http://identifiers.org/hco/1/GRCh38#119140431-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#99048629-C-A

119140431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 99048629-C-T

http://identifiers.org/hco/1/GRCh38#119140492-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/3/GRCm39#99048564-C-A

119140492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 99048564-C-T

119140540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 99048517-G-A

119140540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 99048517-G-T

119140576-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 99048481-G-C

119140576-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 99048481-G-T

119140664-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 99048394-T-G

119140708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: non coding transcript exon variant
orthologous variants: 99048365-G-A

119140708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: non coding transcript exon variant
orthologous variants: 99048365-G-T

http://identifiers.org/hco/1/GRCh38#119140752-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#99048310-A-C

119140752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: non coding transcript exon variant
orthologous variants: 99048310-A-G

119140752-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: non coding transcript exon variant
orthologous variants: 99048310-A-T

http://identifiers.org/hco/1/GRCh38#119140760-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#99048302-C-A

119140760-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: non coding transcript exon variant
orthologous variants: 99048302-C-G

119140760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: non coding transcript exon variant
orthologous variants: 99048302-C-T

119140797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99048271-G-A

119140797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99048271-G-T

http://identifiers.org/hco/1/GRCh38#119140831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#99048233-C-A

119140831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99048233-C-T

http://identifiers.org/hco/1/GRCh38#119140851-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#99048212-A-C

119140851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99048212-A-G

119140950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99048132-A-G

119141372-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99047687-C-G

119141372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99047687-C-T

119141497-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99047570-G-T

119141636-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99047459-C-G

119141636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99047459-C-T

119141757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99047347-T-C

119141812-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 99047281-G-T

119141927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99047192-G-A

119141934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99047180-A-G

119141956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99047157-T-C

119142046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99047071-A-G

http://identifiers.org/hco/1/GRCh38#119142047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#99047070-C-A

http://identifiers.org/hco/1/GRCh38#119142119-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#99047005-C-A

http://identifiers.org/hco/1/GRCh38#119142150-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#99046975-C-A

119142150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99046975-C-T

119142200-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99046925-G-T

119142789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99045597-G-A

119142908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99045464-C-T

119144369-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99044384-T-G

119144549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99044217-T-C

119144581-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99044185-G-C

119144614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99044154-C-T

http://identifiers.org/hco/1/GRCh38#119145147-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#99043899-A-C

119145147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99043899-A-G

119145181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99043811-T-C

119145423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99043649-C-T

119145577-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99043498-T-A

119145723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99043219-G-A

http://identifiers.org/hco/1/GRCh38#119145895-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#99043053-C-A

119145922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99043026-G-A

http://identifiers.org/hco/1/GRCh38#119146275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#99042651-C-A

119146327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99042599-A-G

119146341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99042583-T-C

119146396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99042530-A-G

119146518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99042425-G-A

119146518-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99042425-G-T

119146662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99042233-A-G

119146664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99042231-G-T

119146684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99042199-A-G

http://identifiers.org/hco/1/GRCh38#119146702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#99042111-C-A

119146702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99042111-C-T

119146839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99041935-A-G

119146841-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99041933-G-C

119147904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99041406-A-G

119148051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99041258-T-C

http://identifiers.org/hco/1/GRCh38#119148063-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#99041244-A-C

119148074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99041233-G-A

119157439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99039886-G-A

119157475-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99039853-G-T

119157528-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99039816-C-G

119157528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99039816-C-T

119157872-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99039484-G-T

119159032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99038187-G-A

119159367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99037866-G-A

119159373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99037860-G-A

119159417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99037818-C-T

119159505-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99037738-G-C

119159640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99037608-C-T

119159877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99037373-A-G

119159917-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99037338-G-C

119159989-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99037261-T-A

119160053-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99037199-C-G

119160222-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99037040-T-C

119160465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99036791-G-A

119160845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99036501-A-G

119161241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 99036159-T-C

119162676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99033694-A-G

119162806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99033570-T-C

119162897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99033492-A-G

119163092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99033296-C-T

119163139-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99033198-G-T

119163387-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99032954-T-A

119163498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99032847-G-A

119163498-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99032847-G-T

119163553-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99032796-G-C

119192470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99022520-G-A

119193088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99021910-G-A

119193311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99021730-G-A

119193527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99021521-C-T

119194502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99020633-T-C

119194504-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99020631-G-C

119195393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99020176-T-C

119195419-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99020151-G-C

119195424-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99020146-T-G

http://identifiers.org/hco/1/GRCh38#119195436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#99020134-C-A

