50306172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 3 prime UTR variant
orthologous variants: 32100790-T-C

http://identifiers.org/hco/10/GRCh38#50306178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32100796-C-A

50306178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 3 prime UTR variant
orthologous variants: 32100796-C-T

50306606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 3 prime UTR variant
orthologous variants: 32101218-T-C

50306955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 3 prime UTR variant
orthologous variants: 32101563-T-C

50306955-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 3 prime UTR variant
orthologous variants: 32101563-T-G

50307029-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 3 prime UTR variant
orthologous variants: 32101639-A-G

50307117-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 3 prime UTR variant
orthologous variants: 32101721-G-C

50307145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 32101748-T-C

50307145-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 32101748-T-G

50307356-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32101966-C-G

50307356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32101966-C-T

50307407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32102017-C-T

http://identifiers.org/hco/10/GRCh38#50307419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32102029-C-A

50307419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32102029-C-T

50307437-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32102045-T-A

50307437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32102045-T-C

http://identifiers.org/hco/10/GRCh38#50307440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32102048-C-A

http://identifiers.org/hco/10/GRCh38#50307442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32102050-C-A

50307443-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32102051-A-G

50307464-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32102072-T-A

50307765-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32102394-A-T

http://identifiers.org/hco/10/GRCh38#50307871-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32102496-C-A

50307918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32102560-T-C

50307918-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32102560-T-G

50307962-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32102606-T-G

50308155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 32102799-G-A

50308155-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 32102799-G-T

http://identifiers.org/hco/10/GRCh38#50308192-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32102849-C-A

50308212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32102869-G-T

50308230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32102883-G-A

50308230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32102883-G-T

http://identifiers.org/hco/10/GRCh38#50308235-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32102890-C-A

50308235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32102890-C-T

50308248-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32102903-T-A

50308248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32102903-T-C

50308248-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32102903-T-G

http://identifiers.org/hco/10/GRCh38#50308249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32102904-C-A

50308249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32102904-C-T

50308464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32103126-C-T

50308672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32104079-C-T

50308707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32104096-G-A

50308734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32104123-T-C

50309036-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32104293-G-C

50309181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32104424-A-G

50309334-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32104579-A-T

50309403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32104644-T-C

50309748-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32104973-T-A

50309815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32105021-C-T

50309908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32105103-T-C

50310085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32105271-T-C

50310189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32105371-C-T

50310234-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32105408-G-C

50310333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32105475-C-T

50311151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32106837-A-G

50311380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: missense_variant, undefined
orthologous variants: 32107059-T-C

50311449-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32107119-T-A

50311449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32107119-T-C

50311473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32107143-G-A

50311473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32107143-G-T

50311585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32107227-G-A

50311585-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32107227-G-C

50311585-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32107227-G-T

50311717-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32107332-T-C

http://identifiers.org/hco/10/GRCh38#50311732-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32107345-A-C

50311732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32107345-A-G

50312470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32108161-G-A

50312613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32108309-T-C

50312789-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32108445-G-T

50312801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32108457-G-A

50312899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32108552-A-G

50312984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, undefined
orthologous variants: 32108625-G-T

50313091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32108718-G-A

50313152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32108779-G-A

50313169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32108794-G-A

50313199-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32108824-T-G

50313210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32108830-T-C

50316560-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32110407-T-A

50316804-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32110669-C-G

50316804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32110669-C-T

50316821-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32110684-T-A

50317097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32110800-T-C

50317121-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32110809-A-T

50317261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32110929-G-A

50318108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32111824-T-C

50318329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32112026-C-T

50318495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32112121-G-A

50318570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32112177-C-T

http://identifiers.org/hco/10/GRCh38#50318574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32112181-C-A

50318677-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32112265-C-G

50318863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32112436-A-G

50318868-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32112441-G-T

http://identifiers.org/hco/10/GRCh38#50318904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32112476-C-A

50318904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32112476-C-T

50318954-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32112521-T-G

50319192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32112715-C-T

50319243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32112764-T-C

http://identifiers.org/hco/10/GRCh38#50319262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32112783-C-A

http://identifiers.org/hco/10/GRCh38#50319502-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32112950-A-C

50319635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32113070-T-C

50319801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32113232-T-C

50319837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32113269-C-T

50320173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32113875-C-T

50320411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32114086-G-A

50320455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32114132-T-C

http://identifiers.org/hco/10/GRCh38#50320841-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32114480-C-A

50320841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32114480-C-T

http://identifiers.org/hco/10/GRCh38#50320908-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32114556-A-C

50320914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32114562-A-G

50321197-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32114847-A-T

50321358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32114979-A-G

50321365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32114986-T-C

50321644-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32115287-T-A

50321662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32115305-C-T

50321839-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32115464-A-T

50321858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32115481-C-T

50321972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32115587-A-G

50322281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32115811-G-A

50322973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, undefined
orthologous variants: 32116182-T-C

