46894664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 165436965-G-A

46894664-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 165436965-G-C

46894664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 165436965-G-T

46895085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165437239-T-C

46895085-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165437239-T-G

46895277-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, undefined
orthologous variants: 165437383-G-C

46895545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165437638-C-T

46895650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165437703-G-T

46895651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165437704-T-C

46895852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165437870-A-G

46896525-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165438458-G-T

http://identifiers.org/hco/20/GRCh38#46896667-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#165438593-A-C

46897186-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165439167-T-G

46897633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165439629-A-G

46897979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165439953-G-A

http://identifiers.org/hco/20/GRCh38#46898084-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#165440039-C-A

46898100-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165440054-A-T

46898331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165440227-C-T

46898483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165440344-C-T

46898659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165440545-C-T

46898681-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165440564-G-A

46898681-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165440564-G-T

46898832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165440693-G-A

46898832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165440693-G-T

46899260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165440905-C-T

46899334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165441355-G-A

46899423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165441438-G-A

46899842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165441889-T-C

46899842-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165441889-T-G

46899848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165441907-A-G

46899908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165441977-C-T

46900101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165442151-G-A

46900101-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165442151-G-T

46900267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165442319-G-A

46900279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165442323-A-G

46900391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 165442436-G-A

46900677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 165442736-C-T

46900678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 165442737-G-A

46901067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 165443097-G-A

46901067-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 165443097-G-C

46901074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 165443104-T-C

46901210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 165443245-T-C

46901211-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 165443246-C-G

46901211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 165443246-C-T

46901242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 165443271-A-G

46901484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 165443474-C-T

46901649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 165443641-A-G

http://identifiers.org/hco/20/GRCh38#46901716-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#165443696-C-A

46901716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 165443696-C-T

http://identifiers.org/hco/20/GRCh38#46901751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#165443731-C-A

http://identifiers.org/hco/20/GRCh38#46901873-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#165443864-C-A

46902489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165444427-C-T

46902562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165444496-G-A

46902601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165444505-C-T

46902730-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165444624-C-G

46902949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165444844-T-C

46902972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165444863-C-T

46903020-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165444912-C-G

46903251-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165445058-T-G

46903479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165445279-A-G

46903783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165445624-T-C

46903989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165445831-A-G

46904098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165445924-C-T

46904244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165446023-T-C

http://identifiers.org/hco/20/GRCh38#46904652-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#165446440-A-C

46904654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165446441-A-G

46905111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165446871-G-A

46905111-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165446871-G-C

46905164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165446914-A-G

46905175-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165446925-A-T

46907303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165449495-A-G

46908888-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165451166-T-A

46908935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165451212-A-G

46909115-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165451386-T-G

46909162-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165451433-A-T

46909177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165451448-T-C

46909480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165451686-T-C

46909704-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165451916-T-G

46909734-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165451935-A-T

46909894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165452100-G-A

46910248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165452436-G-A

http://identifiers.org/hco/20/GRCh38#46911151-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#165453335-A-C

http://identifiers.org/hco/20/GRCh38#46911222-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#165453404-C-A

http://identifiers.org/hco/20/GRCh38#46911292-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#165453456-A-C

46911292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165453456-A-G

46911301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165453465-T-C

46912124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165454328-G-A

46914074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165455228-A-G

46914901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165455605-G-A

http://identifiers.org/hco/20/GRCh38#46914999-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#165455697-C-A

46915486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165456178-C-T

http://identifiers.org/hco/20/GRCh38#46915602-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#165456262-A-C

46915859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165456538-C-T

46916208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165457435-G-A

46916239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165457467-C-T

46927047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165463219-A-G

46927144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165463344-A-G

46927185-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165463380-A-T

46927314-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165463533-G-C

46927314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165463533-G-T

46927947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165463653-G-A

46927971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165463677-A-G

46927991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165463697-T-C

46928006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165463712-G-A

46928073-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165463766-G-T

46928082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165463775-C-T

46928141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165463817-A-G

46928377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165464002-G-A

46928377-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165464002-G-T

http://identifiers.org/hco/20/GRCh38#46928378-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#165464003-A-C

