41307273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: 3 prime UTR variant
orthologous variants: 4610450-G-T

41307416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: 3 prime UTR variant
orthologous variants: 4610314-T-C

41307477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: 3 prime UTR variant
orthologous variants: 4610251-T-C

http://identifiers.org/hco/5/GRCh38#41307660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4610107-C-A

http://identifiers.org/hco/5/GRCh38#41307669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4610098-C-A

41307874-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: 3 prime UTR variant
orthologous variants: 4609897-G-T

41307907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: 3 prime UTR variant
orthologous variants: 4609864-G-T

41308029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: 3 prime UTR variant
orthologous variants: 4609742-T-C

41308163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: 3 prime UTR variant
orthologous variants: 4609628-G-A

41308163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: 3 prime UTR variant
orthologous variants: 4609628-G-T

http://identifiers.org/hco/5/GRCh38#41308170-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4609621-C-A

41308170-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: 3 prime UTR variant
orthologous variants: 4609621-C-G

41308175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: 3 prime UTR variant
orthologous variants: 4609616-T-C

41308184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: 3 prime UTR variant
orthologous variants: 4609608-C-T

41308349-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: 3 prime UTR variant
orthologous variants: 4609439-G-T

41308450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: 3 prime UTR variant
orthologous variants: 4609338-T-C

41308474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: 3 prime UTR variant
orthologous variants: 4609321-G-T

41308576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: 3 prime UTR variant
orthologous variants: 4609242-A-G

41308724-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: 3 prime UTR variant
orthologous variants: 4609093-T-G

41308774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: 3 prime UTR variant
orthologous variants: 4609028-C-T

41308813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: 3 prime UTR variant
orthologous variants: 4609001-A-G

41308821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: 3 prime UTR variant
orthologous variants: 4608993-T-C

41308890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: 3 prime UTR variant
orthologous variants: 4608915-A-G

http://identifiers.org/hco/5/GRCh38#41309140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4608659-C-A

41309214-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: 3 prime UTR variant
orthologous variants: 4608586-T-G

41309319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: 3 prime UTR variant
orthologous variants: 4608489-T-C

41309877-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: 3 prime UTR variant
orthologous variants: 4607927-A-T

41309954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: 3 prime UTR variant
orthologous variants: 4607845-T-C

41310011-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: 3 prime UTR variant
orthologous variants: 4607788-T-A

41310015-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: 3 prime UTR variant
orthologous variants: 4607784-T-G

41310087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: 3 prime UTR variant
orthologous variants: 4607667-A-G

41310113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: 3 prime UTR variant
orthologous variants: 4607643-T-C

http://identifiers.org/hco/5/GRCh38#41310294-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4607476-C-A

41310538-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: 3 prime UTR variant
orthologous variants: 4607256-G-C

41310538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: 3 prime UTR variant
orthologous variants: 4607256-G-T

41310638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: 3 prime UTR variant
orthologous variants: 4607185-C-T

41310716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: 3 prime UTR variant
orthologous variants: 4607107-A-G

41310779-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: 3 prime UTR variant
orthologous variants: 4607061-G-T

41310817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: 3 prime UTR variant
orthologous variants: 4607019-C-T

http://identifiers.org/hco/5/GRCh38#41311011-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4606811-C-A

41311037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: 3 prime UTR variant
orthologous variants: 4606785-G-T

41311062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: 3 prime UTR variant
orthologous variants: 4606760-A-G

41311209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: 3 prime UTR variant
orthologous variants: 4606644-T-C

41311279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: 3 prime UTR variant
orthologous variants: 4606573-G-A

41311279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: 3 prime UTR variant
orthologous variants: 4606573-G-T

41311403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: 3 prime UTR variant
orthologous variants: 4606456-C-T

41311493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: 3 prime UTR variant
orthologous variants: 4606258-G-A

41311553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: 3 prime UTR variant
orthologous variants: 4606156-G-T

41311846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: 3 prime UTR variant
orthologous variants: 4605899-T-C

41311932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: 3 prime UTR variant
orthologous variants: 4605812-G-A

41312053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: 3 prime UTR variant
orthologous variants: 4605689-T-C

