http://identifiers.org/hco/13/GRCh38#23979808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60722830-C-A

23979808-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 60722830-C-G

23979808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 60722830-C-T

23979816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 60722838-A-G

23979816-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 60722838-A-T

23979826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 60722848-G-A

http://identifiers.org/hco/13/GRCh38#23979851-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#60722873-C-A

23979851-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 60722873-C-T

23979858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 60722880-A-G

23980017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60722996-A-G

23980018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60722997-A-G

23980260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 60723093-A-G

23980260-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 60723093-A-T

23980280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 60723120-C-T

23982564-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60725263-C-G

23982590-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60725289-T-G

23982900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60725694-C-T

23982981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60725775-A-G

23983280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60726073-T-C

23983286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60726079-C-T

23983295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60726088-G-A

23983295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60726088-G-T

23983375-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60726172-T-A

23983375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60726172-T-C

23983394-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60726191-T-G

http://identifiers.org/hco/13/GRCh38#23983428-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60726224-C-A

23983428-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60726224-C-G

http://identifiers.org/hco/13/GRCh38#23983613-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60726390-A-C

23983659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60726434-A-G

23983659-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60726434-A-T

http://identifiers.org/hco/13/GRCh38#23983677-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60726452-A-C

23983677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60726452-A-G

23983685-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60726460-T-A

http://identifiers.org/hco/13/GRCh38#23983746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60726518-C-A

http://identifiers.org/hco/13/GRCh38#23983771-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60726543-C-A

23983771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 60726543-C-T

23983795-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 60726576-G-T

23983800-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 60726581-T-G

23983823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 60726604-T-C

23983876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 60726652-A-G

23984302-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60727061-C-G

23984462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60727215-G-A

23984508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60727263-A-G

23984511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60727275-T-C

23984877-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60728181-A-T

23984900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60728203-T-C

23984904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60728207-C-T

23984962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60728260-G-A

23985074-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60728350-A-T

23985084-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60728361-G-C

23985134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60728411-C-T

23985157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60728434-T-C

23985159-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60728436-T-A

23985298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60728553-G-A

23985298-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60728553-G-T

23986239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60730368-C-T

23986258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60730384-C-T

23986268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60730394-G-A

23986401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60730528-G-A

23986403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60730530-G-A

http://identifiers.org/hco/13/GRCh38#23986410-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60730537-A-C

23986681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60730697-T-C

23986943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60730971-C-T

23986979-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60730994-T-C

23986990-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60731005-A-T

23987137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60731072-T-C

23987223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60731155-G-A

23987253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60731181-G-A

23987276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60731204-G-A

23987327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60731250-G-A

23987434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60731357-C-T

23987451-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60731374-G-C

http://identifiers.org/hco/13/GRCh38#23987473-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60731396-A-C

23987481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60731404-A-G

23987485-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60731412-T-G

http://identifiers.org/hco/13/GRCh38#23987540-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60731465-A-C

23987617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60731540-G-A

http://identifiers.org/hco/13/GRCh38#23987651-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60731574-A-C

23987651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60731574-A-G

23988431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60732591-G-T

http://identifiers.org/hco/13/GRCh38#23988460-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60732618-A-C

23988460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60732618-A-G

23988811-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60732914-G-C

23988817-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60732920-C-G

23988817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60732920-C-T

23988820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60732923-G-A

http://identifiers.org/hco/13/GRCh38#23988889-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60732993-C-A

23988998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60733098-G-A

23989036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60733136-G-A

23989562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60733345-C-T

23989676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60733457-T-C

23989817-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60733594-G-C

23989963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60733709-C-T

http://identifiers.org/hco/13/GRCh38#23990012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60733739-C-A

23990110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60733825-C-T

23990118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60733833-C-T

23990129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60733844-C-T

23990250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60733950-A-G

23990330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60734011-C-T

23990452-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60734119-A-T

23990476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60734146-C-T

23990617-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60734276-G-T

23990683-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60734343-G-C

23991618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60734729-A-G

http://identifiers.org/hco/13/GRCh38#23991661-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60734797-A-C

23992892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60736925-C-T

http://identifiers.org/hco/13/GRCh38#23993101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60737113-C-A

23993418-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60737518-A-T

23993436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60737531-C-T

http://identifiers.org/hco/13/GRCh38#23993809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60739110-C-A

23993854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60739155-A-G

23993887-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60739189-T-G

23993957-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60739239-T-G

23993978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60739250-T-C

23993983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60739255-T-C

23994013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60739283-A-G

23994013-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60739283-A-T

23994025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60739295-A-G

23994055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60739329-C-T

23994056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60739330-G-A

23994359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60739578-T-C

http://identifiers.org/hco/13/GRCh38#23994376-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60739595-C-A

23994597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60739771-C-T

23994617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60739791-G-A

23994651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60739824-G-A

23994651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60739824-G-T

24003150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60742000-C-T

24003411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60742250-G-A

24003411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60742250-G-T

24004827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60742764-G-A

24005009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60742926-T-C

24005042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60742958-T-C

24005088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60743004-A-G

24005143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60743058-C-T

24005144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60743059-G-A

24005144-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60743059-G-C

24005335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60743252-G-A

24005473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60743393-G-A

http://identifiers.org/hco/13/GRCh38#24005583-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60743647-A-C

http://identifiers.org/hco/13/GRCh38#24005584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60743648-C-A

