56183944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 28534178-C-T

56183949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 28534173-G-A

http://identifiers.org/hco/2/GRCh38#56183974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#28534148-C-A

56183974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 28534148-C-T

56183991-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 28534131-T-A

56183991-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 28534131-T-G

http://identifiers.org/hco/2/GRCh38#56183998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#28534124-C-A

56183998-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 28534124-C-G

56183998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 28534124-C-T

56184002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 28534120-G-A

56184002-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 28534120-G-C

56184002-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 28534120-G-T

http://identifiers.org/hco/2/GRCh38#56184121-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#28534006-A-C

56184121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 28534006-A-G

56184301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 28533846-C-T

56184377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 28533784-G-A

56184578-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 28533584-T-G

56184611-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 28533554-A-T

56184776-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 28533404-A-T

http://identifiers.org/hco/2/GRCh38#56184847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#28533333-C-A

56184847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron_variant, missense_variant, undefined
orthologous variants: 28533333-C-T

56184905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron_variant, undefined
orthologous variants: 28533275-G-A

56184905-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron_variant, undefined
orthologous variants: 28533275-G-T

http://identifiers.org/hco/2/GRCh38#56184949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#28533225-C-A

56184949-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron_variant, undefined
orthologous variants: 28533225-C-G

56184949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron_variant, undefined
orthologous variants: 28533225-C-T

http://identifiers.org/hco/2/GRCh38#56184981-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#28533192-C-A

56184981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron_variant, undefined
orthologous variants: 28533192-C-T

56185135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron_variant, undefined
orthologous variants: 28533031-G-T

56185354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron_variant, undefined
orthologous variants: 28532816-G-A

56185354-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron_variant, undefined
orthologous variants: 28532816-G-T

56185426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron_variant, undefined
orthologous variants: 28532761-G-A

56185426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron_variant, undefined
orthologous variants: 28532761-G-T

http://identifiers.org/hco/2/GRCh38#56185461-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#28532717-A-C

56185461-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron_variant, undefined
orthologous variants: 28532717-A-T

56185554-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron_variant, undefined
orthologous variants: 28532617-T-A

http://identifiers.org/hco/2/GRCh38#56185822-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#28532429-C-A

http://identifiers.org/hco/2/GRCh38#56185858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#28532394-C-A

56185858-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron_variant, undefined
orthologous variants: 28532394-C-G

56185858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron_variant, undefined
orthologous variants: 28532394-C-T

http://identifiers.org/hco/2/GRCh38#56185905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28532346-C-A

56185983-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28532269-C-G

56186048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28532206-A-G

56186111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28532147-C-T

56186210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28532069-G-T

56186389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28531922-A-G

56186392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28531919-G-A

56186445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28531866-G-A

56186495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28531823-G-A

56186495-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28531823-G-C

56186590-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28531734-T-A

56186596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28531728-C-T

56186635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28531690-A-G

56187123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28530795-T-C

56187148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28530770-T-C

56187322-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28530635-A-G

56187693-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28530433-T-A

56187722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28530424-T-C

56187878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28530301-T-C

56187900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28530276-T-C

56188188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28529721-G-A

56188277-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28529638-C-G

56188327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28529589-A-G

56188358-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28529562-C-G

56188444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28529495-G-A

56188515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28529429-A-G

http://identifiers.org/hco/2/GRCh38#56188632-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28529312-C-A

56188656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28529288-T-C

56188666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28529278-C-T

http://identifiers.org/hco/2/GRCh38#56188836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28529113-C-A

56188836-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28529113-C-T

56188913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28529054-C-T

56188928-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28529039-G-T

56188933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28529034-G-A

56188948-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28529019-A-T

56191667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28528046-T-C

56191777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28527938-G-T

56191908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28527864-T-C

56192186-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28527687-T-G

56192214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28527664-A-G

56192461-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28527359-G-C

56192461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28527359-G-T

56192789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: missense variant
orthologous variants: 28527031-A-G

56192795-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: missense variant
orthologous variants: 28527025-T-G

56193053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: synonymous variant
orthologous variants: 28526767-T-C

56193071-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: missense variant
orthologous variants: 28526749-G-A

56193099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: missense variant
orthologous variants: 28526721-G-A

56193099-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: missense variant
orthologous variants: 28526721-G-C

56193172-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: missense variant
orthologous variants: 28526648-C-G

56193172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: synonymous variant
orthologous variants: 28526648-C-T

http://identifiers.org/hco/2/GRCh38#56193203-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28526617-A-C

56193304-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: synonymous variant
orthologous variants: 28526516-G-C