46928378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165464003-A-G

46928388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165464013-T-C

46928443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165464051-T-C

46928498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165464077-C-T

46928699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165464265-T-C

46928852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165464383-T-C

46928898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165464428-C-T

46929146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165464674-G-T

46929253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165464745-T-C

46929260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165464752-C-T

46929271-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165464763-T-A

46929401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165464888-T-C

46929595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165465072-A-G

46929999-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165465954-G-C

46930044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165465999-G-A

46930052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165466011-T-C

46930133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165466083-G-A

46930178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165466130-A-G

46930243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165466195-C-T

46930371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165467029-A-G

46930485-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165467101-C-G

46930503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165467119-G-A

46939027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165470373-T-C

http://identifiers.org/hco/20/GRCh38#46939080-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#165470425-A-C

http://identifiers.org/hco/20/GRCh38#46939376-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#165470689-A-C

46939400-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, undefined
orthologous variants: 165470713-G-C

46939415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165470735-A-G

46939554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165470896-G-A

46939722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165471070-C-T

46939821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165471155-T-C

46940009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165471357-T-C

46940037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165471384-C-T

46940064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165471409-A-G

46940639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165471809-T-C

46940694-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165471862-C-G

46940694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165471862-C-T

46940717-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165471884-G-C

46940729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165471896-C-T

46940868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165472037-G-A

46941303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165472400-C-T

46941314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165472406-C-T

46945235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165475363-A-G

46945782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165475802-G-A

46945790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165475809-G-A

46945818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165475836-C-T

46945853-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165475870-C-G

http://identifiers.org/hco/20/GRCh38#46945987-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#165476009-A-C

46946339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165476730-G-A

46946640-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165477017-C-G

46946810-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165477170-G-T

46946825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165477188-T-C

46946915-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165477243-G-T

46949373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165477844-G-A

46949520-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165477965-G-C

http://identifiers.org/hco/20/GRCh38#46950118-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#165478861-C-A

46950118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165478861-C-T

46950231-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165479040-G-T

46950273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165479082-G-T

46950309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165479105-C-T

46950323-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165479119-A-G

46950460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165479242-G-A

46950884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165479632-G-A

46950976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165479731-C-T

46957098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165480210-C-T

46957120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165480232-G-A

46957171-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165480284-A-T

http://identifiers.org/hco/20/GRCh38#46957291-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#165480434-A-C

46957450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165480835-G-A

46957755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165481100-G-A

http://identifiers.org/hco/20/GRCh38#46959640-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#165482098-A-C

46959646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, undefined
orthologous variants: 165482104-G-A

46959654-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, undefined
orthologous variants: 165482112-A-T

46959662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, undefined
orthologous variants: 165482120-G-A

46959934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165482544-G-A

46960397-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165482910-A-G

46960409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165482921-C-T

46960463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165482975-G-A

46960526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165483037-G-T

46965171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165485640-G-A

46965400-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, undefined
orthologous variants: 165485853-C-T

46965588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165485970-G-A

46965588-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165485970-G-C

46965835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, undefined
orthologous variants: 165486218-C-T

http://identifiers.org/hco/20/GRCh38#46966274-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#165486566-A-C

46966361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165486666-A-G

46966388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165486693-C-T

46969976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165490036-A-G

46969986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165490043-C-T

46969987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165490044-G-A

46969987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165490044-G-T

http://identifiers.org/hco/20/GRCh38#46978299-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#165494819-C-A

46978299-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 165494819-C-G

46978345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 165494845-G-T

46978547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 165494995-A-G

46978551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 165494999-A-G

46978646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165495080-G-T

http://identifiers.org/hco/20/GRCh38#46978736-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#165495171-C-A

