64506058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 105191296-C-T

http://identifiers.org/hco/5/GRCh38#64506218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#105191134-C-A

64506527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 105190819-G-A

64506527-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 105190819-G-C

64506527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 105190819-G-T

64506532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 105190814-C-T

64506654-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 105190691-G-C

64506828-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105190522-T-A

64506828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105190522-T-C

64506828-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105190522-T-G

64507006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105190343-A-G

64507187-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105190171-G-T

64507315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105190006-C-T

64507428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105189900-T-C

64507593-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105189738-T-A

64507593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105189738-T-C

http://identifiers.org/hco/5/GRCh38#64507692-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#105189649-A-C

64507952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105189387-T-C

64507957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105189382-A-G

64507978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105189362-G-T

64508053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105189299-G-A

64508071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105189234-T-C

http://identifiers.org/hco/5/GRCh38#64508306-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#105189009-A-C

64508385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105188938-G-A

64508506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105188779-G-A

64508581-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105188703-C-G

64508750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105188552-G-T

64508791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105188508-C-T

64508797-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105188502-A-T

64509048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105188273-T-C

64509201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105188149-G-A

64509692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105187858-G-A

64509918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105187644-A-G

http://identifiers.org/hco/5/GRCh38#64510172-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#105187393-A-C

64510243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105187318-G-T

64510282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105187282-A-G

64510370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105187194-G-A

64510637-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105186949-T-A

64511092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105186505-G-A

http://identifiers.org/hco/5/GRCh38#64511107-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#105186494-A-C

64511716-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105185664-T-G

64511986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105185410-G-T

64512034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105185356-C-T

64512114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105185296-T-C

64512157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105185254-C-T

64513689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105183613-G-A

http://identifiers.org/hco/5/GRCh38#64513860-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#105183471-C-A

64514046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105183299-C-T

64514621-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105182860-T-G

64514757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105182723-G-A

64514757-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105182723-G-C

64514839-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105182640-A-G

http://identifiers.org/hco/5/GRCh38#64514911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#105182427-C-A

64514959-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105182380-A-T

64515076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105182264-G-T

64515127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105182211-G-A

64515230-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105182133-C-G

64515230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105182133-C-T

64515575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105181830-T-C

http://identifiers.org/hco/5/GRCh38#64516109-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#105181265-A-C

64516303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105181100-C-T

64516622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105180727-C-T

64516730-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105180607-C-G

64516780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105180558-G-A

64516992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105180280-G-A

64517026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105180262-A-G

64517382-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105179938-T-A

http://identifiers.org/hco/5/GRCh38#64517598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#105179741-C-A

64517602-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105179737-G-C

64517833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105179524-G-A

http://identifiers.org/hco/5/GRCh38#64517972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#105179375-C-A

64518504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105178454-G-A

64518522-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105178438-T-C

64518595-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105178369-G-C

http://identifiers.org/hco/5/GRCh38#64518659-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#105178300-A-C

64518659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105178300-A-G

http://identifiers.org/hco/5/GRCh38#64518950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#105178126-C-A

64519067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105178032-A-G

http://identifiers.org/hco/5/GRCh38#64519334-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#105177489-A-C

64519334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105177489-A-G

64519560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105177283-T-C

64519742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105177031-G-T

64519755-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105176940-T-A

64519904-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105176811-G-C

64519999-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105176711-C-G

64520093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105176618-T-C

64520256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105176490-A-G

64520331-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105176421-C-G

64520413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105176347-G-A

64520438-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105176325-T-A

64520707-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105176065-G-C

64521755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105175640-G-A

64521945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105175453-A-G

64522052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105175349-T-C

64522265-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105175154-T-A

64522455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105175006-T-C

http://identifiers.org/hco/5/GRCh38#64522567-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#105174920-C-A

64522605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105174871-T-C

64522721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105174755-C-T

64522734-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105174742-T-A

64522783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105174693-T-C

64522792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105174683-G-A

64523381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105173720-A-G

64523430-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105173674-T-A

64523488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105173627-C-T

http://identifiers.org/hco/5/GRCh38#64523683-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#105173463-A-C

