124823812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59050496-C-T

124823899-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59050581-C-T

124824066-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59050743-T-A

124824066-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59050743-T-G

124827004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59051946-G-A

124827139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59052062-C-T

124827255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59052178-C-T

124827938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59053840-A-G

124828730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59054474-G-A

124828922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59054649-T-C

124829773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59055038-C-T

124829959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59055224-A-G

http://identifiers.org/hco/8/GRCh38#124830104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59055329-C-A

124830108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59055333-T-C

124830199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59055413-A-G

124831162-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59056145-G-T

http://identifiers.org/hco/8/GRCh38#124831180-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59056164-C-A

124831420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59056501-T-C

124831421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59056502-G-A

124831421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59056502-G-T

124831446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59056536-G-A

124831550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59056641-T-C

124831844-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59056895-A-G

124832430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59057628-C-T

124832768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59058483-G-A

124832788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59058507-G-A

124832906-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59058604-T-G

124833051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59058718-G-A

124834160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59059743-G-A

124834323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59059897-G-A

124834323-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59059897-G-C

124834334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59059908-C-T

124834559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 59060070-G-A

124834575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59060086-C-T

124834602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 59060111-T-C

124834726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59060239-C-T

124834750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59060263-C-T

124834751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59060264-G-A

124834818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 59060331-G-A

124834818-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 59060331-G-C

124834818-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 59060331-G-T

http://identifiers.org/hco/8/GRCh38#124834923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59060436-C-A

124834923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59060436-C-T

124834971-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59060484-G-T

124835100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59060617-A-G

124835179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59060695-G-A

124835179-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59060695-G-T

124835325-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59060807-T-G

124835493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59061800-T-C

124835880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59062205-C-T

124835980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59062350-C-T

124835985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59062355-G-T

124836000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59062370-C-T

124836305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59062642-G-T

124838903-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59066398-T-A

124839134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59066619-G-A

124839134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59066619-G-T

124839139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59066624-G-A

124839229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59066708-C-T

124839329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59066783-T-C

124840403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59067661-G-A

124840403-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59067661-G-T

124840406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59067664-A-G

124840406-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59067664-A-T

124840407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59067665-C-T

124840436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 59067700-C-T

124840482-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 59067740-C-G

124840486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59067744-G-A

124840505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59067764-T-C

124840622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59067890-A-G

http://identifiers.org/hco/8/GRCh38#124840639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59067908-C-A

124840935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59068083-A-G

124841003-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59068159-G-T

124841069-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59068226-T-G

124841740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59068488-T-C

124841776-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59068527-G-C

http://identifiers.org/hco/8/GRCh38#124841828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59068578-C-A

124842059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59068872-C-T

124842158-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59069051-G-C

124842160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59069053-G-A

124842473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59069303-G-A

124842606-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59069431-G-A

124842772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59069609-G-A

124843063-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59069900-G-C

124843190-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59070011-G-C

124843418-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59070237-A-G

124843423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59070242-G-A

124843564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59070368-T-C

http://identifiers.org/hco/8/GRCh38#124843840-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59070541-C-A

124844014-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59070645-G-C

124844194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59070812-C-T

124844365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59070994-T-C

124844370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59070999-C-T

124844460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59071100-G-T

124847162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59073369-T-C

124847253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59073461-G-A

124847502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59073708-C-T

124847549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59073755-G-A

124847641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59073828-A-G

124847835-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59074008-T-G

http://identifiers.org/hco/8/GRCh38#124847870-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59074043-C-A

124847892-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59074063-T-C

124847949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59074122-T-C

124847995-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59074169-T-A

124847995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59074169-T-C

124848000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59074174-G-A

124848000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59074174-G-T

124848024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59074190-T-C

124848025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 59074191-G-A

124848042-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 59074208-A-T

124848072-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 59074236-T-A

124848072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 59074236-T-C

124848088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59074252-T-C

124848100-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 59074264-T-G

124848135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 59074303-A-G

http://identifiers.org/hco/8/GRCh38#124848619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59074549-C-A

124848619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59074549-C-T

124848695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59074608-G-A

124848814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59074717-C-T

http://identifiers.org/hco/8/GRCh38#124848857-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59074768-A-C

