90911562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97563469-T-C

90911563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97563468-G-A

90911563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97563468-G-T

90911582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97563449-T-C

90911790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97562529-G-A

90911800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97562518-T-C

90911883-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97562443-T-A

90911919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97562407-G-T

90912008-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97562330-T-A

90912017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97562321-A-G

90912263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97562107-A-G

http://identifiers.org/hco/12/GRCh38#90912264-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97562106-A-C

90912526-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97561614-C-G

90912563-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97561555-G-C

90912606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97561512-A-G

90912723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97561396-A-G

90912786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97561333-T-C

90912844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97561275-T-C

90912846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97561273-A-G

90912876-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97561242-C-G

90915673-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97559885-G-C

90915752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97559809-A-G

90915808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97559767-G-A

90915876-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97559697-T-A

90916001-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97559586-T-C

90916032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97559565-A-G

90916032-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97559565-A-T

90919909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97558935-C-T

90920040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97558808-A-G

90920040-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97558808-A-T

90920374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97558478-C-T

90920480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97558368-A-G

90920481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97558367-C-T

90920553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97558309-A-G

90920594-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97558275-A-G

90920624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97558246-T-C

90920692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97558197-T-C

http://identifiers.org/hco/12/GRCh38#90920719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97558175-C-A

90920727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97558169-C-T

90920928-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97558098-T-G

90920947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97558089-A-G

90920950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97558086-T-C

90920978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97558058-A-G

90920988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97558047-A-G

90921145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97557900-T-C

90921733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97557439-C-T

90921972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97557206-A-G

90922056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97557131-C-T

90922121-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97557063-C-G

http://identifiers.org/hco/12/GRCh38#90922257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97556929-C-A

90922717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97556479-A-G

90922759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97556437-T-C

90922906-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97556299-A-T

90922915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97556290-C-T

90922980-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97556138-T-G

90923222-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97555920-G-T

90923431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97555744-T-C

http://identifiers.org/hco/12/GRCh38#90924073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97555140-C-A

90924073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97555140-C-T

http://identifiers.org/hco/12/GRCh38#90924119-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97555082-A-C

http://identifiers.org/hco/12/GRCh38#90924217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97554984-C-A

90924217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97554984-C-T

90924218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97554983-G-A

90924218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97554983-G-T

90924481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97554725-T-C

http://identifiers.org/hco/12/GRCh38#90924523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97554681-C-A

90924582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97554622-T-C

90924804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97554351-G-A

90924866-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97554288-G-C

90924984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97554177-C-T

90925147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97554018-G-A

90925147-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97554018-G-C

90938819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97551529-G-A

90938819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97551529-G-T

http://identifiers.org/hco/12/GRCh38#90938820-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97551528-C-A

90938820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97551528-C-T

http://identifiers.org/hco/12/GRCh38#90938844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97551505-C-A

90938845-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97551504-A-T

90938848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97551501-G-A

90938890-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97551440-T-A

90938890-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97551440-T-G

90938960-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97551371-A-T

90939030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97551275-C-T

http://identifiers.org/hco/12/GRCh38#90939087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97551198-C-A

90939087-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97551198-C-G

90939087-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97551198-C-T

90939319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97550816-G-A

90939319-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97550816-G-C

http://identifiers.org/hco/12/GRCh38#90939351-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97550796-A-C

90939351-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97550796-A-T

90939373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97550779-C-T

90939381-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97550771-T-G

90939827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97550325-G-A

90939949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97550025-G-A

90939949-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97550025-G-T

90940072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97549930-T-C

90940076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97549926-T-C

90940087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97549915-A-G

90940107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97549890-A-G

90940135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97549852-T-C

90940141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 97549846-T-C

90940141-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 97549846-T-G

http://identifiers.org/hco/12/GRCh38#90940150-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97549837-C-A

90940150-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 97549837-C-G

90940150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 97549837-C-T

90940305-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97549691-A-T

90940384-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97549635-T-A

90940384-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97549635-T-G

90940404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97549616-G-A

90940404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97549616-G-T

90940442-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97549585-T-A

90940442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97549585-T-C

90940828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97549013-A-G

90940828-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97549013-A-T

90941019-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97548811-T-G

90941044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97548780-A-G

90941104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97548721-C-T

http://identifiers.org/hco/12/GRCh38#90941129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#97548697-C-A

90941148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 97548679-G-A

90941180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97548654-G-A

90941221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97548619-T-C

http://identifiers.org/hco/12/GRCh38#90941258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97548584-C-A

http://identifiers.org/hco/12/GRCh38#90941305-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97548536-A-C

