http://identifiers.org/hco/4/GRCh38#56049115-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#76805545-C-A

56049115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 76805545-C-T

http://identifiers.org/hco/4/GRCh38#56049214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76805631-C-A

56049214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: 5 prime UTR variant
orthologous variants: 76805631-C-T

56049282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: 5 prime UTR variant
orthologous variants: 76805684-G-A

56049314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76805714-G-A

56049316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76805716-C-T

56049319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76805719-G-A

56049319-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76805719-G-T

56049320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76805720-C-T

56049379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76805761-G-A

56049379-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76805761-G-C

56049379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76805761-G-T

56049447-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76805814-G-T

56049532-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76805898-C-G

56049532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76805898-C-T

56049584-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76805949-T-A

56049595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76805959-C-T

http://identifiers.org/hco/4/GRCh38#56049626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76805989-C-A

56049699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 76806040-A-G

56049717-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 76806057-C-T

56049775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 76806107-G-A

56049775-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 76806107-G-T

56049788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 76806120-T-C

56049968-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 76806284-G-A

http://identifiers.org/hco/4/GRCh38#56050063-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76806383-C-A

56050122-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76806432-T-A

56050275-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76806589-T-A

56050338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76806647-G-A

56050338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76806647-G-T

56050528-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76806838-A-T

56050686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76806979-C-T

56050758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76807061-G-A

56050796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76807106-G-T

http://identifiers.org/hco/4/GRCh38#56050820-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76807125-A-C

56050820-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76807125-A-T

56051327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76808034-A-G

56051396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76808104-G-T

56051435-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76808133-C-G

56051669-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76808361-C-T

56052038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76808674-A-G

56052039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76808675-A-G

56052157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76808932-A-G

http://identifiers.org/hco/4/GRCh38#56052249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76808973-C-A

56052751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76809491-G-A

56052793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76809533-T-C

56052793-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76809533-T-G

http://identifiers.org/hco/4/GRCh38#56052804-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76809544-C-A

56052838-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76809578-T-G

56053215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76809967-A-G

56053215-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76809967-A-T

56053306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76810059-C-T

56054552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76812140-G-A

http://identifiers.org/hco/4/GRCh38#56054760-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76812325-A-C

56054956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76812523-G-A

56055107-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76812633-C-G

56055179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76812694-G-A

56055289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76812804-A-G

56055380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76812882-G-A

56055437-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76812943-T-G

56055513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76813026-T-C

56055540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76813052-G-A

56055552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76813064-C-T

56055898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76813567-G-A

56055932-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76813602-A-T

56056203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76813864-A-G

56056307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76813971-T-C

56056307-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76813971-T-G

56057089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76814281-G-A

56057089-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76814281-G-T

56057254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76814421-T-C

56057268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76814435-T-C

56057321-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76814488-T-C

56057589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76815046-G-A

56057589-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76815046-G-T

56058852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76815209-A-G

56059100-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76815450-C-G

56059100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76815450-C-T

56061595-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76816830-C-T

56061870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76817062-G-A

56062390-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76817497-A-T

56062418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76817526-C-T

56062419-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76817527-A-G

56062437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76817541-C-T

56062501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76817598-C-T

56062502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76817599-G-A

56062730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76817927-C-T

56062773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76817970-T-C

56062875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76818039-T-C

56062886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76818048-C-T

56062917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76818080-A-G

56062959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76818137-G-A

56063028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76818205-T-C

56063159-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76818334-C-G

56064881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76824868-G-A

56065538-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76825193-T-A

56066140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76825773-G-A

56066150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76825785-G-A

56066299-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76825995-T-G

56066361-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76826059-T-A

56066362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76826060-T-C

http://identifiers.org/hco/4/GRCh38#56068913-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76829106-A-C

56068978-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76829167-T-C

56069064-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76829245-C-T

56069302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76829422-G-A

56069518-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76829636-G-T

56070804-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76831036-A-T

56071139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76831292-A-G

56071597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76831736-C-T

56071643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76831789-G-T

56078200-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76835768-T-A

56078397-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76835969-C-T

56078463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76836039-G-A

56078470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76836047-G-A

56078477-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76836073-G-A

56078826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76836402-A-G

56078831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76836407-G-T

56079043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76836588-T-C

56079275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76836825-A-G

56079352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76836931-C-T

56079353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76836932-A-G

56079372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76836951-C-T

56079465-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76837055-A-T

56079469-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76837057-G-T

56079729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76837182-A-G

56079748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76837202-G-A

56079922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76837351-T-C

56080044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76837471-G-A

56080275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76837525-T-C

56080341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76837584-A-G

http://identifiers.org/hco/4/GRCh38#56080345-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76837588-A-C

56080565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76837793-A-G

http://identifiers.org/hco/4/GRCh38#56080868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76838087-C-A