24005584-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60743648-C-G

24005596-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60743674-A-T

24005613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60743691-G-T

24005614-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60743692-T-G

24005721-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60743792-G-C

24005724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60743795-G-A

24005724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60743795-G-T

24005765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60743838-C-T

24005806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60743879-G-A

24006008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60744058-C-T

24019588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60750198-G-T

24019804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60750446-T-C

24019893-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60750525-T-G

24020066-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60750652-C-G

24020514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 60751206-G-A

24032513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60751703-G-A

24032514-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60751704-G-C

24032578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60751774-G-A

24036243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60752698-A-G

24036244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60752699-C-T

24036250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60752705-T-C

24036287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60752741-T-C

24036394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60752845-T-C

24036534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60753185-C-T

http://identifiers.org/hco/13/GRCh38#24036556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60753204-C-A

24038447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60753943-C-T

24038463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60753960-G-A

24038474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60753978-G-T

24039010-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, undefined
orthologous variants: 60754557-G-T

24039334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60754857-C-T

24039340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60754863-A-G

24039613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60755080-A-G

24039851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60755297-G-A

24039942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60755333-G-A

24040010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60755366-G-A

http://identifiers.org/hco/13/GRCh38#24040099-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60755448-C-A

24040431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60756305-T-C

http://identifiers.org/hco/13/GRCh38#24040442-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60756316-A-C

24040451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60756325-C-T

24040543-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60756408-G-C

24040650-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60756503-T-A

24040650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60756503-T-C

24040687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60756540-C-T

24040778-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60756623-T-A

24040892-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, undefined
orthologous variants: 60757121-A-T

24040893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, undefined
orthologous variants: 60757122-G-A

24040905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60757136-C-T

24040978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, undefined
orthologous variants: 60757196-G-A

24041057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60757242-T-C

24041225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60757400-G-A

24041356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60757537-C-T

24041420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60757661-A-G

http://identifiers.org/hco/13/GRCh38#24041461-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60757714-C-A

24041502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60757764-C-T

24041503-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60757765-A-T

24041518-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60757901-G-C

24041700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60758261-G-A

24042011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60758528-T-C

24042029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60758548-G-A

24042046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60758564-G-A

24042107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60758610-C-T

24042124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60758627-C-T

24042125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60758628-G-T

24042143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60758651-G-A

24042175-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60758689-G-T

http://identifiers.org/hco/13/GRCh38#24042396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60758889-C-A

24042423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60758912-G-T

24042483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60758959-T-C

24042520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60758994-G-A

24042719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60759124-A-G

24042780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60759172-C-T

24042872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60759271-G-A

24042880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60759280-A-G

24042929-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, undefined
orthologous variants: 60759356-G-T

24042950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60759380-C-T

24042953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60759383-C-T

24042974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60759401-C-T

24043040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60759463-G-A

24043049-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60759472-A-T

24043051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60759474-A-G

24043093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60759513-C-T

24043190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60759561-A-G

http://identifiers.org/hco/13/GRCh38#24043201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60759572-C-A

24043736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, undefined
orthologous variants: 60760599-C-T

24043980-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60760848-T-G

24044995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60761036-C-T

24045015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60761056-G-A

24045015-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60761056-G-C

http://identifiers.org/hco/13/GRCh38#24045291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60761322-C-A

24045301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60761332-G-A

24045379-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60761404-G-C

24045613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60761927-G-A

24045645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60761959-G-A

24045703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60762016-G-A

24045860-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60762313-C-G

24045870-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60762440-G-T

24045894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60762466-C-T

24045951-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60762528-G-T

24046014-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60762583-T-A

24046176-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60762765-A-T

http://identifiers.org/hco/13/GRCh38#24046185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60762774-C-A

24046197-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60762786-G-C

24046634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60763108-C-T

http://identifiers.org/hco/13/GRCh38#24046652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60763126-C-A

http://identifiers.org/hco/13/GRCh38#24046653-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60763127-C-A

24046653-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60763127-C-G

24046721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60763193-T-C

24047886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60763535-C-T

24047887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60763536-T-C

24048030-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60763733-C-G

24048130-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60763804-C-G

24048150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60763827-C-T

24048326-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60764007-C-G

24048618-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60764288-T-G

http://identifiers.org/hco/13/GRCh38#24048638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60764309-C-A

24050355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60766201-C-T

24050726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, undefined
orthologous variants: 60766826-A-G

24050786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60766874-G-A

24050978-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60767057-G-C

24051627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60767682-C-T

24051738-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60767773-A-T

24051891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60767930-G-A

24051892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60767931-G-A

24052029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60768027-C-T

24052114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60768119-C-T

24052119-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60768124-C-G

24052178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60768182-G-A

24052183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60768187-G-A

24052315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 60768218-G-A

24052489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60768304-A-G

24052591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60768425-G-A

24052624-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60768442-A-T

24052766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60768582-G-T

24052773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60768589-T-C

24053296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60769084-A-G

24053365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60769156-A-G

24054167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60771007-C-T

24054184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60771024-A-G

24054209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60771049-C-T

24054466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60771328-T-C

24055048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60771534-G-A

24055064-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60771550-T-G

24055094-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60771595-A-T

24055148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60771648-A-G

24055158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60771652-A-G

24055176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60771670-G-A

24055254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60771743-C-T

24055414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60771885-T-C

24055552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60771983-G-A

24055603-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60772034-A-T

24055648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60772065-C-T

24055659-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60772076-T-G

24055896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60772289-A-G

24056097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60772497-G-A

24056112-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60772512-T-G

24056437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60772725-A-G

24056499-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60772754-G-T

24056537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60772789-C-T

24056637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60772881-A-G

24056667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60772911-G-A

24056667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60772911-G-T

24058633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60774726-C-T

24062576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60776647-G-A

24062576-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60776647-G-T

24062580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60776651-G-A

http://identifiers.org/hco/13/GRCh38#24062794-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60777796-C-A

