http://identifiers.org/hco/18/GRCh38#64080619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107628229-C-A

64080666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107628284-A-G

64080685-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107628301-G-C

64080813-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107628829-T-A

64080840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107628856-G-A

64080970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107628999-T-C

http://identifiers.org/hco/18/GRCh38#64080994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107629022-C-A

64080994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107629022-C-T

64081043-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107629074-G-C

http://identifiers.org/hco/18/GRCh38#64081060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107629091-C-A

http://identifiers.org/hco/18/GRCh38#64081137-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107629161-C-A

64081137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107629161-C-T

64081197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107629222-A-G

64081290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107629311-G-A

64081290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107629311-G-T

64081477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107629496-A-G

64082603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107629927-C-T

64082754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107630049-G-A

64082859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107630141-C-T

64082888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107630160-T-C

64083019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107630285-T-C

64083020-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107630286-A-T

http://identifiers.org/hco/18/GRCh38#64083087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107630350-C-A

64083134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107630397-T-C

64083334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107630618-G-A

64083453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107630727-C-T

64083465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107630739-A-G

64083485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107630755-C-T

64083643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107630916-G-A

64083693-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107630951-T-A

64083693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107630951-T-C

64084886-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107632950-T-G

64086213-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107633572-A-T

64086302-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107633663-G-T

64086414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107633775-T-C

64086527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107633875-C-T

64087036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107634357-T-C

64087672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107635418-G-A

64087672-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107635418-G-T

64088202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107635551-A-G

64088379-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107635709-C-G

64091997-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107637132-C-G

64092100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107637227-G-T

64092657-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107637499-C-G

64092716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107637572-C-T

64092854-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107637687-T-A

64093289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107638122-C-T

http://identifiers.org/hco/18/GRCh38#64094297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107638437-C-A

64094297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107638437-C-T

64094313-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107638456-A-T

64094470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107638597-G-A

64094470-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107638597-G-C

64095162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107639312-G-A

64095240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107639387-C-T

64095436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107639572-C-T

64096099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107639982-G-A

64096099-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107639982-G-T

64096157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107640043-A-G

64096282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107640180-G-T

64096370-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107640386-C-G

64096582-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107640702-A-G

64096732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107640825-A-G

64097035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107641140-C-T

64097380-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107641504-A-G

http://identifiers.org/hco/18/GRCh38#64097551-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107641667-C-A

64097693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107641815-A-G

64097693-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107641815-A-T

64097761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107641882-A-G

http://identifiers.org/hco/18/GRCh38#64097772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107641896-C-A

64097865-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107642000-C-G

64097865-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107642000-C-T

http://identifiers.org/hco/18/GRCh38#64097894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#107642025-C-A

64097894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 107642025-C-T

http://identifiers.org/hco/18/GRCh38#64097928-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107642059-A-C

64097932-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107642063-G-A

64098042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 107642151-C-T

http://identifiers.org/hco/18/GRCh38#64098118-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107642226-C-A

64098153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107642261-C-T

64098154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107642262-T-C

64098230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107642330-C-T

64098237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107642337-G-A

64098395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107642494-C-T

64098536-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107642625-G-T

64098597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107642668-T-C

64098737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107642834-T-C

http://identifiers.org/hco/18/GRCh38#64098852-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107642950-C-A

64098852-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107642950-C-T

64098918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107642983-T-C

64098924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107642989-T-C

64098979-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107643038-C-G

64099172-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107643212-A-G

64099220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107643251-G-A

64099412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107643452-G-A

64099446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107643483-A-G

64099651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107643694-G-A

64099820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107643857-A-G

64099998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107644054-A-G

64100035-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107644092-C-G

64100086-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107644139-T-G

64100172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107644253-G-T

64100536-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107644582-C-G

64100699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107644716-C-T

64100845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107644957-T-C

64100937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107645043-G-A

64100940-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107645046-C-G

64100966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107645071-T-C

64101607-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107646716-C-G

64101924-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107647004-G-C

http://identifiers.org/hco/18/GRCh38#64102013-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107647093-C-A