50323118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32116333-T-C

50323225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32116402-T-C

50323353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32116534-C-T

50323378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32116557-C-T

50323487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32116664-T-C

50323809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32116938-T-C

50324076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32117170-T-C

50324641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32117422-C-T

50324695-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32117477-T-A

50324763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32117553-G-A

50324925-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32117674-T-A

50325232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32117937-G-A

50325232-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32117937-G-T

50325352-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron variant
orthologous variants: 32118095-G-C

50325487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, undefined
orthologous variants: 32118230-G-A

50325700-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 32118412-G-C

50325999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32119095-C-T

50326343-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32119373-A-T

50326540-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32119634-T-A

50326736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32119782-G-A

50326852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32119869-G-A

50326852-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32119869-G-C

50326857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32119874-A-G

50326861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32119878-G-A

50327057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32120014-G-A

50327057-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32120014-G-C

50327057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32120014-G-T

http://identifiers.org/hco/10/GRCh38#50327105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#32120047-C-A

50327105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32120047-C-T

50327146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32120086-G-A

50327146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32120086-G-T

http://identifiers.org/hco/10/GRCh38#50327161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32120101-C-A

50327496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32120436-G-A

50328443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32121241-G-A

http://identifiers.org/hco/10/GRCh38#50329728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32122527-C-A

50329728-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32122527-C-G

50329748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32122550-T-C

50329785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32122586-A-G

50329827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32122623-G-A

50329841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32122637-A-G

50329884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32122679-T-C

50329884-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32122679-T-G

http://identifiers.org/hco/10/GRCh38#50330004-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32122783-C-A

50330038-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32122817-C-G

50330680-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32123564-T-C

50330907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32124078-T-C

50331201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32124468-T-C

50331236-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32124514-G-T

50333309-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32126869-T-G

50333492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32127066-C-T

50333571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32127147-C-T

http://identifiers.org/hco/10/GRCh38#50333649-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32127229-A-C

http://identifiers.org/hco/10/GRCh38#50333767-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32127337-C-A

http://identifiers.org/hco/10/GRCh38#50333775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32127345-C-A

http://identifiers.org/hco/10/GRCh38#50336090-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32128662-A-C

50336090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32128662-A-G

http://identifiers.org/hco/10/GRCh38#50336093-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32128665-C-A

50336187-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32128752-T-A

50336280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32128826-T-C

50336283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32128829-G-A

50336493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32129373-G-A

50336575-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32129458-T-G

50336873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32129738-T-C

50337545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32131039-T-C

50338084-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32131926-G-C

http://identifiers.org/hco/10/GRCh38#50339108-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32132779-C-A

50339153-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32132821-A-G

50339155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32132823-C-T

50339737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32133391-T-C

50339860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32133499-G-A

50340279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32133873-G-T

50340358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32133941-T-C

http://identifiers.org/hco/10/GRCh38#50340712-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32134145-C-A

http://identifiers.org/hco/10/GRCh38#50340751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32134175-C-A

50340784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32134210-T-C

http://identifiers.org/hco/10/GRCh38#50341182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32134572-C-A

50341213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32134619-T-C

50341290-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32134693-T-A

50341290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32134693-T-C

50341381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32134754-G-T

50341495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32134841-C-T

50341627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32134946-C-T

50341628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32134948-G-A

50341628-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32134948-G-C

http://identifiers.org/hco/10/GRCh38#50341700-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32135026-C-A

http://identifiers.org/hco/10/GRCh38#50341715-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32135041-C-A

50341764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32135105-C-T

50341893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32135238-G-A

50342144-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32135456-G-T

50342463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32135812-T-C

50342753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32136281-C-T

http://identifiers.org/hco/10/GRCh38#50342846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32136371-C-A

50342846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32136371-C-T

50342869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32136393-A-G

50342869-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32136393-A-T

http://identifiers.org/hco/10/GRCh38#50342873-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32136397-C-A

50342994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32136470-C-T

50343130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32136570-G-A

50343130-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32136570-G-C

50343178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32136615-A-G

50343334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32136765-G-A

50343334-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32136765-G-T

50343404-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32136840-G-C

50343404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32136840-G-T

50343707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 32137139-A-G

50343773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 32137205-C-T

50343956-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 32137388-G-C

50343966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 32137398-C-T

50344182-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant
orthologous variants: 32137615-G-T

50344335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32137753-G-T

50344374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32137792-G-T

50344437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32137859-C-T

50345291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32138361-T-C

50346244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32139086-T-C

50346274-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32139116-T-G

50346282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32139124-T-C

50346368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32139210-T-C

50346374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32139216-C-T

50346453-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32139317-G-C

50346664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32139515-C-T

50347375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32140114-T-C

50347527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32140261-G-A

50347548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32140286-C-T

50347628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32140348-G-A

50347654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32140380-A-G

50347658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32140384-T-C

http://identifiers.org/hco/10/GRCh38#50347664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32140390-C-A

