http://identifiers.org/hco/14/GRCh38#50237570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#69732487-C-A

50237570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 3 prime UTR variant
orthologous variants: 69732487-C-T

50237770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron variant
orthologous variants: 69732687-G-A

50237770-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron variant
orthologous variants: 69732687-G-C

50237812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron variant
orthologous variants: 69732730-G-A

50237812-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron variant
orthologous variants: 69732730-G-T

50242383-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron variant
orthologous variants: 69734361-G-C

50242383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron variant
orthologous variants: 69734361-G-T

50242395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron variant
orthologous variants: 69734373-A-G

50242430-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron variant
orthologous variants: 69734408-A-G

50242452-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69734426-A-T

http://identifiers.org/hco/14/GRCh38#50242466-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#69734440-C-A

50242530-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69734482-T-A

50242530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69734482-T-C

50242558-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69734513-G-A

50242865-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69735154-C-G

http://identifiers.org/hco/14/GRCh38#50242867-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#69735156-C-A

50242895-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69735185-T-A

50242921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69735210-C-T

50243022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69735301-C-T

50243061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69735340-C-T

50243090-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69735369-G-T

50243103-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69735382-G-A

50243103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69735382-G-T

50243278-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69735538-T-A

50243351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69735612-C-T

50243581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69737309-A-G

50244388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69737402-G-A

50244388-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69737402-G-T

50244417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69737429-G-A

50244417-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69737429-G-T

50244459-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69737476-C-G

50244459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69737476-C-T

50244482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69737499-A-G

50244484-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69737501-T-G

50244553-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69737626-G-C

50244553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69737626-G-T

50244571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69737644-T-C

50244693-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69737765-G-A

50244699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69737771-T-C

50244781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69737850-T-C

50244835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69737897-G-A

50244906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69737943-G-A

50244906-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69737943-G-T

50244911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69737948-T-C

http://identifiers.org/hco/14/GRCh38#50244913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#69737950-C-A

50244913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69737950-C-T

50244917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69737953-A-G

50244926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69737962-T-C

50244975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69738001-A-G

50245036-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69738164-T-A

50245038-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69738166-T-A

50245038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69738166-T-C

http://identifiers.org/hco/14/GRCh38#50245042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#69738170-C-A

50245077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69738250-T-C

50245235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69738416-G-A

50245235-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69738416-G-T

50245331-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69738502-C-G

50245331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69738502-C-T

http://identifiers.org/hco/14/GRCh38#50245369-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#69738539-C-A

50245370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69738540-A-G

50245392-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69738564-G-C

50245419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69738592-G-A

50246896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69738909-T-C

50246907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69738920-T-C

50246934-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69738945-T-A

50246934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69738945-T-C

50246939-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69738950-T-A

50246939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69738950-T-C

50246939-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69738950-T-G

50246994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69739011-T-C

50247000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 69739017-T-C

50247034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 3_prime_UTR_variant, intron_variant, splice_region_variant
orthologous variants: 69739051-T-C

50247034-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 3_prime_UTR_variant, intron_variant, splice_region_variant
orthologous variants: 69739051-T-G

50247124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 69739141-A-G

http://identifiers.org/hco/14/GRCh38#50247130-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#69739147-A-C

50247164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron_variant, missense_variant
orthologous variants: 69739181-C-T

http://identifiers.org/hco/14/GRCh38#50247359-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#69739365-C-A

50247359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron variant
orthologous variants: 69739365-C-T

http://identifiers.org/hco/14/GRCh38#50247481-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#69739482-A-C

50247919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron variant
orthologous variants: 69739903-T-C

50247972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron variant
orthologous variants: 69739956-T-C

50248169-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron variant
orthologous variants: 69740920-A-T

http://identifiers.org/hco/14/GRCh38#50248306-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#69741261-A-C

http://identifiers.org/hco/14/GRCh38#50248557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#69741499-C-A

50254581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron variant
orthologous variants: 69741852-T-C

50254609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron variant
orthologous variants: 69741878-T-C

50254671-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron variant
orthologous variants: 69741942-A-T

50261954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron variant
orthologous variants: 69744215-G-A

50261954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron variant
orthologous variants: 69744215-G-T

50262049-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron variant
orthologous variants: 69744334-T-G

50262052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron variant
orthologous variants: 69744337-C-T

50262527-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron variant
orthologous variants: 69744510-T-A

50263099-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron variant
orthologous variants: 69744906-G-C

50263275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron variant
orthologous variants: 69745041-T-C

50263455-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron variant
orthologous variants: 69745215-G-A

50263494-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron variant
orthologous variants: 69745264-G-C

50263608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron variant
orthologous variants: 69745348-T-C

50263622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron variant
orthologous variants: 69745356-G-A

50265154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron variant
orthologous variants: 69746127-C-T

50265242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron variant
orthologous variants: 69746195-T-C

50265270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron variant
orthologous variants: 69746217-A-G

50265535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron variant
orthologous variants: 69746442-A-G

50267129-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron variant
orthologous variants: 69747569-C-G

50267129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron variant
orthologous variants: 69747569-C-T

50267451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron variant
orthologous variants: 69747694-G-A

50267539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron variant
orthologous variants: 69747831-T-C

http://identifiers.org/hco/14/GRCh38#50267601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#69747891-C-A

50267601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron variant
orthologous variants: 69747891-C-T