41312115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: 3 prime UTR variant
orthologous variants: 4605645-G-A

41312115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: 3 prime UTR variant
orthologous variants: 4605645-G-T

41312161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: 3 prime UTR variant
orthologous variants: 4605587-T-C

41312171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: 3 prime UTR variant
orthologous variants: 4605577-T-C

41312313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: 3 prime UTR variant
orthologous variants: 4605454-G-A

http://identifiers.org/hco/5/GRCh38#41312409-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4605369-C-A

41312759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: 3 prime UTR variant
orthologous variants: 4605224-C-T

41312984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: 3 prime UTR variant
orthologous variants: 4604988-A-G

41313235-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: 3 prime UTR variant
orthologous variants: 4604738-G-T

41313283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: 3 prime UTR variant
orthologous variants: 4604688-A-G

41313283-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: 3 prime UTR variant
orthologous variants: 4604688-A-T

41313348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: 3 prime UTR variant
orthologous variants: 4604623-A-G

http://identifiers.org/hco/5/GRCh38#41313467-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4604507-A-C

41313696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: missense variant
orthologous variants: 4604278-T-C

41313738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: missense variant
orthologous variants: 4604236-G-A

http://identifiers.org/hco/5/GRCh38#41313784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4604190-C-A

41313784-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4604190-C-G

41313784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4604190-C-T

http://identifiers.org/hco/5/GRCh38#41313883-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4604108-A-C

41313883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4604108-A-G

41323704-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4598927-T-A

41323848-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4598805-C-T

41324193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4598506-T-C

http://identifiers.org/hco/5/GRCh38#41324381-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4598172-C-A

41324381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4598172-C-T

41324538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4598026-T-C

41324634-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4597935-T-A

41324740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4597838-C-T

41324812-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4597765-A-T

http://identifiers.org/hco/5/GRCh38#41324847-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4597731-A-C

41324863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4597715-A-G

41324957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4597626-T-C

41325119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4597447-G-A

http://identifiers.org/hco/5/GRCh38#41325340-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4597217-C-A

41325399-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4597161-A-T

41329312-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4595050-A-T

http://identifiers.org/hco/5/GRCh38#41329667-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4594714-C-A

41329667-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4594714-C-G

41329667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4594714-C-T

41329691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4594693-T-C

41329773-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4594620-T-A

41329965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4594454-T-C

41333636-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4591961-T-G

41333639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4591958-T-C

41334290-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4591628-C-T

41334398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4591540-A-G

41334529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4591409-C-T

41334786-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4591164-T-G

41334835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4591115-T-C

41334897-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4591054-T-A

41334938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4591013-A-G

41336663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4587647-G-A

41336735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4587579-G-A

41336735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4587579-G-T

41337082-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4587212-G-C

41337180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4587116-G-A

41337264-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4587003-C-G

41337304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4586882-A-G

http://identifiers.org/hco/5/GRCh38#41337326-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4586817-C-A

41337326-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4586817-C-G

41337471-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4586635-T-A

41337599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4585690-G-A

41338114-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4585188-T-A

41338114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4585188-T-C

41338166-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4585135-T-A

http://identifiers.org/hco/5/GRCh38#41338423-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4584883-C-A

http://identifiers.org/hco/5/GRCh38#41338621-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4584683-C-A

41338621-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4584683-C-G

41338621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4584683-C-T

41338635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4584669-A-G

41338925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4584403-G-A

41338973-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4584319-G-T

http://identifiers.org/hco/5/GRCh38#41339275-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4583886-A-C

41339336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4583825-G-A

41339705-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4583455-G-C

41339768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4583378-T-C

http://identifiers.org/hco/5/GRCh38#41340075-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4583012-A-C

http://identifiers.org/hco/5/GRCh38#41340095-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4582990-A-C

41340254-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4582726-C-T

41340303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4582676-C-T

41340304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4582675-T-C

41340602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4582417-T-C

41340605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4582414-C-T

41340610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4582409-C-T

41341276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4581775-C-T

41341348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4581712-C-T

41341380-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4581680-A-T

41341414-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4581651-T-A

http://identifiers.org/hco/5/GRCh38#41341757-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4581365-A-C