24062807-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60777812-T-A

24062807-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60777812-T-C

24062911-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60777916-G-C

24062970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60777974-C-T

24071640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60780324-A-G

24071826-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60780520-T-G

24072269-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60780700-G-A

24072382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60780825-T-C

24072479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60780920-G-A

24075581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60784779-A-G

24075811-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60784990-G-T

24078792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60786545-G-A

24078792-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60786545-G-T

http://identifiers.org/hco/13/GRCh38#24078834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60786585-C-A

24078953-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60786674-G-C

24079318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60786986-G-A

24079350-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60786999-G-C

24079422-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60787063-C-G

24079840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60787906-G-A

24079898-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60787974-C-G

24080203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60788226-C-T

24080232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60788256-C-T

24080306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60788325-C-T

24080628-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60788627-T-G

24080777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60788777-A-G

24080880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60788863-C-T

24081019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60788978-T-C

24081113-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60789081-A-T

24081165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60789138-C-T

24081178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60789148-A-G

24081847-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60789746-G-C

24081847-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60789746-G-T

24081941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60789839-G-A

24082303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60790183-C-T

24082403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60790281-A-G

24082411-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60790289-A-T

24082491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60790347-G-A

24082491-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60790347-G-T

24082520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60790376-A-G

24083200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60791118-A-G

24083417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60791314-G-A

24083589-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60791382-A-T

24083973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60791702-G-A

24084057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60791784-A-G

24084147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60791874-A-G

24084212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60791939-G-A

24084443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60792149-T-C

http://identifiers.org/hco/13/GRCh38#24084564-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60792254-A-C

24084576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60792266-G-A

24084757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60792439-C-T

24086978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60793242-C-T

24086985-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60793249-C-G

24087083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60793375-A-G

24087466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60794299-G-A

24087466-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60794299-G-T

24087822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60794580-T-C

24087857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60794617-G-T

24087859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60794619-C-T

24088110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60794837-C-T

24088954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60795829-G-A

24088966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60795841-C-T

http://identifiers.org/hco/13/GRCh38#24089281-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60796192-C-A

24089577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: -G-A

24089808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: -T-C

24089808-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: -T-G

24089989-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: -G-T

24089998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: -G-A

24091883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60799314-G-T

24091942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60799381-G-A

24092056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60799490-G-A

24092141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60799573-G-A

24092150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60799576-G-A

24092259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60799685-G-T

24092591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60800015-G-A

24092857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60800824-G-T

24092860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60800828-G-A

24093280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60807346-C-T

24093287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60807352-G-A

24093325-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60807387-C-G

http://identifiers.org/hco/13/GRCh38#24093418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60807435-C-A

24093496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60807513-A-G

http://identifiers.org/hco/13/GRCh38#24093716-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60807786-A-C

24104270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60817831-G-T

http://identifiers.org/hco/13/GRCh38#24104294-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60817854-A-C

24104301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60817861-T-C

24104341-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60817914-G-T

24104405-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60817975-C-G

24104505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60818044-A-G

24104656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60818185-A-G

24104754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60818300-G-T

24105006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60818565-C-T

24105058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60818615-A-G

24105088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60818646-T-C

24105097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60818649-T-C

24106578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60824736-C-T

24107424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60825518-T-C

24107507-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60825605-T-C

24110558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60827381-C-T

http://identifiers.org/hco/13/GRCh38#24110567-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60827390-A-C

24110678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60827499-A-G

24110739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60827550-A-G

24110825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60827632-G-A

24113024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60829960-G-T

24113046-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60829982-C-G

24113136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60830072-A-G

24113141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60830077-C-T

24114195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60830542-G-A

24118164-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60830757-C-G

24118164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60830757-C-T

24118293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60830867-G-T

24119362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60834423-G-A

24119383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60834442-G-T

24119941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60834958-A-G

24120088-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60835100-A-T

24120137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60835143-C-T

24120328-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60835280-G-A

24120562-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60835503-G-C

http://identifiers.org/hco/13/GRCh38#24120580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60835521-C-A

24120580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60835521-C-T

24120697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60836515-G-A

24120697-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60836515-G-C

24121018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60836789-C-T

24123842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60836848-T-C

24123857-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60836861-G-C

24123857-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60836861-G-T

24123871-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60837415-G-T

http://identifiers.org/hco/13/GRCh38#24123887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60837431-C-A

24123887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60837431-C-T

24123897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60837446-T-C

http://identifiers.org/hco/13/GRCh38#24123925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60837474-C-A

24123925-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60837474-C-G

http://identifiers.org/hco/13/GRCh38#24124022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60837571-C-A

24124022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60837571-C-T

24124065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60837632-T-C

http://identifiers.org/hco/13/GRCh38#24124356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60838588-C-A

24124450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60838655-G-A

24124571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60838743-T-C

24124690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60839420-A-G

24124723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60839459-T-C

24124758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60839485-A-G

24124993-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, undefined
orthologous variants: 60839620-G-C

http://identifiers.org/hco/13/GRCh38#24125185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#60839769-C-A

24125321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, undefined
orthologous variants: 60839912-G-A

24125609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60840236-G-A

24125657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60840285-A-G

24125686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60840323-C-T

24125743-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60840380-G-T

24128928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60841993-A-G

24129454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60842495-T-C

http://identifiers.org/hco/13/GRCh38#24129643-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60842631-A-C

24129744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60842717-A-G

24130025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60843767-C-T

http://identifiers.org/hco/13/GRCh38#24130040-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60843781-C-A

24130269-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60844017-G-T

24130355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60844123-A-G

24131803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60844165-G-A

24131803-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60844165-G-C

http://identifiers.org/hco/13/GRCh38#24131979-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60844320-C-A

