120855776-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34783873-G-T

120855973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34784062-G-A

120855973-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34784062-G-T

http://identifiers.org/hco/9/GRCh38#120856016-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34784105-C-A

http://identifiers.org/hco/9/GRCh38#120856186-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34784263-C-A

120856186-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34784263-C-G

120856186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34784263-C-T

120856191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34784268-G-A

120856191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34784268-G-T

120856217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34784294-G-A

120856217-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34784294-G-T

120856260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34784337-T-C

http://identifiers.org/hco/9/GRCh38#120856301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34784377-C-A

120856301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34784377-C-T

120856302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34784378-T-C

120856324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34784401-C-T

http://identifiers.org/hco/9/GRCh38#120856409-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34784481-C-A

120856477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34784525-G-A

120856477-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34784525-G-T

http://identifiers.org/hco/9/GRCh38#120856511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34784562-C-A

120856511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34784562-C-T

120856559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34784608-G-T

120856776-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34784810-G-T

http://identifiers.org/hco/9/GRCh38#120856875-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34784905-C-A

120856958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34784951-T-C

120856958-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34784951-T-G

120857114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34784998-G-T

http://identifiers.org/hco/9/GRCh38#120857141-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34785010-C-A

120857141-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34785010-C-G

120857141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34785010-C-T

http://identifiers.org/hco/9/GRCh38#120857197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34785070-C-A

120857201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34785074-A-G

http://identifiers.org/hco/9/GRCh38#120857265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34785137-C-A

120857265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34785137-C-T

120857267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34785139-G-T

120857292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34785164-G-T

http://identifiers.org/hco/9/GRCh38#120857337-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34785208-C-A

120857337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34785208-C-T

120857503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34785333-G-A

120857503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34785333-G-T

120857650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34785460-T-C

120857650-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34785460-T-G

120857677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34785491-G-A

120857677-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34785491-G-T

120857704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34785515-G-A

120857704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34785515-G-T

http://identifiers.org/hco/9/GRCh38#120857723-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34785535-A-C

120857723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34785535-A-G

120857723-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34785535-A-T

120857731-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 34785543-G-A

120858025-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 34785812-C-G

120858088-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 34785875-G-C

120858160-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 34785947-G-C

120858160-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 34785947-G-T

120858172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 34785959-C-T

http://identifiers.org/hco/9/GRCh38#120858232-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34786019-C-A

120858311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34786098-A-G

120858327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34786114-A-G

120858554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34786235-G-T

120858582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34786263-C-T

120858678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34786342-T-C

120860048-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34787027-G-T

120860053-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34787033-T-G

http://identifiers.org/hco/9/GRCh38#120860069-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34787048-C-A

120860069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34787048-C-T

120860143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 34787122-G-A

120860143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 34787122-G-T

120860213-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34787191-T-A

120860213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34787191-T-C

http://identifiers.org/hco/9/GRCh38#120860220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34787198-C-A

120860220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34787198-C-T

http://identifiers.org/hco/9/GRCh38#120860250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34787230-C-A

120860250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34787230-C-T

120860328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34787302-G-T

http://identifiers.org/hco/9/GRCh38#120860360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34787339-C-A

120860360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34787339-C-T

http://identifiers.org/hco/9/GRCh38#120860394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34787372-C-A

120860394-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34787372-C-G

120860394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34787372-C-T

http://identifiers.org/hco/9/GRCh38#120860405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34787380-C-A

120860405-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34787380-C-G

120860405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34787380-C-T

http://identifiers.org/hco/9/GRCh38#120860412-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34787387-A-C

120860539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34787481-A-G

120860570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34787512-A-G

120860570-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34787512-A-T

120860624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34787568-T-C

120860624-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34787568-T-G

120860728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34787681-T-C

http://identifiers.org/hco/9/GRCh38#120860789-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34787741-C-A

