482855G>A
(Homo sapiens)Allele/Variant
Source: rs1030868
Genes: MMP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:55482855G>A
(GRCh38)16:55482889G>C
(Homo sapiens)Allele/Variant
Source: rs774213983
Genes: MMP2 (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: intron_variant
Diseases: Not Available
Variant Name: (GRCh38)16:55482889G>C