122882695-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: 5 prime UTR variant
orthologous variants: 40875547-G-T

http://identifiers.org/hco/11/GRCh38#122882725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40875516-C-A

122882725-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: 5 prime UTR variant
orthologous variants: 40875516-C-G

122882725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: 5 prime UTR variant
orthologous variants: 40875516-C-T

122882742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: 5 prime UTR variant
orthologous variants: 40875499-G-A

122882742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: 5 prime UTR variant
orthologous variants: 40875499-G-T

122882805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: 5 prime UTR variant
orthologous variants: 40875483-A-G

122882864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: 5 prime UTR variant
orthologous variants: 40875442-G-A

122882885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: 5 prime UTR variant
orthologous variants: 40875422-G-A

122882885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: 5 prime UTR variant
orthologous variants: 40875422-G-T

122882897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: 5 prime UTR variant
orthologous variants: 40875410-G-A

122882897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: 5 prime UTR variant
orthologous variants: 40875410-G-T

122883030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 40875292-G-A

122883189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 40875202-C-T

122883190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 40875201-A-G

122883292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 40875117-C-T

122883581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40874856-C-T

122883918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40874343-C-T

122884196-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40874088-T-G

http://identifiers.org/hco/11/GRCh38#122884452-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40873802-A-C

122884594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40873619-C-T

122884676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40873538-A-G

122884720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40873505-G-A

122884999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40873383-G-T

122885223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40873153-T-C

122885278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40873099-C-T

122885728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40872618-G-T

122885756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 40872597-T-C

122885756-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 40872597-T-G

122885775-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: 5 prime UTR variant
orthologous variants: 40872578-A-T

122885865-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: missense variant
orthologous variants: 40872490-C-G

122886075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: missense variant
orthologous variants: 40872280-G-A

122886075-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: missense variant
orthologous variants: 40872280-G-C

122886368-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40872027-T-G

122888265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40870729-C-T

122888303-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40870706-T-C

http://identifiers.org/hco/11/GRCh38#122888357-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40870639-A-C

122888488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40870501-C-T

122888535-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40870452-G-C

122888538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40870449-G-A

122888806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40869881-A-G

122890141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40868880-T-C

122890161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40868861-G-A

122890356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40868669-A-G

122890744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40867606-T-C

122890942-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40867422-A-G

122891611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40866793-T-C

122891671-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40866734-A-T

122891687-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40866718-A-T

122891692-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40866715-A-G

122892123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40865797-T-C

http://identifiers.org/hco/11/GRCh38#122892160-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40865760-A-C

122892748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40865453-A-G

122892834-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40865352-C-G

http://identifiers.org/hco/11/GRCh38#122893021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40865139-C-A

122893300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40864758-C-T

122893328-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40864730-A-T

122893329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40864729-A-G

122893331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40864727-A-G

122893826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40863923-G-A

122893838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40863913-G-A

122893838-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40863913-G-T

122893863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40863894-T-C

122893942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40863821-C-T

122894529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40862835-T-C

122894833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40861563-G-A

122894833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40861563-G-T

122895584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40860818-T-C

122896001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40860365-A-G

122896479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40860062-G-A

122896730-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40859854-C-G

122898722-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40858915-T-A

122898777-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40858869-C-G

122898777-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40858869-C-T

122898794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40858852-G-T

122898901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40858748-C-T

122898995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40858663-A-G

122899039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40858624-C-T

http://identifiers.org/hco/11/GRCh38#122899327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40858359-C-A

122899327-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40858359-C-G

122899387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40858299-C-T

122899436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40858250-C-T

122899637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40858058-G-A

122899665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40858031-G-A

122900780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40857153-T-C

122900780-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40857153-T-G

http://identifiers.org/hco/11/GRCh38#122904014-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40856065-A-C

122904056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: missense variant
orthologous variants: 40856023-C-T

http://identifiers.org/hco/11/GRCh38#122904064-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40856015-C-A

122904103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: missense variant
orthologous variants: 40855976-G-A

122904103-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: missense variant
orthologous variants: 40855976-G-C

122904183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: synonymous variant
orthologous variants: 40855896-G-A

122904183-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: missense variant
orthologous variants: 40855896-G-C

122904258-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: synonymous variant
orthologous variants: 40855821-T-A

122904289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: missense variant
orthologous variants: 40855790-G-A

122904378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: synonymous variant
orthologous variants: 40855701-C-T

122904452-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 40855627-G-A

122904556-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40855526-T-A

http://identifiers.org/hco/11/GRCh38#122904568-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40855514-A-C

122904573-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40855509-C-G

122904573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40855509-C-T

122904583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40855491-G-T

122904605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40855202-T-C

http://identifiers.org/hco/11/GRCh38#122904951-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40854838-C-A

122904989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40854790-C-T

122906759-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40852697-A-T

122906814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40852642-G-A

122907280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40852341-A-G

http://identifiers.org/hco/11/GRCh38#122911002-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40848895-A-C

