216257990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: 3 prime UTR variant
orthologous variants: 72466405-A-G

216258123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: 3 prime UTR variant
orthologous variants: 72466535-G-A

216258123-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: 3 prime UTR variant
orthologous variants: 72466535-G-T

http://identifiers.org/hco/2/GRCh38#216258129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72466541-C-A

216258129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: 3 prime UTR variant
orthologous variants: 72466541-C-T

216258159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: 3 prime UTR variant
orthologous variants: 72466584-G-A

216258159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: 3 prime UTR variant
orthologous variants: 72466584-G-T

http://identifiers.org/hco/2/GRCh38#216258207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72466622-C-A

http://identifiers.org/hco/2/GRCh38#216258240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72466655-C-A

216258240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: 3 prime UTR variant
orthologous variants: 72466655-C-T

216258241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: 3 prime UTR variant
orthologous variants: 72466656-T-C

http://identifiers.org/hco/2/GRCh38#216258368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72466933-C-A

216258368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: 3 prime UTR variant
orthologous variants: 72466933-C-T

216258574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: 3 prime UTR variant
orthologous variants: 72467130-A-G

216258946-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: 3 prime UTR variant
orthologous variants: 72467483-T-G

216258985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: 3 prime UTR variant
orthologous variants: 72467519-C-T

http://identifiers.org/hco/2/GRCh38#216259177-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72467690-C-A

216259177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: 3 prime UTR variant
orthologous variants: 72467690-C-T

http://identifiers.org/hco/2/GRCh38#216259221-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72467732-C-A

216259221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: 3 prime UTR variant
orthologous variants: 72467732-C-T

http://identifiers.org/hco/2/GRCh38#216259223-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72467734-C-A

216259223-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: 3 prime UTR variant
orthologous variants: 72467734-C-G

216259223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: 3 prime UTR variant
orthologous variants: 72467734-C-T

216259405-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: synonymous variant
orthologous variants: 72467894-G-A

216259483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: synonymous variant
orthologous variants: 72467972-G-A

216259483-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: synonymous variant
orthologous variants: 72467972-G-C

216259483-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: synonymous variant
orthologous variants: 72467972-G-T

216259666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: synonymous_variant, undefined
orthologous variants: 72468155-A-G

216259666-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: missense_variant, undefined
orthologous variants: 72468155-A-T

216259723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72468207-A-G

216259724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72468208-G-A

216259724-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72468208-G-C

216259724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72468208-G-T

216259739-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72468219-G-C

216259739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72468219-G-T

216259766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, splice_region_variant, undefined
orthologous variants: 72468251-A-G

216259849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72468382-G-A

216259901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72468411-G-A

216259901-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72468411-G-T

216259918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72468428-T-C

216259971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72468481-G-A

216260250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72468770-T-C

216260454-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72468993-G-A

http://identifiers.org/hco/2/GRCh38#216260663-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#72469207-C-A

216260854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72469376-T-C

216260860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72469382-G-A

216260909-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72469425-G-C

216260925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72469440-G-A

http://identifiers.org/hco/2/GRCh38#216261042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#72469553-C-A

216261050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72469561-G-A

216261257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72469746-T-C

216261274-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72469763-G-C

216261274-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72469763-G-T

216261439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72469924-G-A

216264503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72472664-C-T

216264611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72472758-T-C

216264850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72472978-G-T

216265356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72473702-A-G

216265375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72473720-G-T

216265378-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72473723-T-A

216265378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72473723-T-C

216266047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72475913-A-G

216266202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72476059-C-T

216266210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72476067-C-T

216266214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72476071-A-G

216266224-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72476081-C-G

216266224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72476081-C-T

216266481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72476309-C-T

216266668-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72476821-C-G

216266805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72476959-G-A

216267136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72478988-T-C

216267401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72479158-C-T

216267548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72479297-G-A

http://identifiers.org/hco/2/GRCh38#216267572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72479321-C-A

216267572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72479321-C-T

216267686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72479399-A-G

http://identifiers.org/hco/2/GRCh38#216267845-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72479558-A-C

216267845-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72479558-A-T

216267987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72479713-G-A

216268044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72479768-C-T

216268929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72480383-T-C

216268932-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72480386-G-T

216269197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72480636-T-C

216269243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72480682-T-C

216269469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72480884-C-T

216269543-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72480952-A-G

http://identifiers.org/hco/2/GRCh38#216269815-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72481206-C-A