124848857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59074768-A-G

124848912-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59074815-T-A

http://identifiers.org/hco/8/GRCh38#124848969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59074872-C-A

124848969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59074872-C-T

124849115-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59075031-G-C

124849115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59075031-G-T

124849167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59075084-T-C

124849323-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59075229-G-T

124849355-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59075262-T-A

124849355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59075262-T-C

124849424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59075342-A-G

124849442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59075362-G-T

124851377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59077182-C-T

124851497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59077296-A-G

124851501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59077300-C-T

124851541-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59077337-T-G

124851566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59077363-C-T

124851573-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59077370-A-T

124851582-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59077379-T-G

124851781-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59077568-G-A

124853526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59079713-A-G

124853569-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59079755-G-C

124853646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59079826-T-C

124853815-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59079941-T-G

124853963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59080057-G-A

124854051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59080144-C-T

124854225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59080929-C-T

124855298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59083712-T-C

124855470-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59083947-C-T

124856933-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59084449-C-G

http://identifiers.org/hco/8/GRCh38#124857078-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#59084567-C-A

124857078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59084567-C-T

124857199-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 59084727-G-T

http://identifiers.org/hco/8/GRCh38#124857289-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59084825-C-A

124857289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59084825-C-T

http://identifiers.org/hco/8/GRCh38#124857324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#59084878-C-A

124857394-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59084943-G-T

124857549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59085129-C-T

http://identifiers.org/hco/8/GRCh38#124857589-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59085166-C-A

124857599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59085176-A-G

124857672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59085248-G-A

124857732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59085300-G-A

124857734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59085302-G-T

124857878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59085442-G-A

124857888-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59085452-G-T

124857950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59085507-A-G

http://identifiers.org/hco/8/GRCh38#124857975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59085541-C-A

124857975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59085541-C-T

124858131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59085653-G-A

124860352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59087159-C-T

124860366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59087173-G-A

124860580-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59087365-T-G

124860845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59088178-T-C

124860938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59088222-G-A

124861173-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59088484-C-G

124861180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59088493-C-T

http://identifiers.org/hco/8/GRCh38#124861226-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59088560-A-C

124861256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59088587-T-C

124861260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59088591-G-A

124861321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59088658-G-A

124861373-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59088707-G-T

http://identifiers.org/hco/8/GRCh38#124861777-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59089444-C-A

124861909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59089575-G-A

http://identifiers.org/hco/8/GRCh38#124861930-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59089596-A-C

124862060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59089733-G-A

124862077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59089744-T-C

124862156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59089823-A-G

124862217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59089882-C-T

124862273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59089938-A-G

124862293-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59089958-A-G

124862529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59090166-A-G

124862598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59090228-G-A

124868567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59093642-C-T

124868673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59094148-G-A

124868801-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59094267-A-G

124868807-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59094273-T-G

124869033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59094502-C-T

124872163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59095367-G-A

124872540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59095685-G-A

124872579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59095723-G-A

124872911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59095994-T-C

124873073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59096638-A-G

124873152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59096732-G-A

124877285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59097037-C-T

124877623-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59097484-T-G

http://identifiers.org/hco/8/GRCh38#124877678-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59098855-C-A

124877678-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59098855-C-G

124877678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59098855-C-T

124877686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59098863-G-T

124877688-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59098865-T-G

http://identifiers.org/hco/8/GRCh38#124877709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59098886-C-A

124877709-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59098886-C-G

124877709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59098886-C-T

http://identifiers.org/hco/8/GRCh38#124877726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59098903-C-A

124877726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59098903-C-T

124877767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59098944-A-G

124877795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59098971-C-T

124877838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59099002-A-G

124878750-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59099316-G-C

http://identifiers.org/hco/8/GRCh38#124879080-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59099600-C-A

http://identifiers.org/hco/8/GRCh38#124879665-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59100353-A-C