46978736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165495171-C-T

46978776-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165495202-G-A

46978776-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165495202-G-T

46979141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165495544-G-A

46979141-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165495544-G-T

46979245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165495647-T-C

46979295-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165495714-T-G

46979306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165495725-A-G

46979644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165495980-G-A

46979644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165495980-G-T

46979684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165496018-A-G

46979813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165496160-G-A

46979813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165496160-G-T

46979887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165496233-G-A

46979913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165496264-T-C

46981139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165497230-C-T

46981159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165497249-G-T

46981248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165497331-G-A

46985340-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165503064-G-C

46985980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165503683-C-T

46986130-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165503814-G-C

http://identifiers.org/hco/20/GRCh38#46986156-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#165503839-A-C

46989961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165506667-A-G

46989961-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165506667-A-T

46989997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 165506702-T-C

46990081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: missense variant
orthologous variants: 165506767-G-A

46990081-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: missense variant
orthologous variants: 165506767-G-C

46990095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: missense variant
orthologous variants: 165506782-G-A

46990095-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: missense variant
orthologous variants: 165506782-G-T

46990166-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165506851-G-T

46990501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165507119-A-G

46990846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165507469-A-G

46990872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165507495-C-T

46994279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165515636-G-T

46994353-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, undefined
orthologous variants: 165515711-G-C

46994361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165515719-G-A

46994465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, undefined
orthologous variants: 165515805-G-T

46995333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165516268-C-T

46995378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165516312-C-T

http://identifiers.org/hco/20/GRCh38#46995494-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#165516417-C-A

46995638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165516527-G-A

46995638-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165516527-G-T

http://identifiers.org/hco/20/GRCh38#46995674-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#165516563-C-A

46995694-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165516581-G-C

46995696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165516583-G-A

46995746-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165516633-C-G

46995990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, undefined
orthologous variants: 165516863-T-C

46996033-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, undefined
orthologous variants: 165516906-C-G

46996127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165517002-G-A

46996236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165517076-A-G

http://identifiers.org/hco/20/GRCh38#46996240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#165517080-C-A

46996254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165517095-G-A

http://identifiers.org/hco/20/GRCh38#46998311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#165521797-C-A

46998311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 165521797-C-T

46998314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 165521800-C-T

46998315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 165521801-G-A

46998315-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 165521801-G-C

46998315-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 165521801-G-T

46998385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 165521873-A-G

46998385-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 165521873-A-T

http://identifiers.org/hco/20/GRCh38#46998389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#165521876-C-A

46998389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 165521876-C-T

46998817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165522247-C-T

46998934-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165522365-G-T

46998968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165522393-A-G

http://identifiers.org/hco/20/GRCh38#46999296-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#165522669-C-A

46999297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165522670-A-G

http://identifiers.org/hco/20/GRCh38#46999621-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#165523041-C-A

46999788-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165523163-C-G

46999858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165523197-C-T

46999928-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165523259-A-T

47000085-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165523388-G-C

47000133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165523429-A-G

47000444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165523611-A-G

47000609-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165523722-C-T

47000729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165523844-G-A

http://identifiers.org/hco/20/GRCh38#47001283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#165524627-C-A

47001283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165524627-C-T

http://identifiers.org/hco/20/GRCh38#47001284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#165524628-C-A

47001284-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165524628-C-G

47001342-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165524690-T-G

http://identifiers.org/hco/20/GRCh38#47001344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#165524692-C-A

47001360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165524694-A-G

http://identifiers.org/hco/20/GRCh38#47001384-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#165524716-C-A

47001384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165524716-C-T

http://identifiers.org/hco/20/GRCh38#47001444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#165524773-C-A

47001444-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: synonymous variant
orthologous variants: 165524773-C-G

47001444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: synonymous variant
orthologous variants: 165524773-C-T

47001459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: synonymous variant
orthologous variants: 165524788-C-T