56080891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76838119-C-T

56080941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76838167-T-C

56084468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76839544-A-G

56084616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76839662-G-A

56084816-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76839831-T-G

56084941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76839942-C-T

56085049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76840063-G-T

56085204-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76840177-C-G

56085204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76840177-C-T

56085205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76840178-G-A

56085410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76840380-G-A

http://identifiers.org/hco/4/GRCh38#56085447-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76840419-A-C

http://identifiers.org/hco/4/GRCh38#56085686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76840597-C-A

56085686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76840597-C-T

56085922-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76840796-G-T

56089290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76841792-G-A

56089421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76841924-G-A

56090028-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76842245-G-C

56097975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76844069-G-A

56098221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76844508-G-A

http://identifiers.org/hco/4/GRCh38#56098284-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76844553-A-C

56098424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76844680-C-T

56098543-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76844798-T-G

56099066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76845054-A-G

56099125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76845114-G-A

56099218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76845211-C-T

56099314-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76845275-A-T

56099516-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76845470-C-T

56099717-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76845663-C-G

56099852-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76845786-T-A

56100356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76845966-G-A

56100445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76846062-A-G

56100449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76846076-T-C

56100687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76846264-A-G

http://identifiers.org/hco/4/GRCh38#56100948-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76847121-A-C

56100971-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76847144-A-T

http://identifiers.org/hco/4/GRCh38#56101407-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76847598-A-C

56103782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76851392-T-C

56103786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76851396-A-G

56105975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76852277-C-T

56106167-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76852466-T-A

56106376-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76852658-C-G

56106405-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76852687-T-G

http://identifiers.org/hco/4/GRCh38#56106687-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76853793-C-A

56106687-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76853793-C-G

56106687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76853793-C-T

56106864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76853979-A-G

56110854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76854412-C-T

56111202-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76854695-C-G

56111202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76854695-C-T

56111293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76854775-G-A

56111335-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76854817-T-G

56111340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76854822-G-A

56111340-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76854822-G-C

56111539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76854992-A-G

http://identifiers.org/hco/4/GRCh38#56112925-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76855317-C-A

56112925-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76855317-C-T

56115483-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76855644-G-T

56115729-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76855831-G-C

56115754-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76855856-T-A

56115762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76855865-A-G

56116064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76856142-A-G

56116287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76856389-G-A

56116312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76856420-C-T

http://identifiers.org/hco/4/GRCh38#56116317-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76856425-C-A

56116369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76856498-C-T

56116479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76856602-G-A

56118146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76857500-C-T

56118269-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76857592-C-G

56118269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76857592-C-T

56118392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76857715-A-G

56118559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76857867-C-T

56118809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76857967-C-T

56118835-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76857993-G-C

56118846-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76858004-A-T

56118931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76858079-A-G

56118932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76858080-C-T

56119052-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76859532-G-T

56119118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76859588-A-G

56119226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76859782-G-A

56120504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76860746-A-G

56120555-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76860836-C-G

56120755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76861012-T-C

56120792-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76861059-T-G

56120922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76861199-C-T

56121024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76861288-A-G

56121074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76861332-A-G

56121094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76861365-C-T

56121236-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76861548-T-C

56121382-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76861674-T-G

56122432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76862019-A-G

56122627-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76862183-C-T

56122711-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76862267-C-G

56123199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76862891-G-A

56123353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76863261-A-G

56123358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76863265-G-A

56123471-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76863382-C-G

56123471-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76863382-C-T

56123562-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76863452-C-T

56123622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76863507-C-T

56123664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76863548-A-G

56123753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76863638-A-G

56123776-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76863662-G-C

56124271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76863859-A-G

56124362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76863941-G-A

56124394-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76863978-A-G

56124534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76864115-T-C

56124667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76864206-A-G

56124863-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76864387-T-A

56124867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76864391-G-A

56127639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76867133-G-A

56127651-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76867144-C-G

56127656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76867148-G-T

56127765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76867262-T-C

56128107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76867620-A-G

56128473-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76868101-G-C

56128602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76868219-A-G

56128636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76868257-A-G

56128649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76868270-T-C

56128899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76868589-A-G

56128983-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76868684-T-G

56129315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76868921-G-A

56129543-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, undefined
orthologous variants: 76869048-T-G

56129569-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, undefined
orthologous variants: 76869078-G-C

56129729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76869238-T-C

56129812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76869318-G-A

56130452-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76870000-T-A

56131066-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76874341-A-G

56131263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76874524-C-T

56131292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76874554-A-G

56131309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76874571-T-C

56131309-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76874571-T-G

56131330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76874592-A-G

56132747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76875883-C-T

56133041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76876140-G-A

56133041-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76876140-G-C

56133211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76876286-G-A

56133404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76876443-G-A

56135336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76878478-G-A

56135414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76878560-C-T

56139656-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76880427-A-T

56140273-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76881030-C-G

56140682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76881384-G-A

56143626-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76885606-T-A

56143789-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76885809-C-G

56143793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76885813-T-C

http://identifiers.org/hco/4/GRCh38#56143962-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76885962-C-A