50347711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32140444-C-T

50347716-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32140449-C-G

50347789-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32140518-T-A

50349103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32140918-G-T

50351843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32141360-G-A

50351911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32141426-G-A

50351911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32141426-G-T

http://identifiers.org/hco/10/GRCh38#50351915-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32141430-C-A

50351915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32141430-C-T

http://identifiers.org/hco/10/GRCh38#50351945-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32141459-C-A

50351945-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32141459-C-T

50352262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32141767-G-A

50352287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32141795-T-C

http://identifiers.org/hco/10/GRCh38#50352502-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32141997-A-C

50352560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32142054-C-T

50352561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32142055-G-A

50352561-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32142055-G-T

50352608-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32142094-T-G

50352609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32142095-G-A

50352613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32142099-T-C

50357320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32142493-G-A

50358719-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32142960-C-G

50359341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32143538-A-G

50359716-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32144025-C-G

50359730-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32144039-T-G

50360064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32144377-G-T

50367316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32147214-G-A

50367352-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32147250-T-A

50367487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32147375-C-T

50367828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32147659-C-T

50368802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32148905-G-A

50372938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32151025-G-A

50372990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32151068-A-G

50374234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32151802-C-T

50374235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32151803-A-G

50374242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32151810-C-T

50374455-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32151976-T-A

50374839-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32152342-T-A

50374899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32152404-T-C

50377606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32153388-C-T

50377730-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32153513-T-A

50377730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32153513-T-C

50377840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32153620-G-A

50377840-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32153620-G-C

http://identifiers.org/hco/10/GRCh38#50377850-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32153630-C-A

50377886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32153653-C-T

50378224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32153756-C-T

http://identifiers.org/hco/10/GRCh38#50378680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32154217-C-A

50378680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32154217-C-T

50378836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32154343-C-T

50379020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32154529-A-G

50379273-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32155191-T-G

50379354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32155265-G-A

50379426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32155324-G-A

50379628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32155489-G-T

50379667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32155528-G-A

50380009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32155835-G-A

50380491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32156204-C-T

50380734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32156434-T-C

50381483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32156917-G-A

50381744-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32157582-T-G

50382082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32157974-A-G

50382358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32158421-A-G

50382583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32158602-A-G

http://identifiers.org/hco/10/GRCh38#50382586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32158605-C-A

50382635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32158647-A-G

50382858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32158862-T-C

50382999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32159143-C-T

50383000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32159144-A-G

50383146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32159276-C-T

50383397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32159502-T-C

50383726-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32159794-T-A

50383874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32159946-G-A

50384025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32160152-C-T

50384957-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32160622-C-G

50385195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32160853-A-G

50390761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32161866-C-T

50391256-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32162300-T-G

50391259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32162303-C-T

50391331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32162377-C-T

50392188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32162657-G-A

50392188-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32162657-G-T

50392469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32163303-G-A

50392471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32163305-G-A

50392791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32163575-G-A

50392965-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32163820-A-T

50393049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32163905-G-T

50393139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32163992-A-G

50393154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32164004-C-T

50393381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32164185-C-T

50393422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32164228-A-G

50393964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32165151-A-G

50394096-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32165254-T-G

50394408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32165554-G-A

50394757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32165810-G-A

50394757-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32165810-G-C

50394921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32165940-A-G

50400133-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32168695-C-G

50400315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32168870-T-C

50400375-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32168910-G-C

50401164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32169435-T-C

50401656-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32169933-A-T

50401756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32170018-C-T

50401879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32170139-T-C

50403337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32171456-C-T

50403843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32171945-A-G

50404276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32172409-G-A

50404276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32172409-G-T

50404807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32172932-T-C

50404858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32172982-A-G

50404895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32173019-A-G

http://identifiers.org/hco/10/GRCh38#50405080-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32173188-A-C

50405080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32173188-A-G

50405138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32173240-A-G

50405194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32173318-T-C

http://identifiers.org/hco/10/GRCh38#50405338-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32173462-A-C

50405932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32173957-T-C

50406026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32174216-T-C

50406077-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32174354-A-T

50406105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32174402-T-C

50406444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32174739-G-A

http://identifiers.org/hco/10/GRCh38#50406502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32174797-C-A

50406502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32174797-C-T

50406610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32174892-A-G

50407895-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32174988-G-T

50409445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32175374-G-T

50409490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32175416-A-G

50409729-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32175862-T-A

50409729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32175862-T-C

50410210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32176473-A-G

50410261-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32176522-G-C

50410367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32176622-C-T

50410456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32176679-G-A

50410639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32176822-T-C

50410713-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32176896-C-G

50410742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32176929-C-T

50410771-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32176955-G-C

50410778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32176961-C-T

50410804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32176986-G-A

50410809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32176991-T-C

50413836-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32177706-T-G

50414461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32177920-T-C

http://identifiers.org/hco/10/GRCh38#50414819-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32178263-A-C

50415668-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32179171-T-A

50415668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32179171-T-C

http://identifiers.org/hco/10/GRCh38#50416024-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32179753-C-A