47001521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165524840-T-C

47001540-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165524859-T-A

47001551-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165524876-G-T

http://identifiers.org/hco/20/GRCh38#47001552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#165524877-C-A

47001606-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165524925-G-C

47001606-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165524925-G-T

47004506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165527080-G-A

http://identifiers.org/hco/20/GRCh38#47004816-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#165527348-C-A

47004819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165527351-G-A

47004819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165527351-G-T

47004866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165527397-G-A

http://identifiers.org/hco/20/GRCh38#47004880-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#165527408-A-C

47004888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165527416-A-G

47004888-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165527416-A-T

47004895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165527423-G-A

47004895-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165527423-G-T

47004917-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165527445-T-C

http://identifiers.org/hco/20/GRCh38#47004964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#165527491-C-A

47004964-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: missense variant
orthologous variants: 165527491-C-G

47004964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: missense variant
orthologous variants: 165527491-C-T

47005005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: synonymous variant
orthologous variants: 165527532-G-A

http://identifiers.org/hco/20/GRCh38#47005020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#165527547-C-A

47005159-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165527680-G-C

47005159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165527680-G-T

47005167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165527688-T-C

47005183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165527699-A-G

47005240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165527755-C-T

47005252-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165527768-C-G

47005252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165527768-C-T

47005397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165527867-C-T

47006160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165528508-T-C

47006261-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165528628-C-G

47006313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165528679-G-A

47016032-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165529414-T-G

http://identifiers.org/hco/20/GRCh38#47016064-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#165529435-C-A

47016064-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165529435-C-G

47016066-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165529437-T-G

47016076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165529447-G-A

47016076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165529447-G-T

47016092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165529459-G-A

47016092-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165529459-G-C

47016092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165529459-G-T

47016103-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165529470-G-C

47016103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165529470-G-T

47016117-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165529484-G-T

47016130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165529497-C-T

http://identifiers.org/hco/20/GRCh38#47016173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#165529531-C-A

47016173-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 165529531-C-G

47016173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 165529531-C-T

47016376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165529735-G-A

47016376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165529735-G-T

47016394-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165529753-T-A

47016419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165529778-G-A

47016419-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165529778-G-C

47016419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165529778-G-T

http://identifiers.org/hco/20/GRCh38#47016438-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#165529791-C-A

47016438-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165529791-C-G

47016438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165529791-C-T

47016440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165529793-A-G

47016739-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165530039-C-G

47016741-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165530041-G-T

47016742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165530042-T-C

47016798-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165530096-T-G

47016845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165530125-A-G

47016860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165530138-C-T

47017246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165530457-A-G

47017270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165530468-A-G

47017527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165530595-G-T

47017733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165530711-C-T

47017803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165530777-G-A

47018043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165530975-G-A

http://identifiers.org/hco/20/GRCh38#47018120-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#165531048-A-C