56193304-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: synonymous variant
orthologous variants: 28526516-G-T

http://identifiers.org/hco/2/GRCh38#56193410-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28526419-C-A

56193410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: missense variant
orthologous variants: 28526419-C-T

56193470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28526360-G-A

56193470-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28526360-G-C

56193470-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28526360-G-T

56193549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28526281-A-G

56193586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28526240-T-C

56193586-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28526240-T-G

56194076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28525787-C-T

56194111-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28525757-C-G

56194129-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28525739-T-G

56194544-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28525337-G-C

http://identifiers.org/hco/2/GRCh38#56194901-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28525061-A-C

56196015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28522449-C-T

56196024-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28522441-T-G

56196525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28521955-T-C

56196526-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28521954-C-G

56197519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28514328-T-C

56197761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28514092-T-C

56198270-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28513655-T-A

56198634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28513429-A-G

56198907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28513177-A-G

56199013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28513080-T-C

56199063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28513034-G-A

56199198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28512931-G-A

56200443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28510255-G-A

56200722-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28510021-G-T

56200888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28509864-A-G

56200888-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28509864-A-T

56201000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28509772-G-A

56201177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28509184-A-G

56201327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28509046-G-A

56201331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28509042-T-C

56202458-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28506702-T-A

http://identifiers.org/hco/2/GRCh38#56202664-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28506496-A-C

56202860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28506297-C-T

56203031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28506130-G-A

56203097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28506065-G-A

56204622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28505954-C-T

56204652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28505926-C-T

56204677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28505903-C-T

56204780-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28505809-A-G

56205001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28505404-C-T

56205014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28505391-G-T

56205046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28505369-C-T

56205443-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28504616-A-T

56205487-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28504574-A-G

56205614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28504459-G-T

http://identifiers.org/hco/2/GRCh38#56205821-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28504230-C-A

56205894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28504182-G-A

56205894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28504182-G-T

56205984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28504077-T-C

56206143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28503932-G-A

56206151-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28503924-T-G

56206176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28503906-A-G

56207800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28502501-T-C

56207880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28502419-T-C

http://identifiers.org/hco/2/GRCh38#56207966-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28502328-A-C

56207979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28502316-A-G

56208470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28501990-G-A

56208470-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28501990-G-T

56208639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28501846-A-G

56209239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28501268-C-T

56209669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28500864-G-A

56209803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28500707-T-C

http://identifiers.org/hco/2/GRCh38#56209974-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28500542-A-C

56209974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28500542-A-G

56210287-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28500278-T-C

56210309-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28500265-T-G

56210455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28500137-T-C

56211247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28499861-A-G

56211511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28499603-G-A

56211511-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28499603-G-T

http://identifiers.org/hco/2/GRCh38#56211941-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28499200-A-C

56212022-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28499128-G-T

56212228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28498344-T-C

http://identifiers.org/hco/2/GRCh38#56212309-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28498264-C-A

56212389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28498205-T-C

56212560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28498033-T-C

56212735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28497885-A-G

http://identifiers.org/hco/2/GRCh38#56212797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28497815-C-A

56212797-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28497815-C-G

56212899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28497713-C-T

56212946-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28497669-A-T

56213588-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28497355-T-G

56213640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28497303-T-C

56213683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28497260-C-T

56213709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28497233-T-C

http://identifiers.org/hco/2/GRCh38#56213810-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28497136-A-C

56213810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28497136-A-G

56213830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28497116-G-A

http://identifiers.org/hco/2/GRCh38#56213842-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28497105-A-C

56213842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28497105-A-G

56213906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28497045-T-C

http://identifiers.org/hco/2/GRCh38#56213969-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28496988-A-C

56214242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28496723-T-C

56215632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28493989-C-T

56215639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28493982-A-G

56215639-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28493982-A-T

56215773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28493853-T-C

56215773-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28493853-T-G

56215972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28493672-C-T

56216022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28493624-C-T

56216551-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28493097-C-G

56216551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28493097-C-T

56216603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28492821-G-A

56216603-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28492821-G-T

56220363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28492632-G-T

56220373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28492622-T-C

56220416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28492576-G-A

56220513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28492493-C-T

56220568-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28492440-T-G

56220589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28492419-T-C

56220674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28492327-G-A

56220698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28492303-A-G

56221045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28491983-A-G

56221158-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28491853-A-T

56221187-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28491821-A-T

56221597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28491119-C-T

http://identifiers.org/hco/2/GRCh38#56221768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28490964-C-A

