http://identifiers.org/hco/1/GRCh38#64745104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/4/GRCm39#100926249-C-A

64745104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 100926249-C-T

64745210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: missense variant
orthologous variants: 100926339-G-A

64745210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: missense variant
orthologous variants: 100926339-G-T

http://identifiers.org/hco/1/GRCh38#64745217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100926346-C-A

64745217-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: synonymous variant
orthologous variants: 100926346-C-G

64745217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: synonymous variant
orthologous variants: 100926346-C-T

64745267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: missense variant
orthologous variants: 100926383-G-A

64745267-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: missense variant
orthologous variants: 100926383-G-C

64745267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: missense variant
orthologous variants: 100926383-G-T

http://identifiers.org/hco/1/GRCh38#64745549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100926642-C-A

64745549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: intron variant
orthologous variants: 100926642-C-T

http://identifiers.org/hco/1/GRCh38#64745569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100926662-C-A

64745843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: intron variant
orthologous variants: 100926893-T-C

64746160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: intron variant
orthologous variants: 100927193-C-T

64746414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: intron variant
orthologous variants: 100927697-T-C

64746586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: intron variant
orthologous variants: 100927866-A-G

64746748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: intron variant
orthologous variants: 100927980-G-A

64746870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: intron variant
orthologous variants: 100928088-C-T

64747119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: intron variant
orthologous variants: 100928320-A-G

64748140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: intron variant
orthologous variants: 100929866-C-T

64751234-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: intron variant
orthologous variants: 100933710-A-T

64755409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: intron variant
orthologous variants: 100939429-G-A

64755520-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: intron variant
orthologous variants: 100939510-T-C

64755563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: intron variant
orthologous variants: 100939551-T-C

64755564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: intron variant
orthologous variants: 100939552-T-C

64755831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: intron variant
orthologous variants: 100939800-T-C

64755870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: intron variant
orthologous variants: 100939840-A-G

64760607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: intron variant
orthologous variants: 100941599-G-T

64760619-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: intron variant
orthologous variants: 100941611-G-C

64760692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: intron variant
orthologous variants: 100941666-G-A

64760866-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: intron variant
orthologous variants: 100941846-G-C

64760910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: intron variant
orthologous variants: 100941884-A-G

64761061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: intron variant
orthologous variants: 100942029-T-C

64761063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: intron variant
orthologous variants: 100942036-G-A

64761064-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: intron variant
orthologous variants: 100942037-T-A

64761095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: intron variant
orthologous variants: 100942068-G-A

64761175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: intron variant
orthologous variants: 100942146-A-G

http://identifiers.org/hco/1/GRCh38#64766444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100950992-C-A

64766478-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: intron variant
orthologous variants: 100951026-G-C

64766486-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: intron variant
orthologous variants: 100951034-C-G

64766654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: intron variant
orthologous variants: 100951204-A-G

64766877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: intron variant
orthologous variants: 100951413-T-C

64766980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: intron variant
orthologous variants: 100951486-A-G

64767010-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: intron variant
orthologous variants: 100951511-T-A

64768435-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: intron variant
orthologous variants: 100953284-T-G

64768557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: intron variant
orthologous variants: 100953358-G-T

64768559-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: intron variant
orthologous variants: 100953360-T-G

64768572-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: intron variant
orthologous variants: 100953371-G-T

http://identifiers.org/hco/1/GRCh38#64768629-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100953421-C-A

http://identifiers.org/hco/1/GRCh38#64769212-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100954060-A-C

64776566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: intron variant
orthologous variants: 100957901-C-T

64777074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: intron variant
orthologous variants: 100958529-A-G

64777142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: intron variant
orthologous variants: 100958773-C-T

64777484-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: intron variant
orthologous variants: 100959656-T-G

64777493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: intron variant
orthologous variants: 100959666-T-C

64777498-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: intron variant
orthologous variants: 100959671-A-T

64777539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: intron variant
orthologous variants: 100959701-T-C

64777560-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: intron variant
orthologous variants: 100959724-T-A

64777796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: missense variant
orthologous variants: 100959978-G-A

64777796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: missense variant
orthologous variants: 100959978-G-T

64777831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: synonymous variant
orthologous variants: 100960013-T-C

64777939-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: synonymous variant
orthologous variants: 100960121-A-G

64777941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: missense variant
orthologous variants: 100960123-C-T