41342036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4580757-C-T

41342190-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4580626-A-T

41342212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4580604-C-T

41342535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4580298-A-G

41342977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4579859-T-C

http://identifiers.org/hco/5/GRCh38#41342980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4579856-C-A

41343018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4579811-G-A

http://identifiers.org/hco/5/GRCh38#41343083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4579746-C-A

41343390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4579440-T-C

41344014-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4578296-A-T

41344051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4578259-A-G

http://identifiers.org/hco/5/GRCh38#41344090-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4578220-A-C

http://identifiers.org/hco/5/GRCh38#41344096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4578214-C-A

41344474-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4577836-T-A

41344527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4577785-A-G

41345035-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4577291-T-G

41345671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4576718-C-T

41349552-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4575858-C-G

41349600-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4575812-T-G

41349884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4575534-A-G

41350041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4575410-T-C

41350091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4575361-C-T

41350222-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4574927-C-G

41350222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4574927-C-T

41350379-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4574747-T-A

41350688-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4574423-C-G

41350688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4574423-C-T

41350711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4574399-G-A

41350811-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4574301-T-A

41350811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4574301-T-C

41350847-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4574252-G-A

41351815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4570858-G-A

41351815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4570858-G-T

41351951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4570708-A-G

41353834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4567530-C-T

41354019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4567363-T-C

41354143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4567247-T-C

41354353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4567067-C-T

41354354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4567066-T-C

41354354-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4567066-T-G

41354366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4567054-C-T

41354417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4567005-T-C

41354417-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4567005-T-G

41354458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4566947-C-T

41354749-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4566650-T-A

41354796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4566613-A-G

41354796-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4566613-A-T

41354969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4566466-C-T

41355227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4566231-C-T

41355257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4566200-A-G

41355473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4565989-C-T

41355542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4565924-C-T

http://identifiers.org/hco/5/GRCh38#41356386-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4565177-A-C

41356592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4565004-G-A

41356592-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4565004-G-C

41356593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4565003-A-G

41356747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4564927-C-T

41357043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4564685-A-G

41357113-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4564643-A-T

41357200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4564564-G-A

41357322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4564465-T-C

41357593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4564209-T-C

41363440-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4563760-A-T

41363748-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4563452-C-G

41363762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4563438-G-A

41363767-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4563429-A-T

41363983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4563217-G-A

41363983-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4563217-G-C

41364169-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4563056-G-C

http://identifiers.org/hco/5/GRCh38#41364644-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4562575-C-A

http://identifiers.org/hco/5/GRCh38#41364780-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4562439-A-C

http://identifiers.org/hco/5/GRCh38#41364799-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4562421-A-C

41364881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4562341-G-A

41365058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4562176-C-T

41365067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4562167-A-G

41365261-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4561595-G-T

41365348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4561504-C-T

41365390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4561470-T-C

41365509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4561352-G-A

41365509-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4561352-G-T

41365658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4561175-G-A

http://identifiers.org/hco/5/GRCh38#41365734-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4561073-C-A

41365734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4561073-C-T

41366252-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4560966-G-C

41366292-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4560918-C-G

41366340-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4560870-T-A

41366373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4560838-C-T

41366427-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4560799-A-T

41366462-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4560764-G-C

41368974-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4560466-T-A

http://identifiers.org/hco/5/GRCh38#41369102-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4560352-A-C

41369122-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4560335-G-C

41369337-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4560141-T-A

41369809-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4559992-T-A

41369889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4559912-G-A

41369967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4559832-A-G

41370133-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4559661-A-T

41370243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4559545-A-G

41370244-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4559544-T-A

http://identifiers.org/hco/5/GRCh38#41370322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4559469-C-A