119195926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99019698-A-G

119195926-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99019698-A-T

119196035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99019592-G-A

119196562-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99018873-T-A

119196837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99018599-T-C

119196842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99018592-C-T

119196868-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99018562-T-C

119197035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99018396-A-G

119197256-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99018145-C-G

119197575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99017831-T-C

119197675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99017720-C-T

119204606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99013755-T-C

119204662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99013699-G-T

119204684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99013677-A-G

119204684-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99013677-A-T

119204709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99013655-T-C

119204761-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99013607-T-A

119204919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99013463-C-T

119205010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99013410-G-A

119205014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99013406-C-T

119205037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99013384-T-C

119205353-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99013106-C-G

http://identifiers.org/hco/1/GRCh38#119205408-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#99012724-C-A

119205408-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99012724-C-G

119205408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99012724-C-T

http://identifiers.org/hco/1/GRCh38#119205684-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#99012031-C-A

119205831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99011888-C-T

http://identifiers.org/hco/1/GRCh38#119205856-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#99011863-A-C

http://identifiers.org/hco/1/GRCh38#119205909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#99011831-C-A

119205960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99011800-A-G

119206086-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99011691-T-G

119206456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 99011340-C-T

119207974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98998433-A-G

http://identifiers.org/hco/1/GRCh38#119208095-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#98998310-A-C

119208232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98998170-G-A

119208296-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98998110-A-T

119208461-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98997980-T-A

119209320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98988896-C-T

119209325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98988891-A-G

119209772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98988467-A-G

119210140-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98988119-T-A

119210238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98988035-G-A

http://identifiers.org/hco/1/GRCh38#119210436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#98987844-C-A

119210621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98987682-G-T

119217392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98975467-C-T

119217403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98975457-A-G

119218467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98974471-G-A

119218580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98974363-G-A

119220877-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98962954-T-A

119220877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98962954-T-C

http://identifiers.org/hco/1/GRCh38#119221769-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#98961805-C-A

119221813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98961766-C-T

119221951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98961649-C-T

119222024-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98961538-C-G

119222024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98961538-C-T

119222124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98961424-G-A

119222451-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98961047-T-G

119222534-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98960970-G-T

119222724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98960774-C-T

http://identifiers.org/hco/1/GRCh38#119222746-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#98960752-A-C

http://identifiers.org/hco/1/GRCh38#119222747-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#98960751-C-A

119222747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98960751-C-T

http://identifiers.org/hco/1/GRCh38#119222753-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#98960745-C-A

119222948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98960572-G-A

119223786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98960052-C-T

119223816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98960028-T-C

119223903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98959948-C-T

http://identifiers.org/hco/1/GRCh38#119224092-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#98959765-A-C

119224249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98959607-A-G

119224258-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98959598-G-C

119224411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98959462-C-T

119224712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98959188-T-C

119224989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98958962-C-T

http://identifiers.org/hco/1/GRCh38#119225043-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#98958906-A-C

119225043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98958906-A-G

119225251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98958680-A-G

119225356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98958583-C-T

119225404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98958535-C-T

119225492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98958446-C-T

119225716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98958226-T-C

119225764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98958187-G-A

119225784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98958160-A-G

119226038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98956841-G-A

119226038-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98956841-G-T

119226150-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98956726-T-G

119226190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98956678-C-T

119226238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98956642-A-G

119226242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98956638-A-G

119226242-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98956638-A-T

119226360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98956537-A-G

119226509-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98956394-T-A

119226568-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98956338-T-G

119226644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98956262-C-T

119227672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98954695-G-A

119227672-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98954695-G-C

119227672-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98954695-G-T

119227863-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98954514-C-G

http://identifiers.org/hco/1/GRCh38#119227867-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#98954510-C-A