64524031-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105173125-G-C

64524115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105173042-C-T

64524124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105173033-T-C

64524316-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105172839-C-G

http://identifiers.org/hco/5/GRCh38#64524362-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#105172609-A-C

64524410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105172490-G-T

64525438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105171711-A-G

http://identifiers.org/hco/5/GRCh38#64525464-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#105171685-A-C

64525720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105171444-C-T

64525738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105171426-C-T

http://identifiers.org/hco/5/GRCh38#64526189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#105171238-C-A

http://identifiers.org/hco/5/GRCh38#64526511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#105171019-C-A

64526543-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105170986-T-G

64526797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105170738-G-A

64527124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105170452-G-A

64527580-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105170080-G-T

64527939-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105169657-A-G

http://identifiers.org/hco/5/GRCh38#64527971-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#105169625-A-C

64528226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105169280-T-C

64528279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105169230-G-A

http://identifiers.org/hco/5/GRCh38#64528695-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#105168914-C-A

64529165-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105168483-G-T

64529466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105167928-A-G

64529574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105167826-A-G

64529644-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105167757-A-T

64529802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105167487-C-T

64529922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105167403-G-A

64530053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105167272-G-A

64530053-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105167272-G-C

64530173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105167103-A-G

64530551-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105166730-T-A

64530930-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105166362-A-G

64531000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105166286-G-T

64531220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105166042-A-G

64531385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105165868-C-T

64531450-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105165808-G-C

64531503-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105165753-T-G

64531579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105165685-T-C

64531592-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105165672-C-G

64531742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105165520-A-G

64531821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105165439-A-G

64531994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105165288-T-C

64532588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105164679-G-A

64532688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105164583-G-A

64533520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105162040-C-T

64533791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105161803-C-T

64533794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105161800-C-T

64534279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105161386-G-A

64534367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105161299-G-T

64534420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105161248-C-T

64534567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105161084-A-G

64534809-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105160821-A-T

64534812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105160818-G-A

http://identifiers.org/hco/5/GRCh38#64534848-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#105160782-A-C

64535051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105160366-G-A

64535297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105160140-A-G

http://identifiers.org/hco/5/GRCh38#64535847-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#105159618-A-C

64536099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105159422-A-G

64536099-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105159422-A-T

64536278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105159325-T-C

64536346-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105159261-G-C

64536557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105159050-T-C

http://identifiers.org/hco/5/GRCh38#64536706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#105158910-C-A

http://identifiers.org/hco/5/GRCh38#64536792-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#105158825-C-A

64537133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105158538-A-G

64537823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105158113-G-A

http://identifiers.org/hco/5/GRCh38#64537948-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#105157983-A-C

64539882-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105154278-T-A

64539882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105154278-T-C

64539957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105154215-G-A

64539957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105154215-G-T

64540788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105153531-A-G

64541600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105153227-G-T

64541857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105152989-T-C

64541860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105152986-T-C

64541860-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105152986-T-G

64541949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105152973-C-T

64542137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105152844-C-T

64542178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105152804-C-T

64542179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105152803-G-A

64542234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105152743-A-G

64542235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105152742-T-C

64542348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105152631-T-C

64542704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105152280-C-T

64545648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105151074-T-C

64545912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105150853-G-A

64546133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105150800-G-A

64546181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105150796-A-G

64546409-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105150657-G-C

http://identifiers.org/hco/5/GRCh38#64546464-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#105150602-C-A

64546464-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105150602-C-G

64546464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105150602-C-T

64546572-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105150487-A-T

64546721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105150292-A-G

64546897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105150131-C-T

64547517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105148869-A-G

64547521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105148865-T-C

http://identifiers.org/hco/5/GRCh38#64547703-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#105148689-C-A

64547770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105148625-T-C

64548184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105148255-A-G

64550238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105146211-C-T

64550251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105146198-A-G

64550268-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105146181-A-T

64550297-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105146153-G-C

http://identifiers.org/hco/5/GRCh38#64550470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#105146014-C-A