47018120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165531048-A-G

47018125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165531053-T-C

47018207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165531119-A-G

47018272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165531170-G-T

47018274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165531172-T-C

47018334-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165531219-C-G

47018412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165531285-T-C

47018429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165531296-A-G

47018456-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165531323-G-T

47018471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165531335-A-G

47018479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165531343-A-G

47019030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165531476-A-G

47019149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165531579-T-C

47019491-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165531871-G-T

47019530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165531909-G-A

47027401-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165535419-A-G

47027522-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165535516-T-A

47027634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165535628-G-A

47027684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165535679-T-C

47027684-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165535679-T-G

47027814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165535760-G-A

47031698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165538295-C-T

47031732-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165538329-C-G

47031976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165538484-G-A

47032294-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165538804-A-T

47032295-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165538805-T-A

47032401-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165538911-T-A

47032401-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165538911-T-C

47032464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165538970-T-C

47033265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165540477-T-C

47033266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165540478-A-G

47033475-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165540697-T-G

47033489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165540711-A-G

47033496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165540718-G-A

47033682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165540862-A-G

47033813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165541015-A-G

47033871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165541073-T-C

47033894-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165541096-A-G

47033907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165541109-T-C

47033967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165541200-G-T

47034039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165541273-A-G

47034116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165541350-G-A

47034230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165541464-T-C

47034489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165541636-T-C

47034714-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165541824-C-G

47034714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165541824-C-T

47035135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165542200-G-A

47035140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165542205-A-G

47035140-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165542205-A-T

47035584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165542624-G-A

47035584-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165542624-G-T

47050440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165548399-T-C

47050630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165548573-T-C

47050688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165548621-G-A

47050878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165548771-C-T

47050952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165548840-C-T

47051100-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165548981-G-C

47056490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165550054-C-T

47056524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165550086-T-C

47056547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165550109-C-T

47056570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165550126-G-A

47056586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165550145-A-G

47056701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165550255-C-T

47057826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165552019-G-A

http://identifiers.org/hco/20/GRCh38#47058270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#165552356-C-A

47058302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165552388-T-C

47058315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165552416-G-A

47058347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165552445-G-A

47058348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165552446-C-T

47066695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165553708-G-A

47066695-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165553708-G-T

47066857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165553825-T-C

47066989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165553934-G-A

47067047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165553987-G-A

http://identifiers.org/hco/20/GRCh38#47067067-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#165554007-C-A

http://identifiers.org/hco/20/GRCh38#47072349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#165555580-C-A

47072384-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165555615-G-C

47072384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165555615-G-T

47072404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165555635-G-A

47072404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165555635-G-T

47072530-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165555724-G-C

47072601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165555786-G-A

47073932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165557685-C-T

http://identifiers.org/hco/20/GRCh38#47074031-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#165557769-A-C

http://identifiers.org/hco/20/GRCh38#47074051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#165557785-C-A

47074051-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165557785-C-G

47074051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165557785-C-T

47074138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165557848-G-T

47074166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 165557879-T-C

47074181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 165557894-C-T

47074259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 165557972-G-A

47074259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 165557972-G-T

47074350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165558063-T-C

47075392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165558548-G-A

47077554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165560334-G-A

47077658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165560431-A-G

http://identifiers.org/hco/20/GRCh38#47078067-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#165560816-C-A

47078067-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165560816-C-G

47078067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165560816-C-T

47078499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165561434-C-T

47078578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165561495-C-T

47078739-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165561639-C-T

47078884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165561779-T-C

47087152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165565167-T-C

47089117-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165566470-T-G

http://identifiers.org/hco/20/GRCh38#47089133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#165566485-C-A

47089197-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165566553-G-A

47089294-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 165566649-C-G

47089305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 165566660-G-A

47089305-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 165566660-G-C

47089399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165566754-T-C

47089410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165566762-G-A

47089442-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165566811-G-C

47089472-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165566842-G-T

47089513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165566871-G-A

47089513-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165566871-G-T

47089519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165566877-T-C

47089531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165566889-A-G

47089602-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165566993-T-G

47089673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165567044-G-A

47092476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165569257-A-G

47092584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165569345-A-G

47092692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165569451-G-A

47092726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165569479-A-G

47092948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165569672-A-G

47093150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 165569869-G-A

http://identifiers.org/hco/20/GRCh38#47095783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#165571553-C-A

47095876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 165571642-G-A

47095876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 165571642-G-T

47095933-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 165571712-G-C

47096087-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165571871-T-A

47096104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165571888-A-G

http://identifiers.org/hco/20/GRCh38#47096164-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#165571938-A-C

47096182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165571974-G-A

47096182-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165571974-G-T

47096751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165573173-G-A

47096933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165573359-G-T

47096938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165573364-A-G

http://identifiers.org/hco/20/GRCh38#47097050-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#165573446-A-C

47097050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165573446-A-G

http://identifiers.org/hco/20/GRCh38#47097068-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#165573456-C-A

