22048953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: 5 prime UTR variant
orthologous variants: 70873500-G-A

22049004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: 5 prime UTR variant
orthologous variants: 70873453-G-A

22049090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: 5 prime UTR variant
orthologous variants: 70873362-A-G

22049299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron variant
orthologous variants: 70873179-T-C

22049300-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron variant
orthologous variants: 70873178-C-G

22049300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron variant
orthologous variants: 70873178-C-T

22049301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron variant
orthologous variants: 70873177-C-T

22049358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron variant
orthologous variants: 70873121-G-T

22049394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron variant
orthologous variants: 70873115-G-A

22049560-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron variant
orthologous variants: 70872956-G-C

22049560-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron variant
orthologous variants: 70872956-G-T

22049979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron variant
orthologous variants: 70872686-C-T

22050216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron variant
orthologous variants: 70872443-G-A

22050562-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron variant
orthologous variants: 70872125-C-G

22050735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron variant
orthologous variants: 70871961-C-T

22053419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron variant
orthologous variants: 70867789-G-T

22053514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron variant
orthologous variants: 70867684-G-A

22053514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron variant
orthologous variants: 70867684-G-T

22053531-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron variant
orthologous variants: 70867667-G-T

http://identifiers.org/hco/8/GRCh38#22053577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70867632-C-A

22053577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70867632-C-T

22053626-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70867609-C-G

http://identifiers.org/hco/8/GRCh38#22053681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70867548-C-A

22053681-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70867548-C-G

22053681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70867548-C-T

22053747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70867485-G-A

22053747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70867485-G-T

22053752-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70867480-T-A

22053865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70867379-G-A

22053865-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70867379-G-C

22053865-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70867379-G-T

22053969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70867265-G-A

22054156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70867089-C-T

22054190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70867064-G-A

22054526-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70866769-T-G

22054594-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70866701-T-A

http://identifiers.org/hco/8/GRCh38#22054645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70866665-C-A

22054645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70866665-C-T

http://identifiers.org/hco/8/GRCh38#22054663-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70866647-C-A

22054663-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70866647-C-T

http://identifiers.org/hco/8/GRCh38#22054810-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70866545-C-A

http://identifiers.org/hco/8/GRCh38#22055116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70866247-C-A

22055128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70866234-A-G

22055128-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70866234-A-T

22055354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70866011-G-A

22055354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70866011-G-T

22055455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70865910-G-A

22055455-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70865910-G-T

22055557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70865815-T-C

22055691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70865672-T-C

22055788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70865551-T-C

22055971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70865293-G-A

22056062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70865218-A-G

22056062-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70865218-A-T

22056227-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70865067-G-T

22056360-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70864931-C-G

22056369-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70864922-G-C

http://identifiers.org/hco/8/GRCh38#22056545-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70864771-A-C

22056598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70864739-G-A

22056619-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70864716-A-G

22056784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70864529-A-G

22056799-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70864511-C-G

22056799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70864511-C-T

22056911-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 70864402-A-G

http://identifiers.org/hco/8/GRCh38#22056955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70864358-C-A

22057001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 70864313-G-A

22057081-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 70864231-A-T

22057366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70863934-C-T

22057743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70863575-A-G

22057763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70863555-A-G

22057808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70863523-G-A

22057808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70863523-G-T

http://identifiers.org/hco/8/GRCh38#22057809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70863522-C-A

22057809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70863522-C-T

22057991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70863373-G-T

http://identifiers.org/hco/8/GRCh38#22057998-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70863366-A-C

22057998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70863366-A-G

22058187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70863117-G-A

22059182-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 70862157-G-T

http://identifiers.org/hco/8/GRCh38#22059628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70861811-C-A

22059964-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70861515-G-T

22060364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70861113-T-C

22060364-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70861113-T-G

22064336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70859028-A-G

22064614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70858714-A-G

22064615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70858713-C-T

22064669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70858625-A-G

22064687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70858592-T-C

22064735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70858532-G-A

22064738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70858529-G-A

http://identifiers.org/hco/8/GRCh38#22064967-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70858349-A-C