24131979-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60844320-C-G

24131979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60844320-C-T

http://identifiers.org/hco/13/GRCh38#24131988-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60844329-A-C

24132116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60844453-C-T

24132905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60845768-G-A

24132905-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60845768-G-C

24132905-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60845768-G-T

24133107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60846002-G-T

24133119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60846010-A-G

24133172-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60846063-T-G

24133298-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60846172-G-C

http://identifiers.org/hco/13/GRCh38#24133462-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60846681-A-C

24133495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60846703-C-T

24133541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60846757-A-G

24133604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60846818-C-T

24133877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60847084-C-T

24134317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60848209-G-T

24134934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60849417-A-G

24134990-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60849486-G-T

http://identifiers.org/hco/13/GRCh38#24135028-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60849527-C-A

24135185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60849633-G-A

24135200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60849648-T-C

24135278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60849826-A-G

24135633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60850039-G-A

24135640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60850046-G-A

24135659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60850065-C-T

24135674-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60850073-G-T

24135707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60850106-A-G

24135719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60850164-G-A

24135719-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60850164-G-C

24135721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60850166-G-A

24135910-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, undefined
orthologous variants: 60850343-G-T

http://identifiers.org/hco/13/GRCh38#24135948-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60850384-A-C

24135986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60850422-C-T

24136596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60850934-T-C

24137152-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: -T-A

24139263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60853280-C-T

24139456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60853548-C-T

24139648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60853687-A-G

24146396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60856654-C-T

24146462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60856720-G-T

http://identifiers.org/hco/13/GRCh38#24146555-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60856767-A-C

24151969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60862570-G-A

24151976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60862577-A-G

24152101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60862683-C-T

24152296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60862827-C-T

24157709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60868488-C-T

24157769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60868558-G-A

24157769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60868558-G-T

24157851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60868637-T-C

24158103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60868875-A-G

http://identifiers.org/hco/13/GRCh38#24158348-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60869286-C-A

24158348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60869286-C-T

24158390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60869347-C-T

24158487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60869428-G-A

24158634-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60869515-T-A

24158741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60869614-A-G

24158762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60869635-C-T

24158766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60869639-C-T

24158786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60869661-A-G

24158874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60869747-G-A

24158874-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60869747-G-C

24159245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60870025-A-G

24159348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60870479-G-T

24159811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60871201-G-A

24160170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60871580-C-T

24160591-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, undefined
orthologous variants: 60872007-T-A

24160591-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, undefined
orthologous variants: 60872007-T-G

24160635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60872078-G-A

24160646-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, undefined
orthologous variants: 60872089-T-A

24160647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, undefined
orthologous variants: 60872090-G-A

24160647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, undefined
orthologous variants: 60872090-G-T

24160950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 60872334-G-A

24160950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 60872334-G-T

24160983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 60872357-T-C

24161043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60872407-T-C

24161088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 60872442-C-T

http://identifiers.org/hco/13/GRCh38#24161092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#60872446-C-A

http://identifiers.org/hco/13/GRCh38#24161101-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#60872457-A-C

24161570-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60872891-C-G

24161678-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60872996-T-G

24161685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60872999-A-G

24162351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60873678-G-A

http://identifiers.org/hco/13/GRCh38#24162405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60873737-C-A

http://identifiers.org/hco/13/GRCh38#24162429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60873763-C-A

24162484-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 60873836-G-T

24162503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 60873847-A-G

24162609-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60873943-G-C

24162648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60873976-T-C

http://identifiers.org/hco/13/GRCh38#24162876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60874181-C-A

24162953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60874258-T-C

24162953-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60874258-T-G

24163888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60874781-G-A

24163912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60874798-T-C

24164541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60875133-C-T

24164779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60875335-A-G

24164795-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60875351-T-G

24164865-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60875414-G-C

24164893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60875442-T-C

24165001-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60875528-T-A

24165006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60875534-G-A

24165035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60875554-A-G

24165111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60875616-G-A

24165225-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60875735-C-G

24165225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60875735-C-T

24165258-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60875769-G-C

http://identifiers.org/hco/13/GRCh38#24165375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60875839-C-A

24165375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60875839-C-T

24165519-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60875976-G-C

24166005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60876502-C-T

24166277-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60876757-A-G

http://identifiers.org/hco/13/GRCh38#24166348-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60876827-C-A

24166633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60877017-C-T

24167030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60878817-C-T

24167096-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60878886-T-C

24167234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60879022-G-T

24167255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60879036-T-C

24167274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60879055-C-T

24167281-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60879062-T-C

24168263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60880476-C-T

http://identifiers.org/hco/13/GRCh38#24168730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60880930-C-A

24168730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60880930-C-T

24169062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60881195-C-T

24169208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60881340-A-G

24169251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60881376-C-T

24169394-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60881524-C-G

24169394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60881524-C-T

24169758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60883220-C-T

24169759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60883221-C-T

24169902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60883372-C-T

24170117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60883570-T-C

24170117-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60883570-T-G

24170163-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60884410-T-A

24170208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60884447-T-C

24170414-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60884622-A-T

24170423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60884631-G-A

24170423-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60884631-G-C

24170423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60884631-G-T

24170428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60884636-A-G

24170605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60884778-G-A

24170687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60884849-G-A

24170902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60885123-T-C

24170953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60885160-T-C

24171079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60885258-A-G

24171099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60885278-G-A

24171137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60885327-A-G

24171428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60885591-G-A

24176227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60886549-C-T

24176530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60886882-C-T

24183063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60892653-A-G

24183119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60892694-A-G

24183218-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60892802-T-A

24183236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60892821-A-G

http://identifiers.org/hco/13/GRCh38#24183247-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60892841-A-C