41370766-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4558946-T-G

41370892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4558771-A-G

41370913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4558751-G-T

41371107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4558540-C-T

41371215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4558428-T-C

41371527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4558076-T-C

41373673-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4555525-C-G

41374226-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4554994-A-G

41374303-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4554919-T-A

41374648-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4554561-T-A

41374648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4554561-T-C

41374702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4554503-C-T

41374826-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4554406-G-C

41375110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4554171-A-G

41375223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4554105-T-C

41375363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4553973-G-T

41375394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4553938-T-C

41376176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4553349-G-T

41376259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4553258-G-A

41376329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4553210-T-C

41376692-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4551679-C-G

41376747-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4551625-T-A

41376747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4551625-T-C

41376795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4551581-G-A

41376902-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4551477-A-T

41376996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4551385-T-C

41377071-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4551268-C-T

41377210-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4551071-T-A

41377357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4550928-G-A

41377357-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4550928-G-T

41377412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4550894-T-C

41377541-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4550752-G-C

41377548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4550745-G-A

41377548-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4550745-G-C

http://identifiers.org/hco/5/GRCh38#41377913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4550441-C-A

41377996-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4550363-T-G

41378031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4550328-C-T

41378174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4550196-A-G

41378228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4550141-G-A

41378288-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4550065-T-A

http://identifiers.org/hco/5/GRCh38#41378456-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4549770-C-A

41378456-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4549770-C-T

41378459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4549767-T-C

41378541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4549681-T-C

41378718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4549505-A-G

41378745-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4549481-G-C

http://identifiers.org/hco/5/GRCh38#41378749-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4549477-A-C

41378773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4549453-C-T

41378810-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4549415-C-G

41379327-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4549089-G-T

41379363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4549049-G-A

41379550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4548919-A-G

41379550-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4548919-A-T

41379670-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4548695-T-A

41379863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4548523-T-C

41379898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4548488-A-G

41379899-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4548487-T-A

41379899-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4548487-T-C

41379967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4548421-A-G

41380037-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4548357-T-G

41380068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4548326-C-T

41380190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4548206-T-C

http://identifiers.org/hco/5/GRCh38#41380399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4548014-C-A

41380775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4547674-C-T

41380805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4547647-G-T

41381047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4547369-T-C

41381700-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4546928-T-A

41381701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4546927-A-G

41381737-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4546899-A-G

41381737-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4546899-A-T

41381741-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4546894-A-T

41381753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4546882-T-C

41381756-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4546879-T-A

http://identifiers.org/hco/5/GRCh38#41381762-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4546873-A-C

41381762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4546873-A-G

41381762-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4546873-A-T

41381780-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4546853-A-T

41382027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: missense variant
orthologous variants: 4546606-G-T

41382159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: missense variant
orthologous variants: 4546474-T-C

http://identifiers.org/hco/5/GRCh38#41382612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4546022-C-A

41382612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4546022-C-T

41382657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4545975-A-G

41382657-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4545975-A-T

41382663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4545969-G-A

41382675-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4545957-G-C

41382675-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4545957-G-T

41382904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4545730-T-C

41383062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 4544962-G-A

41383368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4544671-T-C

http://identifiers.org/hco/5/GRCh38#41383515-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4544530-C-A

41383587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4544458-T-C

41383587-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4544458-T-G

41383852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4544253-G-T

41384056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4544051-A-G

41384136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4543971-C-T

41384204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4543900-C-T

41384295-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4543808-T-A

41384661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4542301-C-T

41384694-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4542276-A-T

41384877-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4542088-T-G

http://identifiers.org/hco/5/GRCh38#41385178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4541801-C-A

41385178-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4541801-C-G

41385228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4541755-C-T

41404199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron_variant, undefined
orthologous variants: 4539605-G-A

41404237-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron_variant, undefined
orthologous variants: 4539548-G-C

41404446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron_variant, undefined
orthologous variants: 4539327-C-T

41404449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron_variant, undefined
orthologous variants: 4539324-T-C

http://identifiers.org/hco/5/GRCh38#41405092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#4538749-C-A

41405386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron_variant, undefined
orthologous variants: 4538483-A-G

41405569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron_variant, undefined
orthologous variants: 4538305-G-A

http://identifiers.org/hco/5/GRCh38#41406073-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#4537543-C-A

41406163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron_variant, undefined
orthologous variants: 4537482-C-T

41406431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron_variant, undefined
orthologous variants: 4537255-T-C

41406468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron_variant, undefined
orthologous variants: 4537224-A-G

41406611-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron_variant, undefined
orthologous variants: 4537013-C-G

41406684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron_variant, undefined
orthologous variants: 4536805-G-A