56143962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76885962-C-T

56143963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76885963-G-A

56144065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76886064-A-G

56144106-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76886082-C-G

http://identifiers.org/hco/4/GRCh38#56144267-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76886233-A-C

56148746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76887485-G-T

56148804-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76887536-C-G

56149057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76887601-C-T

56149277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76887779-C-T

56149319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76887821-G-A

56149474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76888075-C-T

56149749-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76888300-T-G

56149759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76888310-A-G

56149946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76888464-G-T

56150149-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76888861-T-G

56150195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76888906-A-G

56150195-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76888906-A-T

56150224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76888935-T-C

56150242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76888953-A-G

56154587-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76891976-C-G

56154718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76892061-C-T

56155053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76892398-C-T

http://identifiers.org/hco/4/GRCh38#56155088-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76892448-A-C

56155216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76892592-A-G

56155419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76892749-C-T

56155547-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76892851-C-G

56155547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76892851-C-T

56155581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76892892-G-A

56155599-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76892910-C-G

56155644-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76892971-C-G

56155656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76892983-A-G

56155724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76893027-A-G

56155738-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76893038-G-C

56158029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76893186-T-C

56158086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76893242-A-G

56158092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76893248-G-T

56158119-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76893275-A-T

56158123-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76893279-C-G

56158583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76894156-A-G

56158723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, undefined
orthologous variants: 76894297-G-A

56158903-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76894452-C-G

56161053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76896282-T-C

56161096-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76896328-T-G

56161143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76896373-C-T

56161144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76896374-G-A

56161173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76896405-G-A

56161190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76896423-A-G

56161239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76896472-A-G

56161301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76896537-A-G

56161311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76896547-G-A

56161384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76896598-T-C

56161404-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76896618-C-G

http://identifiers.org/hco/4/GRCh38#56161565-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76896809-C-A

56161565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76896809-C-T

56162568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76897072-A-G

56162596-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76897100-G-C

56162596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76897100-G-T

56162686-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76897189-C-G

56162723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76897229-G-A

56162989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76897834-A-G

56162989-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76897834-A-T

56163095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76897929-T-C

http://identifiers.org/hco/4/GRCh38#56163179-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76897986-C-A

56163240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76898032-A-G

56163326-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76898091-A-T

http://identifiers.org/hco/4/GRCh38#56163378-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76898138-A-C

56163378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76898138-A-G

56163412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76898172-G-A

56168757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76899098-A-G

56168809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76899143-G-A

56168840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76899183-T-C

56168986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76899267-A-G

56169087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76899468-G-A

56169090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76899471-G-A

56169115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76899495-A-G

56169123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76899503-A-G

56169156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76899531-G-A

56169199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76899575-A-G

56169203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76899579-A-G

56170091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76900111-T-C

56170138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76900158-C-T

http://identifiers.org/hco/4/GRCh38#56170142-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76900162-C-A

56170142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76900162-C-T

56170174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76900194-G-A

56170308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76900301-G-T

56170309-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76900302-T-C

56170337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76900328-G-A

56170705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76900660-G-A

56170708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76900663-G-A

56170854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76900750-A-G

56170854-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76900750-A-T

56170856-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76900752-G-A

56170917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76900812-G-A

56171038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76900899-A-G

56171082-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76900950-A-G

56171082-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76900950-A-T

56171083-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76900951-A-G

56171102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76900965-G-A

56171314-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76901049-T-C

56171498-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76901227-G-C

56172263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76902093-G-A

56172263-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76902093-G-T

56172369-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76902198-T-C

56172387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76902211-A-G

56178554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76906717-G-A

56178554-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76906717-G-C

56178918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76907071-T-C

56178918-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76907071-T-G

56178920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76907073-C-T

56179112-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76907254-C-T

56179120-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76907262-T-G

http://identifiers.org/hco/4/GRCh38#56179184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76907332-C-A

56179184-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76907332-C-G

56179184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76907332-C-T

56179480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76907630-T-C

56179568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76907795-G-T

http://identifiers.org/hco/4/GRCh38#56180188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76908106-C-A

56180188-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76908106-C-G

56183507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76909489-G-T

56183653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, undefined
orthologous variants: 76909602-A-G

56185595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76910083-A-G

56185660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76910133-A-G

56185673-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76910146-G-C

56185673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76910146-G-T

56185692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76910165-G-T

56185802-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76910276-T-A

http://identifiers.org/hco/4/GRCh38#56185854-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76910328-A-C

