http://identifiers.org/hco/10/GRCh38#59176656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#70435100-C-A

59176656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 70435100-C-T

59176666-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 70435090-C-G

59176679-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 70435077-T-A

59176679-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 70435077-T-G

http://identifiers.org/hco/10/GRCh38#59176718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#70435044-C-A

59176718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 70435044-C-T

http://identifiers.org/hco/10/GRCh38#59176893-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#70434896-A-C

59176893-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 70434896-A-T

59176979-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70434814-C-G

http://identifiers.org/hco/10/GRCh38#59177028-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#70434751-C-A

59177028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70434751-C-T

59177166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 70434580-G-A

59177166-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 70434580-G-C

59177194-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 70434552-C-G

59177194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 70434552-C-T

59177202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 70434544-G-A

59177202-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 70434544-G-T

http://identifiers.org/hco/10/GRCh38#59177271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#70434502-C-A

59177271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 70434502-C-T

59177385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 70434424-T-C

http://identifiers.org/hco/10/GRCh38#59177543-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#70434292-A-C

59177543-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 70434292-A-T

59177578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 70434245-A-G

59178205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70433648-A-G

59178728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70433303-A-G

59178790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70433237-G-A

59178883-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70433153-G-C

59179189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70432864-G-A

59179228-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70432826-C-G

59179243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70432811-A-G

59179246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70432808-G-A

59179490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70432583-A-G

http://identifiers.org/hco/10/GRCh38#59179743-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#70432326-A-C

59179743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70432326-A-G

59179743-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70432326-A-T

59179752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70432311-A-G

59179916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70432177-T-C

59180003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70432037-G-A

59180235-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70431763-T-A

59180235-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70431763-T-G

http://identifiers.org/hco/10/GRCh38#59180283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#70431715-C-A

59180283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70431715-C-T

59180336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70431645-A-G

59180336-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70431645-A-T

59180341-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70431640-T-A

59180345-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70431636-T-G

59180353-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70431628-T-A

59180353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70431628-T-C

59180416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70431580-A-G

59181055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70430973-C-T

59181223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70430810-G-A

59181405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70430520-T-C

59181437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70430492-C-T

59181521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70430411-T-C

59181680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70430256-A-G

http://identifiers.org/hco/10/GRCh38#59181704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#70430223-C-A

59181845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 70430075-G-A

59182024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70429903-C-T

59182273-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70429679-C-T

http://identifiers.org/hco/10/GRCh38#59182308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#70429644-C-A

59182308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70429644-C-T

59182323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70429627-A-G

59182323-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70429627-A-T

59182809-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70429398-T-A

59182949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70429269-C-T

59183463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70428681-T-C

59183547-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70428594-T-G

59183559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70428579-T-C

59184007-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70428131-G-T

59184422-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70427684-T-G

59184564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70427557-A-G

59189818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70426419-A-G

59190680-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70425367-G-C

59190698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70425352-G-A

59190727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70425324-A-G

59190838-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70425239-T-G

59190849-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70425228-T-C

59190934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70425149-T-C

http://identifiers.org/hco/10/GRCh38#59191014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#70425072-C-A

59191014-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70425072-C-G

59191115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70424972-A-G

59191146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70424944-C-T

59191209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70424896-T-C

59191223-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70424882-G-C

59191229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70424876-T-C

59191452-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70424643-T-A

http://identifiers.org/hco/10/GRCh38#59191720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#70424374-C-A

59191850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70424250-T-C

59191888-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70424207-G-C

59191942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70424151-C-T

59192045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70423558-T-C

59192064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70423537-T-C

59192079-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70423522-C-G

http://identifiers.org/hco/10/GRCh38#59192115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#70423496-C-A

59192207-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70423413-T-A

59192334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70423276-A-G

59192361-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70423248-T-A

59192376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70423233-C-T

59192425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70423183-T-C

http://identifiers.org/hco/10/GRCh38#59192773-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#70421992-A-C

59192872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70421894-G-A

59192914-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70421853-G-C

59193011-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70421744-T-G

59193033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70421722-T-C

59193336-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70421480-T-A

59193472-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70421365-G-T

http://identifiers.org/hco/10/GRCh38#59193521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#70421317-C-A

