http://identifiers.org/hco/16/GRCh38#2339203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24572466-C-A

2339203-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24572466-C-G

2339320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24572349-G-T

2339336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24572333-G-A

2339451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24572257-T-C

2339853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24571820-G-A

2340118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24571582-C-T

2340300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24571440-C-T

2340428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24571350-G-A

2340428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24571350-G-T

http://identifiers.org/hco/16/GRCh38#2340586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#24571210-C-A

2340586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 24571210-C-T

2340588-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 24571208-G-C

2340588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 24571208-G-T

2340636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24571162-G-A

2340636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24571162-G-T

2340704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24571091-G-A

2340704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24571091-G-T

http://identifiers.org/hco/16/GRCh38#2340808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#24570975-C-A

2340808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24570975-C-T

2341055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 24570648-T-C

2341175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 24570526-C-T

2341176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 24570525-T-C

2341191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 24570510-A-G

http://identifiers.org/hco/16/GRCh38#2341331-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#24570430-C-A

2341331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 24570430-C-T

2341338-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 24570423-T-G

2341352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 24570411-G-A

http://identifiers.org/hco/16/GRCh38#2341432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24570372-C-A

2341432-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24570372-C-G

2341518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24570314-T-C

2341518-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24570314-T-G

2341577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24570270-G-A

2341577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24570270-G-T

2341602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24570258-C-T

http://identifiers.org/hco/16/GRCh38#2341763-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24570171-A-C

2341841-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24570126-G-C

http://identifiers.org/hco/16/GRCh38#2341855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24570115-C-A

2341918-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24570081-G-T

2341943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24570056-C-T

2341947-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24570052-G-C

2342138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24569977-A-G

2342271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24569837-G-A

2342271-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24569837-G-C

2342271-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24569837-G-T

2342385-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24569721-A-T

2342618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24569500-G-T

2342790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24569372-A-G

2342813-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24569349-C-G

2342813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24569349-C-T

2342835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24569328-T-C

2342844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24569319-T-C

http://identifiers.org/hco/16/GRCh38#2342894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24569280-C-A

http://identifiers.org/hco/16/GRCh38#2342957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24569236-C-A

2343029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24569165-T-C

2343031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24569163-G-T

2343039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24569155-A-G

2344820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24568840-C-T

2344851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24568813-C-T

2344910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24568756-T-C

2345006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24568673-T-C

2345051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24568641-G-T

2360690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24566851-A-G

http://identifiers.org/hco/16/GRCh38#2360844-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24566699-A-C

2360844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24566699-A-G

http://identifiers.org/hco/16/GRCh38#2361009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24566517-C-A

2361080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24566298-A-G

2361096-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24566278-C-G

2361096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24566278-C-T

2361146-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: non coding transcript exon variant
orthologous variants: 24566222-G-C

2361525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24565396-A-G

2362497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24563854-T-C

http://identifiers.org/hco/16/GRCh38#2362534-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24563817-C-A

2362534-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24563817-C-G

2362534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24563817-C-T

http://identifiers.org/hco/16/GRCh38#2362589-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24563744-C-A

2362619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24563717-G-T

2362781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24563565-G-A

2362781-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24563565-G-T

2363023-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24563342-T-G

http://identifiers.org/hco/16/GRCh38#2363155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24563223-C-A

2363155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24563223-C-T

2363181-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24563194-C-G

2363181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24563194-C-T

2365333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24556740-T-C

2365749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: non coding transcript exon variant
orthologous variants: 24554566-T-C

http://identifiers.org/hco/16/GRCh38#2365847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24554468-C-A

2365847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24554468-C-T

2365914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24554412-A-G

2366507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24553648-G-A

2366830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24553387-A-G

2366904-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24553318-G-C

2366904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24553318-G-T

2366910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24553312-G-A

2366911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24553311-C-T

http://identifiers.org/hco/16/GRCh38#2366954-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24553271-C-A

2366954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 24553271-C-T

2366956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 24553269-T-C

2367106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: non coding transcript exon variant
orthologous variants: 24553116-G-T

2367145-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24553077-G-C

2367145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24553077-G-T

2367523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24552945-T-C

2367610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24552853-A-G

2367665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24552801-G-A

2368590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24549099-C-T

2368634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24549057-G-T

2368724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24548996-C-T

2368753-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24548971-G-T

2368770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24548954-C-T

2368997-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24548734-T-G

2369176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24548559-T-C

http://identifiers.org/hco/16/GRCh38#2369319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24548401-C-A

2369394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24548330-G-A

2369734-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24548071-T-A

2369764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24548041-T-C

http://identifiers.org/hco/16/GRCh38#2369890-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24547926-C-A

