28180425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 53045410-G-T

28181436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53046352-G-A

28182130-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53046990-G-C

28182507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53047363-G-A

28182520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53047376-C-T

28182527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53047380-G-A

28182619-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53047479-C-G

28182619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53047479-C-T

28182944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53047786-G-T

28183285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53048005-G-A

28183341-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53048062-A-T

28183499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53048208-G-A

28183500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53048209-C-T

28183545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53048275-C-T

28183607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53048348-T-C

28183607-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53048348-T-G

28183712-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53048456-A-T

28183820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53048552-C-T

28183821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53048553-G-A

28184222-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53048908-G-T

28184348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53049070-A-G

28184460-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53049172-T-G

28184539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53049250-A-G

28185816-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53050092-C-T

28185857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53050123-A-G

28185871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53050151-T-C

28185871-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53050151-T-G

28185879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53050159-T-C

http://identifiers.org/hco/7/GRCh38#28185884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#53050164-C-A

28185884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53050164-C-T

28186032-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53050308-A-G

28186976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53051738-G-A

28186996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53051758-T-C

28187016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53051776-A-G

28187078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53051841-G-A

28187245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53052011-A-G

28187641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53052418-C-T

28187968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53053102-C-T

28187989-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53053123-C-G

28187992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53053126-C-T

28188116-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53053230-T-G

28188500-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53053614-G-C

28188778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53054263-A-G

28189528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53055141-G-A

28189859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53055445-A-G

28189892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53055477-G-A

28189981-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53055569-T-G

http://identifiers.org/hco/7/GRCh38#28189995-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#53055583-A-C

28189995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53055583-A-G

28190639-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53056170-T-C

28190704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53056237-G-A

http://identifiers.org/hco/7/GRCh38#28191081-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#53056663-C-A

28192260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53058066-T-C

28192418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53058175-T-C

28192455-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53058212-C-G

28192591-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53058348-G-C

28192997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53058839-A-G

28193109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53058937-C-T

http://identifiers.org/hco/7/GRCh38#28196546-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#53062186-C-A

28198388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53063424-G-A

28199011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53063714-A-G

28199011-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53063714-A-T

28199209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53063876-G-A

28199239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53063905-T-C

28199358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53063997-C-T

http://identifiers.org/hco/7/GRCh38#28199383-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#53064022-A-C

28199483-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53064102-G-T

28199503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53064122-A-G

http://identifiers.org/hco/7/GRCh38#28200105-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#53064331-A-C

28200105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53064331-A-G

28200153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53064377-T-C

28200153-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53064377-T-G

28200194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53064409-C-T

28200271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53064480-A-G

28200285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53064494-T-C

28200295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53064504-G-T

28201001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53065953-G-A

28201217-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53066165-T-C

28210969-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53068979-T-G

http://identifiers.org/hco/7/GRCh38#28211775-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#53069825-C-A

28214457-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53071524-A-T

28214458-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53071525-A-T

28215351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53072103-A-G

http://identifiers.org/hco/7/GRCh38#28215469-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#53072228-A-C

28216098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53072502-A-G

28216272-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53072660-T-G

28217113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53073517-A-G

28217129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53073533-A-G

28217343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 53074574-C-T

http://identifiers.org/hco/7/GRCh38#28217891-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#53075553-A-C

28217974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53075638-C-T

28218095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53075763-G-A

28218282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53076002-G-T

28218341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53076061-A-G

28218368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53076088-G-T

http://identifiers.org/hco/7/GRCh38#28218382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#53076102-C-A

28218926-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53076709-T-A

28218983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53076762-C-T

28219111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53076888-A-G

28219212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53076984-T-C

28219213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53076985-A-G

28219328-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53077097-T-C

28219353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53077121-T-C

28219413-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53077178-T-A

28219525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53077270-G-A

28219750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53077488-G-A

28220129-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53084432-A-T

28220135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53084438-A-G

28222903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53091153-C-T

28223288-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53091467-A-G

28223351-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53091531-G-T

28223363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53091543-A-G

http://identifiers.org/hco/7/GRCh38#28223383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#53091564-C-A

28223431-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53091599-T-A

28223627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53092331-G-A

28223817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53092496-G-A

28224193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53092929-A-G

http://identifiers.org/hco/7/GRCh38#28224194-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#53092930-A-C

http://identifiers.org/hco/7/GRCh38#28224245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#53093175-C-A