216269828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72481223-C-T

216269954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72481337-A-G

216270017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72481401-C-T

216270073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72481453-C-T

http://identifiers.org/hco/2/GRCh38#216270539-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72481616-C-A

216270638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72481721-C-T

216270712-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72481794-T-A

216271139-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72482073-T-C

216271310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72482238-C-T

216271329-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72482256-C-G

216271562-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72482468-G-T

216271612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72482527-C-T

216271691-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72482599-G-C

216271765-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72482669-T-G

216272372-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72482877-T-A

216272372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72482877-T-C

216272463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72482999-A-G

216272512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72483032-G-A

http://identifiers.org/hco/2/GRCh38#216272903-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72483422-A-C

216273017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72483530-G-A

216273057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72483570-G-A

216273141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72483609-A-G

216273217-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72483683-T-G

216273414-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72483873-T-A

216273478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72483890-G-A

216273478-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72483890-G-T

216274135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72483951-A-G

216274212-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72484010-G-C

216274216-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72484014-C-G

216274278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72484086-C-T

216274419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72484179-G-T

216274618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72484333-G-A

216274763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72484462-C-T

216274789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72484484-C-T

216276498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72484584-G-A

216276751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72484836-G-A

216276751-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72484836-G-C

216276873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72484988-C-T

http://identifiers.org/hco/2/GRCh38#216277249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72485922-C-A

216277341-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72485987-T-G

216277344-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72485990-A-G

216277373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72486019-C-T

216277453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72486096-G-A

216277467-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72486110-G-T

216277494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72486137-C-T

216277545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72486188-A-G

http://identifiers.org/hco/2/GRCh38#216277549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72486192-C-A

216277549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72486192-C-T

http://identifiers.org/hco/2/GRCh38#216277573-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72486215-A-C

http://identifiers.org/hco/2/GRCh38#216277581-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72486223-C-A

216277581-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72486223-C-T

http://identifiers.org/hco/2/GRCh38#216277588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72486229-C-A

http://identifiers.org/hco/2/GRCh38#216277648-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72486292-A-C

http://identifiers.org/hco/2/GRCh38#216277655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72486299-C-A

216277655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72486299-C-T

http://identifiers.org/hco/2/GRCh38#216277659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72486303-C-A

216277659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72486303-C-T

216277733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: synonymous variant
orthologous variants: 72486376-G-A

216277817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: synonymous variant
orthologous variants: 72486460-G-A

http://identifiers.org/hco/2/GRCh38#216277844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72486487-C-A

216277844-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: synonymous variant
orthologous variants: 72486487-C-G

216277844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: synonymous variant
orthologous variants: 72486487-C-T

216277927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72486567-C-T

http://identifiers.org/hco/2/GRCh38#216277940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72486580-C-A

216277940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72486580-C-T

216277993-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72486630-G-T

216278094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72486729-G-A

216278146-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72486776-A-T

216278543-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72486850-T-G

216278597-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72486904-T-A

216278697-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72487004-G-T

http://identifiers.org/hco/2/GRCh38#216278979-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72487275-C-A

216279589-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72487472-G-T

216279622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72487489-C-T

216280353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72488412-A-G

216280422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72488479-C-T

216280423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72488480-C-T

216280563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72488603-C-T

216280604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72488644-A-G

216280688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72488770-C-T

http://identifiers.org/hco/2/GRCh38#216280817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72488893-C-A

216280817-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72488893-C-G

216281028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72489080-A-G

216281223-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72489277-T-C

216281250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72489332-A-G

216281386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72489465-G-A

216281395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72489474-C-T

216281420-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72489499-T-A

216281420-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72489499-T-G

216281474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72489541-T-C

216281474-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72489541-T-G

http://identifiers.org/hco/2/GRCh38#216282327-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72490280-C-A

216282327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72490280-C-T

http://identifiers.org/hco/2/GRCh38#216282436-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72490365-A-C

216282436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72490365-A-G

216282541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72490452-T-C

216282778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72490838-G-T

216282861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72490930-C-T

216282867-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72490936-T-A

216282940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72491012-C-T

216283036-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72491111-G-C

216283036-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72491111-G-T

216283045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72491120-C-T

216283136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72491216-C-T

216283213-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72491295-G-C

216283213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72491295-G-T

216283254-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72491340-T-A

216283311-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72491389-A-T

216283315-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72491393-T-G

216283335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72491413-T-C

http://identifiers.org/hco/2/GRCh38#216283490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72491529-C-A

216283490-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72491529-C-G

http://identifiers.org/hco/2/GRCh38#216283540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72491581-C-A