56222402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28490579-A-G

56222482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28490511-G-A

56222482-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28490511-G-C

56222560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28490412-G-A

56223124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28489914-G-A

56223196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28489850-T-C

56223196-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28489850-T-G

56223541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28489541-G-A

56223854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28489274-C-T

56224101-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28488930-T-A

56224124-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28488907-T-G

56224189-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28488844-G-C

56234598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28486244-A-G

56234832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28486051-A-G

56234868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28486015-C-T

56234878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28486005-G-A

56235045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28485847-A-G

56235123-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28485777-G-T

http://identifiers.org/hco/2/GRCh38#56235124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28485776-C-A

56235124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28485776-C-T

http://identifiers.org/hco/2/GRCh38#56235229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#28485674-C-A

56235229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron_variant, undefined
orthologous variants: 28485674-C-T

56235463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28485310-A-G

56235478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28485295-T-C

56235601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28485180-T-C

56235606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28485175-T-C

56235717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28485102-A-G

56235891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28485042-C-T

56235998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28484944-A-G

56236037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28484908-A-G

56236255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28484681-G-A

56236357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28484609-G-A

56236372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28484594-G-A

56236372-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28484594-G-T

56236435-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28484534-C-G

56236435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28484534-C-T

56236460-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28484509-T-A

56236485-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28484484-G-T

56236559-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28484455-C-G

56236559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28484455-C-T

56236601-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28484431-C-G

56236652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28484379-A-G

56236892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28484143-A-G

56236892-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28484143-A-T

http://identifiers.org/hco/2/GRCh38#56236929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28484106-C-A

56236929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28484106-C-T

56236991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28484044-T-C

56237372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28483321-A-G

56237394-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28483288-T-G

56237709-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28482985-T-A

56237884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28482819-G-A

56238740-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28482223-C-G

56238925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28482059-T-C

56238956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28482034-A-G

56239117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28481881-G-A

http://identifiers.org/hco/2/GRCh38#56239159-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28481840-C-A

56239253-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28481747-A-G

56239253-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28481747-A-T

56239258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28481742-C-T

56239266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28481733-A-G

56239462-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28481560-C-G

56239462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28481560-C-T

56240058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28481001-T-C

56240166-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28480897-C-G

56246882-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28474932-T-G

56246907-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28474908-T-C

56247000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28474817-T-C

56247129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28474694-A-G

56247169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28474681-C-T

56247487-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28474471-T-A

56247494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28474463-C-T

56247559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28474399-G-A

56247559-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28474399-G-C

56247896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28474187-G-A

56248183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28473913-A-G

56248215-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28473881-C-T

56248547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28473554-A-G

56248637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28473145-T-C

http://identifiers.org/hco/2/GRCh38#56248883-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28472686-C-A

56248906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28472663-A-G

56249309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28472284-A-G

56249338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28472261-C-T

56249480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28472134-G-A

http://identifiers.org/hco/2/GRCh38#56249499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28472115-C-A

56249557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28472058-G-A

56249606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28472012-A-G

56249634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28471984-T-C

56249769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28471860-G-A

56250421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28470820-T-C

56250497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28470742-T-C

56250548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28470676-G-T

56251533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28469727-C-T

56251649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28469644-T-C

56251747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28469571-A-G

56251747-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28469571-A-T

56252020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28469375-C-T

56253039-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28469205-T-A

56253271-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28468987-G-T

56253368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28468938-G-A

56253796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28468735-G-A

56253906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28468640-T-C

56253948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28468600-A-G

56254032-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28468552-G-T

56254083-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28468501-T-A

56254280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28467948-C-T

56254323-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28467910-G-C

http://identifiers.org/hco/2/GRCh38#56254577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28467703-C-A

56254577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28467703-C-T

56254583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28467698-T-C

http://identifiers.org/hco/2/GRCh38#56254637-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28467642-A-C

56254637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28467642-A-G

http://identifiers.org/hco/2/GRCh38#56254701-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28467581-A-C

56254805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28467486-G-A

56254860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28467436-G-A

56254966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28467336-C-T

56255054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28467245-G-A

56255164-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28467130-G-C

56255469-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28466737-A-T

56255568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28466654-C-T

56255642-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28466595-A-T

56255712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28466521-A-G

56255895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28466375-A-G

56256570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28465209-C-T

56256626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28465157-C-T

56257533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28464487-C-T

56257574-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28464446-G-T

56257683-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28464354-C-G

56257690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28464347-G-T

56257741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28464304-G-A

http://identifiers.org/hco/2/GRCh38#56257799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28464246-C-A