122911228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40848721-T-C

122911324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40848626-A-G

122911342-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40848606-C-G

122911376-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40848586-T-G

122912859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40848093-T-C

122912904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40848048-G-A

122914368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40845721-T-C

122914380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40845713-T-C

122915175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40845282-T-C

122915265-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40845194-G-C

122915330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40845128-G-A

122918698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40844067-T-C

122918876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40843888-C-T

122920454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40839196-C-T

122920497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40839156-A-G

122920544-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40839112-T-G

122920577-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40839076-C-G

122920577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40839076-C-T

http://identifiers.org/hco/11/GRCh38#122921348-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40837965-A-C

122921371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40837942-T-C

122921497-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40837853-T-G

122921714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40837765-C-T

122921742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40837737-C-T

122922051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40837518-T-C

122922051-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40837518-T-G

122922065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40837504-G-A

122922092-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40837477-A-G

122922399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40836685-A-G

122922502-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40836582-C-G

http://identifiers.org/hco/11/GRCh38#122924747-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40834232-C-A

122924747-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40834232-C-G

122924747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40834232-C-T

http://identifiers.org/hco/11/GRCh38#122924800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40834182-C-A

122924801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40834181-A-G

122924828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40834155-A-G

122924845-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40834138-C-G

122924849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40834134-G-A

122924849-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40834134-G-C

122924849-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40834134-G-T

122924906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron_variant, missense_variant
orthologous variants: 40834058-C-T

122925140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40833831-G-A

122925140-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40833831-G-T

122925280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40833701-A-G

122925285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40833696-A-G

122925299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40833682-A-G

122925489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40833539-G-A

122925527-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40833514-A-T

122925536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40833505-A-G

122925543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40833498-T-C

122926292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40833393-A-G

122926362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40833171-A-G

122926470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40833064-C-T

122926602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40832934-A-G

122932094-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40831346-T-G

122932147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40831293-C-T

122932202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40831239-A-G

122932305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40831136-T-C

122932800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40830439-C-T

122932869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40830370-G-A

122933104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40830110-A-G

122933447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40829688-T-C

122933447-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40829688-T-G

122933527-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40829606-G-C

http://identifiers.org/hco/11/GRCh38#122933540-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40829593-A-C

122933596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40829536-C-T

122933792-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40829337-T-G

122934040-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40829144-T-A

122934121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40829076-C-T

122934499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: missense variant
orthologous variants: 40828860-A-G

122934522-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: missense variant
orthologous variants: 40828837-C-G

http://identifiers.org/hco/11/GRCh38#122934620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40828739-C-A

122934638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: synonymous variant
orthologous variants: 40828721-A-G

122934702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: missense variant
orthologous variants: 40828657-A-G

122934717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: missense variant
orthologous variants: 40828642-G-A

122934717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: missense variant
orthologous variants: 40828642-G-T

122934725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: synonymous variant
orthologous variants: 40828634-G-A

http://identifiers.org/hco/11/GRCh38#122934774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40828588-C-A

122934774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: missense variant
orthologous variants: 40828588-C-T

122934848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: synonymous variant
orthologous variants: 40828523-A-G

122934868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: missense variant
orthologous variants: 40828503-A-G

http://identifiers.org/hco/11/GRCh38#122934948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40828420-C-A

122934948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: missense variant
orthologous variants: 40828420-C-T

122935122-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40827634-G-C

122935180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40827580-G-A

122935180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40827580-G-T

http://identifiers.org/hco/11/GRCh38#122935226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40827535-C-A

122935226-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40827535-C-G

122935226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40827535-C-T

122935875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40827216-C-T

122936163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40826159-T-C

122936171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40826151-G-A

http://identifiers.org/hco/11/GRCh38#122936248-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40826082-A-C

122936299-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40826032-C-G

122936355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40825980-G-A

122936449-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40825891-G-T

122936465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40825875-C-T

122946200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40823278-A-G

122946294-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40822914-T-C

122946322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40822887-G-A

122946470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40822544-G-A

122946470-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40822544-G-C

122946470-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 40822544-G-T

122946673-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 40822349-T-A

122946673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 40822349-T-C

122946802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40822220-G-A

122946875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40822164-A-G

http://identifiers.org/hco/11/GRCh38#122946900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40822139-C-A

122946900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40822139-C-T

http://identifiers.org/hco/11/GRCh38#122946911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40822127-C-A

122946911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40822127-C-T

http://identifiers.org/hco/11/GRCh38#122946970-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40822068-C-A

122946970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40822068-C-T

122947003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40822035-G-A

122947003-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40822035-G-T

122947027-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40822011-T-G

http://identifiers.org/hco/11/GRCh38#122947028-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40822010-C-A

http://identifiers.org/hco/11/GRCh38#122947126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40821927-C-A

