62232450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: non coding transcript exon variant
orthologous variants: 179755300-G-A

62232450-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: non coding transcript exon variant
orthologous variants: 179755300-G-T

62232534-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: non coding transcript exon variant
orthologous variants: 179755361-G-T

62232537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: non coding transcript exon variant
orthologous variants: 179755364-G-A

62232595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: non coding transcript exon variant
orthologous variants: 179755395-G-T

62232638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: non coding transcript exon variant
orthologous variants: 179755438-A-G

62232646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: non coding transcript exon variant
orthologous variants: 179755446-T-C

http://identifiers.org/hco/20/GRCh38#62232651-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#179755451-C-A

62232651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: non coding transcript exon variant
orthologous variants: 179755451-C-T

62232653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: non coding transcript exon variant
orthologous variants: 179755453-G-A

62232653-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: non coding transcript exon variant
orthologous variants: 179755453-G-T

http://identifiers.org/hco/20/GRCh38#62232708-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#179755498-C-A

62232717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: non coding transcript exon variant
orthologous variants: 179755507-C-T

62232778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: non coding transcript exon variant
orthologous variants: 179755574-T-C

http://identifiers.org/hco/20/GRCh38#62232855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#179755842-C-A

http://identifiers.org/hco/20/GRCh38#62233228-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#179756228-C-A

62233228-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: non coding transcript exon variant
orthologous variants: 179756228-C-G

http://identifiers.org/hco/20/GRCh38#62233232-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#179756232-C-A

62233238-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: non coding transcript exon variant
orthologous variants: 179756238-C-G

62233238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: non coding transcript exon variant
orthologous variants: 179756238-C-T

62233287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: non coding transcript exon variant
orthologous variants: 179756270-T-C

62233323-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: non coding transcript exon variant
orthologous variants: 179756293-T-A

62233336-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: non coding transcript exon variant
orthologous variants: 179756306-G-C

62233356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: non coding transcript exon variant
orthologous variants: 179756321-G-A

62233443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: non coding transcript exon variant
orthologous variants: 179756405-A-G

62233445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: non coding transcript exon variant
orthologous variants: 179756407-G-A

62233476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: non coding transcript exon variant
orthologous variants: 179756455-C-T

62233495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: non coding transcript exon variant
orthologous variants: 179756502-G-A

http://identifiers.org/hco/20/GRCh38#62233513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#179756520-C-A

62233555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: non coding transcript exon variant
orthologous variants: 179756560-G-A

http://identifiers.org/hco/20/GRCh38#62233658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#179756646-C-A

62233663-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: non coding transcript exon variant
orthologous variants: 179756651-G-C

62233664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: non coding transcript exon variant
orthologous variants: 179756652-G-A

62233664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: non coding transcript exon variant
orthologous variants: 179756652-G-T

62233676-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: non coding transcript exon variant
orthologous variants: 179756663-T-A

62233676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: non coding transcript exon variant
orthologous variants: 179756663-T-C

62233711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: non coding transcript exon variant
orthologous variants: 179756695-G-A

62233711-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: non coding transcript exon variant
orthologous variants: 179756695-G-C

62233711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: non coding transcript exon variant
orthologous variants: 179756695-G-T

http://identifiers.org/hco/20/GRCh38#62233963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#179757035-C-A

62234108-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179757105-C-G

62234108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179757105-C-T

62234713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 179757651-C-T

62235053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 179757971-G-A

62235053-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 179757971-G-T

62235096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 179758019-T-C

http://identifiers.org/hco/20/GRCh38#62235500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#179758386-C-A

62235500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 179758386-C-T

62235522-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 179758407-G-C

62235554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 179758445-G-T

62235629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 179758525-G-T

http://identifiers.org/hco/20/GRCh38#62235737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#179758752-C-A

62235737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 179758752-C-T

http://identifiers.org/hco/20/GRCh38#62235774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#179758784-C-A

62235820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 179758843-G-A

62235820-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 179758843-G-C

62235820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 179758843-G-T

62235932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 179758917-G-A

62235932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 179758917-G-T

http://identifiers.org/hco/20/GRCh38#62236124-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#179759054-A-C

62236124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 179759054-A-G

http://identifiers.org/hco/20/GRCh38#62236128-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#179759058-C-A

62236209-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 179759128-G-C

62236209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 179759128-G-T

62236249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 179759167-T-C

62236362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: intron variant
orthologous variants: 179759230-C-T

62236420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: intron variant
orthologous variants: 179759294-C-T

62236442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: intron variant
orthologous variants: 179759335-T-C

http://identifiers.org/hco/20/GRCh38#62236751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#179759620-C-A

62236944-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 179759831-A-T

62236987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 179759872-C-T

62237124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: intron variant
orthologous variants: 179759958-T-C