2370298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24547784-T-C

2370651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24547466-G-A

2370651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24547466-G-T

2370891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24547257-C-T

2373927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24546753-A-G

2373936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24546744-T-C

2373943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24546737-G-A

2373943-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24546737-G-T

2374030-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: non coding transcript exon variant
orthologous variants: 24546651-T-G

2374114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24546571-G-A

2374125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24546561-A-G

2374140-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24546546-G-T

2374141-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24546545-G-T

2374157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24546529-T-C

2374280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24546474-C-T

2374412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24546377-C-T

2374747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24545999-A-G

2374946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24545823-G-T

2374970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24545799-T-C

2375281-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24545482-G-T

2377174-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24530277-T-A

2377263-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24530188-C-G

2379375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24526624-T-C

http://identifiers.org/hco/16/GRCh38#2379381-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24526618-C-A

2379616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24526394-G-A

2386085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24519436-G-A

http://identifiers.org/hco/16/GRCh38#2386136-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24519383-A-C

2386136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: non coding transcript exon variant
orthologous variants: 24519383-A-G

2386153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: non coding transcript exon variant
orthologous variants: 24519366-A-G

2386159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: non coding transcript exon variant
orthologous variants: 24519360-T-C

2386203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: non coding transcript exon variant
orthologous variants: 24519316-G-A

2386203-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: non coding transcript exon variant
orthologous variants: 24519316-G-C

2386203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: non coding transcript exon variant
orthologous variants: 24519316-G-T

http://identifiers.org/hco/16/GRCh38#2386271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24519254-C-A

2386271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24519254-C-T

2386275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24519250-A-G

2386277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24519248-G-A

http://identifiers.org/hco/16/GRCh38#2386278-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24519247-C-A

2386278-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24519247-C-G

2386278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24519247-C-T

2395946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 24515228-C-T

2403410-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24514540-T-G

2403454-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24514502-T-G

2403533-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24514405-T-A

http://identifiers.org/hco/16/GRCh38#2403955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24514328-C-A

2403955-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24514328-C-G

2403988-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24514296-T-A

2404104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24514182-A-G

2404104-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24514182-A-T

http://identifiers.org/hco/16/GRCh38#2404117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24514169-C-A

http://identifiers.org/hco/16/GRCh38#2404129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24514157-C-A

2404179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24514106-C-T

2404447-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24513261-C-G

2404481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24513226-G-T

2405366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24512372-T-C

2405366-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24512372-T-G

2405394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24512344-C-T

2406517-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24510910-G-T

http://identifiers.org/hco/16/GRCh38#2406525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24510903-C-A

2406644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: non coding transcript exon variant
orthologous variants: 24510790-A-G

2406684-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: non coding transcript exon variant
orthologous variants: 24510750-T-A

http://identifiers.org/hco/16/GRCh38#2406768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24510666-C-A

2406822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: non coding transcript exon variant
orthologous variants: 24510612-T-C

2406822-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: non coding transcript exon variant
orthologous variants: 24510612-T-G

http://identifiers.org/hco/16/GRCh38#2406825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24510609-C-A

2406825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: non coding transcript exon variant
orthologous variants: 24510609-C-T

http://identifiers.org/hco/16/GRCh38#2406941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24510498-C-A

2406941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24510498-C-T

2406973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24510466-G-A

2406973-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24510466-G-T

2407101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24510341-G-A

2410000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24508769-A-G

2410013-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24508756-C-G

2410015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24508754-G-A

2410016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24508753-G-A

2410057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24508714-A-G

2410058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24508713-G-A

2410071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24508700-G-A

2410138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24508634-G-A

2410138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24508634-G-T

2410193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: non coding transcript exon variant
orthologous variants: 24508564-C-T

2410204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: non coding transcript exon variant
orthologous variants: 24508553-G-T

2410436-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 24508321-A-T

2410471-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24508286-T-A

2410471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24508286-T-C

2410471-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24508286-T-G

http://identifiers.org/hco/16/GRCh38#2410496-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24508254-A-C

http://identifiers.org/hco/16/GRCh38#2410733-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24508060-C-A

2410733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: non coding transcript exon variant
orthologous variants: 24508060-C-T

2410787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: non coding transcript exon variant
orthologous variants: 24508006-G-A

2410787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: non coding transcript exon variant
orthologous variants: 24508006-G-T

2410834-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24507959-T-A

2410834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24507959-T-C

2410858-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24507936-T-A

2410858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24507936-T-C

2410858-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24507936-T-G

http://identifiers.org/hco/16/GRCh38#2410879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24507919-C-A

http://identifiers.org/hco/16/GRCh38#2410906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24507890-C-A

2410906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24507890-C-T

2411032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24507797-G-A

http://identifiers.org/hco/16/GRCh38#2411047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24507782-C-A

2411125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24507710-A-G

2411734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24505291-C-T

2411945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24505020-G-A

2411945-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24505020-G-T

2411946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24505019-C-T

http://identifiers.org/hco/16/GRCh38#2411993-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24504971-C-A