50416024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32179753-C-T

50416028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32179757-C-T

50416627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32180270-T-C

50417454-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32187575-T-A

50417570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32187675-G-A

50417570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32187675-G-T

50417627-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32187721-A-G

50417787-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32187895-T-A

50417821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32187925-T-C

50417969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32188067-G-A

50418126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 32188279-G-A

50418126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 32188279-G-T

http://identifiers.org/hco/10/GRCh38#50418379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32188365-C-A

50418404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32188391-G-T

50418408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32188395-G-T

50418879-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32188792-T-A

50419417-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32189229-T-A

50419704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32189505-G-T

50419974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32190803-C-T

50419979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32190808-T-C

50420258-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32191045-C-G

50420258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32191045-C-T

50420947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32191542-G-T

50420960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32191555-G-A

50421072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32191665-A-G

50421073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32191666-C-T

50421143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32191733-T-C

50421960-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32191974-C-G

50421979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32191986-C-T

50422059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32192071-C-T

50422122-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32192126-C-G

50422204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32192189-G-A

50422306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32192278-C-T

50422309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32192281-A-G

50422643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32192625-C-T

50423150-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32193049-C-G

50423175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32193086-C-T

50423476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32193540-G-A

50423896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32193885-C-T

50426599-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32194399-G-C

50426599-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32194399-G-T

http://identifiers.org/hco/10/GRCh38#50426631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#32194808-C-A

50426631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32194808-C-T

50426849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32195910-C-T

50427537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32196313-A-G

50427776-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32196528-G-T

50430872-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32197521-C-G

50430872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32197521-C-T

50431001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32197616-T-C

50431076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32197685-A-G

50431179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32197777-T-C

50431541-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32198134-T-G

50432098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32198618-A-G

50432402-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32199290-G-A

50432669-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32199508-G-C

50432838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32199594-A-G

50433064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32200279-T-C

50433223-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32200424-C-G

http://identifiers.org/hco/10/GRCh38#50433276-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32200476-C-A

50433326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32200518-A-G

50433408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32200840-C-T

50433476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 32200909-G-A

50433554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 32200988-C-T

50433760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32201085-C-T

50433801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32201107-C-T

50435083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32201929-C-T

50435850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32202886-C-T

50435919-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32202937-C-G

50436000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32203032-T-C

http://identifiers.org/hco/10/GRCh38#50436053-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32203085-A-C

50436053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32203085-A-G

50436493-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32203973-G-C

50436495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32203975-G-A

50437158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32204641-G-A

50437408-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32204895-C-G

http://identifiers.org/hco/10/GRCh38#50437585-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32205054-A-C

50437585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32205054-A-G

http://identifiers.org/hco/10/GRCh38#50437604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32205073-C-A

50437604-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32205073-C-G

50437682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32205151-T-C

50437743-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32205204-T-A

50437743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32205204-T-C

50437990-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32206611-A-T

50438256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32206857-A-G

50438578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32207139-G-A

50438670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32207235-G-A

50438969-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32207426-C-G

50438969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32207426-C-T

50438975-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32207432-G-C

50439183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32207642-G-A

50439239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32207770-C-T

50439307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32207842-G-A

50439326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32207859-G-A

http://identifiers.org/hco/10/GRCh38#50439527-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32208061-C-A

50439527-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32208061-C-G

50439527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32208061-C-T

50439618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32208133-C-T

50439810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32208283-G-A

50439819-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32208292-T-G

50439836-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32208309-C-G

50439859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32208333-A-G

50439929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32208401-C-T

50440049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32208504-C-T

50440173-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32208629-C-T

50440221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32208656-T-C

50440350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32208739-C-T

50440388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32208764-A-G

50440407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32208782-C-T

50441993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32210210-G-A

50442031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32210248-T-C

50447238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32214159-A-G

50447757-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32214715-A-T

50447920-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32214869-C-G

50447932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32214881-A-G

50449178-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32216436-G-C

50449179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32216437-G-A

50449179-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32216437-G-C

50449179-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32216437-G-T

50449649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32216831-G-A

50449691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32216857-C-T

50449793-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32216929-T-A

50456694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32217122-G-A

50456959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32217367-G-A

50457996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32218264-C-T

50458088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32218359-A-G

50458837-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32218860-T-C

50459213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32219253-G-A

50459213-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32219253-G-C

50460748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32219953-T-C

50460750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32219955-T-C

http://identifiers.org/hco/10/GRCh38#50460794-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32219997-C-A

50460824-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32220027-A-T

50460855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32220059-G-A

50460881-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32220085-G-T

50461570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32220682-T-C

50461614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32220712-C-T

50461852-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32220873-T-G

50461923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-C

50462845-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32221917-T-A

50462845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32221917-T-C

http://identifiers.org/hco/10/GRCh38#50463144-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32222149-A-C