56257799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28464246-C-T

56257800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28464245-A-G

56258156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28463909-A-G

56259635-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28463584-T-A

56259683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28463538-T-C

56260258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28463024-A-G

56260345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28462886-G-T

56261703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28462003-T-C

56261831-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28461951-C-G

56261831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28461951-C-T

56262017-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28461781-A-T

56262213-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28461606-T-G

56262252-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28461568-A-T

http://identifiers.org/hco/2/GRCh38#56262334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28461493-C-A

56262565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28461008-A-G

56262584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28460989-G-A

56262963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28460627-A-G

56262963-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28460627-A-T

56263439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28460203-A-G

56263479-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28460169-C-T

56263774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28459911-A-G

56263832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28459854-A-G

56264435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28459163-T-C

56264535-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28459018-C-G

http://identifiers.org/hco/2/GRCh38#56264638-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28458919-A-C

56264638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28458919-A-G

56264679-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28458901-A-G

http://identifiers.org/hco/2/GRCh38#56264687-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28458893-C-A

56264734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28458852-T-C

56264784-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28458807-T-G

56264859-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28458739-C-G

56264859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28458739-C-T

56264860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28458738-G-A

56264906-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28458680-G-C

http://identifiers.org/hco/2/GRCh38#56266839-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28457573-A-C

56266839-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28457573-A-T

56266910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28457488-G-A

56267154-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28457243-G-C

http://identifiers.org/hco/2/GRCh38#56267459-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28456946-C-A

56267474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28456931-C-T

56267609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28456796-G-A

56267609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28456796-G-T

56267632-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28456776-T-A

56267765-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28456654-T-A

56269222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28454771-C-T

56269330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28454671-C-T

56273164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28452666-A-G

56273479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28452364-A-G

56273525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28452319-T-C

http://identifiers.org/hco/2/GRCh38#56273708-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28452172-A-C

56280257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28447213-T-C

56280278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28447192-T-C

http://identifiers.org/hco/2/GRCh38#56280421-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28447059-A-C

56280421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28447059-A-G

56280616-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28447006-A-T

56280742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28446910-A-G

56280877-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28446785-C-G

56280945-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28446717-T-G

56286300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28444983-A-G

56286647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28444664-T-C

56286948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28444371-A-G

56287235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28444116-C-T

56287349-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28444010-C-G

56287976-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28443503-G-C

56288029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron_variant, undefined
orthologous variants: 28443451-C-T

56288255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron_variant, undefined
orthologous variants: 28443269-A-G

56288377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron_variant, undefined
orthologous variants: 28443155-G-A

56288377-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron_variant, undefined
orthologous variants: 28443155-G-T

56288639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28442888-G-A

56288669-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28442859-C-G

56288685-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28442843-A-T

56288802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28442708-T-C

56289098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28442433-G-A

http://identifiers.org/hco/2/GRCh38#56289143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28442390-C-A

56289152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28442381-T-C

56289260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28442283-T-C

56289352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28442191-G-A

56289437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28442115-A-G

56289578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28441982-T-C

56289580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28441980-C-T

56289606-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28441954-A-T

http://identifiers.org/hco/2/GRCh38#56289667-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28441894-A-C

56289667-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28441894-A-T

56290151-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28441448-G-A

56290327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28441271-T-C

56290329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28441269-C-T

56290448-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28441167-G-C

56290450-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28441165-G-C

56290481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28441124-G-A

http://identifiers.org/hco/2/GRCh38#56290724-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28440897-A-C

56290751-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28440870-T-G

56290757-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28440864-C-G

56290893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28440708-G-A

56290893-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28440708-G-C

56290893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28440708-G-T

56290920-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28440681-C-G

56291008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28440593-A-G

56291141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28440465-G-A

56291141-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28440465-G-T

56291300-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28440354-A-T

56291488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28440149-A-G

56291491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28440146-C-T

56291518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28440064-T-C

56291744-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28439866-T-C

56295453-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28438609-G-T

http://identifiers.org/hco/2/GRCh38#56295713-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28438379-C-A

56295792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28438299-A-G

56295926-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28438197-C-G

56296076-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28438055-T-G

56296312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28437788-G-A

56296313-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28437787-C-G

56296389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28437714-T-C

56296436-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28437671-T-G

56296466-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28437642-G-C

56296477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28437631-C-T

56296745-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28437339-A-T

56296958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28437141-T-C

56296959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28437140-A-G

http://identifiers.org/hco/2/GRCh38#56297103-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28436996-A-C

http://identifiers.org/hco/2/GRCh38#56297202-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28436917-A-C