41406756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron_variant, undefined
orthologous variants: 4536739-C-T

41406803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron_variant, undefined
orthologous variants: 4536704-G-T

41407158-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron_variant, undefined
orthologous variants: 4536372-T-G

41407170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron_variant, undefined
orthologous variants: 4536360-T-C

41407586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron_variant, undefined
orthologous variants: 4535946-T-C

41407638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron_variant, undefined
orthologous variants: 4535897-C-T

41407717-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron_variant, undefined
orthologous variants: 4535819-T-A

41407867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron_variant, undefined
orthologous variants: 4535667-T-C

41408271-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron_variant, undefined
orthologous variants: 4534240-G-T

41408365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron_variant, undefined
orthologous variants: 4534156-C-T

41408532-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron_variant, undefined
orthologous variants: 4533933-G-C

41408801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron_variant, undefined
orthologous variants: 4533695-A-G

41408925-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron_variant, undefined
orthologous variants: 4533569-G-C

41409059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron_variant, undefined
orthologous variants: 4533438-T-C

41409087-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron_variant, undefined
orthologous variants: 4533405-G-C

41409252-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4533237-C-T

41409277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4533209-C-T

41410474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4532326-G-A

41410474-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4532326-G-C

41410567-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4532228-C-G

41410567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4532228-C-T

41410647-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4532146-T-G

41410896-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4531898-T-A

41410925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron_variant, undefined
orthologous variants: 4531872-C-T

41411044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4531756-A-G

41411705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4531099-T-C

http://identifiers.org/hco/5/GRCh38#41412325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4530882-C-A

41412834-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4530164-C-G

41412834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4530164-C-T

http://identifiers.org/hco/5/GRCh38#41413813-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4529677-C-A

41413857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4529625-T-C

41413880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4529603-G-A

41413888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4529595-G-A

41415269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4529019-A-G

http://identifiers.org/hco/5/GRCh38#41415289-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4528994-C-A

http://identifiers.org/hco/5/GRCh38#41415638-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4528647-A-C

41416483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4527799-T-C

41416585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4527697-T-C

http://identifiers.org/hco/5/GRCh38#41417591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4526944-C-A

41417591-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4526944-C-G

41417618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4526917-A-G

41417621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4526914-T-C

41417687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4526856-G-A

41417750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4526807-G-A

41417963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4525649-G-A

41417963-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4525649-G-C

41418671-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4524948-C-G

41418815-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4524810-A-T

41419010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron_variant, undefined
orthologous variants: 4524659-G-A

41419103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron_variant, undefined
orthologous variants: 4524582-A-G

41419140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron_variant, undefined
orthologous variants: 4524548-A-G

41419408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4523786-G-T

41419450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4523746-A-G

41420422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4522923-G-T

41422108-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4521624-G-T

41422280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4521487-A-G

41422471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4521340-A-G

41422480-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4521331-T-G

41422734-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4521093-T-G

41422828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4521006-C-T

http://identifiers.org/hco/5/GRCh38#41422850-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4520996-A-C

41423338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4520518-G-A

41423382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4520475-T-C

41423493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4520383-T-C

41423601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4520335-G-A

41423874-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4520193-G-A

41423973-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4519972-T-G

41425349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4518821-G-A

41430082-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4506200-A-T

41430090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4506192-G-A

41430272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4506049-C-T

41430392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4505965-T-C

41430517-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4505832-G-A

41430529-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4505820-G-C

41430543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4505806-G-A

http://identifiers.org/hco/5/GRCh38#41430969-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4504551-A-C

41431045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4504493-A-G

41431096-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4504444-G-C

41431113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4504422-T-C

41431326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4504239-T-C

41431408-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4504148-T-A

41431576-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4503982-C-G

41431576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4503982-C-T

41431597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4503961-T-C

41431610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4503948-C-T

41432197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4503504-C-T

41432380-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4503324-T-A

41432380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4503324-T-C

41432420-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4503285-G-C

41432636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4493290-C-T

41432891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4492194-G-A

http://identifiers.org/hco/5/GRCh38#41433015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4492081-C-A