50463429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32222396-C-T

50466929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32225433-C-T

50467357-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32225917-C-G

50467581-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32226147-A-T

50468276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32226923-A-G

http://identifiers.org/hco/10/GRCh38#50468307-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32226953-A-C

http://identifiers.org/hco/10/GRCh38#50468325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32226970-C-A

50468496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32227124-A-G

50468521-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32227151-T-C

50468609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32227228-T-C

http://identifiers.org/hco/10/GRCh38#50468861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32227654-C-A

50468886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32227679-C-T

50470144-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32229338-T-A

50470287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32229496-G-A

50470290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32229499-T-C

50470980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32230316-T-C

http://identifiers.org/hco/10/GRCh38#50470999-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32230334-A-C

50471012-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32230365-T-A

50471058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32230396-C-T

50471641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32231080-T-C

50471787-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32231215-T-A

50471830-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32231237-G-C

50471866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32231273-C-T

50472870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32231465-A-G

50472974-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32231538-T-A

50473121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32231701-T-C

50473126-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32231706-T-G

50473884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32232541-G-A

50473884-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32232541-G-C

http://identifiers.org/hco/10/GRCh38#50474070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32232697-C-A

50474070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32232697-C-T

50474142-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32232761-G-T

50474182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32232817-G-A

50474182-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32232817-G-T

http://identifiers.org/hco/10/GRCh38#50474360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32232953-C-A

50474360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32232953-C-T

50474790-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32233346-A-T

50474859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32233413-T-C

50475074-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32233640-T-A

50475108-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32233678-A-G

50475158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32233742-T-C

50477990-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32234940-G-C

50478123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32235054-T-C

50478659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32236405-C-T

50478696-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32236438-G-C

50478825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32236556-C-T

50478865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32236584-G-A

50489948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32238357-T-C

http://identifiers.org/hco/10/GRCh38#50490333-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32238706-A-C

50490362-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32238739-A-T

50498002-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32241460-C-G

50498909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32244024-T-C

50498975-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32244091-G-C

50498975-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32244091-G-T

50499211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32244353-C-T

50499347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32244467-G-A

http://identifiers.org/hco/10/GRCh38#50499481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32244600-C-A

50499501-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32244612-G-C

50499646-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32244761-G-A

http://identifiers.org/hco/10/GRCh38#50499923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32244973-C-A

50500123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32245080-G-A

50500414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32245205-T-C

50500477-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32245257-C-G

http://identifiers.org/hco/10/GRCh38#50501467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32247518-C-A

50501467-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32247518-C-G

50501814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32248675-G-A

50502277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32249133-C-T

50502287-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32249143-T-A

50502287-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32249143-T-G

50502300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32249156-A-G

50502301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32249157-G-A

50502489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32249320-C-T

50502624-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32249405-T-A

50502624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32249405-T-C

50502819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32249554-T-C

50502919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32249653-G-A

50502952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32249694-G-A

50503263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32249998-G-A

50503292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32250027-C-T

50504224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32250485-C-T

50504669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32250836-A-G

http://identifiers.org/hco/10/GRCh38#50504677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32250844-C-A

50504677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32250844-C-T

50505838-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32251916-G-C

50506158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32252152-A-G

http://identifiers.org/hco/10/GRCh38#50506506-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32252485-A-C

50506900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32252644-T-C

http://identifiers.org/hco/10/GRCh38#50506954-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#32252689-C-A

http://identifiers.org/hco/10/GRCh38#50506992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32252727-C-A

50507012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32252751-G-A

50507093-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32252807-A-T

50507228-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32252943-C-G

50507291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32253002-C-T

50507329-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32253042-G-A

50507329-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32253042-G-C

50507488-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32253185-T-A

50507517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32253216-C-T

http://identifiers.org/hco/10/GRCh38#50507846-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32253921-C-A

http://identifiers.org/hco/10/GRCh38#50507878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32253953-C-A

50507946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32254019-C-T

50507995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32254067-A-G

50508925-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32254380-A-T

50509039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32254484-T-C

50509099-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32254531-A-T

50509608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32254827-T-C

50509793-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32254981-C-G

http://identifiers.org/hco/10/GRCh38#50510043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32255246-C-A

50510246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32255418-A-G

50510570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32255764-C-T

50510644-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32255921-A-T

50510650-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32255927-A-T

50510803-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32256277-T-G

http://identifiers.org/hco/10/GRCh38#50510818-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32256292-A-C

50510984-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32256413-A-T

http://identifiers.org/hco/10/GRCh38#50511270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32256997-C-A

50511270-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32256997-C-G

50511777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32257432-T-C

50511871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32257513-G-A

50511888-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32257530-C-T

50511940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32257589-G-T

50511984-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32257633-G-C

50511997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32257648-G-A

50512186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32257831-C-T

50512310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32257944-A-G

50512315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32257949-T-C

http://identifiers.org/hco/10/GRCh38#50512317-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32257951-C-A

50512493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32258152-G-A

50512889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32258600-G-A

http://identifiers.org/hco/10/GRCh38#50512921-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32258639-A-C