216283540-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72491581-C-G

216283540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72491581-C-T

216283610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: synonymous variant
orthologous variants: 72491637-G-A

216283757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72491790-G-T

216283771-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72491803-G-C

216283771-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72491803-G-T

http://identifiers.org/hco/2/GRCh38#216283814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#72491841-C-A

216283814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72491841-C-T

216283818-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72491845-G-C

216283818-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72491845-G-T

216283844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72491895-G-A

216283844-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72491895-G-C

216283844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72491895-G-T

216284396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72492341-G-A

216284502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72492464-G-A

216284638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72492679-T-C

216284808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72493123-G-T

216284931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72493236-A-G

216285215-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72493500-C-G

216285215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72493500-C-T

216285322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72493596-G-A

216285423-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72493676-T-G

216285524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72493789-A-G

216285579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72493845-C-T

216285665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72493919-T-C

216285876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72494121-C-T

216285933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72494176-G-A

216285985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72494228-T-C

216286017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72494272-G-A

216286017-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72494272-G-C

216286098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72494347-G-A

http://identifiers.org/hco/2/GRCh38#216286158-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72494395-C-A

216287136-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72495281-C-G

216287349-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72495452-G-T

216287514-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72495586-T-G

216288311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72495812-A-G

216288326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72495827-C-T

216289751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72496476-G-A

216290035-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72496751-G-C

216290121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72496815-A-G

216290131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72496825-G-A

216290187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72496880-G-A

216290832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72497961-G-A

216290859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72497988-G-A

216290869-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72497997-G-C

216290913-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72498034-C-G

216290954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72498074-C-T

216291030-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72498141-G-T

216291112-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72498222-A-T

216291145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72498254-T-C

216291229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72498327-A-G

216291255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72498354-G-A

216291697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72499506-T-C

216292438-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72500229-T-G

216292535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72500367-T-C

216292597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72500441-C-T

216292686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72500574-G-A

216292697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72500589-C-T

216293036-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72500843-C-G

216293141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72500941-G-A

216293141-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72500941-G-C

216293310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72501066-G-A

216293316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72501075-A-G

http://identifiers.org/hco/2/GRCh38#216293588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72501336-C-A

216293754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72501501-A-G

216293913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72501663-T-C

216294030-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72501780-T-A

216294030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72501780-T-C

216294232-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72501978-G-T

216294449-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72502194-T-A

216294804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72502522-A-G

216297007-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72504521-C-G

216297015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72504529-A-G

216297105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72504618-G-A

216297500-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72504936-G-T

216297597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72505034-C-T

216297807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72505355-C-T

216298098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72505649-C-T

216298144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72505705-G-A

216298703-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72505920-T-A

216298740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72505961-T-C

216298751-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72505972-T-A

216298854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72506050-T-C

216298854-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72506050-T-G

216298919-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72506111-A-T

216298950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72506148-T-C

216299113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72506296-T-C

216299284-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72506430-A-G

216299405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72506547-C-T

http://identifiers.org/hco/2/GRCh38#216299564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72506692-C-A

216299564-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72506692-C-G

216299564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72506692-C-T

http://identifiers.org/hco/2/GRCh38#216299847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72506934-C-A

216300115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72507175-A-G

216300652-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72507361-T-A

216300691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72507387-G-A

216300691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72507387-G-T

http://identifiers.org/hco/2/GRCh38#216300720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72507408-C-A

216300720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72507408-C-T

216300779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72507461-T-C

216301177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72507862-C-T

216301352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72508023-A-G

216301434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72508109-G-A

216301516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72508627-T-C

216301741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72508842-A-G

216301785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72508886-A-G

216301872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72508969-T-C

216301917-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72509009-A-T

http://identifiers.org/hco/2/GRCh38#216301979-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72509074-C-A

216302015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72509110-G-A

216302095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72509174-G-A

216302121-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72509201-C-G

216302161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72509241-A-G

216303322-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72510653-T-G

http://identifiers.org/hco/2/GRCh38#216303380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#72510741-C-A

216303380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72510741-C-T

216303425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72510780-T-C

216303547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72510905-G-T

216303591-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72510952-G-T

216303748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72511444-G-A

216303906-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72511609-T-A

216303906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72511609-T-C

216304140-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72511875-T-G

216304284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72512034-G-A

216304346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72512075-C-T

216304379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72512092-T-C

http://identifiers.org/hco/2/GRCh38#216304433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#72512144-C-A

http://identifiers.org/hco/2/GRCh38#216304513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#72512193-C-A

http://identifiers.org/hco/2/GRCh38#216304585-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#72512263-C-A