56297398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28436698-T-C

56297431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28436674-A-G

56297561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28436394-C-T

56297570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28436385-T-C

56297617-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28436261-G-T

56297643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28436244-G-A

56297667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28436227-T-C

56297765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28436130-G-A

56297765-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28436130-G-C

56297796-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28435878-C-G

56298097-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28435570-T-A

56298097-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28435570-T-G

56298101-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28435566-A-T

56298116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28435548-T-C

56298186-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28435478-G-C

56298186-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28435478-G-T

56298223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28435441-G-A

56298233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28435431-G-A

56298261-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28435403-G-T

56298276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28435387-A-G

56298278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28435385-T-C

56298339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28435328-A-G

56298417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28435252-G-A

56298539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28434992-A-G

56298593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28434938-G-A

56298611-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28434925-C-G

http://identifiers.org/hco/2/GRCh38#56298854-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28434695-C-A

56298862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28434687-A-G

56298908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28434651-G-A

56299001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28434567-G-A

56299072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28434494-A-G

56299422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28434148-G-A

56299536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28434033-C-T

56299539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28434030-G-A

56299589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28433985-T-C

56299627-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28433947-C-G

56299788-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28433830-G-T

56300053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28433563-G-A

56300453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28433053-C-T

56300549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28432969-T-C

56300608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28432909-A-G

56300699-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28432839-A-G

56300932-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28432610-C-T

56301079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28432459-C-T

http://identifiers.org/hco/2/GRCh38#56301138-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28432413-A-C

56301202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28432359-A-G

56301371-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28432191-C-G

56302583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28430316-T-C

56302695-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28430223-G-C

56302984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28429998-A-G

56303020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28429961-G-A

56303020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28429961-G-T

56303331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28429666-A-G

http://identifiers.org/hco/2/GRCh38#56303531-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28429463-A-C

56303533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28429461-G-A

56303680-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28429356-A-G

56303865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28429180-G-A

56303872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28429171-A-G

56303880-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28429163-T-C

56304153-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28428868-G-C

56304306-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28428516-A-G

56304379-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28428444-A-G

56304434-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28428389-G-C

56304461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28428373-C-T

56304512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28428314-G-A

56304512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28428314-G-T

56305205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28428048-A-G

56305419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28427856-T-C

56305565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28427736-G-A

56305716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28427585-G-A

56305843-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28427461-T-A

56305890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28427414-G-A

56306821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28423818-C-T

56306849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28423788-A-G

56306982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28423655-A-G

56307054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28423594-T-C

56308674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28421854-T-C

56308811-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28421721-T-C

http://identifiers.org/hco/2/GRCh38#56309008-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28421546-A-C

56309342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28421170-C-T

56309355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28421157-C-T

56309498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28421011-G-A

56309806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28420734-G-A

56309848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28420692-G-A

56310026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28420547-T-C

56310065-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28420508-A-G

56310065-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28420508-A-T

56310094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28420479-G-A

56310094-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28420479-G-T

56310190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28420386-C-T

http://identifiers.org/hco/2/GRCh38#56310387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28420181-C-A

56310414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28420154-G-A

56310540-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28420028-A-G

56310553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28420015-A-G

56310997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28419560-G-T

56311157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28419404-C-T

56311288-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28419314-T-G

http://identifiers.org/hco/2/GRCh38#56311403-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28419222-A-C

56311457-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28419168-G-T

http://identifiers.org/hco/2/GRCh38#56312223-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28418401-C-A

http://identifiers.org/hco/2/GRCh38#56312514-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28418090-A-C

56312691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28417917-C-T

56312913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28417668-G-A

http://identifiers.org/hco/2/GRCh38#56312963-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28417620-A-C

56312985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28417599-A-G

56312992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28417592-G-A

56313120-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28417499-T-G

56313434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28417264-T-C

56313590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28417074-T-C

56313662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28417003-G-A

http://identifiers.org/hco/2/GRCh38#56313726-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28416941-A-C

56313742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28416925-A-G

56313897-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28416848-T-A

56313897-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28416848-T-G

56314261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28416578-G-A

56314269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28416570-A-G

56314279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28416560-T-C

56314510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28416370-T-C

56314885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28416078-G-A

56314925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28416035-G-A

56314980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28415991-G-A

56315139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28415835-A-G

56315207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28415789-G-A

56315336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28415666-G-A

56315372-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28415633-T-G

56315536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28415527-C-T

56315682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28415413-G-A

56315753-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28415353-G-T

56316570-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28411899-T-G

56316727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28411749-G-A

56317176-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28411302-G-C

http://identifiers.org/hco/2/GRCh38#56317596-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28410889-A-C