62237442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: intron_variant, undefined
orthologous variants: 179760243-G-A

62237601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: intron variant
orthologous variants: 179760350-C-T

62237658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: intron variant
orthologous variants: 179760384-C-T

http://identifiers.org/hco/20/GRCh38#62237903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#179760624-C-A

62237956-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: intron_variant, undefined
orthologous variants: 179760673-C-T

62238178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: intron_variant, undefined
orthologous variants: 179760843-C-T

62238324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: intron_variant, undefined
orthologous variants: 179760988-C-T

62238352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: intron_variant, undefined
orthologous variants: 179761016-A-G

62238374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: intron_variant, undefined
orthologous variants: 179761040-G-T

62238419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: intron_variant, undefined
orthologous variants: 179761084-G-A

62238419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: intron_variant, undefined
orthologous variants: 179761084-G-T

62238461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: intron_variant, undefined
orthologous variants: 179761125-A-G

62238478-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: intron variant
orthologous variants: 179761148-G-T

62238489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 179761159-G-T

62238535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 179761204-G-A

62238539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 179761207-T-C

http://identifiers.org/hco/20/GRCh38#62238616-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#179761276-C-A

62238616-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 179761276-C-T

http://identifiers.org/hco/20/GRCh38#62238620-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#179761280-A-C

62238788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 179761487-G-A

62238840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 179761519-G-A

62238840-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 179761519-G-T

62238855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 179761536-G-A

62238855-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 179761536-G-T

62243965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 179767953-G-A

62245928-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 179769320-G-A

62254820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 179776537-A-G

62256066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 179778781-G-A

62256066-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 179778781-G-T

62256217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 179778901-C-T

62257618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 179779473-C-T

62259967-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 179779992-C-G

62260129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 179780154-T-C

62262100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 179781118-T-C

62262100-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 179781118-T-G

62262428-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 179781904-C-G

62262428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 179781904-C-T

62262604-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 179782054-C-G

62262757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 179782154-G-A

62262976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 179782335-G-A

http://identifiers.org/hco/20/GRCh38#62263537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#179782809-C-A

62263537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 179782809-C-T

http://identifiers.org/hco/20/GRCh38#62263613-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#179782895-C-A

62263613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 179782895-C-T

62263622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 179782904-G-A

62264314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 179783306-A-G

62271654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 179786192-G-A

62271654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 179786192-G-T

62271712-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 179786268-A-T

62271732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant, splice_donor_variant
orthologous variants: 179786288-G-A

62271732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant, splice_donor_variant
orthologous variants: 179786288-G-T

62271768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 179786328-G-A

62271768-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 179786328-G-C

62271768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 179786328-G-T

http://identifiers.org/hco/20/GRCh38#62271807-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#179786379-C-A

62271807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 179786379-C-T

62271809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 179786381-G-A

62271809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 179786381-G-T

62271840-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 179786411-G-C

62271840-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 179786411-G-T

62271872-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 179786452-A-T

62271878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 179786458-G-A

62271878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 179786458-G-T

62272003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 179786544-G-A

62272003-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 179786544-G-T

http://identifiers.org/hco/20/GRCh38#62272033-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#179786574-C-A

62272033-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 179786574-C-G

62272244-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 179786744-C-G

62272244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 179786744-C-T

http://identifiers.org/hco/20/GRCh38#62273287-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#179786860-C-A

62273287-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 179786860-C-G

62273287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 179786860-C-T

http://identifiers.org/hco/20/GRCh38#62273293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#179786866-C-A

62273293-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 179786866-C-G

62273293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 179786866-C-T

62273491-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 179787049-A-T

62273538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 179787096-G-T

http://identifiers.org/hco/20/GRCh38#62273549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#179787108-C-A

62277000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 179788916-G-A

62277078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 179789016-G-A

62277119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 179789053-C-T

http://identifiers.org/hco/20/GRCh38#62277195-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#179789107-A-C

62277391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 179789282-G-A

62277815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 179789686-C-T

62277983-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 179789849-T-G

http://identifiers.org/hco/20/GRCh38#62279065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#179790108-C-A

62279065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 179790108-C-T

http://identifiers.org/hco/20/GRCh38#62279120-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#179790170-C-A

62279407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 179790459-A-G

62279408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 179790460-G-A

62279408-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 179790460-G-C

62279408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 179790460-G-T

http://identifiers.org/hco/20/GRCh38#62279643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#179790615-C-A

62279643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 179790615-C-T

62279880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 179790805-A-G

62279928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 179790855-T-C

62279928-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 179790855-T-G

62279941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 179790868-G-A

62279965-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 179790880-T-G

62280158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 179791108-G-A

62280158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 179791108-G-T

62280286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 179791293-G-T

http://identifiers.org/hco/20/GRCh38#62280295-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#179791303-A-C