216305298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72512689-A-G

216305563-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72513092-G-A

216306464-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72513549-T-G

216306584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72513664-T-C

http://identifiers.org/hco/2/GRCh38#216306766-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#72513812-A-C

216306766-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72513812-A-T

216306827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72513870-G-T

http://identifiers.org/hco/2/GRCh38#216306969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#72514013-C-A

216306977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72514021-C-T

216308444-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72520632-T-A

216308512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72520704-G-A

216308520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72520712-A-G

216308557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72520743-T-C

216308558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72520744-G-A

216308571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72520757-C-T

216308579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72520765-G-A

http://identifiers.org/hco/2/GRCh38#216308853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#72521037-C-A

216308853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72521037-C-T

216308913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72521095-G-A

216308949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72521131-C-T

216309068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72521243-C-T

216309177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72521350-T-C

216309272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72521444-G-T

216309335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72521507-G-A

216309448-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72521594-C-G

216309448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72521594-C-T

216309454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72521600-G-T

http://identifiers.org/hco/2/GRCh38#216309692-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#72521821-C-A

216309692-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72521821-C-G

216309813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72521961-C-T

216309906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72522040-C-T

216309941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72522079-T-C

216309971-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72522108-T-G

216310145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72522256-G-A

216313603-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72526412-A-T

216314029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72526862-G-A

http://identifiers.org/hco/2/GRCh38#216314779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#72527263-C-A

216314827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72527309-G-A

216315922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72529307-C-T

216315972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72529356-G-T

216316180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72529565-G-A

216316456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72529902-A-G

http://identifiers.org/hco/2/GRCh38#216316621-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#72530037-C-A

216316957-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72530283-T-A

216317061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72530347-C-T

216323035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72531800-T-C

216323092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72531856-T-C

216323126-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72531889-T-A

216323126-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72531889-T-G

216323361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72532131-A-G

http://identifiers.org/hco/2/GRCh38#216327348-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72532578-C-A

216327463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72532648-T-C

216327732-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72532912-A-T

216327966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72533159-A-G

216327966-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72533159-A-T

216332994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72538686-T-C

216332994-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72538686-T-G

216333045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72538732-A-G

216333090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72538761-T-C

216333158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72538831-A-G

216333248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72538909-G-A

216333517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72539176-A-G

216333753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72539394-C-T

216333793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72539437-G-A

216333823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72539470-C-T

216333903-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72539550-A-T

216333904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72539551-T-C

216333920-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72539571-A-T

216333937-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72539588-C-G

216333937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72539588-C-T

216334095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72539737-G-A

216334095-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72539737-G-T

216334858-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72540669-T-C

216334948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72540749-A-G

216335019-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72540814-T-G

216335343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72541149-T-C

http://identifiers.org/hco/2/GRCh38#216335940-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72541222-A-C

216336022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72541286-T-C

216336023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72541287-G-A

216336025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72541289-A-G

http://identifiers.org/hco/2/GRCh38#216336027-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72541291-C-A

216336058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72541317-A-G

216336094-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72541354-A-T

216336107-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72541366-T-A

216336264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72541561-G-A

http://identifiers.org/hco/2/GRCh38#216336288-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72541591-A-C

216336288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72541591-A-G

216336408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: -C-T

216336516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72541817-C-T

216336522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72541823-A-G

216336560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72541874-T-C

216336738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72542185-G-A

216336738-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72542185-G-C

216336738-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72542185-G-T

http://identifiers.org/hco/2/GRCh38#216336792-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72542223-C-A

216336797-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72542228-G-T

216337557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72542637-A-G

216337778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72542775-C-T

216338749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72543262-A-G

216338785-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72543298-C-G

216338785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72543298-C-T

216338893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72543406-C-T

216339120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72543590-T-C

216339133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72543604-G-A

216339273-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72543746-T-A

216339406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72543868-C-T

216339762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72544194-A-G

216339762-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72544194-A-T

216339825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72544256-C-T

http://identifiers.org/hco/2/GRCh38#216339887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72544318-C-A

216339972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72544392-C-T

216340054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72544457-C-T

216340102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72544482-G-A

216340102-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72544482-G-T

216340103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72544483-C-T

216340114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72544494-A-G

216340125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72544505-G-A

216340153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72544520-C-T

http://identifiers.org/hco/2/GRCh38#216340234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72544582-C-A