56317812-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28410694-T-G

56317877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28410634-A-G

56317944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28410589-T-C

56317984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28410550-A-G

56318067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28410466-A-G

56318073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28410460-A-G

56318276-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28410276-A-T

56318359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28410194-T-C

56318708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28409534-G-A

56318726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28409515-C-T

56318769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28409463-C-T

56318772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28409460-T-C

56318801-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28409432-C-T

56318875-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28409357-G-C

http://identifiers.org/hco/2/GRCh38#56318966-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28409274-A-C

56318970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28409270-T-C

http://identifiers.org/hco/2/GRCh38#56318980-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28409260-A-C

56318980-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28409260-A-G

56318983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28409257-A-G

http://identifiers.org/hco/2/GRCh38#56319187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28409076-C-A

56319219-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28409044-G-C

http://identifiers.org/hco/2/GRCh38#56319527-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28408799-A-C

56319550-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28408776-G-C

56319602-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28408728-C-G

56319761-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28408581-T-A

56319817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28408533-A-G

56323536-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28408162-A-T

56323676-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28408016-A-G

56323730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28407962-T-C

56323748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28407944-G-T

56323776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28407916-C-T

56323782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28407912-A-G

56324076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28407639-T-C

56324076-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28407639-T-G

56324134-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28407581-T-G

56324211-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28407519-G-A

56324249-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28407478-G-T

http://identifiers.org/hco/2/GRCh38#56324577-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28407155-C-A

56324577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28407155-C-T

56324726-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28407002-C-G

56324753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28406975-T-C

http://identifiers.org/hco/2/GRCh38#56324914-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28406839-C-A

56325266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28406514-G-A

56325266-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28406514-G-C

56325514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28405754-T-C

56325923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28405567-A-G

56326040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28405465-G-A

56326041-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28405464-C-G

56326041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28405464-C-T

56326124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28405394-A-G

56326287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28405237-G-T

http://identifiers.org/hco/2/GRCh38#56326459-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28405069-A-C

56328490-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28400940-C-T

56328732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28400689-G-A

56328969-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28400322-T-G

56329008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28400283-A-G

56329246-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28400079-G-A

56329246-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28400079-G-C

56329246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28400079-G-T

56329527-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28399833-A-T

http://identifiers.org/hco/2/GRCh38#56329825-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28399616-A-C

56329933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28399519-T-C

56330038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28399463-G-A

56330038-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28399463-G-T

56330249-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28399242-G-C

56331744-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28391825-G-A

56331744-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28391825-G-C

56331873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28391694-T-C

56331934-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28391631-C-G

56331934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28391631-C-T

56332027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28391555-G-A

56332085-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28391495-G-A

http://identifiers.org/hco/2/GRCh38#56332290-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28391277-C-A

56332538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28391090-G-T

56332590-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28391037-A-T

http://identifiers.org/hco/2/GRCh38#56332739-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28390979-A-C

56333194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28390734-G-A

56333194-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28390734-G-C

56333194-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28390734-G-T

56333405-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28390544-G-C

56333481-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28390468-A-G

56333638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28390342-G-A

56333886-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28390145-A-T

56334309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28389853-C-T

56334324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28389838-G-A

http://identifiers.org/hco/2/GRCh38#56334331-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28389831-A-C

56334364-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28389795-C-G

56334468-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28389706-G-C

56334574-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28389612-G-C

56334633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28389580-C-T

56334637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28389576-T-C

56334722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28389492-G-A

56334741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28389479-C-T

http://identifiers.org/hco/2/GRCh38#56334751-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28389469-A-C

56334751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28389469-A-G

http://identifiers.org/hco/2/GRCh38#56334794-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28389428-A-C

56334794-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28389428-A-T

56334827-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28389407-C-G

56334839-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28389395-A-T

56334865-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28389369-G-C

56334889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28389355-A-G

56335112-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28389137-A-G

56335435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28388864-A-G

56335435-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28388864-A-T

56335491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28388805-C-T

56335543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28388762-G-A

56335589-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28388716-G-C

56338790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28387676-C-T

56338804-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28387670-G-C

56338817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28387655-G-A

56338996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28387496-C-T

56339017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28387476-T-C

56339059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28387449-C-T

56339240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28387285-T-C

56339285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28387240-C-T

56339339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28387202-T-C

56339504-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28386899-G-C

56339646-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28386763-G-C

56339775-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28386638-T-G

56339784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28386629-G-A

56340095-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28386390-G-T

56340249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28385246-G-A

56340254-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28385241-T-A

56340278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28385213-A-G

56340359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28385127-G-A

56340359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28385127-G-T

56340374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28385112-G-T

56341413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28385086-G-A

56341413-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28385086-G-C

56341413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28385086-G-T

56341477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28385016-A-G

56341500-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28384993-C-G

56341500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28384993-C-T

56341727-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28384789-G-T

56341847-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28384642-C-G

56342058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28384425-T-C

56342685-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28384329-G-C

http://identifiers.org/hco/2/GRCh38#56342808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28384226-C-A