62280321-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 179791329-T-C

62280449-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 179791430-T-G

62280542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 179791524-C-T

62280849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 179791780-A-G

62280876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 179791807-A-G

62280895-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 179791826-A-T

http://identifiers.org/hco/20/GRCh38#62280933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#179791860-C-A

62281139-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 179792053-T-A

62281139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 179792053-T-C

62281299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 179792270-A-G

62281397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 179792378-T-C

http://identifiers.org/hco/20/GRCh38#62281402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#179792383-C-A

62281402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 179792383-C-T

http://identifiers.org/hco/20/GRCh38#62281436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#179792427-C-A

62281436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 179792427-C-T

62281469-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 179792475-T-A

http://identifiers.org/hco/20/GRCh38#62281485-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#179792495-A-C

62281485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 179792495-A-G

http://identifiers.org/hco/20/GRCh38#62281669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#179792685-C-A

62281669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 179792685-C-T

62281689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 179792707-G-A

62281689-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 179792707-G-C

62281689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 179792707-G-T

62281700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 179792718-G-A

http://identifiers.org/hco/20/GRCh38#62281907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#179792917-C-A

62281907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 179792917-C-T

http://identifiers.org/hco/20/GRCh38#62281911-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#179792921-A-C

62281911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 179792921-A-G

62281960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 179792957-G-A

62281960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 179792957-G-T

http://identifiers.org/hco/20/GRCh38#62282007-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#179792984-C-A

62282007-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 179792984-C-G

62282025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 179793001-C-T

http://identifiers.org/hco/20/GRCh38#62284118-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#179795064-A-C

62284872-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 179795370-T-G

http://identifiers.org/hco/20/GRCh38#62285144-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#179795648-A-C

62286480-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 179796972-T-A

62286480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 179796972-T-C

62286496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 179796995-G-A

62286496-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 179796995-G-C

62286496-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 179796995-G-T

62286570-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 179797047-T-G

62286594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 179797071-C-T

62286624-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 179797113-C-G

62286624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 179797113-C-T

62286732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 179797221-T-C

http://identifiers.org/hco/20/GRCh38#62286735-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#179797224-C-A

62286735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 179797224-C-T

http://identifiers.org/hco/20/GRCh38#62286772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#179797262-C-A

62286773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 179797263-A-G

http://identifiers.org/hco/20/GRCh38#62286807-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#179797306-C-A

62286807-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 179797306-C-G

62286807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 179797306-C-T

http://identifiers.org/hco/20/GRCh38#62286817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#179797316-C-A

62286817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 179797316-C-T

62289158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 179799575-A-G

62289167-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 179799584-A-T

62289377-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 179799766-T-G

62289383-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 179799772-G-C

62289383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 179799772-G-T

62289385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 179799774-G-A

62289533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 179799904-G-A

http://identifiers.org/hco/20/GRCh38#62289766-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#179800162-A-C

62289802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 179800197-G-A

62289829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 179800224-C-T

62291672-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 179800803-G-T

62291917-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 179800968-G-C

62292133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 179801166-C-T

62292327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 179801320-C-T

62292649-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 179801635-T-A

http://identifiers.org/hco/20/GRCh38#62294018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#179803477-C-A

62294018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 179803477-C-T

62294062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 179803516-T-C

http://identifiers.org/hco/20/GRCh38#62294150-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#179803593-C-A

62294150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 179803593-C-T

62294167-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 179803610-T-A

http://identifiers.org/hco/20/GRCh38#62294168-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#179803611-C-A

62294168-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 179803611-C-G

62294168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 179803611-C-T

62294178-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 179803619-T-A

62294178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 179803619-T-C

62294198-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 179803639-T-A

http://identifiers.org/hco/20/GRCh38#62294262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#179803698-C-A

62294262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 179803698-C-T

62294305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 179803740-G-T

http://identifiers.org/hco/20/GRCh38#62294323-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#179803762-A-C

http://identifiers.org/hco/20/GRCh38#62294329-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#179803767-A-C

62294334-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 179803772-G-T

62294352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 179803775-G-T

62294769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 179804145-G-T

62294781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 179804157-A-G

62294906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 179804269-T-C

62295447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 179804447-C-T

62295499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 179804497-T-C

62295590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 179804582-G-A

62295590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 179804582-G-T

62295685-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 179804666-G-T

http://identifiers.org/hco/20/GRCh38#62295696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#179804680-C-A

62295713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 179804695-G-T

http://identifiers.org/hco/20/GRCh38#62295719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#179804701-C-A

62295719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 179804701-C-T

62295732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 179804714-A-G

62295832-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 179804797-G-C

http://identifiers.org/hco/20/GRCh38#62295985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#179804943-C-A

62295985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 15761
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 179804943-C-T