64102149-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107647228-A-G

64102325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107647393-A-G

64102326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107647394-G-A

64102381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107647433-A-G

64103657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107648569-C-T

64103681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107648595-T-C

64103687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107648601-C-T

64103827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107648776-T-C

64103831-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107648780-G-C

64103831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107648780-G-T

64103854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107648803-C-T

64104000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107648941-G-A

64104000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107648941-G-T

64104073-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107649017-T-G

64104129-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107649079-T-A

http://identifiers.org/hco/18/GRCh38#64104310-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107649251-C-A

64104310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107649251-C-T

64104474-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107649403-C-G

64104474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107649403-C-T

http://identifiers.org/hco/18/GRCh38#64104506-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107649435-C-A

64104694-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107649627-G-C

64104819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107649687-G-A

64104924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107649792-G-A

http://identifiers.org/hco/18/GRCh38#64104967-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107649836-C-A

64105065-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107649916-C-G

http://identifiers.org/hco/18/GRCh38#64105471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107650364-C-A

64105491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107650384-A-G

http://identifiers.org/hco/18/GRCh38#64105718-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107650601-C-A

64106157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107651029-C-T

64106369-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107651244-C-G

64106438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107651310-C-T

64106474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107651346-G-A

64106487-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107651361-C-G

64106733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107651585-A-G

64106734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107651586-G-A

64106783-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107651617-G-C

64106999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107651832-G-A

64107011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107651840-T-C

64107069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107651890-T-C

64107076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107651897-A-G

64107177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107651985-G-A

64107622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107652391-T-C

64107793-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107652540-G-C

64107824-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107652572-C-G

64107911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107652657-G-A

64107911-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107652657-G-T

http://identifiers.org/hco/18/GRCh38#64107953-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107652675-A-C

64108177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107652895-C-T

64108182-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107652900-T-G

http://identifiers.org/hco/18/GRCh38#64108259-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107653001-A-C

64108288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107653030-G-A

64108593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107653311-G-A

http://identifiers.org/hco/18/GRCh38#64108738-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107653438-C-A

64108764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107653465-A-G

64108915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107653558-G-A

64109107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107653750-A-G

http://identifiers.org/hco/18/GRCh38#64109219-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107653827-A-C

http://identifiers.org/hco/18/GRCh38#64110451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107654301-C-A

64110456-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107654303-T-G

64110462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107654309-G-A

64110509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107654358-G-A

http://identifiers.org/hco/18/GRCh38#64110602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107654422-C-A

64110649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107654468-G-A

64110666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107654479-T-C

64110746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107654552-C-T

64110957-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107654768-G-C

64111097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107654907-C-T

64111155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107654963-A-G

64111271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107655072-C-T

http://identifiers.org/hco/18/GRCh38#64111276-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107655077-A-C

64111368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107655164-C-T

64111385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107655181-C-T

64111386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107655182-G-A

64111410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107655206-A-G

64111724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107656020-T-C

64112164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107656464-C-T

64112169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107656469-T-C

64112179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107656479-G-A

64112194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107656494-C-T

64112239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107656539-T-C

64112239-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107656539-T-G

64112274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107656574-A-G

64112289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107656589-C-T

64112290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107656590-G-A

http://identifiers.org/hco/18/GRCh38#64116332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107660251-C-A

64116894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107660638-G-A

64116894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107660638-G-T

64117106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107660836-A-G

http://identifiers.org/hco/18/GRCh38#64117512-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107661251-A-C

64117642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107661397-G-A

64117713-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107662036-C-T

64117783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107662102-G-A

64117869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107662184-A-G

64117885-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107662200-A-T

64117887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107662202-G-T

64118387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107662676-G-A

64118431-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107662723-T-A

64118533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107662815-A-G

http://identifiers.org/hco/18/GRCh38#64118761-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107663986-C-A

64119105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107664569-G-A

64119441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107664943-T-C

64119450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107664952-A-G

http://identifiers.org/hco/18/GRCh38#64120179-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107666294-C-A

64120209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107666323-C-T

64120719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107667063-C-T

64121004-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107667347-T-A

64121109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107667449-C-T

64124424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107669891-C-T

64124799-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107670251-T-A

64124965-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107670407-G-C

64125061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107670504-G-A

64126786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107674694-G-A

64126836-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107674738-A-T

64126953-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107674839-T-A

64127289-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107675146-T-G

64127382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 107675238-C-T

64127384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 107675240-G-A

64127384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant, splice_acceptor_variant
orthologous variants: 107675240-G-T