22064967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70858349-A-G

22066567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70855936-T-C

22066593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70855905-G-A

22066593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70855905-G-T

22066658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 70855885-G-A

http://identifiers.org/hco/8/GRCh38#22066825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70855741-C-A

22066825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 70855741-C-T

22066839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 70855727-G-A

22066839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 70855727-G-T

22066911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70855658-G-A

22066911-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70855658-G-C

22066911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70855658-G-T

http://identifiers.org/hco/8/GRCh38#22066941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#70855625-C-A

22066941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70855625-C-T

22066945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70855621-T-C

http://identifiers.org/hco/8/GRCh38#22067167-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70855385-C-A

22067167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 70855385-C-T

22067203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70855351-G-A

22067203-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70855351-G-C

22067203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70855351-G-T

22067259-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70855305-G-C

22067259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70855305-G-T

22067263-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70855301-T-A

22067263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70855301-T-C

22067263-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70855301-T-G

22067328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70855223-C-T

22067413-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70854989-A-T

22067498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70854908-A-G

22067688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70854717-G-A

22067691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70854714-G-A

22067691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70854714-G-T

22067696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70854709-T-C

22067699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70854706-T-C

22067699-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70854706-T-G

http://identifiers.org/hco/8/GRCh38#22067703-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70854702-C-A

22067703-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70854702-C-G

22067703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70854702-C-T

22067740-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70854682-T-G

22068067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70854450-G-A

22068343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70854287-A-G

22068556-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70854146-G-C

22068860-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70853715-G-C

http://identifiers.org/hco/8/GRCh38#22068903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70853662-C-A

22068947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70853615-T-C

http://identifiers.org/hco/8/GRCh38#22069123-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70853466-C-A

22069123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70853466-C-T

http://identifiers.org/hco/8/GRCh38#22069199-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70853385-C-A

22069199-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70853385-C-G

22069199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70853385-C-T

22069240-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70853346-T-A

22069240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70853346-T-C

22069312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70853258-G-A

22069312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70853258-G-T

http://identifiers.org/hco/8/GRCh38#22069314-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70853256-A-C

22069327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70853245-G-A

22069327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70853245-G-T

22069342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70853230-G-A

22069342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70853230-G-T

22069361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 70853211-T-C

22069532-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70853035-G-A

22069532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70853035-G-T

22069739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70852841-G-A

22069743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70852837-G-A

22069743-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70852837-G-C

22069744-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70852836-G-C

22069744-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70852836-G-T

22069763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70852825-G-A

22069763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70852825-G-T

22069803-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70852811-T-A

22069959-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70852650-C-G

22069959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70852650-C-T

22069998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70852619-T-C

22069998-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70852619-T-G

22070009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70852608-G-A

22070032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70852589-A-G

22070110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70852519-G-A

22070110-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70852519-G-C

22070110-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70852519-G-T

22070111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 70852518-G-A

22070131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 70852486-A-G

http://identifiers.org/hco/8/GRCh38#22070229-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70852386-A-C

22070229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 70852386-A-G

http://identifiers.org/hco/8/GRCh38#22070262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70852353-C-A

22070343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron variant
orthologous variants: 70852271-G-A

http://identifiers.org/hco/8/GRCh38#22070375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70852242-C-A

22070375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron variant
orthologous variants: 70852242-C-T

22070398-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron variant
orthologous variants: 70852219-T-A

22070398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron variant
orthologous variants: 70852219-T-C

22070399-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron variant
orthologous variants: 70852218-C-G

22070399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron variant
orthologous variants: 70852218-C-T

22070451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron variant
orthologous variants: 70852171-G-A

22070451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron variant
orthologous variants: 70852171-G-T

22070454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron variant
orthologous variants: 70852168-T-C

http://identifiers.org/hco/8/GRCh38#22070473-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70852157-C-A

22070473-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron variant
orthologous variants: 70852157-C-G

22070473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron variant
orthologous variants: 70852157-C-T

22070475-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron variant
orthologous variants: 70852155-C-T

http://identifiers.org/hco/8/GRCh38#22072478-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70850703-C-A

22072478-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron variant
orthologous variants: 70850703-C-G

22072478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron variant
orthologous variants: 70850703-C-T

22072924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron variant
orthologous variants: 70850580-T-C