24183305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60892903-C-T

24183764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60893125-G-A

24183775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60893136-T-C

24183832-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60893191-T-G

24183912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 60893262-C-T

24183956-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60893314-T-C

24184216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60893492-T-C

24184940-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60894342-C-G

24184945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60894347-A-G

24185039-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 60894421-G-C

24185073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60894455-G-A

24185102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60894482-T-C

24185125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 60894503-T-C

24185152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60894526-C-T

24185158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60894532-G-A

24185168-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60894544-G-A

24185197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60894569-T-C

24185310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60894667-C-T

24185700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60895064-T-C

24185791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60895154-G-A

24186172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60897061-A-G

24186281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60897162-A-G

24186310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60897194-A-G

24186501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60897383-C-T

24186886-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60898520-T-G

24186927-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60898561-A-T

24186955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60898587-A-G

24186990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60898628-T-C

24187056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60898691-A-G

24187104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60898736-A-G

24187380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60898935-A-G

24192466-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60899239-C-G

24192466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60899239-C-T

24192569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60899298-G-A

24192615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60899342-A-G

24192786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60899490-T-C

24192944-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60899576-C-G

24192944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60899576-C-T

24193035-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60899673-C-G

24193236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60899829-G-A

24193251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60899842-G-A

24193271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60899860-A-G

24193473-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60900592-T-G

24193580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60900691-G-A

24193757-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60900896-G-C

http://identifiers.org/hco/13/GRCh38#24193769-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60900908-A-C

http://identifiers.org/hco/13/GRCh38#24194008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60901628-C-A

24194036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60901653-A-G

24194036-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60901653-A-T

24194042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60901659-C-T

24194093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60901702-G-A

24194179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60901795-G-A

24194211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60901828-A-G

24194220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60901837-T-C

24194276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 60901890-A-G

24194289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60901903-T-C

24194320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60901935-G-A

http://identifiers.org/hco/13/GRCh38#24194366-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60901979-A-C

24194427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60902031-A-G

http://identifiers.org/hco/13/GRCh38#24195136-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60902385-C-A

24195157-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60902406-C-G

24195281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60902526-G-A

24195337-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60902576-G-C

24195414-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60902657-T-G

24195423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60902666-A-G

24195572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60902816-A-G

24195621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60902861-T-C

24195757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60902978-G-A

24195986-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60903231-A-T

24196019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60903263-T-C

24196167-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60903365-T-A

24196229-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60903422-C-G

24198521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60906746-A-G

24198542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60906767-G-A

24198882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60907054-C-T

http://identifiers.org/hco/13/GRCh38#24198942-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60907114-C-A

24202146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60907679-C-T

24202617-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60907855-G-T

24202708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60907937-A-G

24202761-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60907984-G-T

24202856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60908078-C-T

24203706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60908760-G-A

24204524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60909630-A-G

http://identifiers.org/hco/13/GRCh38#24204792-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60909863-A-C

24204813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60909881-A-G

24204907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60910019-A-G

24207456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60910092-G-A

24207847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60910472-C-T

24207861-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60910486-G-C

24207894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60910522-C-T

24207946-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60910570-T-G

24208157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60910905-A-G

24208171-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60910919-C-G

24208333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60911042-A-G

24208451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60911124-C-T

24210764-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60913121-G-T

24210809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60913150-G-A

24211034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60913309-T-C

24211133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60913389-G-A

24211179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60913438-A-G

24211205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60913485-G-A

24211260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60913643-A-G

24211457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60913913-A-G

24211475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60913927-T-C

24211475-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60913927-T-G

24211657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60914175-C-T

24211667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60914185-T-C

24211705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60914234-C-T

24211873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60914414-C-T

24212368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60914716-C-T

24212689-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60915041-A-T

24212712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 60915064-A-G

24212743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60915095-T-C

24212847-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 60915173-T-C

24212897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 60915217-A-G

24213016-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60915314-G-C

24213020-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60915322-T-A

24213020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60915322-T-C

24213157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60915437-G-A

24213180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60915450-G-A

24213676-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60916207-T-A

24215639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60920177-A-G

24215719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60920238-G-A

24215740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60920256-A-G

24215767-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60920282-G-C

24216470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60920855-C-T

24216492-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60920880-C-T

24216633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60921018-G-T

24216645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60921030-T-C

24216645-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60921030-T-G

24217517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60923127-C-T

24217553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60923161-G-A

24217553-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60923161-G-C

24217947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60923630-G-A

24218004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60923668-C-T

24218067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60923722-G-A

24218109-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60923761-C-G

24218111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60923763-C-T

24218404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60924164-C-T

24218418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60924177-G-A

24218426-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60924185-A-G

24218442-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60924189-T-G

24218999-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60924762-T-A

24218999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60924762-T-C

24219113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60924866-C-T

24219181-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60924938-A-T

24219225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60924981-T-C

24219326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60925081-G-A

24220015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60926100-T-C

24220015-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60926100-T-G

24220372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60926490-T-C

24220466-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60926593-G-T

24220621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60926707-C-T

24220656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60926757-A-G

24220872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60926958-G-A

24221218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60927278-G-A

24221309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60927354-A-G

24221346-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60927421-T-G

24221451-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60927520-C-G

24222483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60927991-A-G

24222483-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60927991-A-T

24222650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60928123-A-G

24222702-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60928154-G-T

24222739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60928191-G-A

24222739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60928191-G-T

http://identifiers.org/hco/13/GRCh38#24222756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60928212-C-A