90941582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97548245-G-A

90941638-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97548195-T-G

90941639-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97548194-T-A

http://identifiers.org/hco/12/GRCh38#90941690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97548143-C-A

90942040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97544496-G-A

90942298-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97544252-G-C

http://identifiers.org/hco/12/GRCh38#90942602-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97544033-A-C

90942602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97544033-A-G

90942642-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97544012-A-T

90942645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97544009-A-G

http://identifiers.org/hco/12/GRCh38#90942781-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97543919-A-C

90943134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97543603-G-T

90943263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97543486-C-T

http://identifiers.org/hco/12/GRCh38#90943299-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97543450-C-A

90943302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97543447-G-A

90943394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97543355-C-T

http://identifiers.org/hco/12/GRCh38#90943451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97543299-C-A

90943570-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97543181-A-T

90943656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97543118-G-A

90943794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97543036-T-C

90943812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97543020-T-C

90943843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97542991-T-C

90943900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97542928-T-C

90944483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97542326-A-G

90944826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97541955-T-C

90945162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97540694-G-A

90945175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97540682-T-C

90945298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97540578-A-G

90945365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97540514-T-C

90945437-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97540449-T-A

90945603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97540280-T-C

90945667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97540217-T-C

90945696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97540195-T-C

90945696-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97540195-T-G

90945901-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97540028-C-G

90945901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97540028-C-T

90946025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97539914-G-A

90946025-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97539914-G-T

90946215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97539709-T-C

90946291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97539598-A-G

http://identifiers.org/hco/12/GRCh38#90946308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97539581-C-A

90946308-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97539581-C-G

90946869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97537417-A-G

http://identifiers.org/hco/12/GRCh38#90946897-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97537389-A-C

http://identifiers.org/hco/12/GRCh38#90947021-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97537299-A-C

90947079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97537239-A-G

90947156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97537179-G-A

90947274-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97537076-C-G

90947326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97537017-G-A

90947445-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97536913-T-A

90947449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97536909-T-C

90947809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97536556-T-C

http://identifiers.org/hco/12/GRCh38#90948308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97536150-C-A

90948308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97536150-C-T

90948427-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97536031-G-C

90948480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97535978-A-G

90948571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97535909-T-C

90948791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97535691-A-G

90948827-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97535634-A-T

90948836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97535621-T-C

90948864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97535596-G-A

90949004-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97535250-T-G

90949481-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97534888-T-C

90949899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97534537-A-G

90949899-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97534537-A-T

90950340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97534137-T-C

90950454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97534033-T-C

90950495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97534000-A-G

90950703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97533665-A-G

90950966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97533329-G-A

http://identifiers.org/hco/12/GRCh38#90951194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97533123-C-A

90951229-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97533101-G-T

90951487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97532842-C-T

90952019-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97531958-G-C

90952174-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97531804-T-A

90952174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97531804-T-C

90952213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97531769-G-A

90952213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97531769-G-T

90952214-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97531768-G-C

90952214-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 97531768-G-T

http://identifiers.org/hco/12/GRCh38#90952285-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97531720-C-A

90952425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97531609-G-T

90952571-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97531470-C-G

90952597-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97531446-A-G

90952681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 97531353-T-C

90953175-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97530890-A-T

90953434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97530636-C-T

90953446-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97530624-T-C

http://identifiers.org/hco/12/GRCh38#90953795-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97530278-A-C

90953809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 97530264-C-T

90953862-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 97530208-A-T

90954109-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 97529967-C-G

90954183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 97529893-G-T

90954216-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 97529860-T-A

90954216-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 97529860-T-C

90954267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 97529809-G-A

90954267-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 97529809-G-C

90954267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 97529809-G-T

90954280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 97529796-G-A

90954280-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 97529796-G-T

http://identifiers.org/hco/12/GRCh38#90954331-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97529745-C-A

90954331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 97529745-C-T

http://identifiers.org/hco/12/GRCh38#90954346-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97529730-A-C

90954408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 97529668-T-C

90954459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 97529617-G-A

90954459-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 97529617-G-T

http://identifiers.org/hco/12/GRCh38#90954602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97529456-C-A

90954602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 97529456-C-T

90954730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 97529349-G-A

90954730-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 97529349-G-C

90954730-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 97529349-G-T

90954776-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97529303-C-G

90954776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97529303-C-T

90954801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97529276-G-T

90954840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97529243-T-C

90955064-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97529029-A-T

http://identifiers.org/hco/12/GRCh38#90955067-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#97529026-C-A

90955067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97529026-C-T

90955075-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97529018-T-A

90955075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97529018-T-C

90955075-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97529018-T-G

90955085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97529008-C-T

90955110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97528983-G-A

90955110-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28373
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 97528983-G-T