22072943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron variant
orthologous variants: 70850561-C-T

22072954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron variant
orthologous variants: 70850550-A-G

22072954-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron variant
orthologous variants: 70850550-A-T

22073014-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron variant
orthologous variants: 70850493-T-A

22073150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron variant
orthologous variants: 70850409-G-A

22073299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron variant
orthologous variants: 70850292-A-G

22073701-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron variant
orthologous variants: 70850240-T-G

22073778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: missense variant
orthologous variants: 70850163-T-C

22073817-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: missense variant
orthologous variants: 70850124-C-G

22073817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: missense variant
orthologous variants: 70850124-C-T

http://identifiers.org/hco/8/GRCh38#22073888-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70850044-C-A

22073901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron variant
orthologous variants: 70850031-T-C

22073906-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron variant
orthologous variants: 70850026-T-A

22073919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron variant
orthologous variants: 70850013-A-G

http://identifiers.org/hco/8/GRCh38#22073929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70850004-C-A

22073929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron variant
orthologous variants: 70850004-C-T

http://identifiers.org/hco/8/GRCh38#22073952-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70849978-C-A

22073952-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron variant
orthologous variants: 70849978-C-G

22073952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron variant
orthologous variants: 70849978-C-T

22073972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron variant
orthologous variants: 70849961-A-G

22073973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron variant
orthologous variants: 70849960-G-A

22073973-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron variant
orthologous variants: 70849960-G-T

22074199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron variant
orthologous variants: 70849755-C-T

22074200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron variant
orthologous variants: 70849754-G-A

22074201-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron variant
orthologous variants: 70849753-C-T

22079846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron variant
orthologous variants: 70843660-T-C

http://identifiers.org/hco/8/GRCh38#22080054-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70843493-C-A

22080054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron variant
orthologous variants: 70843493-C-T

22080103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron variant
orthologous variants: 70843474-G-A

22080103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron variant
orthologous variants: 70843474-G-T

22080137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron variant
orthologous variants: 70843440-A-G

22080152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron variant
orthologous variants: 70843426-G-T

22080162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron variant
orthologous variants: 70843416-C-T

http://identifiers.org/hco/8/GRCh38#22080163-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70843415-C-A

22080231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: missense variant
orthologous variants: 70843345-C-T

22080493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron variant
orthologous variants: 70843102-G-A

22080497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron variant
orthologous variants: 70843098-G-A

22080725-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron variant
orthologous variants: 70842882-G-C

22080987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron variant
orthologous variants: 70842610-G-T

22081062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron variant
orthologous variants: 70842534-G-A

22081062-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron variant
orthologous variants: 70842534-G-C

22081062-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron variant
orthologous variants: 70842534-G-T

http://identifiers.org/hco/8/GRCh38#22081068-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70842526-C-A

http://identifiers.org/hco/8/GRCh38#22081232-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70842367-C-A

22081232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron variant
orthologous variants: 70842367-C-T

22081311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: intron variant
orthologous variants: 70842309-T-C

22081350-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 70842292-A-G

22081550-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: 3 prime UTR variant
orthologous variants: 70842032-T-G

22081699-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: 3 prime UTR variant
orthologous variants: 70841893-T-A

22081699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: 3 prime UTR variant
orthologous variants: 70841893-T-C

22081729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: 3 prime UTR variant
orthologous variants: 70841869-G-T

22081732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: 3 prime UTR variant
orthologous variants: 70841866-C-T

http://identifiers.org/hco/8/GRCh38#22082055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70841557-C-A

22082055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: 3 prime UTR variant
orthologous variants: 70841557-C-T

http://identifiers.org/hco/8/GRCh38#22082370-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70841278-C-A

22082480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: 3 prime UTR variant
orthologous variants: 70841152-G-A

22082480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: 3 prime UTR variant
orthologous variants: 70841152-G-T

http://identifiers.org/hco/8/GRCh38#22082483-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#70841149-A-C

22082483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: 3 prime UTR variant
orthologous variants: 70841149-A-G

22082518-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3382
most severe consequence: 3 prime UTR variant
orthologous variants: 70841117-G-T