216340257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72544606-C-T

216340279-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72544629-G-C

216340426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72544769-G-A

http://identifiers.org/hco/2/GRCh38#216340513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72544842-C-A

216340620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72544946-A-G

216340852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72545105-C-T

216341005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72545260-C-T

216341124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72545389-C-T

216341391-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72545635-G-C

216341855-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72546025-T-A

216341855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72546025-T-C

216341856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72546026-G-A

216341967-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72546119-T-A

216342044-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72546199-C-G

216342100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72546254-G-T

216342296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72546373-G-A

http://identifiers.org/hco/2/GRCh38#216342297-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72546374-A-C

216342327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72546403-A-G

216342387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72546466-C-T

216342432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72546507-G-A

216342537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72546609-G-A

216342844-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72546894-T-G

216342845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72546895-C-T

216343104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72547099-G-A

216343151-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72547146-C-G

216343495-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72547454-A-T

216343549-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72547472-A-T

216343643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72547519-G-A

http://identifiers.org/hco/2/GRCh38#216343959-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72547867-C-A

216344043-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72548000-C-G

216344586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72548792-A-G

216344677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72548868-T-C

216344731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72548926-T-C

216344731-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72548926-T-G

216344839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72549021-C-T

216344897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72549097-G-A

216344897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72549097-G-T

http://identifiers.org/hco/2/GRCh38#216345160-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72549608-C-A

216345229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72549687-G-A

http://identifiers.org/hco/2/GRCh38#216345250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72549709-C-A

216345953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72550424-A-G

216346215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72550672-A-G

http://identifiers.org/hco/2/GRCh38#216346268-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72550712-A-C

216346272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72550716-G-A

216346272-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72550716-G-C

216346361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72550802-G-A

216349204-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72552073-A-T

216349377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72552225-C-T

216349399-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72552247-T-G

216349445-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72552296-C-G

216349445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72552296-C-T

216349669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72552786-G-A

216349835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72552953-A-G

http://identifiers.org/hco/2/GRCh38#216350199-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72553243-C-A

216350199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72553243-C-T

216350285-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72553334-T-A

216350290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72553339-T-C

216350337-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72553387-C-G

216350507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72553516-C-T

http://identifiers.org/hco/2/GRCh38#216350893-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72553838-A-C

216350922-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72553867-T-A

216351176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72554111-C-T

http://identifiers.org/hco/2/GRCh38#216351265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72554194-C-A

216351265-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72554194-C-G

216351310-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72554233-T-C

http://identifiers.org/hco/2/GRCh38#216351612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72554385-C-A

216351612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72554385-C-T

216351706-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72554467-T-A

216351712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72554473-C-T

216351841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72554581-A-G

216351846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72554586-G-A

216351943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72554697-A-G

http://identifiers.org/hco/2/GRCh38#216352231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72554906-C-A

216352231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72554906-C-T

216352363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72554977-C-T

216352429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72555026-G-A

216352908-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72555293-C-T

216352924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72555310-G-A

216352924-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72555310-G-C

216353238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72555559-A-G

216353284-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72555603-C-G

216353324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72555649-T-C

216353351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72555667-T-C

216353671-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72555800-C-G

216353671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72555800-C-T

216353945-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72555941-G-T

216354189-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72556198-C-G

216354189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72556198-C-T

216354314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72556348-T-C

216354476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72556472-A-G

216354482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72556478-G-A

216354725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72556729-G-T

216354782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72556786-C-T

216355525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72557128-G-A

216356010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72557475-A-G

216356342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72557830-G-A

216356374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72557861-G-A

216356388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72557875-A-G

216356417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72557904-C-T

216357726-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72559977-A-G

216357825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72560074-T-C

216358137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72560375-C-T

216358612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72561113-C-T

216359278-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72561524-A-T

216360165-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72562395-G-T

216360286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72562517-C-T

216360323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72562553-T-C

216360381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72562611-A-G

216360707-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72562827-C-G

216361414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72563317-C-T

216361534-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72563430-G-A

216361534-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72563430-G-C

216361770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72563673-C-T

216362590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72564874-G-A

216362590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72564874-G-T

216362624-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72564900-G-C

216362625-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72564901-G-T

http://identifiers.org/hco/2/GRCh38#216362852-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72566939-A-C

216363449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72567739-T-C

http://identifiers.org/hco/2/GRCh38#216363458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72567765-C-A