59193757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70420942-A-G

59193971-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70420718-T-A

59194354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70420514-A-G

59194595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70420285-A-G

59215911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70419384-A-G

http://identifiers.org/hco/10/GRCh38#59216628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#70418610-C-A

59217041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70418179-C-T

59217042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70418178-C-T

59217510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70417272-T-C

59217972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70416381-G-T

59218307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70416057-T-C

59218307-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70416057-T-G

59220331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70415782-A-G

59220606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70415405-G-A

59220837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70415176-T-C

http://identifiers.org/hco/10/GRCh38#59221561-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#70414207-A-C

59221561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70414207-A-G

59221594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70414174-T-C

http://identifiers.org/hco/10/GRCh38#59221730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#70414021-C-A

59221804-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70413948-A-T

59221834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70413926-A-G

59222161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70413548-A-G

http://identifiers.org/hco/10/GRCh38#59222284-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#70413420-A-C

59222747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70412994-A-G

59223100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70412685-A-G

59223296-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70412486-T-G

59223314-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70412468-C-G

59223314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70412468-C-T

59223336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70412446-A-G

59223336-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70412446-A-T

59233841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70407440-T-C

59233847-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70407434-A-T

59233871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70407410-A-G

59234015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70407264-C-T

http://identifiers.org/hco/10/GRCh38#59234086-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#70407193-C-A

http://identifiers.org/hco/10/GRCh38#59234235-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#70407028-C-A

59234235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70407028-C-T

59234423-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 70406728-T-G

http://identifiers.org/hco/10/GRCh38#59234459-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#70406692-A-C

59234480-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 70406671-T-G

59234883-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70406358-A-T

59235184-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70406100-G-T

59235857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70405440-T-C

59235920-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70405348-A-T

59236032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70405241-T-C

59236361-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70404988-T-A

59236361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70404988-T-C

59236362-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70404987-C-G

59236362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70404987-C-T

59236375-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70404974-T-A

59236458-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70404929-T-G

59236931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 70404472-T-C

59237262-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 70404197-T-G

59237435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 70404036-C-T

59237834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 70401869-G-A

59238022-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 70401737-T-G

59238132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 70401575-G-T

59238438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 70401259-A-G

59238489-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 70401216-T-A

59238489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 70401216-T-C

http://identifiers.org/hco/10/GRCh38#59238490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#70401215-C-A

59238490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 70401215-C-T

59238571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 70401133-T-C

59238638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 70401069-G-A

59238638-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 70401069-G-T

59238644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 70401063-C-T

59240165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70399928-C-T

59240171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70399922-A-G

59240178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70399915-A-G

59240697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70399739-A-G

59240700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70399736-A-G

59240769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70399676-G-A

59240973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70399485-A-G

59240974-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70399484-T-C

59240987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70399471-T-C

59241145-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70399270-G-T

59241233-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70399094-T-A

59243584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70398521-G-A

http://identifiers.org/hco/10/GRCh38#59243818-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#70398285-A-C

59243982-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70398150-A-T

59244634-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70395967-T-G

http://identifiers.org/hco/10/GRCh38#59244670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#70395940-C-A

59244771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70395848-G-A

59244771-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70395848-G-C

59244894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70395775-A-G

http://identifiers.org/hco/10/GRCh38#59244915-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#70395756-A-C

59244939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70395726-G-A

59244939-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70395726-G-C

59244939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70395726-G-T

59244989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70395677-T-C

59245008-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70395658-G-A

59245008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70395658-G-T

http://identifiers.org/hco/10/GRCh38#59245015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#70395651-C-A

59245037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 70395629-C-T

59245328-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 70395338-T-A

59245614-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 70395056-T-G

59246650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 70394089-G-A

http://identifiers.org/hco/10/GRCh38#59247196-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#70393592-C-A

59247196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 70393592-C-T

59247236-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 70393554-G-T

http://identifiers.org/hco/10/GRCh38#59247360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#70393428-C-A

59247360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 70393428-C-T

59247377-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 70393412-G-T

59247378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 70393411-G-T

59247516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 70393282-C-T

59247538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 70393260-A-G

59247556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 70393242-A-G

59247743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29378
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 70393060-A-G