Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: MSTN (Hsa) Molecular Consequence: 3 prime UTR variant
(GRCh38)2:190056684C>T
(Homo sapiens)Allele/Variant
Source: rs114597606
Genes: C2orf88 (Hsa), MSTN (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)2:190056684C>T
(GRCh38)2:190056185C>A
(Homo sapiens)Allele/Variant
Source: rs886055370
Genes: C2orf88 (Hsa), MSTN (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)2:190056185C>A
(GRCh38)2:190057217C>A
(Homo sapiens)Allele/Variant
Source: rs762191502
Genes: C2orf88 (Hsa), MSTN (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)2:190057217C>A
(GRCh38)2:190056474C>T
(Homo sapiens)Allele/Variant
Source: rs776456900
Genes: C2orf88 (Hsa), MSTN (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)2:190056474C>T
(GRCh38)2:190057137T>C
(Homo sapiens)Allele/Variant
Source: rs886055372
Genes: C2orf88 (Hsa), MSTN (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)2:190057137T>C
(GRCh38)2:190055744G>C
(Homo sapiens)Allele/Variant
Source: rs12105165
Genes: C2orf88 (Hsa), MSTN (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)2:190055744G>C
(GRCh38)2:190055808A>G
(Homo sapiens)Allele/Variant
Source: rs144167726
Genes: C2orf88 (Hsa), MSTN (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)2:190055808A>G
(GRCh38)2:190056195T>C
(Homo sapiens)Allele/Variant
Source: rs1685421811
Genes: C2orf88 (Hsa), MSTN (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)2:190056195T>C
(GRCh38)2:190056516G>A
(Homo sapiens)Allele/Variant
Source: rs72909336
Genes: C2orf88 (Hsa), MSTN (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)2:190056516G>A
(GRCh38)2:190056563T>G
(Homo sapiens)Allele/Variant
Source: rs1042335329
Genes: C2orf88 (Hsa), MSTN (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)2:190056563T>G
(GRCh38)2:190056863T>G
(Homo sapiens)Allele/Variant
Source: rs16823986
Genes: C2orf88 (Hsa), MSTN (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)2:190056863T>G
(GRCh38)2:190056765C>T
(Homo sapiens)Allele/Variant
Source: rs16832285
Genes: C2orf88 (Hsa), MSTN (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)2:190056765C>T
(GRCh38)2:190056985G>C
(Homo sapiens)Allele/Variant
Source: rs150145410
Genes: C2orf88 (Hsa), MSTN (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)2:190056985G>C
(GRCh38)2:190057131A>G
(Homo sapiens)Allele/Variant
Source: rs923518162
Genes: C2orf88 (Hsa), MSTN (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)2:190057131A>G
(GRCh38)2:190057123C>T
(Homo sapiens)Allele/Variant
Source: rs60490864
Genes: C2orf88 (Hsa), MSTN (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)2:190057123C>T
(GRCh38)2:190056922G>T
(Homo sapiens)Allele/Variant
Source: rs1685447206
Genes: C2orf88 (Hsa), MSTN (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)2:190056922G>T
(GRCh38)2:190056968G>A
(Homo sapiens)Allele/Variant
Source: rs537956645
Genes: C2orf88 (Hsa), MSTN (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)2:190056968G>A
(GRCh38)2:190056055C>G
(Homo sapiens)Allele/Variant
Source: rs3187415
Genes: C2orf88 (Hsa), MSTN (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)2:190056055C>G
(GRCh38)2:190055896T>C
(Homo sapiens)Allele/Variant
Source: rs377503267
Genes: C2orf88 (Hsa), MSTN (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)2:190055896T>C
(GRCh38)2:190055926T>C
(Homo sapiens)Allele/Variant
Source: rs3791782
Genes: C2orf88 (Hsa), MSTN (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)2:190055926T>C
(GRCh38)2:190056335A>G
(Homo sapiens)Allele/Variant
Source: rs886055371
Genes: C2orf88 (Hsa), MSTN (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)2:190056335A>G
(GRCh38)2:190057218C>A
(Homo sapiens)Allele/Variant
Source: rs141652279
Genes: C2orf88 (Hsa), MSTN (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)2:190057218C>A
(GRCh38)2:190055942G>C
(Homo sapiens)Allele/Variant
Source: rs1253469843
Genes: C2orf88 (Hsa), MSTN (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)2:190055942G>C
(GRCh38)2:190056999T>C
(Homo sapiens)Allele/Variant
Source: rs578136956
Genes: C2orf88 (Hsa), MSTN (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)2:190056999T>C
(GRCh38)2:190055985G>A
(Homo sapiens)Allele/Variant
Source: rs1195446819
Genes: C2orf88 (Hsa), MSTN (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)2:190055985G>A
(GRCh38)2:190056561A>G
(Homo sapiens)Allele/Variant
Source: rs186458339
Genes: C2orf88 (Hsa), MSTN (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)2:190056561A>G