119228744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98953468-A-G

119228859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98953365-T-C

119228953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98953271-A-G

119229019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98953204-G-A

119229367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98952858-G-A

119229388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98952850-G-A

119229485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98952764-T-C

119229600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98952653-G-A

119230065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98952172-A-G

119230134-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98952102-A-T

119230528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98951991-G-A

119230765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98951757-T-C

119230880-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98951639-G-C

119230980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98951547-A-G

119231044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98951478-G-A

119231256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98951132-G-A

119238167-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98950172-G-T

119238299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98950043-A-G

119238350-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98949995-T-A

119238544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98949780-T-C

119239514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98949471-G-A

119239574-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98949428-T-A

119239771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98949250-C-T

119239980-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98949040-G-T

119244675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98939151-T-C

119244780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98939073-C-T

119244912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98938931-A-G

119244941-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98938903-C-G

119244967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98938877-T-C

119245681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98938800-G-A

119245802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98938711-G-T

119245868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98938651-G-A

119245942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98938581-A-G

http://identifiers.org/hco/1/GRCh38#119246430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#98938057-C-A

119246431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98938056-A-G

119246635-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98937851-A-T

http://identifiers.org/hco/1/GRCh38#119246722-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#98937764-C-A

119246827-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98937660-A-G

119248794-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98934975-C-G

119248873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98934885-G-A

119248934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98934826-C-T

119249053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98934701-C-T

119249320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98934454-G-A

119249409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98934364-C-T

119249626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98934161-C-T

119250341-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98933489-A-T

119252345-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98932730-G-C

119252853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98932289-C-T

119253516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98931877-A-G

119253516-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98931877-A-T

119253522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98931790-A-G

http://identifiers.org/hco/1/GRCh38#119253553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#98931752-C-A

119253687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98931652-T-C

http://identifiers.org/hco/1/GRCh38#119253694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#98931645-C-A

119253896-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98931477-G-T

119254078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98931265-C-T

119254092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98931253-T-C

http://identifiers.org/hco/1/GRCh38#119254136-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#98931206-A-C

119254136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98931206-A-G

119257637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98930883-G-A

119257794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98930701-A-G

http://identifiers.org/hco/1/GRCh38#119259383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#98930331-C-A

119259408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98930305-C-T

119259518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98930212-T-C

119259664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98930079-A-G

119259817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98929950-T-C

119260141-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98929643-G-C

119260141-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98929643-G-T

http://identifiers.org/hco/1/GRCh38#119260187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#98929587-C-A

119260187-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98929587-C-G

119260187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98929587-C-T

119260191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98929583-T-C

http://identifiers.org/hco/1/GRCh38#119260232-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#98929487-C-A

119260232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98929487-C-T

119260248-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98929471-G-T

119260268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98929451-G-T

119260322-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98929398-A-T

119260477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98929237-T-C

119260609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98929108-G-T

119260894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98928824-G-A

119261273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98928458-C-T

119261399-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98928340-A-T

119261480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98928258-T-C

119261482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98928256-A-G

http://identifiers.org/hco/1/GRCh38#119261497-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#98928241-C-A

119261497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98928241-C-T

119261610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98928124-A-G

119261866-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98927496-C-G

119262968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98926396-G-A

119262968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98926396-G-T

119263309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98926131-T-C

http://identifiers.org/hco/1/GRCh38#119263560-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#98925915-C-A

http://identifiers.org/hco/1/GRCh38#119263660-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#98925810-A-C

119263970-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98925399-C-G

119263970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98925399-C-T

119264128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98925258-C-T

119269412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98924421-G-T

119269460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98924379-A-G

119269532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98924308-T-C

119269532-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98924308-T-G

119269545-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98924295-T-A

119269591-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98924233-A-G

119269736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98924006-T-C

119269932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98923809-C-T

119269972-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98923767-T-A

119270025-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98923725-G-T

119270029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98923721-A-G

119270223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98923544-T-C

119270339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98923430-A-G

119270572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98922754-A-G

http://identifiers.org/hco/1/GRCh38#119270621-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#98922695-A-C

http://identifiers.org/hco/1/GRCh38#119270688-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#98922628-A-C

119270820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98922511-G-A

119270887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98922441-C-T

119273879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98904151-A-G

119274048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 98903994-T-C

119275318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98902924-C-T

119275346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98902896-A-G

http://identifiers.org/hco/1/GRCh38#119275479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#98902775-C-A

http://identifiers.org/hco/1/GRCh38#119275562-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#98902395-C-A

119275573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98902384-A-G

http://identifiers.org/hco/1/GRCh38#119275638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#98902319-C-A

119275638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98902319-C-T

119275660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98902022-T-C

119275660-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98902022-T-G

http://identifiers.org/hco/1/GRCh38#119275731-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/3/GRCm39#98901962-A-C

119275778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40612
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 98901937-A-G