122947126-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40821927-C-G

122947126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40821927-C-T

http://identifiers.org/hco/11/GRCh38#122947284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40821807-C-A

122947284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40821807-C-T

122947311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40821780-A-G

122947328-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40821763-A-T

http://identifiers.org/hco/11/GRCh38#122947374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40821748-C-A

122947376-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40821746-T-G

122947378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40821744-G-T

122947379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 40821743-T-C

122950602-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40820904-A-T

122950960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40820576-A-G

122951042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40820464-G-T

122951562-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40819936-T-G

122951594-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40819900-T-A

122951660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40819829-T-C

122951738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40819755-G-A

http://identifiers.org/hco/11/GRCh38#122951743-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40819750-A-C

122951869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40819607-T-C

122952319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40819104-T-C

122952994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40818413-T-C

http://identifiers.org/hco/11/GRCh38#122953028-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40818379-A-C

http://identifiers.org/hco/11/GRCh38#122953596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40817911-C-A

122953596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40817911-C-T

122953836-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40817741-C-G

122954052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40817516-A-G

122954188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40817377-T-C

122955881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40816365-C-T

122956188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40809867-T-C

http://identifiers.org/hco/11/GRCh38#122956243-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40809819-A-C

122956392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40809668-T-C

http://identifiers.org/hco/11/GRCh38#122956416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40809644-C-A

122956416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40809644-C-T

122956582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40809496-T-C

122956647-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40809437-G-C

122956665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40809419-A-G

122956675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40809409-A-G

http://identifiers.org/hco/11/GRCh38#122956745-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40809340-C-A

122956811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40809273-G-A

122956821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40809263-G-A

122956822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40809262-T-C

122956841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40809244-A-G

122956931-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40809157-G-T

122956971-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40809117-C-G

122956971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40809117-C-T

http://identifiers.org/hco/11/GRCh38#122957224-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40808873-C-A

122957224-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40808873-C-G

http://identifiers.org/hco/11/GRCh38#122957225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40808872-C-A

122957225-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40808872-C-G

http://identifiers.org/hco/11/GRCh38#122957229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40808867-C-A

122957229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40808867-C-T

122957288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40808828-A-G

122957317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40808815-G-A

122957444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: missense variant
orthologous variants: 40808690-C-T

122957511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40808624-G-A

122957511-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40808624-G-T

122957834-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40808446-T-G

122958125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40808200-T-C

122958172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40808151-A-G

122958263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40808066-G-A

122958408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40807945-G-A

122958445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40807910-T-C

http://identifiers.org/hco/11/GRCh38#122958561-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40807810-C-A

122958561-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40807810-C-G

122958561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40807810-C-T

122958619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40807753-A-G

122958876-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40807397-T-C

122958930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40807339-T-C

122959102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: intron variant
orthologous variants: 40807164-A-G

http://identifiers.org/hco/11/GRCh38#122959448-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40806830-A-C

122959448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: 3 prime UTR variant
orthologous variants: 40806830-A-G

http://identifiers.org/hco/11/GRCh38#122959499-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40806785-A-C

122959499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: 3 prime UTR variant
orthologous variants: 40806785-A-G

http://identifiers.org/hco/11/GRCh38#122959512-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40806774-C-A

122959609-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: 3 prime UTR variant
orthologous variants: 40806704-T-G

122959610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: 3 prime UTR variant
orthologous variants: 40806703-A-G

122959694-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: 3 prime UTR variant
orthologous variants: 40806619-T-A

122959694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: 3 prime UTR variant
orthologous variants: 40806619-T-C

122959844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: 3 prime UTR variant
orthologous variants: 40806511-T-C

122959844-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: 3 prime UTR variant
orthologous variants: 40806511-T-G

http://identifiers.org/hco/11/GRCh38#122959855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40806500-C-A

122959935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: 3 prime UTR variant
orthologous variants: 40806419-T-C

122959937-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: 3 prime UTR variant
orthologous variants: 40806417-T-A

122961916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: 3 prime UTR variant
orthologous variants: 40806293-A-G

http://identifiers.org/hco/11/GRCh38#122962078-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40806172-A-C

122962086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: 3 prime UTR variant
orthologous variants: 40806165-A-G

122962170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: 3 prime UTR variant
orthologous variants: 40806045-G-A

122962170-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: 3 prime UTR variant
orthologous variants: 40806045-G-C

122962175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: 3 prime UTR variant
orthologous variants: 40805987-A-G

http://identifiers.org/hco/11/GRCh38#122962194-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#40805942-A-C

122963321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: 3 prime UTR variant
orthologous variants: 40805432-C-T

122963403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: 3 prime UTR variant
orthologous variants: 40805149-A-G

122963426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: 3 prime UTR variant
orthologous variants: 40805128-C-T

122963450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: 3 prime UTR variant
orthologous variants: 40805104-G-A

122963464-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 26288
most severe consequence: 3 prime UTR variant
orthologous variants: 40805090-G-T