24222756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60928212-C-T

24222797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60928281-C-T

24222852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 60928339-A-G

24222867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 60928354-G-A

24223001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 60928470-G-A

24223011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 60928480-G-A

24223097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 60928566-T-C

http://identifiers.org/hco/13/GRCh38#24223114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60928583-C-A

http://identifiers.org/hco/13/GRCh38#24223184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60928653-C-A

24223199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 60928668-C-T

24223208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 60928677-G-A

24223217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 60928686-G-A

24223232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 60928701-A-G

24223253-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 60928722-C-G

http://identifiers.org/hco/13/GRCh38#24223529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60928974-C-A

24223529-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 60928974-C-G

24223565-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 60929010-C-G

24223628-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 60929052-C-G

24223628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 60929052-C-T

24223649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 60929073-G-A

24223949-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 60929376-G-C

http://identifiers.org/hco/13/GRCh38#24224049-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#60929488-A-C

24224051-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 60929490-G-C

http://identifiers.org/hco/13/GRCh38#24224052-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#60929491-C-A

24224052-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 60929491-C-G

24224052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 60929491-C-T

24224441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 60929847-G-A

http://identifiers.org/hco/13/GRCh38#24224466-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60929872-C-A

24224466-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 60929872-C-G

24224466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 60929872-C-T

24224499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 60929908-G-A

24224499-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 60929908-G-T

24224526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 60929944-G-A

24224526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 60929944-G-T

24224662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 60930079-T-C

http://identifiers.org/hco/13/GRCh38#24224682-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60930103-C-A

24224682-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 60930103-C-G

24224695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 60930116-T-C

http://identifiers.org/hco/13/GRCh38#24224857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60930354-C-A

24224857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60930354-C-T

24226545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60930790-C-T

24226580-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60930823-G-T

24226621-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60930863-T-G

24226731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60930955-A-G

24226820-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60931154-G-C

24226879-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60931216-G-T

24226884-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60931221-G-C

24230828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60934770-G-A

http://identifiers.org/hco/13/GRCh38#24233668-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60937607-A-C

24233668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60937607-A-G

24234038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60937931-T-C

24234077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60937972-G-A

24234298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60939034-G-A

24234484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60939203-G-A

24245035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60940455-C-T

24245127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60940546-C-T

24245280-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60940677-G-T

http://identifiers.org/hco/13/GRCh38#24245290-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60940691-A-C

24246015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60941075-T-C

24246326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60941401-T-C

http://identifiers.org/hco/13/GRCh38#24249425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60944110-C-A

24249425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60944110-C-T

24249429-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60944115-A-T

http://identifiers.org/hco/13/GRCh38#24249459-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60944146-C-A

24249459-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60944146-C-G

24249459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60944146-C-T

24249659-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 60944348-C-G

http://identifiers.org/hco/13/GRCh38#24249689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60944378-C-A

24249757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: missense variant
orthologous variants: 60944443-G-A

24250023-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60944695-G-C

24250225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60944897-G-T

24250273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60945033-G-A

24250273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60945033-G-T

24250301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60945056-T-C

24250354-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60945150-A-T

24250477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60945305-T-C

24250724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60945557-G-T

24250854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60945845-A-G

24251471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60946640-T-C

24251636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60946792-G-A

24251860-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 5_prime_UTR_variant, missense_variant, splice_region_variant
orthologous variants: 60947016-A-G

24252055-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60947150-G-T

24252084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60947167-C-T

24252208-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60947277-G-C

24252267-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60947331-G-C

24252356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60947405-A-G

24252487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60947533-T-C

24252508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60947554-T-C

24252548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60947594-A-G

24252654-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60947694-T-A

24252757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 60947798-G-T

24254180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60949943-G-A

24254180-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60949943-G-C

24254223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60949988-A-G

24254275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 60950034-G-T

24254364-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 60950107-T-G

24254423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 60950170-T-C

24254431-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 60950178-C-G

24254431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 60950178-C-T

24254450-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60950197-G-A

24254450-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60950197-G-T

24254520-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60950253-G-A

24254520-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60950253-G-T

24254584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60950312-C-T

24254590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60950319-G-A

24254719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60950445-C-T

24254720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60950446-G-A

24255312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60951116-C-T

24255456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60951194-C-T

24255631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60951328-G-A

24255716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60951400-A-G

24255729-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60951413-C-G

24255770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60951451-T-C

24259664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60959361-C-T

24260731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60960893-C-T

24260982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60961144-A-G

24261036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60961195-G-A

24261129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60961289-G-A

24261752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60962010-G-A

24261775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60962033-A-G

24262335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60963357-G-T

24262601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60963636-G-T

24262686-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60963713-A-T

24262941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60963902-A-G

24262944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60963905-C-T

24263803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60965019-A-G

24264020-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60965227-G-C

24264034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60965239-G-T

http://identifiers.org/hco/13/GRCh38#24264057-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60965263-A-C

24264169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60965514-T-C

24264210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60965579-A-G

24264241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60965610-C-T

24264242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60965611-G-A

24264339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60965681-C-T

24270271-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60970046-T-G

http://identifiers.org/hco/13/GRCh38#24270280-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60970055-A-C

24270280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60970055-A-G

24270560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60970347-G-T

http://identifiers.org/hco/13/GRCh38#24270799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#60970550-C-A

24270800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 60970551-C-T

24270911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, splice_region_variant, undefined
orthologous variants: 60970654-G-T

24270948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, undefined
orthologous variants: 60970680-A-G

24271171-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60970805-A-T

24271359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60970970-G-A

24271385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60971007-G-A

24271620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60971194-C-T

24271700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, undefined
orthologous variants: 60971258-G-A