216363458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72567765-C-T

http://identifiers.org/hco/2/GRCh38#216363896-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72568426-C-A

216363905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72568429-T-C

216363905-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72568429-T-G

216364021-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72568545-T-C

216364092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72568615-T-C

216364165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72568686-C-T

216364245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72568805-T-C

216364245-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72568805-T-G

216364474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72569019-C-T

216364932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72569385-T-C

216365109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72569564-C-T

http://identifiers.org/hco/2/GRCh38#216365194-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72569637-C-A

216365970-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72570310-A-T

216366151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72570467-T-C

http://identifiers.org/hco/2/GRCh38#216366407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72570707-C-A

216366407-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72570707-C-G

216366578-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72570881-T-A

http://identifiers.org/hco/2/GRCh38#216366657-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72570960-A-C

216366727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72571034-C-T

http://identifiers.org/hco/2/GRCh38#216366748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72571055-C-A

216366886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72571207-C-T

216367110-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72571378-G-T

http://identifiers.org/hco/2/GRCh38#216367468-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72571688-A-C

216367768-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72571983-T-A

216367768-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron_variant, undefined
orthologous variants: 72571983-T-C

216368122-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72572307-G-C

http://identifiers.org/hco/2/GRCh38#216368575-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72572734-C-A

216368629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72572782-C-T

216368831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72572971-T-C

216369450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72573496-T-C

216369699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72573735-A-G

216369700-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72573736-C-T

216369702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72573738-T-C

216369735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: intron variant
orthologous variants: 72573774-G-T

216369894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: missense variant
orthologous variants: 72573933-C-T

216369903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: missense variant
orthologous variants: 72573942-C-T

216369990-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: missense variant
orthologous variants: 72574026-T-A

216369990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: missense variant
orthologous variants: 72574026-T-C

216370006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: synonymous variant
orthologous variants: 72574042-C-T

216370063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: synonymous variant
orthologous variants: 72574102-G-A

216370063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: synonymous variant
orthologous variants: 72574102-G-T

http://identifiers.org/hco/2/GRCh38#216370222-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72574261-C-A

216370222-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: missense variant
orthologous variants: 72574261-C-G

216370352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: 5 prime UTR variant
orthologous variants: 72574385-G-A

216370352-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: 5 prime UTR variant
orthologous variants: 72574385-G-T

216370354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: 5 prime UTR variant
orthologous variants: 72574387-T-C

216370354-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: 5 prime UTR variant
orthologous variants: 72574387-T-G

http://identifiers.org/hco/2/GRCh38#216370501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72574531-C-A

216370501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: 5 prime UTR variant
orthologous variants: 72574531-C-T

216370573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: 5 prime UTR variant
orthologous variants: 72574606-A-G

216370601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: 5 prime UTR variant
orthologous variants: 72574634-G-A

216370601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: 5 prime UTR variant
orthologous variants: 72574634-G-T

216370723-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: 5 prime UTR variant
orthologous variants: 72574730-G-T

216370918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: 5 prime UTR variant
orthologous variants: 72574906-G-A

216370918-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: 5 prime UTR variant
orthologous variants: 72574906-G-T

216370957-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: 5 prime UTR variant
orthologous variants: 72574945-A-G

216370969-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: 5 prime UTR variant
orthologous variants: 72574952-G-T

216371194-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: 5 prime UTR variant
orthologous variants: 72575154-G-T

216371210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: 5 prime UTR variant
orthologous variants: 72575174-A-G

216371242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: 5 prime UTR variant
orthologous variants: 72575206-G-A

216371242-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: 5 prime UTR variant
orthologous variants: 72575206-G-T

http://identifiers.org/hco/2/GRCh38#216371552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72575515-C-A

216371552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: 5 prime UTR variant
orthologous variants: 72575515-C-T

216371685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: 5 prime UTR variant
orthologous variants: 72575645-C-T

216371708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: 5 prime UTR variant
orthologous variants: 72575668-G-T

http://identifiers.org/hco/2/GRCh38#216371812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72575776-C-A

216371812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: 5 prime UTR variant
orthologous variants: 72575776-C-T

http://identifiers.org/hco/2/GRCh38#216371834-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#72575798-C-A

216371834-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: 5 prime UTR variant
orthologous variants: 72575798-C-T

216371863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: 5 prime UTR variant
orthologous variants: 72575827-G-T

216371966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: 5 prime UTR variant
orthologous variants: 72575934-G-T

http://identifiers.org/hco/2/GRCh38#216372159-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29269
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#72576124-C-A