64550523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105145952-G-A

http://identifiers.org/hco/5/GRCh38#64551992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#105144020-C-A

http://identifiers.org/hco/5/GRCh38#64552877-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#105143309-A-C

http://identifiers.org/hco/5/GRCh38#64553203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#105142996-C-A

64553203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105142996-C-T

http://identifiers.org/hco/5/GRCh38#64553211-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#105142988-C-A

64553211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105142988-C-T

64553392-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105142776-G-C

64553412-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105142736-T-G

64553452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105142697-G-A

64553465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105142683-C-T

64553466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105142682-C-T

64554601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105141752-C-T

64554633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105141720-G-A

64554694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105141641-A-G

http://identifiers.org/hco/5/GRCh38#64555014-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#105141324-A-C

64555296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105141111-G-A

64555742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105140879-T-C

64555821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105140859-T-C

64555866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105140821-C-T

64555995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105140698-T-C

64556277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105140432-T-C

http://identifiers.org/hco/5/GRCh38#64556309-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#105140400-A-C

http://identifiers.org/hco/5/GRCh38#64556414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#105140304-C-A

http://identifiers.org/hco/5/GRCh38#64556417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#105140301-C-A

http://identifiers.org/hco/5/GRCh38#64556688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#105140087-C-A

64556702-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105140073-T-G

64557013-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105139776-T-G

64557034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105139754-C-T

64557156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105139482-T-C

64557491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105139030-T-C

64557517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105139004-C-T

64557695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105138834-A-G

64557695-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105138834-A-T

64557801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105138742-C-T

64559584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105138088-A-G

64559622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105138057-G-A

64559647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105138032-G-A

http://identifiers.org/hco/5/GRCh38#64559966-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#105137690-A-C

64560241-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105137048-G-C

64560272-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105137017-T-A

64560481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105136794-C-T

64560539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105136750-C-T

http://identifiers.org/hco/5/GRCh38#64560716-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#105136605-C-A

64560720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105136602-G-A

64560785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105136529-T-C

64560971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105136386-C-T

http://identifiers.org/hco/5/GRCh38#64561084-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#105136273-C-A

64561102-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105136255-C-G

64561102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105136255-C-T

64561116-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105136241-T-A

64561130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105136227-G-T

64561727-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105135990-T-G

http://identifiers.org/hco/5/GRCh38#64561812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#105135884-C-A

64561812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105135884-C-T

64562089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105135625-G-A

64562089-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105135625-G-T

64562356-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105135400-T-G

64562402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105135355-A-G

64562526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105135300-A-G

64564017-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105134591-T-G

http://identifiers.org/hco/5/GRCh38#64564197-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#105134451-A-C

64564271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105134399-A-G

64564523-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105134144-G-C

64564609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105134060-C-T

64565651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105127533-G-A

64565793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105127400-C-T

64566892-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105126710-G-C

64568009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105126114-A-G

64568016-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105126107-A-T

64568600-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105125444-T-G

64568667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105125181-G-A

http://identifiers.org/hco/5/GRCh38#64568702-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#105125148-A-C

http://identifiers.org/hco/5/GRCh38#64568890-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#105124985-C-A

64568912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105124964-T-C

64569061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105124834-A-G

64569066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105124829-A-G

64569219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105124679-A-G

64569226-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105124672-G-T

64569327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105124583-A-G

64569614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105124315-C-T

http://identifiers.org/hco/5/GRCh38#64569618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#105124311-C-A

