Version: 8.0.0Date: Tue Jan 28 2025
Allele/Variant Genes: MSTN (Hsa)
(GRCh38)2:190057285C>T
(Homo sapiens)Allele/Variant
Source: NC_000002.12:g.190057285C>T
Genes: C2orf88 (Hsa), MSTN (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:190057285C>T
(GRCh38)2:190060054T>C
(Homo sapiens)Allele/Variant
Source: rs185201680
Genes: C2orf88 (Hsa), MSTN (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:190060054T>C
(GRCh38)2:190060079G>C
(Homo sapiens)Allele/Variant
Source: rs770535740
Genes: C2orf88 (Hsa), MSTN (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:190060079G>C
(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)2:190057766G>A
(Homo sapiens)Allele/Variant
Source: rs138328192
Genes: C2orf88 (Hsa), MSTN (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:190057766G>A
(GRCh38)2:190060088A>G
(Homo sapiens)Allele/Variant
Source: rs776358005
Genes: C2orf88 (Hsa), MSTN (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:190060088A>G
(GRCh38)2:190060351T>C
(Homo sapiens)Allele/Variant
Source: rs1805086
Genes: C2orf88 (Hsa), MSTN (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:190060351T>C
(GRCh38)2:190060423A>C
(Homo sapiens)Allele/Variant
Source: rs142195885
Genes: C2orf88 (Hsa), MSTN (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:190060423A>C
(GRCh38)2:190062291G>A
(Homo sapiens)Allele/Variant
Source: rs34191156
Genes: C2orf88 (Hsa), MSTN (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:190062291G>A
(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)2:190062433G>A
(Homo sapiens)Allele/Variant
Source: NC_000002.12:g.190062433G>A
Genes: C2orf88 (Hsa), MSTN (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:190062433G>A
(GRCh38)2:190057301C>T
(Homo sapiens)Allele/Variant
Source: rs375423318
Genes: C2orf88 (Hsa), MSTN (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:190057301C>T
(GRCh38)2:190057391G>C
(Homo sapiens)Allele/Variant
Source: rs757027065
Genes: C2orf88 (Hsa), MSTN (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:190057391G>C
(GRCh38)2:190057590T>G
(Homo sapiens)Allele/Variant
Source: rs1390302339
Genes: C2orf88 (Hsa), MSTN (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:190057590T>G
(GRCh38)2:190062499A>G
(Homo sapiens)Allele/Variant
Source: rs1685625618
Genes: C2orf88 (Hsa), MSTN (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:190062499A>G
(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)2:190057274C>T
(Homo sapiens)Allele/Variant
Source: rs772177439
Genes: C2orf88 (Hsa), MSTN (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:190057274C>T
(GRCh38)2:190060175A>C
(Homo sapiens)Allele/Variant
Source: NC_000002.12:g.190060175A>C
Genes: C2orf88 (Hsa), MSTN (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:190060175A>C
(GRCh38)2:190062417G>A
(Homo sapiens)Allele/Variant
Source: rs35321585
Genes: C2orf88 (Hsa), MSTN (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:190062417G>A
(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)2:190060280T>G
(Homo sapiens)Allele/Variant
Source: rs191779769
Genes: C2orf88 (Hsa), MSTN (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:190060280T>G
(GRCh38)2:190062695C>T
(Homo sapiens)Allele/Variant
Source: rs1685633250
Genes: C2orf88 (Hsa), MSTN (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: 5_prime_UTR_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:190062695C>T
(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)2:190060108C>T
(Homo sapiens)Allele/Variant
Source: NC_000002.12:g.190060108C>T
Genes: C2orf88 (Hsa), MSTN (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:190060108C>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)2:190057324A>G
(Homo sapiens)Allele/Variant
Source: rs761053215
Genes: C2orf88 (Hsa), MSTN (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:190057324A>G
(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)2:190057489G>A
(Homo sapiens)Allele/Variant
Source: rs773422984
Genes: C2orf88 (Hsa), MSTN (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:190057489G>A
(GRCh38)2:190057641G>A
(Homo sapiens)Allele/Variant
Source: rs374256136
Genes: C2orf88 (Hsa), MSTN (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: splice_region_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:190057641G>A
(GRCh38)2:190060296C>T
(Homo sapiens)Allele/Variant
Source: rs1685556708
Genes: C2orf88 (Hsa), MSTN (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:190060296C>T
(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)2:190057505C>G
(Homo sapiens)Allele/Variant
Source: rs1266075720
Genes: C2orf88 (Hsa), MSTN (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:190057505C>G
(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)2:190057217C>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)2:190057588C>T
(Homo sapiens)Allele/Variant
Source: rs35791082
Genes: C2orf88 (Hsa), MSTN (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:190057588C>T
(GRCh38)2:190060343G>T
(Homo sapiens)Allele/Variant
Source: rs35493945
Genes: C2orf88 (Hsa), MSTN (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:190060343G>T
(GRCh38)2:190060356T>C
(Homo sapiens)Allele/Variant
Source: rs758969290
Genes: C2orf88 (Hsa), MSTN (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: non_coding_transcript_variant, synonymous_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:190060356T>C
(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)2:190060293T>G
(Homo sapiens)Allele/Variant
Source: rs200908904
Genes: C2orf88 (Hsa), MSTN (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:190060293T>G
(GRCh38)2:190060319C>T
(Homo sapiens)Allele/Variant
Source: rs35781413
Genes: C2orf88 (Hsa), MSTN (Hsa)
Synonyms: Not Available
Variant Type: SNP
Molecular Consequence: missense_variant, non_coding_transcript_variant, intron_variant
Diseases: Not Available
Variant Name: (GRCh38)2:190060319C>T
(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