41433015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4492081-C-T

41433016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4492080-G-A

41433086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4492002-C-T

41433396-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4491732-A-T

41433635-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4491506-T-C

41433693-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4491448-A-T

41433729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4491411-G-A

41433729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4491411-G-T

41433788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4491354-T-C

41433810-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4491328-G-T

41433854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4491284-C-T

http://identifiers.org/hco/5/GRCh38#41433982-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4491144-C-A

41433984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4491142-A-G

41434357-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4490786-T-G

http://identifiers.org/hco/5/GRCh38#41434518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4490657-C-A

41434744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4490449-T-C

41434770-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4490422-G-C

41435272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4489955-C-T

http://identifiers.org/hco/5/GRCh38#41435377-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4489863-A-C

41435426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4489742-T-C

41436095-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4481913-G-C

41436110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4481906-C-T

41436447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4481589-T-C

41436548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4481493-C-T

41436911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4481047-G-A

41437744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4478984-G-A

41438166-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4478564-T-G

http://identifiers.org/hco/5/GRCh38#41438187-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4478541-A-C

41438200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4478528-A-G

41438884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4477834-T-C

41438992-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4477751-A-T

http://identifiers.org/hco/5/GRCh38#41439139-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4477619-C-A

41439139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4477619-C-T

41439289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4477472-A-G

41439415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4477353-A-G

41439499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4477272-A-G

41439539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4477238-T-C

http://identifiers.org/hco/5/GRCh38#41439555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4477225-C-A

41439555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4477225-C-T

41444057-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4472388-C-G

41444171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4472274-T-C

41444960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4471060-T-C

41444988-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4471031-T-A

41445040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4470980-T-C

41445041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4470979-G-A

41445242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4470782-T-C

41445277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4470747-T-C

41445277-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4470747-T-G

41446286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4470298-G-T

41446288-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4470296-A-T

41446333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4470251-T-C

41446977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4469921-A-G

41446986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4469912-A-G

41447011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4469887-A-G

41447019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4469879-A-G

41447677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4469213-T-C

41447978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4468919-A-G

41448236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4468699-G-A

41448993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4465738-T-C

http://identifiers.org/hco/5/GRCh38#41449004-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4465725-A-C

41450018-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4464838-A-T

41450753-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4463894-G-T

http://identifiers.org/hco/5/GRCh38#41450906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4463743-C-A

41450993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4463662-C-T

41450995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4463660-C-T

41451238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4463440-T-C

41451431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4463059-T-C

41451631-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4462883-T-A

41451807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4462563-G-A

41452049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4462328-G-A

41452100-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4461922-T-C

41452100-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4461922-T-G

41452198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4461827-G-A

41452751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4461337-A-G

41452867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4460787-T-C

41452988-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4460679-T-G

41456353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4459705-C-T

41456441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4459629-A-G

41456505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4459558-T-C

41456507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4459556-G-A

41456507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4459556-G-T

41456558-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4458626-A-T

41456571-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4458613-G-T

41456584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4458600-C-T

41456619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4458582-T-C

http://identifiers.org/hco/5/GRCh38#41457022-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4458191-A-C

http://identifiers.org/hco/5/GRCh38#41457129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4458086-C-A

41457394-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4457891-G-C

41457682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4457657-C-T

41457704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4457633-A-G

http://identifiers.org/hco/5/GRCh38#41457770-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4457567-A-C

41457774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4457563-G-A

41457947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4457360-G-A

41457947-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4457360-G-C

41458196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4457108-T-C

41458252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4457055-T-C

41458524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4456819-T-C

http://identifiers.org/hco/5/GRCh38#41459072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4456388-C-A

http://identifiers.org/hco/5/GRCh38#41459193-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4456242-A-C

http://identifiers.org/hco/5/GRCh38#41459504-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4455943-A-C

41459505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4455942-C-T

41459519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4455913-G-A

41459765-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4455385-C-G

http://identifiers.org/hco/5/GRCh38#41460090-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4454995-A-C

41460090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4454995-A-G

41460457-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4454655-G-C

http://identifiers.org/hco/5/GRCh38#41460588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4454391-C-A