28224245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53093175-C-T

28224283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53093213-A-G

28224586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53093546-T-C

28224619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53093609-G-A

28224789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53094094-G-A

http://identifiers.org/hco/7/GRCh38#28224924-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#53094245-A-C

28224925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53094246-A-G

28224990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53094308-C-T

28225102-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53094425-T-G

28225235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53094537-C-T

28225236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53094538-G-A

28225366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53094672-G-A

28225459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53094765-A-G

28225780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53095072-G-A

28225941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53095240-G-A

28226018-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53095312-C-G

28226191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53095399-C-T

28226237-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53095447-C-G

28226390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53095585-A-G

28226450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53095647-T-C

28226485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53095693-T-C

28226518-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53095730-T-G

28228270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53096283-T-C

28228270-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53096283-T-G

28228487-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53096467-A-T

28228519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53096499-C-T

28228527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53096507-G-A

28228713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53096688-G-T

28228739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53096716-G-A

28228739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53096716-G-T

28228743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53096720-A-G

28228788-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53096764-T-G

28228923-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53097423-T-A

28229633-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53098020-A-T

28229638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53098025-G-A

28229641-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53098028-G-T

28231165-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53098145-T-G

28231205-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53098210-G-T

28231400-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53100812-G-C

28231416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53100833-G-A

28231418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53100835-A-G

28231499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53100914-T-C

http://identifiers.org/hco/7/GRCh38#28231660-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#53101067-C-A

28231660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53101067-C-T

28231689-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53101095-G-C

28231689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53101095-G-T

28231754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53101154-G-A

28232038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53101398-G-A

28232038-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53101398-G-C

28232049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53101410-G-A

28232049-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53101410-G-C

28232060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53101421-G-A

28232116-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53101511-A-T

http://identifiers.org/hco/7/GRCh38#28232326-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#53101626-C-A

28232326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53101626-C-T

28232360-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53101660-T-A

28232360-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53101660-T-G

28232398-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53101698-T-C

28233461-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53102470-G-C

http://identifiers.org/hco/7/GRCh38#28233469-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#53102483-A-C

28233555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53102543-T-C

28233606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53102597-T-C

28233625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53102616-A-G

28234465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53102950-G-A

28234513-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53102991-C-G

28236970-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53104414-T-A

28236984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53104428-C-T

28237018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53104467-A-G

28237283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53104684-G-T

http://identifiers.org/hco/7/GRCh38#28237325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#53104702-C-A

28237458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53104815-T-C

28237535-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53104887-T-A

28237598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53104940-C-T

28237939-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53106386-T-A

28237939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53106386-T-C

28237946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53106393-T-C

http://identifiers.org/hco/7/GRCh38#28238271-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#53107063-A-C

28238271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53107063-A-G

28238473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53107247-G-A

28238925-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 53107522-A-T

28239906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53108179-G-A

28239906-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53108179-G-T

28239971-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53108246-G-C

28239971-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 53108246-G-T

http://identifiers.org/hco/7/GRCh38#28240139-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#53108396-A-C

28241327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: non coding transcript exon variant
orthologous variants: 53109333-T-C

28241328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: non coding transcript exon variant
orthologous variants: 53109334-A-G

28241328-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: non coding transcript exon variant
orthologous variants: 53109334-A-T

28241374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: non coding transcript exon variant
orthologous variants: 53109380-C-T

28241413-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: non coding transcript exon variant
orthologous variants: 53109415-G-C

28241413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: non coding transcript exon variant
orthologous variants: 53109415-G-T

28241462-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: non coding transcript exon variant
orthologous variants: 53109464-G-T

28241998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: non coding transcript exon variant
orthologous variants: 53110540-T-C

28242207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: non coding transcript exon variant
orthologous variants: 53110738-G-A

28242816-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: non coding transcript exon variant
orthologous variants: 53111283-G-T

28243075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: non coding transcript exon variant
orthologous variants: 53111501-A-G

28243124-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: non coding transcript exon variant
orthologous variants: 53111549-A-G

28243188-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: non coding transcript exon variant
orthologous variants: 53111604-G-T

28243196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: non coding transcript exon variant
orthologous variants: 53111612-C-T

28243197-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: non coding transcript exon variant
orthologous variants: 53111613-T-A

28243198-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: non coding transcript exon variant
orthologous variants: 53111614-C-G

28243237-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: non coding transcript exon variant
orthologous variants: 53111646-G-T

28243318-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 41218
most severe consequence: non coding transcript exon variant
orthologous variants: 53111693-T-A