56185854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76910328-A-G

56185855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76910329-T-C

56186114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76910560-G-A

56186114-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76910560-G-C

56186372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76910778-G-A

56186372-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76910778-G-T

56186396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76910803-A-G

56186445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76910853-A-G

56186581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76911011-T-C

56186722-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76911150-G-C

56187295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76911377-C-T

56188105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76912041-A-G

56188479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76912536-C-T

56188610-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76912654-G-C

56188610-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76912654-G-T

56191299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76913568-G-A

56191580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76913792-C-T

56194131-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76914876-G-C

56194279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76915010-A-G

56194351-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76915201-G-C

56195668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76916762-G-T

56195938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76917647-C-T

56196005-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76917714-A-T

56196122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76917843-T-C

56196212-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76917930-T-A

56196246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76917978-G-A

56196246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76917978-G-T

56196264-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76917993-T-A

56196264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76917993-T-C

56196282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76918014-T-C

56196553-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76918288-G-C

56196553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76918288-G-T

56196579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76918316-T-C

56196597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76918327-C-T

56196783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76918522-C-T

56197015-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76918732-T-A

http://identifiers.org/hco/4/GRCh38#56197294-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76919326-C-A

56197408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76919430-A-G

56197503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76919522-C-T

56197607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76919649-A-G

http://identifiers.org/hco/4/GRCh38#56197624-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76919664-A-C

56197624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76919664-A-G

56200590-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76921997-G-C

56200712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76922099-C-T

56201053-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76922645-T-G

56201248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76922861-G-A

56201280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76922882-A-G

56201581-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76923171-A-G

56201783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76923333-G-A

56201967-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76923633-G-C

56201967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76923633-G-T

http://identifiers.org/hco/4/GRCh38#56202055-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76923705-A-C

56203853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76928175-A-G

56203942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76928254-G-A

56203954-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76928266-T-G

http://identifiers.org/hco/4/GRCh38#56204043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76928342-C-A

56204071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76928374-G-A

56215422-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76929727-G-T

56215654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76929951-G-A

56216017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76930331-G-A

56216017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76930331-G-T

56216152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 76930432-G-A

56216152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 76930432-G-T

http://identifiers.org/hco/4/GRCh38#56216237-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76930491-C-A

56216354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76930601-G-A

http://identifiers.org/hco/4/GRCh38#56216559-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76930805-C-A

56219028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76931789-A-G

56219306-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76932000-G-C

56219721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76932083-T-C

56219878-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76932225-G-C

56219878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76932225-G-T

56219903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76932253-A-G

http://identifiers.org/hco/4/GRCh38#56219978-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76932306-A-C

56220091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76932413-G-A

56220115-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76932437-G-A

56220135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76932460-G-A

56220213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76932533-A-G

56220332-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76932662-G-T

56224336-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76934824-T-G

56224406-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76934898-T-C

56224753-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76935074-G-T

56225196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76935375-A-G

56225237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76935420-A-G

56225263-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76935446-T-G

56225488-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76935677-C-G

56225797-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76935938-T-C

56225842-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76935986-G-C

56225960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76936110-T-C

56226124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76936283-G-A

56226320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76936638-G-A

http://identifiers.org/hco/4/GRCh38#56226521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76936836-C-A

56227201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76937495-A-G

56227317-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76937600-G-T

56227437-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76937724-C-T

56227562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76937835-T-C

56227658-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76937922-C-G

56227674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76937938-G-A

56227755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76938027-G-A

56227755-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76938027-G-C

56227836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76938250-A-G

56228207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76938852-A-G

56228886-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76940175-A-G

56228911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76940199-T-C

56229069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76940361-A-G

56229134-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76940420-A-G

56229261-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76940504-G-T

56229268-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76940525-C-G

56229288-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76940545-C-G

http://identifiers.org/hco/4/GRCh38#56229319-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76940584-C-A

56229477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76940769-T-C

56229555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76940849-G-A

56230002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76941280-T-C

56230235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76941522-T-C

56230312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76941779-G-T

56230553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76942028-C-T

56230873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76942531-A-G

56234743-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76945616-G-T

56234804-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76945674-A-T

56234991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76945828-G-T

56235124-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76945946-T-A

56235189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76946023-G-A

56235318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76946160-A-G

56235429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76946311-G-A

56235429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76946311-G-T

56239479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76949018-G-A

56239535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76949061-A-G

56239549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76949075-A-G

http://identifiers.org/hco/4/GRCh38#56239823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76950141-C-A

56240155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76950639-C-T

56240439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76950879-G-A

56241571-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76951995-G-C

56241633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76952089-T-C

56241751-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76952220-G-C

56241813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76952265-A-G

56242001-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76952483-T-G

56242018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76952500-A-G

56242061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76952551-G-A

http://identifiers.org/hco/4/GRCh38#56242277-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76952759-A-C