47097068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165573456-C-T

http://identifiers.org/hco/20/GRCh38#47097234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#165573838-C-A

47097237-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165573841-G-T

47097245-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165573849-T-A

47097245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165573849-T-C

47097245-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165573849-T-G

47097246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165573850-G-A

47097246-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165573850-G-C

47097246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165573850-G-T

47097269-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165573870-C-G

47097269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165573870-C-T

http://identifiers.org/hco/20/GRCh38#47097286-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#165573888-C-A

47097286-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165573888-C-G

47097286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165573888-C-T

47097549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165574139-C-T

47097552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165574142-C-T

47097554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165574144-G-A

47097827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165574389-C-T

47097828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165574390-G-A

47097860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165574427-A-G

47097952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165574521-C-T

http://identifiers.org/hco/20/GRCh38#47097954-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#165574523-C-A

47097982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165574548-C-T

47098214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165574773-G-A

47098261-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165574809-A-T

47098530-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165575033-G-C

47098708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165575204-C-T

47099939-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165575508-A-G

47100109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165575657-G-A

47100363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165575933-G-A

47100505-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165576067-T-G

http://identifiers.org/hco/20/GRCh38#47100752-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#165576256-C-A

47101022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165576750-A-G

47101111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165576804-G-T

47101414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165577059-A-G

47101785-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165577365-G-C

47101856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165577429-G-A

47101896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165577464-G-A

47101919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165577488-A-G

47102005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165577555-G-T

47102051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165577602-A-G

47102109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165577716-C-T

47102321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165578053-G-T

47102327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165578059-C-T

47102472-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165578181-G-T

47102747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165578452-A-G

47102828-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165578518-G-T

47103141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165578856-T-C

47106151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165580972-T-C

47106244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165581041-C-T

47106318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165581099-C-T

47106725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165581476-G-A

47106729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165581480-G-T

47106832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165581586-C-T

47106992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165581822-C-T

47107109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165581947-G-A

47107346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165582156-G-A

47109015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165582537-G-A

47117815-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165582995-A-G

47118373-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165583523-A-T

47118643-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165583758-T-C

47119327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165584313-C-T

47119580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165584544-C-T

47125704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165587443-A-G

47125832-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165587571-C-G

47125882-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165587621-G-T

47125885-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165587624-T-G

47126195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, undefined
orthologous variants: 165587918-G-A

47126470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165588182-G-A

47126696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165588637-A-G

47127108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165589008-T-C

47128509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165589347-G-A

47128585-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165589411-A-T

47128635-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165589460-G-T

http://identifiers.org/hco/20/GRCh38#47128680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#165589530-C-A

47128697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165589548-T-C

47128813-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165589675-T-C

47128889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165589761-G-A

47128889-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165589761-G-C

47136331-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165590185-T-A

47136430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165590293-G-A

47136438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165590301-C-T

47137044-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165590605-T-A

47137044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165590605-T-C

47137333-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165590853-C-G

47137496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165590958-G-A

47137585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165591035-C-T

47139952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165592993-A-G

47140132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165593123-C-T

47140133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165593124-G-A

47140133-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165593124-G-C

47140194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165593173-A-G

47140421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165593397-G-A

47140499-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165593487-A-T

47143028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, undefined
orthologous variants: 165596331-G-A

47143028-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, undefined
orthologous variants: 165596331-G-T

47143070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 165596372-G-A

http://identifiers.org/hco/20/GRCh38#47143079-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#165596381-C-A

47143079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 165596381-C-T

47143115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 165596417-T-C

47143115-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 165596417-T-G

47143162-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, undefined
orthologous variants: 165596464-G-C