64569618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105124311-C-T

64569770-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105124187-C-G

64569770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105124187-C-T

64569771-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105124186-A-T

64570453-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105123949-T-G

64570963-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105123456-G-T

64571048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105123375-A-G

64571093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105123338-C-T

64571371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105123073-A-G

64571580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105122864-G-A

64571589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105122855-G-A

64571629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105122814-A-G

64571629-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105122814-A-T

64571713-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105122734-T-A

64571901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105122565-A-G

64571901-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105122565-A-T

64571907-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105122552-A-T

64572023-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105122436-A-T

64572059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105122400-T-C

64572059-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105122400-T-G

64572237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105122225-T-C

64572783-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105121512-T-G

64574706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105120554-T-C

64574883-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105120380-A-T

64574975-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105120297-A-T

64575107-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105120172-G-C

64575236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105120043-A-G

64575673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105119607-G-A

64575673-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105119607-G-C

64575673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105119607-G-T

64575970-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105119306-T-A

64575970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105119306-T-C

64576033-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105119266-A-T

64576081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105119227-G-A

64576157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105119143-G-A

64576194-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105119105-G-T

64576422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105118875-A-G

64576434-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105118863-T-G

64576628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105118665-C-T

64576670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105118634-C-T

64576802-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105118524-C-G

64576992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105118345-T-C

64577546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105118155-T-C

64577744-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105118013-T-A

64577744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105118013-T-C

64578385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105115783-T-C

64578400-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105115768-T-A

64579089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105115391-T-C

64579588-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105115272-T-A

64579588-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105115272-T-G

64579593-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105115267-T-A

64579636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105115219-A-G

64579732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105115124-A-G

http://identifiers.org/hco/5/GRCh38#64580020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#105114829-C-A

64580035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105114814-C-T

64580082-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105114753-T-G

64580121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105114715-G-A

64580123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105114713-A-G

http://identifiers.org/hco/5/GRCh38#64580133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#105114702-C-A

64580152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105114683-A-G

64580194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105114641-T-C

64580223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105114622-G-A

64580258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105114588-C-T

64580373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105114530-G-A

64580498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105114417-G-A

64580818-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105113696-G-C

http://identifiers.org/hco/5/GRCh38#64580832-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#105113682-A-C

64581434-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105113395-T-A

64581454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105113375-G-A

64581460-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105113369-C-G

64581596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105113233-T-C

64582066-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105112739-G-C

64582089-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105112716-A-T

64582299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105112525-T-C

64582349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105112451-A-G

64583005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105111782-G-A

64583145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105111653-T-C

64583163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105111635-A-G

64583287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105111603-A-G

64583368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105111566-G-A

64583368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105111566-G-T

64583513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105111470-G-A

64583794-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105111222-A-G

64584448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105111133-A-G

64584523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105111072-G-A

64584662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105110931-G-T

64584854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105110747-G-A

64584894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105110708-G-A

64584965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105110637-G-A

64584991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105110612-T-C

64585041-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105110563-T-G

64585042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105110562-G-A

64585344-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105110297-G-C

64585481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105110153-G-A

64585583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105110054-C-T

http://identifiers.org/hco/5/GRCh38#64585691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#105109950-C-A

64585691-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105109950-C-G

64585691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105109950-C-T

64585809-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105109844-A-T

64586213-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105109436-G-C

64586241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105109399-G-A

64586280-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105109367-T-A

64586440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105109208-T-C

64586831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105108862-G-A

64586847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105108854-T-C

64586953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105108746-T-C

http://identifiers.org/hco/5/GRCh38#64586974-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#105108725-A-C

64586983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105108716-G-A

64587081-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105108647-G-C

64587093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105108639-A-G

64587543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105108177-G-A

http://identifiers.org/hco/5/GRCh38#64587766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#105107988-C-A

64587766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105107988-C-T

http://identifiers.org/hco/5/GRCh38#64587963-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#105107802-A-C

64589050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105107326-C-T

64589622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105107089-T-C

64589666-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105107055-G-T

64589670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105107051-A-G

http://identifiers.org/hco/5/GRCh38#64589918-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#105106941-C-A

64590065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105106790-T-C

64590227-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105105976-A-T

64592878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105105792-T-C

http://identifiers.org/hco/5/GRCh38#64593021-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#105105673-A-C

64593161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105105533-G-T

64593207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105105493-A-G

64593351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105105373-T-C

64593358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105105365-G-A

64593437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105105314-T-C

64593719-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105104771-T-G

64594169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105104329-C-T

64594314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105104185-C-T

64594467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105104037-G-A

http://identifiers.org/hco/5/GRCh38#64594561-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#105103760-C-A