56242571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76953047-G-A

56242669-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76953141-A-T

56242707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76953175-C-T

56242787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76953248-A-G

56242935-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76953387-G-C

56244077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76955544-T-C

56244179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76955638-G-A

56244179-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76955638-G-C

56244241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76955705-A-G

56244242-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76955706-T-A

56244242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76955706-T-C

56244296-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76955772-A-T

56244325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76955795-G-A

56244914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76956394-T-C

56244940-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76956421-T-G

56244965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76956446-C-T

56245069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76956550-A-G

56245109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76956593-A-G

56245141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76956624-C-T

56245195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76956659-C-T

56245232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76956696-T-C

56245234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76956698-G-T

http://identifiers.org/hco/4/GRCh38#56245437-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76956888-A-C

56245533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76956979-A-G

56246083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76957482-T-C

56246221-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76957580-G-C

56246274-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76957640-T-A

56246383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76957709-G-A

56246383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76957709-G-T

56246388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76957714-A-G

56246430-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76957754-G-C

http://identifiers.org/hco/4/GRCh38#56246537-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76957863-C-A

56246537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 76957863-C-T

56246611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 76957938-A-G

56246624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 76957956-T-C

56246632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 76957964-T-C

56246633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 76957965-G-A

56246633-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 76957965-G-T

56246682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 76958016-G-A

56246682-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 76958016-G-T

56246718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76958052-T-C

56247005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76958243-G-A

56247180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76958397-C-T

56247202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76958417-C-T

56249592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76960833-T-C

56249775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76961010-C-T

56249936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76961166-C-T

56249976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76961206-G-A

56250138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76961356-A-G

56250343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76961484-C-T

56250387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76961540-A-G

http://identifiers.org/hco/4/GRCh38#56250389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76961542-C-A

56250453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76961591-A-G

56250556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76961699-A-G

http://identifiers.org/hco/4/GRCh38#56250705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76961844-C-A

56251259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76962594-G-T

56251334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76962665-G-A

56251369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76962700-A-G

56251378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76962709-G-T

56251423-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76962765-G-C

56251540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76962927-T-C

56251750-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76963100-C-G

56251814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76963166-C-T

56251960-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76963289-A-T

56251962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76963291-A-G

56251966-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76963295-A-T

56252194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76963486-G-A

56252366-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76963640-C-G

56252763-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76964033-T-A

56252786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76964056-G-T

56252890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76964147-C-T

56252977-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76964616-G-A

56253258-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76964884-A-T

56261156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76965640-G-A

56261219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76965702-C-T

56261300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, undefined
orthologous variants: 76965769-G-A

56265379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76966351-G-A

56265700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76967135-A-G

56265838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76967223-C-T

http://identifiers.org/hco/4/GRCh38#56266082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76967604-C-A

56266082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76967604-C-T

56266389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76967892-T-C

56266603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76968099-G-A

56266638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76968151-A-G

http://identifiers.org/hco/4/GRCh38#56266837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76968332-C-A

56266844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76968335-G-A

56266932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76968435-A-G

56271365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76969743-G-T

56271686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76970039-A-G

56272301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76970293-G-A

http://identifiers.org/hco/4/GRCh38#56272398-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76970392-C-A

56272398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 76970392-C-T

56272401-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 76970395-G-T

56272542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76970534-G-A

56272542-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76970534-G-T

56272647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76970602-T-C

56273126-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76970727-T-C

56273345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76970953-G-A

56273345-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76970953-G-C

56273736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76971385-A-G

56273988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76971530-A-G

56274025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76971567-G-A

56275885-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76972850-C-T

http://identifiers.org/hco/4/GRCh38#56276212-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76973157-C-A

56276212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76973157-C-T

56276318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76973425-A-G

56276402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76973508-T-C

56276467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76973568-T-C

56276580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76973667-G-A

56276675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76973757-A-G

56276913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76973933-A-G

56277052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76974064-A-G

56280520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76975621-C-T

56280541-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76975641-C-G

56280613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76975712-T-C

56280710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76975807-G-T

56281586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76976173-A-G

56281647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76976230-A-G

56282006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76976546-G-A

56282006-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76976546-G-C

56282061-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76976640-A-G

56282381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76976984-G-A

56286695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76977678-G-A

56286954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76977927-C-T

http://identifiers.org/hco/4/GRCh38#56287915-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76978342-C-A

56287915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76978342-C-T

56287966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76978395-G-A

http://identifiers.org/hco/4/GRCh38#56288159-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76978560-C-A

56288201-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76978614-T-G

56288218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76978629-C-T

56291090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76980397-C-T

56291111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76980418-G-T

56291184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76980488-G-A

56291231-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76980546-T-A

56291235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76980550-A-G

56291255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76980573-G-A

56291274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76980592-A-G

56291465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76980779-A-G

56291589-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76980909-G-C

56291598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76980918-A-G

http://identifiers.org/hco/4/GRCh38#56295639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76985884-C-A