2412047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24504942-A-G

2412090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24504912-T-C

2412112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24504878-G-A

2412168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24504825-A-G

2412266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24504741-G-T

2421011-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24488442-G-C

2422453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24486832-G-A

2422453-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24486832-G-T

http://identifiers.org/hco/16/GRCh38#2422463-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24486822-C-A

2422463-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24486822-C-G

2422463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24486822-C-T

2422472-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24486815-G-T

2422493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24486788-G-T

2422511-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24486774-G-T

2422519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24486766-A-G

2422673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: non coding transcript exon variant
orthologous variants: 24486616-G-A

2422673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: non coding transcript exon variant
orthologous variants: 24486616-G-T

2422682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: non coding transcript exon variant
orthologous variants: 24486607-G-A

2423347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 24485769-C-T

2423491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24485627-T-C

2423506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24485612-A-G

2424019-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24485147-G-T

2424068-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24485107-T-G

2424118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24485049-A-G

2424128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24485039-G-A

2424128-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24485039-G-T

http://identifiers.org/hco/16/GRCh38#2424129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24485038-C-A

2424129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24485038-C-T

2424208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24484963-G-A

2424208-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24484963-G-T

2424408-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24484762-G-C

2424408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24484762-G-T

http://identifiers.org/hco/16/GRCh38#2424410-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24484760-C-A

2424410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24484760-C-T

2424429-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24484742-G-C

2424429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24484742-G-T

2424438-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24484733-A-T

2424476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24484698-A-G

2424476-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24484698-A-T

http://identifiers.org/hco/16/GRCh38#2424478-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24484696-C-A

2424486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24484687-T-C

http://identifiers.org/hco/16/GRCh38#2424543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24484621-C-A

2424543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24484621-C-T

http://identifiers.org/hco/16/GRCh38#2424555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24484609-C-A

2424555-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24484609-C-G

2424555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24484609-C-T

2424678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: non coding transcript exon variant
orthologous variants: 24484484-G-A

2424703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: non coding transcript exon variant
orthologous variants: 24484459-G-A

2424722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: non coding transcript exon variant
orthologous variants: 24484440-G-A

2424722-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: non coding transcript exon variant
orthologous variants: 24484440-G-T

2424774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 24484388-G-A

2424802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24484373-G-A

http://identifiers.org/hco/16/GRCh38#2424836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24484341-C-A

2424836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24484341-C-T

2424837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24484340-G-A

2424837-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24484340-G-C

2424837-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24484340-G-T

2425045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: non coding transcript exon variant
orthologous variants: 24484181-G-A

2425045-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: non coding transcript exon variant
orthologous variants: 24484181-G-T

http://identifiers.org/hco/16/GRCh38#2425058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24484168-C-A

2425058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24484168-C-T

2425142-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24484141-G-T

2425173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24484120-G-A

2425173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24484120-G-T

http://identifiers.org/hco/16/GRCh38#2425176-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24484117-A-C

2425176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24484117-A-G

2425189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24484104-C-T

2425230-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24484063-A-T

2425254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24484039-C-T

2425445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24483854-G-A

2425445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24483854-G-T

http://identifiers.org/hco/16/GRCh38#2425472-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24483825-C-A

http://identifiers.org/hco/16/GRCh38#2425484-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24483813-C-A

2425490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24483807-C-T

2425499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24483788-T-C

2425504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24483783-C-T

2425509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24483778-T-C

2425509-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24483778-T-G

2425518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24483763-G-A

2425518-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24483763-G-T

2425539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24483538-A-G

2425678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: non coding transcript exon variant
orthologous variants: 24483391-G-T

2425736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: non coding transcript exon variant
orthologous variants: 24483327-T-C

http://identifiers.org/hco/16/GRCh38#2425742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24483321-C-A

2425742-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: non coding transcript exon variant
orthologous variants: 24483321-C-G

2425742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: non coding transcript exon variant
orthologous variants: 24483321-C-T

2425758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: non coding transcript exon variant
orthologous variants: 24483305-T-C

http://identifiers.org/hco/16/GRCh38#2425826-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24483264-C-A

2425826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: non coding transcript exon variant
orthologous variants: 24483264-C-T

http://identifiers.org/hco/16/GRCh38#2425857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24483236-C-A

http://identifiers.org/hco/16/GRCh38#2425867-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: non coding transcript exon variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#24483226-C-A

2425867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: non coding transcript exon variant
orthologous variants: 24483226-C-T

2425870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: non coding transcript exon variant
orthologous variants: 24483223-G-A

2425872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: non coding transcript exon variant
orthologous variants: 24483221-G-A

2425872-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 32972
most severe consequence: non coding transcript exon variant
orthologous variants: 24483221-G-T