24271885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, undefined
orthologous variants: 60971410-G-A

24271933-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, undefined
orthologous variants: 60971457-G-C

24274257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60973837-G-A

24274479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60974031-G-A

24274547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60974079-G-A

24274712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60974220-C-T

http://identifiers.org/hco/13/GRCh38#24275362-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60975066-A-C

24275362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60975066-A-G

24275980-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60975736-A-T

24276045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60975786-T-C

24276062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60975803-G-A

http://identifiers.org/hco/13/GRCh38#24276148-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60975904-C-A

24276180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60975937-C-T

24276685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60976472-C-T

24276686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60976473-A-G

24277051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60976857-G-A

24279671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60978353-T-C

24279750-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60978429-G-T

24279783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60978458-A-G

24279847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60978499-C-T

24279859-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60978511-G-C

24279874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60978526-G-T

24280165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60978754-C-T

24280828-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60979370-A-T

24280953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, undefined
orthologous variants: 60979489-G-A

24280953-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, undefined
orthologous variants: 60979489-G-T

24281129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60979640-C-T

24281141-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60979647-T-A

24281141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60979647-T-C

24281148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60979654-G-A

24281330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60979811-T-C

24281548-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60979974-T-C

24281566-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60979992-A-T

24281567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60979993-C-T

24281624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60980026-G-T

24281648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60980050-G-A

http://identifiers.org/hco/13/GRCh38#24284114-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60983069-C-A

24284125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60983084-T-C

24284154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: synonymous variant
orthologous variants: 60983113-T-C

24284278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 60983237-G-A

24284303-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60983251-C-G

24284303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60983251-C-T

24284361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60983293-T-C

http://identifiers.org/hco/13/GRCh38#24285940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60983915-C-A

24286148-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60984099-A-T

http://identifiers.org/hco/13/GRCh38#24286155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60984106-C-A

http://identifiers.org/hco/13/GRCh38#24286179-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60984127-C-A

24286179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60984127-C-T

http://identifiers.org/hco/13/GRCh38#24286199-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60984147-A-C

24286199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60984147-A-G

http://identifiers.org/hco/13/GRCh38#24286282-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60984231-A-C

24286436-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60984389-A-T

24286520-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60984474-G-T

24286603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60984682-G-A

http://identifiers.org/hco/13/GRCh38#24286614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60984695-C-A

24286614-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60984695-C-G

24286614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60984695-C-T

24286641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60984769-A-G

24286652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60984780-A-G

24286670-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60984798-G-T

http://identifiers.org/hco/13/GRCh38#24286688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60984814-C-A

http://identifiers.org/hco/13/GRCh38#24286812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60984937-C-A

24286812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 60984937-C-T

24286911-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 60985036-C-T

24287776-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60985357-T-A

24288195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60985685-C-T

24288856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60987127-G-A

24288860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, undefined
orthologous variants: 60987131-G-A

24288860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron_variant, undefined
orthologous variants: 60987131-G-T

24288878-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60987147-T-A

http://identifiers.org/hco/13/GRCh38#24288966-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60987379-C-A

24289046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: synonymous variant
orthologous variants: 60987459-G-A

24289046-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: synonymous variant
orthologous variants: 60987459-G-T

http://identifiers.org/hco/13/GRCh38#24289209-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60987618-C-A

24289234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60987646-C-T

http://identifiers.org/hco/13/GRCh38#24289235-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60987647-A-C

24289235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60987647-A-G

24289785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60987839-G-A

24289852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60987892-A-G

24289853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60987893-A-G

24290000-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60988045-A-T

24290042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60988077-G-A

24290042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60988077-G-T

24290050-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60988085-A-T

24290115-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60988160-G-C

24290209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60988252-A-G

24290259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60988301-C-T

24290575-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60989037-G-C

http://identifiers.org/hco/13/GRCh38#24290578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60989040-C-A

24290623-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60989056-G-C

24290696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: synonymous variant
orthologous variants: 60989128-G-A

24290696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: synonymous variant
orthologous variants: 60989128-G-T

http://identifiers.org/hco/13/GRCh38#24290699-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60989131-C-A

24290699-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: synonymous variant
orthologous variants: 60989131-C-G

24290699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: synonymous variant
orthologous variants: 60989131-C-T

24290910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60989335-G-A

24290910-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60989335-G-T

http://identifiers.org/hco/13/GRCh38#24290919-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60989344-A-C

24290919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60989344-A-G

24290920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60989345-C-T

http://identifiers.org/hco/13/GRCh38#24290923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60989348-C-A

24290923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60989348-C-T

24290939-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60989362-G-C

24290939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60989362-G-T

24290954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60989382-A-G

24290954-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60989382-A-T

24290963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60989391-T-C

24290964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60989392-A-G

24293589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60990238-G-A

24294021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60990625-T-C

24294033-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60990637-G-C

24294403-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60990914-A-T

24294428-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60990937-T-A

24294538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60991047-G-A

http://identifiers.org/hco/13/GRCh38#24294613-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60991106-C-A

24294613-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60991106-C-G

24294613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60991106-C-T

24294632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60991120-T-C

24294633-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60991121-T-A

24294633-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60991121-T-G

24294687-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60991175-C-G

24294710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60991198-G-A

http://identifiers.org/hco/13/GRCh38#24294856-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60991347-C-A

24294856-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: synonymous variant
orthologous variants: 60991347-C-T

24294890-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60991378-T-A

24295011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60991486-T-C

24295945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60992230-G-A

24296313-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60992571-T-G

24296337-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60992595-A-T

24296443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60992701-T-C

24296582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60992825-C-T

24296598-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60992836-T-A

24296615-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60992853-G-T

24296654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60992910-G-A

24297515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: synonymous variant
orthologous variants: 60993813-G-A