56295882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76986481-C-T

56295981-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76986799-G-C

56296082-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76986894-G-C

56296232-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76987018-G-T

56296452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76987149-C-T

56296508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76987206-A-G

56296547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76987238-C-T

56296644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76987290-T-C

56296688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76987336-G-A

56296699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76987347-C-T

56297272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76987856-T-C

56297691-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76988120-T-A

56297691-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76988120-T-G

56297694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76988123-C-T

56297706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76988135-A-G

56297936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 76988348-T-C

56298008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76988408-T-C

http://identifiers.org/hco/4/GRCh38#56298140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76988545-C-A

56298140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76988545-C-T

56298412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76988844-G-T

56298493-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76988926-T-A

56298583-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76989005-T-G

56299098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76989170-G-A

56299204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76989254-G-A

56299204-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76989254-G-T

56300330-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76989934-G-C

56301082-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76990884-T-A

56301082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76990884-T-C

56301264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76991061-A-G

56301321-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76991117-T-C

56301336-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, undefined
orthologous variants: 76991132-G-C

56301340-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, undefined
orthologous variants: 76991136-G-T

56301439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76991220-G-A

56301691-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76991498-G-T

56301864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76991650-T-C

56301906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76991683-A-G

56302037-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76991810-T-A

56302058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76991846-C-T

56302556-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76992338-A-T

56302596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76992377-G-A

56302784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76992590-G-A

56302956-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76992764-C-G

56303036-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76992831-C-G

56303622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76993040-T-C

56303671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76993090-G-A

http://identifiers.org/hco/4/GRCh38#56303713-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76993130-C-A

56303713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76993130-C-T

56303714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76993131-G-A

56303773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76993180-T-C

56303875-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76993248-G-A

56304037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76993380-G-T

56304084-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76993408-C-G

56304282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76993593-C-T

56304351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76993673-G-T

56305090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76994260-C-T

56305671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76994771-C-T

56305718-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76994831-C-T

56305755-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76994873-T-G

http://identifiers.org/hco/4/GRCh38#56305953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76995091-C-A

56305969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76995107-G-A

56306000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76995140-G-A

56306006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76995146-T-C

56306226-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76995390-G-T

56306630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76995810-A-G

http://identifiers.org/hco/4/GRCh38#56306647-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76995827-C-A

56306687-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76995873-C-G

http://identifiers.org/hco/4/GRCh38#56307089-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76996266-C-A

56307147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76996330-T-C

56307447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76996579-G-A

56307485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, undefined
orthologous variants: 76996614-T-C

http://identifiers.org/hco/4/GRCh38#56307507-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76996636-A-C

56307571-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 76996700-T-G

56307580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: 5_prime_UTR_variant, missense_variant, undefined
orthologous variants: 76996709-G-A

56307580-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: 5_prime_UTR_variant, missense_variant, undefined
orthologous variants: 76996709-G-T

56307606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: synonymous variant
orthologous variants: 76996735-T-C

http://identifiers.org/hco/4/GRCh38#56307744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#76996881-C-A

56307938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76997054-A-G

56307953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76997072-C-T

56308016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76997153-G-A

56308027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76997164-A-G

56308027-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76997164-A-T

56308050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76997188-T-C

56308050-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76997188-T-G

56308224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76997360-T-C

56308248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76997378-A-G

56308337-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76997477-G-C

56308344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76997484-T-C

http://identifiers.org/hco/4/GRCh38#56308701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76997617-C-A

56308723-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 76997636-G-T

56308819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 76997737-G-A

56308819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 76997737-G-T

56308832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 76997748-G-T

56309017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76997935-A-G

http://identifiers.org/hco/4/GRCh38#56309078-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76997994-C-A

56310263-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76998787-G-T

56310265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76998789-G-A

56310302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76998817-C-T

http://identifiers.org/hco/4/GRCh38#56310529-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76999023-A-C

56310529-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76999023-A-T

http://identifiers.org/hco/4/GRCh38#56310549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76999043-C-A

56310549-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76999043-C-G

56310549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76999043-C-T

56310561-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76999079-T-A

56310561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76999079-T-C

56310576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76999094-G-A

56310713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 76999230-T-C

56310818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76999306-G-A

56310818-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76999306-G-C

56310818-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 76999306-G-T

56310902-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76999363-T-A

56310923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76999384-G-A

56310958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76999421-C-T

56311004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76999468-T-C

56311031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76999496-G-A

56311031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76999496-G-T

http://identifiers.org/hco/4/GRCh38#56311039-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76999504-A-C

56311039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76999504-A-G

http://identifiers.org/hco/4/GRCh38#56311065-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#76999541-A-C