64777981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: synonymous variant
orthologous variants: 100960163-A-G

64778041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: synonymous variant
orthologous variants: 100960223-A-G

64778066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 100960248-A-G

64778141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100960324-G-A

64778178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100960370-T-C

64778178-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100960370-T-G

64778196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100960382-G-A

64778816-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100962008-A-T

64779008-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100962116-T-G

64779032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100962137-T-C

64779801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100962798-C-T

64779805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100962802-A-G

64779973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100962928-C-T

64780217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100963154-T-C

64780397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100963328-A-G

64780480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100963564-A-G

64780943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100964024-C-T

http://identifiers.org/hco/1/GRCh38#64781418-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100964438-A-C

http://identifiers.org/hco/1/GRCh38#64781634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100964634-C-A

64781634-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100964634-C-G

64781634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100964634-C-T

http://identifiers.org/hco/1/GRCh38#64781647-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100964647-C-A

64781655-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100964652-A-T

http://identifiers.org/hco/1/GRCh38#64781664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100964661-C-A

64781664-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100964661-C-G

64781664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100964661-C-T

64781665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100964662-G-A

64781665-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100964662-G-T

http://identifiers.org/hco/1/GRCh38#64781670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100964667-C-A

64781670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100964667-C-T

http://identifiers.org/hco/1/GRCh38#64781692-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100964689-C-A

64781716-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100964733-A-T

http://identifiers.org/hco/1/GRCh38#64781717-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100964734-A-C

64781717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100964734-A-G

64782026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100964980-C-T

64782406-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100965339-A-T

64782438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100965380-A-G

64782664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100965608-T-C

64782684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100965620-C-T

64788077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100977162-G-A

64788114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100977189-C-T

64788162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100977240-T-C

64789027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100977304-C-T

64789121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100977404-A-G

64789157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100977443-C-T

64789173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100977459-G-A

64789208-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100977490-C-G

64789254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100977524-A-G

http://identifiers.org/hco/1/GRCh38#64789296-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100977563-C-A

64789296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100977563-C-T

64789355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100977617-T-C

64789355-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100977617-T-G

http://identifiers.org/hco/1/GRCh38#64789380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100977642-C-A

64789380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 100977642-C-T

http://identifiers.org/hco/1/GRCh38#64789456-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100977718-C-A

64789495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 100977757-T-C

64789556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100977813-G-A

64789556-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100977813-G-T

64789569-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100977825-T-A

64789583-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100977844-A-T

64789678-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100977930-C-G

64789820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100978077-C-T

http://identifiers.org/hco/1/GRCh38#64789857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100978115-C-A

64789857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100978115-C-T

64790016-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100978251-C-T

64790827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100978443-G-A

64790841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100978457-C-T

64790910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100978496-A-G

64790933-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100978518-T-G

64791120-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100978713-C-G

64791123-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100978716-T-G

64802484-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100987710-G-T

64802591-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100987971-T-A

64802870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100988363-T-C

64802951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100988428-A-G

64803077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100988563-T-C

http://identifiers.org/hco/1/GRCh38#64803969-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100989937-A-C

64804017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100989974-C-T

64804071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100990003-C-T

64804080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100990011-T-C

http://identifiers.org/hco/1/GRCh38#64804210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100990112-C-A

64804386-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100990274-T-C

http://identifiers.org/hco/1/GRCh38#64804488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100990368-C-A

64804489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100990369-C-T

64804650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100990703-G-A

64804650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100990703-G-T

64804699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100990751-A-G

64804721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100990771-G-A

64804721-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100990771-G-T

http://identifiers.org/hco/1/GRCh38#64804782-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100990832-C-A

64804782-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 100990832-C-G

64804782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 100990832-C-T

http://identifiers.org/hco/1/GRCh38#64804875-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100990899-C-A

64804932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100990951-A-G

64804936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100990955-T-C

64804941-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100990960-T-A

64804944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100990972-G-T

http://identifiers.org/hco/1/GRCh38#64804947-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100990975-A-C

64804947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100990975-A-G

64804947-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100990975-A-T

64804975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100991036-T-C

64805005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 100991066-T-C

64805089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 100991147-T-C

64805134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100991190-A-G

http://identifiers.org/hco/1/GRCh38#64805169-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100991225-A-C

64805174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100991230-T-C

http://identifiers.org/hco/1/GRCh38#64805241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100991293-C-A