50267639-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron variant
orthologous variants: 69747949-A-T

50267659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron variant
orthologous variants: 69747969-G-T

50267713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron variant
orthologous variants: 69748016-A-G

http://identifiers.org/hco/14/GRCh38#50267923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#69748228-C-A

50267923-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron variant
orthologous variants: 69748228-C-G

50267923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron variant
orthologous variants: 69748228-C-T

50267929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron variant
orthologous variants: 69748234-A-G

50267940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron variant
orthologous variants: 69748248-T-C

50267949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron variant
orthologous variants: 69748257-A-G

http://identifiers.org/hco/14/GRCh38#50268060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#69748367-C-A

50268060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron variant
orthologous variants: 69748367-C-T

50268737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron variant
orthologous variants: 69748641-T-C

50268741-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron variant
orthologous variants: 69748645-C-G

50269013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron variant
orthologous variants: 69748836-G-A

50269013-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron variant
orthologous variants: 69748836-G-T

http://identifiers.org/hco/14/GRCh38#50269025-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#69748848-A-C

50269036-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron variant
orthologous variants: 69748857-T-A

50269036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron variant
orthologous variants: 69748857-T-C

50269036-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron variant
orthologous variants: 69748857-T-G

50269042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron variant
orthologous variants: 69748863-G-T

50269044-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron variant
orthologous variants: 69748865-T-A

50269045-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron variant
orthologous variants: 69748866-T-A

50269093-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron variant
orthologous variants: 69748906-G-T

http://identifiers.org/hco/14/GRCh38#50269118-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#69748935-C-A

50269118-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron variant
orthologous variants: 69748935-C-T

http://identifiers.org/hco/14/GRCh38#50269159-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#69748973-C-A

50269357-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69749173-T-C

50269447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69749783-G-A

50269447-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69749783-G-C

50269447-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69749783-G-T

50269774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69747949-A-G

50278504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 69752523-G-A

50278504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 69752523-G-T

50278538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 69752557-A-G

50278690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69752705-T-C

50279054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69753238-G-A

50279054-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69753238-G-C

50279116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69753304-T-C

50279120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69753308-T-C

50283322-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69753764-G-C

50283323-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69753765-C-G

50283347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69753787-C-T

50283365-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69753805-C-G

50283365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69753805-C-T

50284054-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69754081-G-T

50284058-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69754091-A-G

50284297-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69754767-T-C

50284433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69754897-G-A

50284433-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69754897-G-T

50284616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69755058-T-C

50284689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69755130-T-C

50284751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69755171-A-G

50285255-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69755500-G-C

50285271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69755516-T-C

50285275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69755524-A-G

50285542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69755757-C-T

50285823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69755986-C-T

50286018-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69756157-T-C

50286432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69756451-C-T

50286541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69756557-T-C

50286910-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69756872-A-T

50286933-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69756895-T-A

50286933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69756895-T-C

50287003-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69756962-T-C

50287215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69757149-A-G

50287296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69757229-G-T

50287369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69757320-C-T

50287403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69757333-C-T

50287558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69757407-C-T

50287705-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69757468-T-A

50287709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69757472-T-C

50287909-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69757548-G-C

50287917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 69757556-C-T

50294171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 69759452-G-A

50294171-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 69759452-G-C

50294317-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69759597-T-A

50294317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69759597-T-C

50294334-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69759615-T-A

50294334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69759615-T-C

50294381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69759658-C-T

50294424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69759703-C-T

50294817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69760470-T-C

50295008-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69760648-C-G

50301190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69767319-A-G

50301198-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69767336-T-C

50301459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69767576-T-C

50301654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69767771-T-C

50301663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69767780-G-A

50301686-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69767799-A-T

50302125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 69768194-T-C

http://identifiers.org/hco/14/GRCh38#50302143-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#69768212-A-C

50302201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69768280-T-C

50302212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69768291-T-C

50302387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69768443-C-T

50302410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69768458-C-T

50302424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69768472-C-T

50302468-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69768514-T-G

http://identifiers.org/hco/14/GRCh38#50302481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#69768526-C-A

50302481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69768526-C-T

50302702-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69768716-A-T

http://identifiers.org/hco/14/GRCh38#50302784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#69768747-C-A

50302784-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69768747-C-G

http://identifiers.org/hco/14/GRCh38#50302787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#69768750-C-A

50303021-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 69768971-C-G

50303089-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69769196-T-A

50303089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69769196-T-C

50303089-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69769196-T-G

50311314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: NMD_transcript_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 69770816-G-A

50311395-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 69770884-C-G

50311395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 69770884-C-T

50311514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69770952-T-C

50311514-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69770952-T-G

50311516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69770954-A-G

50311537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69770989-G-A

50311537-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69770989-G-C

50311542-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69770994-G-T

http://identifiers.org/hco/14/GRCh38#50311570-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#69771018-A-C

50311570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69771018-A-G

50311790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69771219-C-T

50311794-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69771223-C-G

50311794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69771223-C-T

http://identifiers.org/hco/14/GRCh38#50311913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#69771335-C-A

50311917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69771339-G-A

50311917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69771339-G-T

50311930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69771351-G-A

50311930-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 69771351-G-T

50311935-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69771356-G-C

50311935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 69771356-G-T

50312053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 69771473-C-T

50312105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 69771525-G-A

50312105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20499
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 69771525-G-T