64594573-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105103748-T-A

64594574-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105103747-T-G

http://identifiers.org/hco/5/GRCh38#64594610-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#105103711-C-A

64594610-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105103711-C-G

64594625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105103697-A-G

64594656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105103666-T-C

64594658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105103664-C-T

64594802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 105103542-G-A

64594829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 105103515-G-A

64594931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105103439-A-G

64594972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105103395-A-G

64594978-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105103389-G-C

64594980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105103387-G-A

64594980-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105103387-G-T

64595368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105103247-T-C

64595377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105103241-C-T

http://identifiers.org/hco/5/GRCh38#64595661-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#105102986-A-C

64595831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105102816-T-C

64596015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105102636-T-C

http://identifiers.org/hco/5/GRCh38#64596079-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#105102568-C-A

64596265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105102412-G-A

64596342-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105102317-C-G

64596884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105101837-C-T

64598057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105100909-T-C

64598073-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105100894-G-C

64598100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105100867-G-A

http://identifiers.org/hco/5/GRCh38#64598235-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#105100783-C-A

64598235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105100783-C-T

64598483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105100553-T-C

64598633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105100429-G-A

64598698-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105100363-T-G

64598751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105100278-C-T

64598999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105099921-T-C

64599016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105099908-T-C

64599447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105099464-T-C

64599513-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105099398-T-G

64599518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105099392-T-C

64599641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105099262-G-A

http://identifiers.org/hco/5/GRCh38#64599729-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#105099131-A-C

64600397-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105098445-T-A

64600397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105098445-T-C

64600599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105098263-G-A

64600754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105098130-T-C

64600832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105098061-G-A

64600832-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105098061-G-C

64601054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105097846-G-A

64601157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105097750-T-C

http://identifiers.org/hco/5/GRCh38#64601319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#105097588-C-A

64601345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105097563-G-T

64601362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105097553-G-T

64601505-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105097427-T-A

64601505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105097427-T-C

64601505-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105097427-T-G

http://identifiers.org/hco/5/GRCh38#64601531-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#105097400-C-A

64601599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105097330-T-C

64601608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105097321-A-G

64601608-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105097321-A-T

http://identifiers.org/hco/5/GRCh38#64601620-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#105097309-A-C

64601620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105097309-A-G

http://identifiers.org/hco/5/GRCh38#64601633-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#105097296-C-A

64601633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105097296-C-T

64601976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105096953-C-T

64603361-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-T

64603381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

64603688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-C

64603688-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-G

64603826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

64603943-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-T

64603944-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-T

64603948-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-A

64604029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

64604086-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-T

64604185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

64604351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -C-T

64604405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-G

64605489-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105091427-G-C

64606197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105090538-T-C

64606267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105090470-G-A

64606600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105090243-C-T

64606927-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105089918-T-G

64607044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105089798-A-G

64608134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105089395-A-G

64608182-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105089353-A-G

64608687-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105088567-C-G

64608687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105088567-C-T

64608848-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105088424-T-G

64608872-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105088400-C-G

64609118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105088131-T-C

64609145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 105088104-T-C

64609250-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 105087999-T-A

64609250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 105087999-T-C

64609254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 105087995-T-C

http://identifiers.org/hco/5/GRCh38#64609257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#105087992-C-A

64609257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 105087992-C-T

http://identifiers.org/hco/5/GRCh38#64609274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#105087976-C-A

64609274-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 105087976-C-G

64609318-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 105087930-A-T

64609444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 105087705-G-A

64609567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 105087578-T-C

64610438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 105086709-G-T

64610526-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 105086642-G-C

64610526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 105086642-G-T

http://identifiers.org/hco/5/GRCh38#64611029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#105086152-C-A

64611264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 105085933-T-C

64611266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 105085931-A-G

64611332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 105085864-T-C

64611610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 105085570-T-C

http://identifiers.org/hco/5/GRCh38#64611778-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#105085402-C-A

64611922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 105085218-G-A

64611922-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 105085218-G-T

http://identifiers.org/hco/5/GRCh38#64611982-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#105085162-C-A

64612199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23271
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 105084952-A-G