64805382-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100991431-G-A

64805404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100991453-C-T

64805573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100991619-C-T

64805581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100991627-A-G

64805606-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100991651-C-G

64806013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100992046-A-G

64806652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100992740-G-A

64806744-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100992834-T-G

http://identifiers.org/hco/1/GRCh38#64807049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100993074-C-A

http://identifiers.org/hco/1/GRCh38#64807099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100993131-C-A

64807099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100993131-C-T

64807261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 100993249-A-G

64807261-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 100993249-A-T

64807303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 100993291-G-A

64807303-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 100993291-G-T

64807336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 100993324-G-A

64807336-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 100993324-G-T

64807337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 100993325-G-A

64807369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 100993357-G-A

64807369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 100993357-G-T

64812429-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100994400-G-C

64812449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100994420-T-C

http://identifiers.org/hco/1/GRCh38#64812699-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100994869-C-A

64812699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100994869-C-T

64812888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100995050-T-C

http://identifiers.org/hco/1/GRCh38#64812966-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100995127-C-A

64813510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100995498-C-T

64813647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100995584-A-G

64813652-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100995589-A-T

64813749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100995672-G-A

64813749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100995672-G-T

64813764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100995687-G-T

64814139-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 100995951-G-T

64814798-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 100996386-A-G

64814825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 100996413-T-C

http://identifiers.org/hco/1/GRCh38#64814851-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100996439-C-A

64814851-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 100996439-C-G

64814851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 100996439-C-T

http://identifiers.org/hco/1/GRCh38#64814852-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100996440-C-A

64814852-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 100996440-C-G

64814852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 100996440-C-T

64814880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 100996468-G-A

64814880-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 100996468-G-C

64814880-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 100996468-G-T

64814896-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 100996484-G-C

64814896-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 100996484-G-T

64814998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 100996568-G-A

64815105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 100996662-G-A

64815105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 100996662-G-T

64815216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 100996741-G-A

64815219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 100996744-G-T

64815291-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 100996815-T-G

http://identifiers.org/hco/1/GRCh38#64815305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#100996829-C-A

64815316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 100996840-C-T

64815356-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 100996882-T-A

64815368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 100996894-A-G

http://identifiers.org/hco/1/GRCh38#64822475-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101001789-A-C

64822529-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: intron variant
orthologous variants: 101001829-C-G

64822776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: intron variant
orthologous variants: 101001993-A-G

64822786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: intron variant
orthologous variants: 101002001-A-G

64823007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: intron variant
orthologous variants: 101002171-T-C

64823409-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: intron variant
orthologous variants: 101002875-T-G

64823561-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: intron variant
orthologous variants: 101003019-A-G

64823733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: intron variant
orthologous variants: 101003174-A-G

64830259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: intron variant
orthologous variants: 101007041-T-C

64830488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: intron variant
orthologous variants: 101007208-G-A

64830494-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: intron variant
orthologous variants: 101007210-T-C

64830828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: intron variant
orthologous variants: 101007518-T-C

64830829-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: intron variant
orthologous variants: 101007519-T-A

http://identifiers.org/hco/1/GRCh38#64830919-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101007609-C-A

64831393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: 3 prime UTR variant
orthologous variants: 101008061-C-T

64831442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: 3 prime UTR variant
orthologous variants: 101008100-A-G

64831604-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: 3 prime UTR variant
orthologous variants: 101008244-T-G

64831875-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: 3 prime UTR variant
orthologous variants: 101008490-G-C

64832301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: 3 prime UTR variant
orthologous variants: 101008790-C-T

64832735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: 3 prime UTR variant
orthologous variants: 101009197-T-C

64832783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: 3 prime UTR variant
orthologous variants: 101009232-G-T

http://identifiers.org/hco/1/GRCh38#64832809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101009258-C-A

64832809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: 3 prime UTR variant
orthologous variants: 101009258-C-T

64832910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: 3 prime UTR variant
orthologous variants: 101009312-A-G

64833029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: 3 prime UTR variant
orthologous variants: 101009397-A-G

64833074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: 3 prime UTR variant
orthologous variants: 101009427-G-T

64833077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: 3 prime UTR variant
orthologous variants: 101009430-G-A

64833152-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: 3 prime UTR variant
orthologous variants: 101009486-A-T

http://identifiers.org/hco/1/GRCh38#64833153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25577
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#101009487-C-A