56342808-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28384226-C-G

56343005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28384029-G-A

56343005-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28384029-G-C

56343005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28384029-G-T

56343034-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28384000-G-T

56343091-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28383955-G-T

56343097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28383949-G-A

http://identifiers.org/hco/2/GRCh38#56343226-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28383864-A-C

56343285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28383810-G-A

56343664-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28383440-C-G

56343664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28383440-C-T

56344761-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28382896-C-G

56345110-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28382313-A-G

56345231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28382210-A-G

56346790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28374358-T-C

56347090-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28374083-T-A

56347099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28374074-A-G

56347116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28374058-T-C

56347116-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28374058-T-G

56347234-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28373929-T-A

56347234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28373929-T-C

56347238-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28373925-G-T

56347431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28373776-C-T

http://identifiers.org/hco/2/GRCh38#56347558-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28373687-A-C

http://identifiers.org/hco/2/GRCh38#56347660-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28373592-A-C

56347862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28373408-G-A

56347862-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28373408-G-T

56347878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28373392-C-T

56347888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28373387-A-G

56348165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28373126-A-G

56348264-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28373039-C-G

56348264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28373039-C-T

56348760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28372558-G-A

56348920-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28372402-T-A

56348920-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28372402-T-G

56349017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28372254-G-T

56349417-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28371938-A-T

56349438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28371916-A-G

56349453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28371901-G-A

56349551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28371813-A-G

56349607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28371757-G-A

56352679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28371262-T-C

56352679-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28371262-T-G

56352743-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28371205-T-C

56352813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28371135-A-G

56353096-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28370858-C-G

56353096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28370858-C-T

56353120-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28370835-G-A

56353139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28370816-G-A

56353336-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28370632-A-T

56353338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28370630-G-A

56353338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28370630-G-T

56353445-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28370525-T-G

56353496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28370476-T-C

56353514-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28370448-C-T

56354103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28368954-A-G

56354103-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28368954-A-T

http://identifiers.org/hco/2/GRCh38#56354107-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28368950-A-C

56354432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28367872-G-A

56354592-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28367721-A-G

56354628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28367685-A-G

56355339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28367022-C-T

http://identifiers.org/hco/2/GRCh38#56355382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28367003-C-A

56355424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28366967-G-A

http://identifiers.org/hco/2/GRCh38#56355592-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28366657-A-C

56355690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28366545-A-G

56355761-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28366487-G-C

56355802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28366446-T-C

56355885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28366365-T-C

56355943-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28366318-C-G

56355943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28366318-C-T

http://identifiers.org/hco/2/GRCh38#56355974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28366287-C-A

56355985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28366276-A-G

56356119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28366144-C-T

56356158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28366113-A-G

56356253-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28365936-T-A

56356253-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28365936-T-C

56357797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28365158-C-T

56358117-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28364860-A-T

56358229-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28364770-G-A

http://identifiers.org/hco/2/GRCh38#56358271-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28364729-A-C

56358527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28364499-G-A

56358528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28364498-T-C

56358679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28364330-C-T

56358681-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28364328-G-C

56359090-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28364183-A-G

56359090-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28364183-A-T

56359092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28364181-G-T

56359191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28364107-C-T

56359248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28364065-T-C

56359313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28364043-G-A

56359350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28364014-C-T

56359425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28363960-G-T

http://identifiers.org/hco/2/GRCh38#56359476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28363910-C-A

56359476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28363910-C-T

56359505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28363882-T-C

56359937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28363495-A-G

56359959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28363472-A-G

56360239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28363214-T-C

56360300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28363153-C-T

56360312-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28363141-A-T

56360319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28363134-G-A

56360337-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28363117-T-A

56360369-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28363085-G-C

56365382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28357991-T-C

56365446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28357933-G-A

http://identifiers.org/hco/2/GRCh38#56365505-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28357873-C-A

56365524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28357854-G-A

56365524-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28357854-G-C

56365757-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28357453-T-A

56365988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28357254-A-G

56366092-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28357148-T-G

56366132-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28357109-A-T

56366200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28357033-T-C

56366565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28356375-T-C

56366770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28356142-A-G

56367168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28355805-T-C

56367316-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28355659-G-C

56367362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28355626-G-A

56369020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28352918-C-T

56369154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28352792-C-T

56369366-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28352604-G-T

http://identifiers.org/hco/2/GRCh38#56369373-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28352597-A-C