56311065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76999541-A-G

56311080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76999554-G-A

56311082-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76999556-G-C

56311126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76999596-G-T

56311199-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 77000494-T-C

56311210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 77000502-G-A

http://identifiers.org/hco/4/GRCh38#56311220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77000512-C-A

56311220-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77000512-C-G

56311220-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77000512-C-T

http://identifiers.org/hco/4/GRCh38#56311292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77000581-C-A

56311292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77000581-C-T

56311324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77000615-G-T

56311365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77000654-G-T

56311409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77000699-G-A

56311409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77000699-G-T

56311505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77000824-G-A

56311992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 77002113-G-A

http://identifiers.org/hco/4/GRCh38#56312018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77002139-C-A

http://identifiers.org/hco/4/GRCh38#56313134-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77002717-C-A

56313136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 77002719-G-A

56313136-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 77002719-G-T

http://identifiers.org/hco/4/GRCh38#56313142-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77002725-C-A

56313142-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 77002725-C-G

56313142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 77002725-C-T

56313182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 77002767-T-C

56313313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: synonymous variant
orthologous variants: 77002898-C-T

56313326-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: missense variant
orthologous variants: 77002911-G-T

56313413-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 77002996-T-G

56313426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 77003009-T-C

56313451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 77003038-G-T

56313501-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 77003089-T-A

56313501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 77003089-T-C

56313501-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 77003089-T-G

56313519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 77003107-T-C

56313628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 77003208-T-C

56313947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 77004099-A-G

56313960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 77004115-G-A

56313960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 77004115-G-T

http://identifiers.org/hco/4/GRCh38#56314005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77004143-C-A

56314005-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 77004143-C-G

56314024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 77004162-T-C

56314099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: synonymous variant
orthologous variants: 77004237-C-T

56314229-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: missense variant
orthologous variants: 77004367-G-T

56314315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: synonymous variant
orthologous variants: 77004453-G-A

http://identifiers.org/hco/4/GRCh38#56314359-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77004542-C-A

56314359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: missense variant
orthologous variants: 77004542-C-T

56314403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: missense variant
orthologous variants: 77004589-G-A

http://identifiers.org/hco/4/GRCh38#56314418-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77004604-A-C

56314418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: missense variant
orthologous variants: 77004604-A-G

http://identifiers.org/hco/4/GRCh38#56314519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77004759-C-A

56314519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: synonymous variant
orthologous variants: 77004759-C-T

56314522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: synonymous variant
orthologous variants: 77004762-G-A

56314522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: missense variant
orthologous variants: 77004762-G-T

56314524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: missense variant
orthologous variants: 77004785-T-C

56314529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: missense variant
orthologous variants: 77004790-G-A

56314529-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: stop gained
orthologous variants: 77004790-G-T

http://identifiers.org/hco/4/GRCh38#56314532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77004793-C-A

56314532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: missense variant
orthologous variants: 77004793-C-T

56314533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: missense variant
orthologous variants: 77004794-G-A

56314533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: missense variant
orthologous variants: 77004794-G-T

56314534-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: synonymous variant
orthologous variants: 77004795-G-T

56314543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: synonymous variant
orthologous variants: 77004819-G-A

56314543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: missense variant
orthologous variants: 77004819-G-T

56314546-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: synonymous variant
orthologous variants: 77004822-G-A

56314546-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: missense variant
orthologous variants: 77004822-G-C

56314546-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: missense variant
orthologous variants: 77004822-G-T

56314558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: synonymous variant
orthologous variants: 77004834-A-G

http://identifiers.org/hco/4/GRCh38#56314566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77004857-C-A

56314566-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: missense variant
orthologous variants: 77004857-C-G

56314566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: missense variant
orthologous variants: 77004857-C-T

56314669-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: synonymous variant
orthologous variants: 77004984-T-A

56314696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: synonymous variant
orthologous variants: 77005011-G-A

56314770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: missense variant
orthologous variants: 77005148-T-C

56314910-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: missense variant
orthologous variants: 77005291-G-C

56314917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: missense variant
orthologous variants: 77005298-A-G

56314933-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: synonymous variant
orthologous variants: 77005314-T-G

http://identifiers.org/hco/4/GRCh38#56315131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77005509-C-A

56315131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: synonymous variant
orthologous variants: 77005509-C-T

56315194-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: synonymous variant
orthologous variants: 77005572-G-T

56315282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: missense variant
orthologous variants: 77005657-A-G

56315291-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: missense variant
orthologous variants: 77005666-C-G

http://identifiers.org/hco/4/GRCh38#56315500-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77005854-A-C

56315537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: missense variant
orthologous variants: 77005891-G-A

56315551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: synonymous variant
orthologous variants: 77005905-G-A