64127417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107675271-A-G

64127554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107675412-G-A

64127554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107675412-G-T

64127706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107675572-G-A

64127773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107675625-T-C

64128037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107676407-T-C

64128225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107676590-T-C

64128495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107676863-C-T

64128674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107677040-G-A

http://identifiers.org/hco/18/GRCh38#64128781-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107677146-A-C

64128781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107677146-A-G

64129219-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107677550-C-G

64129243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107677574-C-T

http://identifiers.org/hco/18/GRCh38#64129245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107677576-C-A

64129500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107677808-A-G

64129730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107678032-T-C

64129730-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107678032-T-G

64129752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107678071-T-C

64130326-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107678699-A-T

64130330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107678703-C-T

64130369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107687535-G-A

64130369-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107687535-G-C

64130499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107687644-C-T

64130553-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107687694-C-G

64130572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107687711-G-A

64130572-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107687711-G-T

64130939-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107688029-C-G

64131002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107688092-T-C

64131233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107688314-C-T

64131362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107688443-C-T

64131545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107688626-T-C

64132184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107689264-A-G

http://identifiers.org/hco/18/GRCh38#64132549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107689586-C-A

64132549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107689586-C-T

64132623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107689661-G-A

64132670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107689706-A-G

64132670-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107689706-A-T

64132781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107689846-G-A

64132898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107689945-C-T

64132936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107689983-G-A

64132936-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107689983-G-C

64132936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107689983-G-T

64133155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107690178-G-A

64133899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107692539-G-A

64133901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107692541-C-T

64133916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107692556-C-T

64134148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107693476-T-C

64134451-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107693776-T-G

64134477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107693802-C-T

64134593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107693911-G-A

64134609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 107693927-G-A

64134666-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107693987-C-G

64137215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107694314-A-G

http://identifiers.org/hco/18/GRCh38#64137322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107694420-C-A

64137570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107694568-G-T

http://identifiers.org/hco/18/GRCh38#64138515-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107695511-C-A

64138515-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107695511-C-G

http://identifiers.org/hco/18/GRCh38#64138631-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107695624-A-C

64138840-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107695882-G-T

64139040-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107696078-G-T

http://identifiers.org/hco/18/GRCh38#64139331-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107696353-C-A

64139331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107696353-C-T

64139593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107696594-G-A

http://identifiers.org/hco/18/GRCh38#64141801-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107701882-C-A

64142105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107702174-G-A

64142105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107702174-G-T

64142398-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107702563-G-C

http://identifiers.org/hco/18/GRCh38#64142612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107702776-C-A

64143109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107703861-G-A

64143243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107703964-C-T

64145784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107705183-G-A

http://identifiers.org/hco/18/GRCh38#64145871-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107705261-A-C

64145909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107705304-C-T

64145922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107705317-A-G

64145977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107705372-T-C

64146015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107705408-G-A

64146017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107705410-G-T

64146060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107705461-T-C

64146174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107706637-T-C

64146572-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107707025-T-A

64146572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107707025-T-C

http://identifiers.org/hco/18/GRCh38#64146610-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107707054-C-A

64146702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107707128-T-C

64146873-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107707344-C-G

64147045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107707523-T-C

64147359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107707779-G-T

64147411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107707829-T-C

64147685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107708017-C-T

64147815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107708164-G-A

64147880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107708265-G-A

64148171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107709210-T-C

http://identifiers.org/hco/18/GRCh38#64148228-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107709243-C-A

64148414-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107709405-T-A

64148655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107709601-T-C

64148681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107709624-T-C

64148744-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 107709664-A-T

64148779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107709699-T-C

64148782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107709702-A-G

64148806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107709716-G-T

64148860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 107709775-G-A

64148860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 107709775-G-T

http://identifiers.org/hco/18/GRCh38#64148964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107709850-C-A

64148967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107709853-G-T

http://identifiers.org/hco/18/GRCh38#64148969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107709857-C-A

http://identifiers.org/hco/18/GRCh38#64149028-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#107709897-C-A

64149044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107709913-G-A

64149044-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107709913-G-C

64149044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 28597
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 107709913-G-T