120860794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34787746-G-A

120860898-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34787850-G-T

120860910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34787855-A-G

120860911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34787856-G-A

120860911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34787856-G-T

120860923-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34787868-G-T

120860943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34787909-G-A

120860948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34787914-G-A

120860948-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34787914-G-T

120860997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34787961-A-G

120861199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34788190-A-G

120861199-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34788190-A-T

120861215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34788207-G-A

120861215-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34788207-G-C

120861215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34788207-G-T

http://identifiers.org/hco/9/GRCh38#120861225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34788217-C-A

120861240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34788253-C-T

120861299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34788309-C-T

120861346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34788362-G-A

120861346-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34788362-G-C

120861501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34788525-G-A

120861501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34788525-G-T

120861590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34788608-T-C

120861707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34788720-C-T

120861759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34788774-G-T

120861840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34788859-T-C

120862011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 34789029-G-A

120862114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34789145-G-T

http://identifiers.org/hco/9/GRCh38#120862138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34789158-C-A

120862138-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34789158-C-G

120862143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34789163-A-G

120862157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34789177-G-A

120862413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34789387-G-A

120862461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34789409-A-G

http://identifiers.org/hco/9/GRCh38#120862463-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34789411-C-A

http://identifiers.org/hco/9/GRCh38#120862464-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34789412-C-A

http://identifiers.org/hco/9/GRCh38#120862493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34789442-C-A

120862493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34789442-C-T

120862506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34789455-G-A

120862506-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34789455-G-T

120862529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34789533-T-C

120862543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34789553-C-T

http://identifiers.org/hco/9/GRCh38#120862625-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34789632-A-C

120862625-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 34789632-A-T

120862695-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 34789702-G-T

120862845-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34789840-T-A

120862845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34789840-T-C

http://identifiers.org/hco/9/GRCh38#120862851-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34789846-C-A

120862851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34789846-C-T

http://identifiers.org/hco/9/GRCh38#120862968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34789908-C-A

120862968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34789908-C-T

120862970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34789910-T-C

120863241-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34790123-C-G

http://identifiers.org/hco/9/GRCh38#120863497-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34790489-A-C

120863571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34790691-G-A

120863648-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34790739-G-C

120863718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34790795-G-A

120863718-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34790795-G-C

120863884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34790932-T-C

120863928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34790958-G-T

120863934-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34790964-G-T

120863957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34790981-G-A

120863957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34790981-G-T

120863972-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34790996-T-G

http://identifiers.org/hco/9/GRCh38#120864006-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#34791031-C-A

120864042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 34791065-C-T

120864051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 34791074-G-A

120864051-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 34791074-G-C

http://identifiers.org/hco/9/GRCh38#120864191-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34791209-C-A

http://identifiers.org/hco/9/GRCh38#120864209-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34791224-C-A

120864348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34791430-T-C

http://identifiers.org/hco/9/GRCh38#120864440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34791498-C-A

120865384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34792842-T-C

120865607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34793059-A-G

http://identifiers.org/hco/9/GRCh38#120865637-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34793089-C-A

120865666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34793118-A-G

120865915-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34793304-G-C

120865915-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34793304-G-T

120865962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 34793313-G-A

120866100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 34793436-T-C

120866184-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34793535-C-G

120866184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34793535-C-T

120866314-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34793642-C-G

120866693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34793964-G-A

120866708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34793979-G-A

120866890-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 34794087-C-G

120866890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 34794087-C-T

http://identifiers.org/hco/9/GRCh38#120867005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34794198-C-A

120867005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34794198-C-T

120867803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34794283-G-A

http://identifiers.org/hco/9/GRCh38#120867825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34794305-C-A

120868390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34794478-A-G

120868400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34794488-C-T

120868464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34794537-G-A

120868464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34794537-G-T

120868484-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 34794557-G-T

120868678-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34794749-C-G

120868678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34794749-C-T

http://identifiers.org/hco/9/GRCh38#120868695-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#34794777-C-A

120868695-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34794777-C-G

120868695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34794777-C-T

http://identifiers.org/hco/9/GRCh38#120868697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34794779-C-A

http://identifiers.org/hco/9/GRCh38#120868724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34794805-C-A

120868732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34794823-G-T

http://identifiers.org/hco/9/GRCh38#120868759-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#34794878-C-A