56315571-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: missense variant
orthologous variants: 77005922-A-G

56315584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: synonymous variant
orthologous variants: 77005935-T-C

56315584-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: synonymous variant
orthologous variants: 77005935-T-G

http://identifiers.org/hco/4/GRCh38#56315689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77006040-C-A

56315689-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: synonymous variant
orthologous variants: 77006040-C-G

56315689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: synonymous variant
orthologous variants: 77006040-C-T

56315696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: missense variant
orthologous variants: 77006047-G-A

56315725-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: synonymous variant
orthologous variants: 77006076-A-G

56315725-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: missense variant
orthologous variants: 77006076-A-T

56315782-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: missense variant
orthologous variants: 77006133-G-T

56316141-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: missense variant
orthologous variants: 77006462-A-T

56316210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: missense variant
orthologous variants: 77006531-G-A

56316295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: synonymous variant
orthologous variants: 77006619-G-A

56316316-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: synonymous variant
orthologous variants: 77006640-G-A

56316325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: synonymous variant
orthologous variants: 77006649-C-T

56316460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: synonymous variant
orthologous variants: 77006784-A-G

56316511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: synonymous variant
orthologous variants: 77006835-G-A

http://identifiers.org/hco/4/GRCh38#56316565-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77006880-C-A

56316565-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: synonymous variant
orthologous variants: 77006880-C-G

56316565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: synonymous variant
orthologous variants: 77006880-C-T

56316644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: missense variant
orthologous variants: 77006956-A-G

56316742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 77007045-G-A

56316742-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 77007045-G-C

56316763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 77007069-G-A

56316763-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 77007069-G-T

http://identifiers.org/hco/4/GRCh38#56318484-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77010396-C-A

56318484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 77010396-C-T

56318567-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 77010443-A-T

56320861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77013422-A-G

56320861-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77013422-A-T

56320884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77013442-G-A

56320884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77013442-G-T

56320886-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77013444-A-G

56320886-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 77013444-A-T

56323108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 77013649-G-A

56323305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 77013787-T-C

http://identifiers.org/hco/4/GRCh38#56323330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77013806-C-A

56323411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: synonymous variant
orthologous variants: 77013881-T-C

56323435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: synonymous variant
orthologous variants: 77013905-G-A

56323463-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: missense variant
orthologous variants: 77013933-T-G

56323477-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: missense variant
orthologous variants: 77013947-G-C

56323584-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 77014057-T-A

56323908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 77014872-G-A

http://identifiers.org/hco/4/GRCh38#56323969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77014925-C-A

56323969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 77014925-C-T

http://identifiers.org/hco/4/GRCh38#56323973-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77014929-C-A

56323973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 77014929-C-T

http://identifiers.org/hco/4/GRCh38#56323978-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77014934-A-C

56323978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 77014934-A-G

http://identifiers.org/hco/4/GRCh38#56323987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77014943-C-A

56324073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 77014992-A-G

56324151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 77015066-T-C

56324256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 77015171-G-A

56324321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 77015233-G-A

56324340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 77015276-G-A

56325530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 77016152-G-T

56326997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 77017878-C-T

56327023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 77017903-A-G

56327447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 77018190-G-A

56327520-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 77018244-A-T

56327532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 77018262-A-G

56327536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 77018266-A-G

http://identifiers.org/hco/4/GRCh38#56327558-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77018292-C-A

56327558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 77018292-C-T

56327597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 77018326-T-C

56327624-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: intron variant
orthologous variants: 77018346-T-G

56327657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: missense_variant, synonymous_variant
orthologous variants: 77018377-C-T

http://identifiers.org/hco/4/GRCh38#56327687-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77018407-A-C

56327829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: 3 prime UTR variant
orthologous variants: 77018549-T-C

http://identifiers.org/hco/4/GRCh38#56327945-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77018666-C-A

56328160-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: 3 prime UTR variant
orthologous variants: 77018880-T-A

56328160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: 3 prime UTR variant
orthologous variants: 77018880-T-C

56328366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: 3 prime UTR variant
orthologous variants: 77019058-T-C

56328413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: 3 prime UTR variant
orthologous variants: 77019102-A-G

http://identifiers.org/hco/4/GRCh38#56328416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77019105-C-A

http://identifiers.org/hco/4/GRCh38#56328463-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77019147-C-A

56328463-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: 3 prime UTR variant
orthologous variants: 77019147-C-G

56328463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: 3 prime UTR variant
orthologous variants: 77019147-C-T

56329434-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: 3 prime UTR variant
orthologous variants: 77020089-G-C

56329545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: 3 prime UTR variant
orthologous variants: 77020199-A-G

http://identifiers.org/hco/4/GRCh38#56330220-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#77020999-C-A

56330231-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29219
most severe consequence: 3 prime UTR variant
orthologous variants: 77021007-G-T