50512981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32258700-C-T

50512996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32258715-T-C

50513059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32258758-T-C

50513061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32258760-C-T

50513073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32258772-T-C

50513275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32258952-T-C

50513410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32259052-C-T

50513452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32259092-C-T

50513592-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32259229-T-A

50513663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32259294-A-G

http://identifiers.org/hco/10/GRCh38#50513849-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32259437-A-C

50514693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32261763-A-G

50514709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32261779-T-C

50515201-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32262239-C-G

50515201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32262239-C-T

50515202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32262240-T-C

50515576-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32262660-A-T

50516088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32263179-G-A

50516769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32263859-G-A

50516951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32264031-T-C

50517258-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32264996-A-T

50519508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32266698-G-A

50519620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32266766-G-T

http://identifiers.org/hco/10/GRCh38#50519727-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32266839-C-A

50519728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32266840-A-G

50519728-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32266840-A-T

50519755-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32266865-C-G

50519815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32266925-G-A

50519815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32266925-G-T

50519870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32266987-A-G

50521284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32267834-T-C

50521294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32267850-A-G

50521320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32267877-T-C

50521880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32268334-C-T

50522188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32268840-C-T

50522392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32269019-C-T

50522453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32269075-C-T

http://identifiers.org/hco/10/GRCh38#50522552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32269156-C-A

50522561-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32269165-G-T

50522666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32269265-C-T

50522794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32269371-C-T

50523807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32270275-T-C

50523807-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32270275-T-G

50524263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32270670-C-T

50524745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32271125-T-C

50524812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32271189-C-T

50524822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32271198-G-A

http://identifiers.org/hco/10/GRCh38#50525935-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32272151-A-C

50525935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32272151-A-G

50525979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32272196-C-T

http://identifiers.org/hco/10/GRCh38#50526023-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32272238-A-C

50526023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32272238-A-G

50526567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32272373-T-C

50526660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32272469-C-T

50526766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32272560-A-G

50529601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32275515-G-T

http://identifiers.org/hco/10/GRCh38#50529801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32275708-C-A

50529829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32275731-G-A

http://identifiers.org/hco/10/GRCh38#50529924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32275826-C-A

50530089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32275967-A-G

50530093-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32275971-C-G

50530093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32275971-C-T

50530120-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32275992-A-T

50530171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32276041-T-C

50530424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32277466-C-T

50531516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32278437-G-T

50531529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32278450-C-T

50531597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32278514-C-T

50531724-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32278632-C-G

50531724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32278632-C-T

50536457-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32282680-G-C

50536551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32282771-C-T

50536735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32282941-T-C

50536735-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32282941-T-G

50537178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32283629-T-C

http://identifiers.org/hco/10/GRCh38#50537242-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32283681-C-A

50537242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32283681-C-T

50537297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32283737-A-G

50537299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32283739-C-T

50538974-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32285288-C-G

50538975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32285289-C-T

50539058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32285481-G-A

50539287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32285677-C-T

50539762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32286681-C-T

50539936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32287754-C-T

50539943-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32287761-G-T

50540001-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32287800-G-T

50540165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32287951-A-G

50540432-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32288462-T-A

50540432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32288462-T-C

50540491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32288510-T-C

50540505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32288526-T-C

50541540-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32290569-T-G

50541644-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32290682-G-A

50541684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32290717-C-T

50541916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32290917-C-T

50550018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32292541-C-T

http://identifiers.org/hco/10/GRCh38#50550505-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32292892-C-A

50552217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32295934-C-T

http://identifiers.org/hco/10/GRCh38#50552380-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32296065-A-C

50552491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32296160-T-C

50552663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32296334-G-A

50552756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32296448-T-C

50552764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32296456-T-C

http://identifiers.org/hco/10/GRCh38#50553148-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#32297101-C-A

50553148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32297101-C-T

50553157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32297110-T-C

50553241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32297193-C-T

50553674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32297600-A-G

50553742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32297662-C-T

50553743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32297663-G-A

http://identifiers.org/hco/10/GRCh38#50553918-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32297854-A-C

50554022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32297902-A-G

50554041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32297920-C-T

50554864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32298748-G-A

50555196-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32298985-T-A

50555471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32299234-A-G

50555529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32299289-A-G

50555556-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32299319-T-A

50555556-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32299319-T-C

50555620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32299379-T-C

50555632-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32299391-G-T

50556226-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32299958-A-T

50556272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32300004-G-A

50556276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32300008-A-G

50556547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32300218-C-T

50556785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32300425-T-C

50556988-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32300628-G-A

50557056-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32300692-G-T

http://identifiers.org/hco/10/GRCh38#50557385-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32300986-C-A

50557490-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32301086-T-G

http://identifiers.org/hco/10/GRCh38#50557672-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32301273-C-A

50557708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32301309-G-A

http://identifiers.org/hco/10/GRCh38#50557710-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32301311-C-A