24297515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: synonymous variant
orthologous variants: 60993813-G-T

http://identifiers.org/hco/13/GRCh38#24298582-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60995511-A-C

24298584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60995513-G-A

24298584-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60995513-G-C

24298599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60995539-G-A

http://identifiers.org/hco/13/GRCh38#24298835-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60995740-A-C

24298929-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60995815-T-A

24298993-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60995876-T-A

24298993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60995876-T-C

24299008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60995901-G-T

24299050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60995941-G-A

24299063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60995945-G-A

http://identifiers.org/hco/13/GRCh38#24299066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60995948-C-A

24299358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60996179-G-A

24299489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60996256-G-A

24299573-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60996286-G-C

24299637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60996346-G-A

24299832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60996548-C-T

24300009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60996659-C-T

24300055-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60996703-T-A

24300110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60996760-T-C

http://identifiers.org/hco/13/GRCh38#24300255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60996898-C-A

24300255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60996898-C-T

http://identifiers.org/hco/13/GRCh38#24300360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60996991-C-A

http://identifiers.org/hco/13/GRCh38#24300382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60997013-C-A

24300402-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 60997033-A-T

24300506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60997137-A-G

24300506-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: 60997137-A-T

http://identifiers.org/hco/13/GRCh38#24302566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60998292-C-A

24302614-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: synonymous variant
orthologous variants: 60998341-T-A

24302614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: synonymous variant
orthologous variants: 60998341-T-C

24302636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: synonymous variant
orthologous variants: 60998363-C-T

24302644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: synonymous variant
orthologous variants: 60998371-C-T

http://identifiers.org/hco/13/GRCh38#24302680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60998407-C-A

24302680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: synonymous variant
orthologous variants: 60998407-C-T

24302683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: synonymous variant
orthologous variants: 60998410-C-T

24302786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: 60998515-G-A

24302835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: 60998562-T-C

24302847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: 60998571-C-T

http://identifiers.org/hco/13/GRCh38#24302848-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60998572-A-C

24302855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: 60998579-G-A

24302937-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: 60998658-G-T

24302962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: 60998683-G-A

24302962-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: 60998683-G-T

24302973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: 60998690-T-C

http://identifiers.org/hco/13/GRCh38#24302993-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60998710-C-A

24302993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: 60998710-C-T

http://identifiers.org/hco/13/GRCh38#24303011-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60998721-C-A

24303018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: 60998728-G-A

24303018-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: 60998728-G-C

24303018-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: 60998728-G-T

24303020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: 60998730-G-A

24303020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: 60998730-G-T

24303053-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: 60998763-T-A

24303053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: 60998763-T-C

24303053-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: 60998763-T-G

24303096-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: 60998795-G-T

http://identifiers.org/hco/13/GRCh38#24303109-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60998802-C-A

24303122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: 60998815-A-G

24303148-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: 60998839-T-G

24303247-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: 60998952-T-A

24303247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: 60998952-T-C

24303248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: 60998953-T-C

24303248-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: 60998953-T-G

24303342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: 60999015-A-G

24303345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: 60999018-G-A

24303345-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: 60999018-G-C

24303345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: 60999018-G-T

24303430-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: 60999092-T-A

24303430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: 60999092-T-C

24303527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: 60999173-C-T

http://identifiers.org/hco/13/GRCh38#24303583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60999191-C-A

24303583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: 60999191-C-T

24303628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: 60999240-G-A

24303628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: 60999240-G-T

24303635-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: 60999247-G-T

24304328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: 60999545-A-G

24304405-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: 60999610-A-T

24304445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: 60999645-A-G

24304449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: 60999649-T-C

24304534-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: 60999734-G-T

http://identifiers.org/hco/13/GRCh38#24304574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60999747-C-A

24304574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: 60999747-C-T

http://identifiers.org/hco/13/GRCh38#24304610-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#60999786-C-A

24304610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: 60999786-C-T

24304632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: 60999808-T-C

24304643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: 60999819-A-G

24304689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: 60999840-T-C

24304689-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: 60999840-T-G

24304733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: 60999888-C-T

24304752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: 60999903-G-A

24304757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: 60999908-T-C

24304802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: 60999946-G-T

http://identifiers.org/hco/13/GRCh38#24304875-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#61000019-C-A

24304875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: 61000019-C-T

24305167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: 61000296-G-A

24305167-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: 61000296-G-T

http://identifiers.org/hco/13/GRCh38#24305199-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#61000324-A-C

24305199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: 61000324-A-G

24305277-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: 61000396-A-T

24305525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: 61000640-C-T

24305662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: 61000756-T-C

24305784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: 61000858-G-A

24306026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: 61001036-T-C

http://identifiers.org/hco/13/GRCh38#24306035-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#61001052-A-C

http://identifiers.org/hco/13/GRCh38#24306158-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#61001145-C-A

24306164-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: 61001151-A-T

24306174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: 61001161-T-C

24306239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: 61001238-A-G

24306239-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: 61001238-A-T

http://identifiers.org/hco/13/GRCh38#24306311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#61001307-C-A

http://identifiers.org/hco/13/GRCh38#24306322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#61001318-C-A

24306571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: 61001484-A-G

24306581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: 61001494-G-A

24306581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: 61001494-G-T

24306633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: 61001555-G-A

24306764-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: 61001701-T-G

24306875-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: 61001805-C-G

24306926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: 61001850-A-G

24306926-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: 61001850-A-T

24306962-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: 61001898-G-T

24307021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23222
most severe consequence: 3 prime UTR variant
orthologous variants: 61001947-G-T