120868759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 34794878-C-T

120868786-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34794916-G-C

120868786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 34794916-G-T

120868859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34795036-G-A

120868859-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34795036-G-C

120868859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 34795036-G-T

120868985-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34795201-C-G

120868985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34795201-C-T

120868986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34795202-C-T

120869035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, undefined
orthologous variants: 34795285-C-T

120869053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34795315-A-G

http://identifiers.org/hco/9/GRCh38#120869101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#34795383-C-A

120869114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, undefined
orthologous variants: 34795396-G-A

120869114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, undefined
orthologous variants: 34795396-G-T

http://identifiers.org/hco/9/GRCh38#120869122-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#34795404-C-A

120869122-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, undefined
orthologous variants: 34795404-C-G

120869122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, undefined
orthologous variants: 34795404-C-T

120869126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, undefined
orthologous variants: 34795408-T-C

http://identifiers.org/hco/9/GRCh38#120869151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#34795431-C-A

120869151-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, undefined
orthologous variants: 34795431-C-G

120869151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, undefined
orthologous variants: 34795431-C-T

120869174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 34795454-T-C

120869223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: synonymous_variant, undefined
orthologous variants: 34795503-G-A

120869256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: synonymous_variant, undefined
orthologous variants: 34795536-G-A

120869256-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: synonymous_variant, undefined
orthologous variants: 34795536-G-C

120869345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, undefined
orthologous variants: 34795625-G-A

120869345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, undefined
orthologous variants: 34795625-G-T

120869736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 34796327-C-T

120869746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 3_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 34796337-G-A

120869746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 3_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 34796337-G-T

120869776-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 3_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 34796367-T-A

120869776-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 3_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 34796367-T-C

120869793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 34796404-C-T

http://identifiers.org/hco/9/GRCh38#120869823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34796442-C-A

120869823-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 34796442-C-G

120869830-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 3_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 34796449-G-C

120869830-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 3_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 34796449-G-T

120869911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 5_prime_UTR_variant, stop_gained, synonymous_variant, undefined
orthologous variants: 34796536-G-A

120869911-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 5_prime_UTR_variant, missense_variant, synonymous_variant, undefined
orthologous variants: 34796536-G-C

120869911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 5_prime_UTR_variant, missense_variant, synonymous_variant, undefined
orthologous variants: 34796536-G-T

120869959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34796584-G-A

120869959-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34796584-G-T

120869984-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34796614-A-T

120869998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34796628-C-T

120870082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34796712-T-C

120870434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34797008-T-C

http://identifiers.org/hco/9/GRCh38#120870650-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34798096-A-C

120870650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34798096-A-G

http://identifiers.org/hco/9/GRCh38#120870661-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34798107-C-A

120870661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34798107-C-T

http://identifiers.org/hco/9/GRCh38#120870678-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34798124-C-A

120870772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34798213-G-A

120871150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34798486-G-A

120871195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34798530-G-A

120871300-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34798637-T-C

120871374-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34798705-C-G

120871751-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34799171-T-G

120871933-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34799396-G-C

120871958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34799440-A-G

120872355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34799953-G-A

120872984-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34800329-T-A

120872984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34800329-T-C

120873209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34800492-G-T

120873226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34800509-C-T

120873452-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34800717-G-C

120873455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34800720-C-T

120873457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34800722-T-C

120873487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34800734-A-G

120873627-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, undefined
orthologous variants: 34800841-C-G

120873757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, undefined
orthologous variants: 34800975-C-T

http://identifiers.org/hco/9/GRCh38#120873833-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#34801024-A-C

120873833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, undefined
orthologous variants: 34801024-A-G

120873833-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, undefined
orthologous variants: 34801024-A-T

120873893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34801104-G-A

120873893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34801104-G-T

120873951-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34801154-G-A

120873951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34801154-G-T

120873952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34801155-G-A

120873952-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34801155-G-T

120874093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34801297-A-G

120874522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34801599-G-T

120874710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: missense variant
orthologous variants: 34801777-C-T

120874902-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34801913-G-C

120874902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34801913-G-T

120875466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, undefined
orthologous variants: 34802429-G-A