50557710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32301311-C-T

50557883-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32301470-T-G

http://identifiers.org/hco/10/GRCh38#50557973-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32301570-C-A

50557982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32301579-A-G

50557983-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32301580-C-G

50558164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32301723-T-C

50558205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32301758-C-T

50558341-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32301879-T-C

50558357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32301895-T-C

50558411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32301925-G-A

http://identifiers.org/hco/10/GRCh38#50558435-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32301949-A-C

50559054-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32302131-T-A

50559567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32302600-T-C

50559952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32303006-T-C

50559969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32303023-G-A

50559991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32303044-C-T

50560058-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32303124-T-G

50560818-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32303260-G-C

50560827-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32303269-C-T

http://identifiers.org/hco/10/GRCh38#50563029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32303653-C-A

50563043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32303667-G-A

50563204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32303805-G-T

50563899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32304164-C-T

50564224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32304565-C-T

50564248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32304587-T-C

50564255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32304595-G-A

50565493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32306397-A-G

50565493-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32306397-A-T

50565724-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32306628-T-A

50565724-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32306628-T-G

50567186-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32306755-T-A

50567213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32306781-G-A

50567225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32306793-G-A

50567234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32306802-C-T

50567241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32306809-G-A

50567351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32306835-G-A

50567351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32306835-G-T

50567427-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32306891-A-T

50567481-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32306941-A-T

50567527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32306999-C-T

50567571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32307043-C-T

50567819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32307274-G-A

50567841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32307292-T-C

50567901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32307352-T-C

50567990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32307429-A-G

50568143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32307579-G-A

50568143-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32307579-G-T

50568409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32307834-G-A

50568409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32307834-G-T

50568411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32307836-C-T

50568495-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32307933-T-A

50568524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32307962-C-T

50569770-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32308290-T-G

50570236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32308683-C-T

50570351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32308788-C-T

50570374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32308811-G-A

50571261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32310456-G-A

50571556-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32310752-T-C

50571617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32310804-C-T

50571618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32310805-G-A

50572027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32311150-T-C

50572122-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32311247-T-A

50576711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32318924-A-G

http://identifiers.org/hco/10/GRCh38#50577124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32319397-C-A

50577124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32319397-C-T

50577132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32319405-G-A

50577194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32319476-G-A

50577194-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32319476-G-C

50577194-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32319476-G-T

50577208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32319490-T-C

50577216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32319498-G-A

50577216-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32319498-G-C

50577244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32319525-T-C

50577355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32319622-T-C

http://identifiers.org/hco/10/GRCh38#50577658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32319826-C-A

50577718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32319881-A-G

50577742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32319901-C-T

50577753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32319912-A-G

50577753-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32319912-A-T

50577871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32320029-C-T

50577952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32320103-A-G

50578340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32320471-A-G

50578340-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32320471-A-T

50578417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32320549-T-C

50578660-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32320781-G-C

50578965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32321103-C-T

50579243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32321390-G-A

50579559-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32322007-C-G

50579772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 32322198-A-G

50580102-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32322493-T-G

http://identifiers.org/hco/10/GRCh38#50580218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32322578-C-A

50580218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32322578-C-T

50580643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32322931-G-A

50580643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32322931-G-T

50581550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32323347-C-T

50581609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32323405-G-A

50581651-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32323448-T-A

50581651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32323448-T-C

50581722-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32323516-A-T

http://identifiers.org/hco/10/GRCh38#50582315-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32324101-A-C

50582601-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32324345-C-G

50582601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32324345-C-T

50582702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32324417-T-C

http://identifiers.org/hco/10/GRCh38#50582855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32324556-C-A

50582921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32324597-G-A

50582921-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32324597-G-T

50583007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32324621-C-T

50583109-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32324723-C-G

50583261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32324862-A-G

50583281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32324882-G-A

50583763-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32325278-A-T

50583766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32325281-A-G

50584521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32326165-G-A

50584521-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32326165-G-T

50584543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32326177-T-C

50584768-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32326396-C-T

50584821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32326448-T-C

50585532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32327100-C-T

50585705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32327158-A-G

50586168-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32327529-G-C

50586177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32327538-T-C

50586235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32327566-A-G

50586512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32327792-A-G

50586603-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32327879-T-A

50586819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32328097-C-T

50588556-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32328628-A-T

50590156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32329348-T-C

50590226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32329402-G-A

50590226-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 32329402-G-T

http://identifiers.org/hco/10/GRCh38#50590519-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32329676-A-C

50590962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32330130-A-G

50591039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32330226-A-G

50591309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32330474-T-C

50591309-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32330474-T-G

50591363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32330519-C-T

50591744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32330880-C-T

50591971-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32331057-C-G

50591971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32331057-C-T

50591979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32331065-T-C

50592129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32331185-C-T

50592727-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32331844-C-G

50592727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32331844-C-T

50592753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32331870-T-C

50593044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32332302-A-G

50593130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32332817-C-T

http://identifiers.org/hco/10/GRCh38#50593369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32332995-C-A