47143209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165596506-G-T

47143213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165596510-A-G

47143218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165596513-G-A

47143256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165596877-T-C

47143449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165597051-G-A

47143542-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165597142-G-T

47143598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165597195-A-G

47146371-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165598297-T-A

47164099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165601401-C-T

47164187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165601477-G-A

47164368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165601655-C-T

47164374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165601661-A-G

47164374-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165601661-A-T

47164421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165601693-G-A

47164421-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165601693-G-C

47164970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165602741-C-T

47169129-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165603814-T-A

47172650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165605570-G-A

47172650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165605570-G-T

47172722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: synonymous_variant, undefined
orthologous variants: 165605632-C-T

47172785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: synonymous_variant, undefined
orthologous variants: 165605695-C-T

47172824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: synonymous_variant, undefined
orthologous variants: 165605734-G-A

47179036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165607623-G-A

47179089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165607677-G-A

47179089-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165607677-G-T

47179297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165607756-G-A

http://identifiers.org/hco/20/GRCh38#47179311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#165607770-C-A

47179311-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165607770-C-G

47179311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165607770-C-T

47179321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165607780-G-A

47179321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165607780-G-T

47179367-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165607818-T-G

47179483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165607914-G-A

47179652-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165608035-T-C

47179826-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, synonymous_variant, undefined
orthologous variants: 165608163-C-G

47179929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, undefined
orthologous variants: 165608266-A-G

47180050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165608340-T-C

47180050-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165608340-T-G

47180634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165608787-G-A

47180692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165608841-G-T

http://identifiers.org/hco/20/GRCh38#47180704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#165608855-C-A

47183245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165611097-G-A

47183245-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165611097-G-C

47183245-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165611097-G-T

47183257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165611111-G-T

47183287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 165611141-G-A

47183287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 165611141-G-T

47183417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165611269-G-A

47183417-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165611269-G-T

47183434-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165611292-A-T

47183446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165611303-G-A

47183475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165611329-T-C

47183498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165611358-T-C

47183911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165611732-T-C

47183934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165611755-G-A

47184057-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165611877-G-C

47188040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165612940-T-C

47188040-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron variant
orthologous variants: 165612940-T-G

47188049-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 165612950-T-A

47188049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 165612950-T-C

47188103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: synonymous variant
orthologous variants: 165613004-G-A

47188103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: synonymous variant
orthologous variants: 165613004-G-T

http://identifiers.org/hco/20/GRCh38#47188140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#165613041-C-A

47188140-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: 3 prime UTR variant
orthologous variants: 165613041-C-G

47188140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: 3 prime UTR variant
orthologous variants: 165613041-C-T

http://identifiers.org/hco/20/GRCh38#47188153-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#165613055-A-C

http://identifiers.org/hco/20/GRCh38#47188158-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#165613060-C-A

47188158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: 3 prime UTR variant
orthologous variants: 165613060-C-T

http://identifiers.org/hco/20/GRCh38#47188241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#165613128-C-A

47188241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: 3 prime UTR variant
orthologous variants: 165613128-C-T

47188268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: 3 prime UTR variant
orthologous variants: 165613154-G-T

http://identifiers.org/hco/20/GRCh38#47188348-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#165613179-C-A

47188348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: 3 prime UTR variant
orthologous variants: 165613179-C-T

47188506-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: 3 prime UTR variant
orthologous variants: 165613289-T-G

47188524-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: 3 prime UTR variant
orthologous variants: 165613307-T-A

47188524-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: 3 prime UTR variant
orthologous variants: 165613307-T-G

47188630-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: 3 prime UTR variant
orthologous variants: 165613366-G-A

47188630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: 3 prime UTR variant
orthologous variants: 165613366-G-T

47188649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: 3 prime UTR variant
orthologous variants: 165613385-A-G

47188655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: 3 prime UTR variant
orthologous variants: 165613391-G-A

47188655-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: 3 prime UTR variant
orthologous variants: 165613391-G-C

47188655-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: 3 prime UTR variant
orthologous variants: 165613391-G-T

47188775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: 3 prime UTR variant
orthologous variants: 165613481-G-A

47188775-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3520
most severe consequence: 3 prime UTR variant
orthologous variants: 165613481-G-T