56369852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28352163-C-T

56370868-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28351158-G-C

56370896-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28351128-A-T

56370959-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28351077-T-G

56371011-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28351026-G-A

56371134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28350914-T-C

56371192-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28350788-G-A

56371236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28350706-G-A

56371302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28350576-A-G

http://identifiers.org/hco/2/GRCh38#56371390-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28350370-A-C

56371459-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28350306-T-G

56371788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28350021-T-C

56371914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28349917-T-C

56371930-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28349901-T-C

56372130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28349712-A-G

56372256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28349596-T-C

56372343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron_variant, splice_acceptor_variant
orthologous variants: 28349509-G-A

56372343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron_variant, splice_acceptor_variant
orthologous variants: 28349509-G-T

56372561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28349284-G-A

56372578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28349267-A-G

56372614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28349248-G-A

56372621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28349241-G-T

56372699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28349157-C-T

56372751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28349123-G-A

56372777-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28349111-T-A

56372777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28349111-T-C

56372918-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28348977-G-T

56373134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28348691-G-A

56373142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28348684-A-G

56373151-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28348675-A-G

56373307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28348281-T-C

56373422-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28348184-A-T

http://identifiers.org/hco/2/GRCh38#56373709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28347907-C-A

56373729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28347890-T-C

56373753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28347866-A-G

56373793-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28347824-T-G

56373837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28347781-A-G

56373883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28347739-C-T

56373898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28347725-A-G

56374233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28347418-G-A

56374334-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28347321-T-A

56374334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28347321-T-C

56374877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28347082-G-A

http://identifiers.org/hco/2/GRCh38#56374930-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28347035-A-C

56375112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28346861-T-C

56375284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28346731-G-A

56375393-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28346600-C-G

56375393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28346600-C-T

56375577-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28346431-G-C

56375732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28346247-G-A

56375978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28346015-G-A

56376015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28345981-G-A

56376015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28345981-G-T

56376053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28345943-T-C

56376053-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28345943-T-G

56376570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28345500-T-C

56376620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28345459-T-C

56376644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28345439-C-T

56376652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28345431-A-G

56376684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28345396-A-G

56376914-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28345200-A-G

56377086-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28345034-A-G

56377285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28344845-T-C

56377390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28344741-A-G

56377445-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28344686-C-G

56377913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28344469-G-T

http://identifiers.org/hco/2/GRCh38#56377918-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28344463-A-C

56378240-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28344238-C-G

56378335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28344170-T-C

56378354-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28344152-C-G

56378609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28343927-G-A

56378704-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28343871-G-C

56378813-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28343783-G-A

56378874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28343719-T-C

56379296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28343378-A-G

56379338-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28343348-A-T

56380362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28342396-C-T

http://identifiers.org/hco/2/GRCh38#56380622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28342325-C-A

56381302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28341767-A-G

56381403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28341487-C-T

56381612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28341298-G-A

56381612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28341298-G-T

56381696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28341207-A-G

56382182-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28340759-C-G

56382379-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28340582-T-A

56382380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28340581-T-C

56382386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28340575-C-T

56383203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28339880-G-T

56383212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28339871-G-A

56383336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28339761-A-G

56383419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28339692-T-C

56383419-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28339692-T-G

56383475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28339638-T-C

56383499-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28339620-G-T

56383629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28339548-A-G

56383720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28339475-C-T

56384011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28339213-C-T

http://identifiers.org/hco/2/GRCh38#56384156-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28339049-C-A

56384156-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28339049-C-G

56384156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28339049-C-T

56384194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28339012-A-G

http://identifiers.org/hco/2/GRCh38#56384241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#28338971-C-A

56384241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: intron variant
orthologous variants: 28338971-C-T

56384358-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: 3 prime UTR variant
orthologous variants: 28338854-T-A

56384358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: 3 prime UTR variant
orthologous variants: 28338854-T-C

56384686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: 3 prime UTR variant
orthologous variants: 28338549-G-A

56384686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: 3 prime UTR variant
orthologous variants: 28338549-G-T

56384831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: 3 prime UTR variant
orthologous variants: 28338413-G-A

56385206-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: 3 prime UTR variant
orthologous variants: 28338069-C-G

56385294-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: 3 prime UTR variant
orthologous variants: 28337980-G-C

56385317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: 3 prime UTR variant
orthologous variants: 28337954-T-C

56385697-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29400
most severe consequence: 3 prime UTR variant
orthologous variants: 28337617-A-T