41460588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4454391-C-T

41460630-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4454354-C-G

41460814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4454170-G-A

41460902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4454109-C-T

41461699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4453121-C-T

41462210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4452493-G-A

41462456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4452241-G-A

41462635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4452056-G-A

41462635-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4452056-G-T

41463621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4451047-T-C

41463634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4451035-T-C

41463639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4451030-G-A

41463639-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4451030-G-T

41463676-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4450989-C-G

41463735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4450931-G-A

http://identifiers.org/hco/5/GRCh38#41463775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4450894-C-A

41464611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4442048-G-A

41464915-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4441754-G-T

41465228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4441466-T-C

41465310-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4441374-A-T

41465338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4441347-C-T

41465355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4441332-T-C

41465359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4441328-T-C

41465370-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4441314-T-A

41465371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4441313-T-C

41465385-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4441299-T-A

41465385-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4441299-T-G

41465528-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4441195-A-G

41465528-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4441195-A-T

41465555-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4441168-C-G

41465688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4441050-C-T

http://identifiers.org/hco/5/GRCh38#41466277-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4440490-A-C

41469875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4440236-A-G

41469884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4440229-G-T

41469895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4440217-G-A

41469895-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4440217-G-C

http://identifiers.org/hco/5/GRCh38#41469977-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4440141-A-C

41472669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4432617-G-A

41472758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4432511-G-A

41472759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4432510-T-C

41472882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4432394-C-T

http://identifiers.org/hco/5/GRCh38#41473095-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4432181-A-C

41477459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4429232-T-C

41477520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4429171-A-G

41477558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4429135-G-T

41477920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4428812-T-C

41478298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4427014-C-T

41478708-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4426668-A-G

41479250-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4426275-G-C

41479252-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4426273-T-A

41479252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4426273-T-C

41480210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4425324-T-C

http://identifiers.org/hco/5/GRCh38#41480524-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4425027-A-C

41480976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4424914-T-C

41481090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4424813-A-G

41481101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4424802-G-A

41481101-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4424802-G-T

41481550-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4423368-C-T

41481563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4423347-A-G

41481691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4423227-G-A

41482552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4422389-T-C

41482553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4422388-G-A

41483158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4421783-C-T

41483373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4421579-T-C

41483600-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4421396-G-C

41483600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4421396-G-T

41483646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4421315-A-G

41483899-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4420735-C-G

41485121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4419573-A-G

41485122-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4419572-T-A

41485122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4419572-T-C

41485561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4419144-C-T

41502988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4413090-T-C

41503119-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4412990-A-G

41503291-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4412829-G-C

41503380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4412741-T-C

41503417-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4412704-G-C

41503742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4412384-G-A

41503784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4412342-T-C

41503970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4412198-T-C

http://identifiers.org/hco/5/GRCh38#41504164-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4411852-C-A

http://identifiers.org/hco/5/GRCh38#41504248-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4411772-A-C

41504248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4411772-A-G

41504265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4411753-G-A

http://identifiers.org/hco/5/GRCh38#41504323-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4411677-C-A

41504323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4411677-C-T

41504411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4411602-C-T

http://identifiers.org/hco/5/GRCh38#41504449-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#4411572-A-C

41504723-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4411388-T-G

41504819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4411320-A-G

41505143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4411114-C-T

41505956-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4410280-T-A

41506241-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4410003-T-A

41506596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4409622-A-G

41506823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4409254-G-A

41506896-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4409192-T-G

41507245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4408855-T-C

41507325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4408806-A-G

41507677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4408445-T-C

41507687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4408435-G-A

41508355-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4407295-T-A

41508355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4407295-T-C

41508394-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron_variant, undefined
orthologous variants: 4407263-T-C

41508521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4407108-G-A

41508913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4406742-A-G

41509110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4406560-C-T

41509159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron variant
orthologous variants: 4406499-T-C

41510127-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron_variant, undefined
orthologous variants: 4405520-A-T

41510292-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron_variant, undefined
orthologous variants: 4405396-T-A

41510292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron_variant, undefined
orthologous variants: 4405396-T-C

41510292-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: intron_variant, undefined
orthologous variants: 4405396-T-G

41510542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 31822
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 4405177-G-A