50593485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32333072-C-T

50593523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32333091-G-A

http://identifiers.org/hco/10/GRCh38#50593614-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32333177-A-C

50593991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32333560-C-T

50594131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32333700-C-T

50594461-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32334011-T-G

50596761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32337373-G-A

50596969-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32337567-G-C

50602331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32341163-G-A

50602348-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32341180-C-G

50602503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32341319-G-A

50602503-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32341319-G-C

50602518-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32341336-G-T

50602539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32341357-T-C

http://identifiers.org/hco/10/GRCh38#50603003-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32342211-A-C

50603026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32342465-G-T

50603100-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32342530-A-T

50603762-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32343580-G-T

50603785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32343596-T-C

50603793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32343604-A-G

50603829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32343641-A-G

http://identifiers.org/hco/10/GRCh38#50603913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32343720-C-A

50603913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32343720-C-T

50604096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32343900-C-T

50604120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32343925-A-G

http://identifiers.org/hco/10/GRCh38#50605471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32349953-C-A

50605471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32349953-C-T

50605614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32350094-T-C

50606030-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32350426-A-G

50606405-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32350769-C-G

50606670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32351031-G-A

50606772-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32351098-T-A

50606838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32351161-G-A

http://identifiers.org/hco/10/GRCh38#50606863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32351194-C-A

50607442-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32351440-C-T

50608022-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32351984-G-C

50608227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32352182-A-G

50608375-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32352320-G-A

50609518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32352706-A-G

50609518-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32352706-A-T

50609629-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32352803-C-G

50609799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32352981-G-A

50610181-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32353256-C-G

50610199-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32353267-A-T

50610631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32353705-G-A

50612397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32354592-G-A

50612433-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32354632-T-G

50613998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32355663-G-A

http://identifiers.org/hco/10/GRCh38#50614128-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32355803-A-C

50614128-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32355803-A-T

50614132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32355807-G-T

50614250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32355884-T-C

50614252-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32355886-G-C

50614646-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32356185-G-T

50614686-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32356225-C-G

50614719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32356266-G-A

50614987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32356562-T-C

50614989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32356564-C-T

50614992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32356567-C-T

50615020-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32356594-T-A

50615044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32356616-G-A

50615818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32358894-C-T

50616056-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32359122-T-C

50619906-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32362485-T-G

50619947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32362549-C-T

50619975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32362580-G-A

http://identifiers.org/hco/10/GRCh38#50620036-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32362640-C-A

50620135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32362742-G-A

50620218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32362827-A-G

50620285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32362883-T-C

50621432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32363469-G-A

50622131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32364106-C-T

50622642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32364585-G-A

50622642-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32364585-G-T

50622822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32364749-G-A

50622832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32364754-C-T

50622841-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32364763-G-C

50622885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32364805-G-A

50623504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32365422-C-T

50623513-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32365431-C-G

50623513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32365431-C-T

50623628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32365539-A-G

50623628-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32365539-A-T

50623633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32365544-G-A

50623633-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32365544-G-C

50623648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32365559-G-A

50623648-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32365559-G-T

50623682-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32365595-T-A

50623682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32365595-T-C

50623749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32365666-G-T

http://identifiers.org/hco/10/GRCh38#50623757-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#32365675-C-A

50623772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 32365689-G-A

50623772-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 32365689-G-C

http://identifiers.org/hco/10/GRCh38#50623802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#32365718-C-A

50623802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 32365718-C-T

50623816-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32365732-G-A

50623816-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32365732-G-C

http://identifiers.org/hco/10/GRCh38#50623883-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#32365799-C-A

50623883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 32365799-C-T

50624040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32365951-G-A

50624040-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32365951-G-C

50624101-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32365997-C-G

50624101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32365997-C-T

50624118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32366009-G-A

50624215-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32366127-G-C

50624215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32366127-G-T

50624230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32366143-T-C

50624230-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32366143-T-G

50624526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32366471-G-A

50624526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32366471-G-T

http://identifiers.org/hco/10/GRCh38#50624527-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32366472-C-A

50624527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32366472-C-T

http://identifiers.org/hco/10/GRCh38#50624540-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32366482-A-C

50624540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32366482-A-G

50624540-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32366482-A-T

50624619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 32366544-C-T

50624707-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 32366632-T-C

50624707-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 32366632-T-G

50624809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32366721-G-T

http://identifiers.org/hco/10/GRCh38#50624812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#32366724-C-A

50624812-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32366724-C-G

50624812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32366724-C-T

50624831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32366741-G-A

50624831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32366741-G-T

50624873-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32366781-G-A

50624873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32366781-G-T

50624887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 32366792-G-A

50624887-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 32366792-G-C

50624887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 32366792-G-T

http://identifiers.org/hco/10/GRCh38#50624910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#32366812-C-A

50624910-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 32366812-C-G

50624910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 32366812-C-T

50624978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32366878-G-A

50624978-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29799
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32366878-G-T