120875626-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34802554-T-A

120875631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34802559-C-T

120875834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34802705-G-A

120875834-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34802705-G-T

120875875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, undefined
orthologous variants: 34802740-G-A

120875875-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, undefined
orthologous variants: 34802740-G-T

120875932-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 34802798-C-G

120876017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 34802888-A-G

120876018-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 34802889-G-C

120876018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 34802889-G-T

120876143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 34803005-G-T

120876169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 34803031-G-A

120876169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 34803031-G-T

120876173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 34803035-G-T

http://identifiers.org/hco/9/GRCh38#120876188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34803047-C-A

120876188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 34803047-C-T

http://identifiers.org/hco/9/GRCh38#120876394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34803261-C-A

120876394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 34803261-C-T

http://identifiers.org/hco/9/GRCh38#120876423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34803283-C-A

120876423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 34803283-C-T

120876899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34803761-C-T

http://identifiers.org/hco/9/GRCh38#120876957-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34803811-A-C

120876957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34803811-A-G

120876957-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34803811-A-T

http://identifiers.org/hco/9/GRCh38#120876995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 5_prime_UTR_variant, intron_variant, stop_gained, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#34803849-C-A

120876998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, undefined
orthologous variants: 34803852-G-A

120876998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, undefined
orthologous variants: 34803852-G-T

http://identifiers.org/hco/9/GRCh38#120877003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#34803857-C-A

120877003-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, undefined
orthologous variants: 34803857-C-G

120877019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 34803875-T-C

120877179-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 34804037-C-G

120877179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 34804037-C-T

http://identifiers.org/hco/9/GRCh38#120877253-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#34804111-A-C

120877253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, undefined
orthologous variants: 34804111-A-G

120877253-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, undefined
orthologous variants: 34804111-A-T

120877310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34804166-G-A

120877310-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34804166-G-T

120877704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34804436-A-G

120877857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34804523-A-G

120878337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34804801-G-A

120878529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34804979-G-A

120878645-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34805094-C-G

120878667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34805116-C-T

120879045-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron_variant, undefined
orthologous variants: 34805399-G-T

120879115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34805413-G-A

120882358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34811496-A-G

120882407-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34811546-G-C

120882455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34811596-T-C

120882938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34811780-T-C

120883128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34811919-A-G

120883261-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34812026-C-T

120883381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34812149-G-T

120888411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34814354-T-C

120888453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34814391-T-C

120888779-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34814653-C-G

120888910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34814747-T-C

120888949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34814780-A-G

120889010-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34814834-G-C

120890240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34815586-G-A

120890392-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34815728-G-T

120890486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34815814-T-C

120890717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34816029-G-A

120890808-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34816119-T-A

120890972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34816329-C-T

120891173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34816511-G-A

120891173-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34816511-G-C

http://identifiers.org/hco/9/GRCh38#120891176-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34816514-C-A

120891176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34816514-C-T

120891788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34816843-A-G

120891915-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34816939-C-G

120892269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34817472-C-T

120892534-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34817665-T-G

http://identifiers.org/hco/9/GRCh38#120892547-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34817677-C-A

120892808-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34817925-T-A

120892830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34817950-T-C

120892857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34817977-A-G

120893033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34818115-C-T

120893558-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: intron variant
orthologous variants: 34818573-T-G

120902365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 5 prime UTR variant
orthologous variants: 34832085-T-C

http://identifiers.org/hco/9/GRCh38#120902586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34832252-C-A

120902586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant
orthologous variants: 34832252-C-T

120902604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant
orthologous variants: 34832270-G-A

120902604-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant
orthologous variants: 34832270-G-T

120902610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant
orthologous variants: 34832276-G-A

120902626-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant
orthologous variants: 34832292-G-T

http://identifiers.org/hco/9/GRCh38#120902744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34832397-C-A

120902744-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant
orthologous variants: 34832397-C-G

120902746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant
orthologous variants: 34832399-G-A

http://identifiers.org/hco/9/GRCh38#120902760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 24566
most severe consequence: 3_prime_UTR_variant, 5_prime_UTR_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#34832410-C-A