124879665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59100353-A-G

124879845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59100533-C-T

124879996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59101018-T-C

124880684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59101458-G-A

124880684-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59101458-G-T

124880946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59102189-T-C

124880955-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59102198-T-A

124881026-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59102270-C-T

124881173-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59102392-T-A

124881237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59102458-A-G

124881363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59102555-G-A

124881363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59102555-G-T

124881548-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59102698-T-C

124882564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59103127-G-A

124882581-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59103144-T-G

124882603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59103166-C-T

124882614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59103176-A-G

124893456-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59112192-G-T

124896086-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59120538-C-G

http://identifiers.org/hco/8/GRCh38#124896534-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59121091-C-A

124896688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59121243-A-G

124896766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59121317-A-G

124897032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59121542-C-T

124913386-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59122436-G-T

124913607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59122640-G-A

124913998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59123038-G-A

124914341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59123348-A-G

124914373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59123378-A-G

124914725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59123693-G-A

http://identifiers.org/hco/8/GRCh38#124915639-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59123982-A-C

124915843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59124147-C-T

124916059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59124324-T-C

124916278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59124508-C-T

124916711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59124730-C-T

124916713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59124732-G-A

124916713-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59124732-G-T

124916819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59124841-T-C

124917553-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59125035-C-G

124917553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59125035-C-T

124917971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59126463-C-T

124918012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59126504-C-T

124918053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59126545-G-A

124918248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59126731-C-T

124918905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59127558-A-G

124919603-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59128226-G-C

124919603-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59128226-G-T

124919825-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59128421-A-T

http://identifiers.org/hco/8/GRCh38#124920184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59128761-C-A

124920184-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59128761-C-T

124920316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59128873-T-C

http://identifiers.org/hco/8/GRCh38#124922964-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59129005-A-C

124922964-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59129005-A-T

124922968-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59129009-T-G

124923607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59129394-G-A

124924168-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59129919-G-C

http://identifiers.org/hco/8/GRCh38#124925034-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59130741-C-A

124925324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59131001-G-A

124925324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59131001-G-T

124925704-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59131328-C-G

124925822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59131460-C-T

124925936-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59131578-G-T

124926078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59131698-A-G

124926233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59131857-C-T

124926622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59132244-G-A

124926622-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59132244-G-T

124926698-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59132320-T-G

http://identifiers.org/hco/8/GRCh38#124927180-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59132762-A-C

124927209-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59132818-C-G

124927226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59132835-G-A

124927504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59133089-T-C

124927808-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59133379-C-T

124928525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59134119-G-A

124928620-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59134219-T-C

http://identifiers.org/hco/8/GRCh38#124929718-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59134756-A-C

124929942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59134973-G-A

http://identifiers.org/hco/8/GRCh38#124930020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59135080-C-A

124930114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59135175-A-G

124930367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59135405-C-T

124930843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59135847-C-T

124931036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59136034-G-A

124931354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59136340-T-C

124931426-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59136399-G-C

http://identifiers.org/hco/8/GRCh38#124932161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59137378-C-A

124932721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59137944-A-G

124932789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59137995-T-C

124932828-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59138038-A-T

124935456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59139614-T-C

124935743-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59140077-T-A

124936074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59140401-A-G

124936476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59140877-G-A

124936556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59140950-C-T

124936588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59140981-T-C

124936746-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59141146-G-T

http://identifiers.org/hco/8/GRCh38#124936811-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59141198-A-C

124936811-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59141198-A-T

http://identifiers.org/hco/8/GRCh38#124936920-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59141308-C-A

124937529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59141914-G-A

124937586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59141958-G-A

124937586-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59141958-G-T

124937589-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59141976-G-T

124937678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59142064-A-G

124937720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59142105-G-A

124937723-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59142108-A-T

http://identifiers.org/hco/8/GRCh38#124937724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59142109-C-A

124937724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59142109-C-T

http://identifiers.org/hco/8/GRCh38#124937728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59142113-C-A

124937815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59142204-G-A

124937815-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59142204-G-C

124937815-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59142204-G-T

124937966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59142322-C-T

124938072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59142405-T-C

124938126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59142467-C-T

124938159-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59142501-G-C

124938798-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59143096-G-C

124939235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59143499-G-A

124939255-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59143517-T-G

124939259-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59143521-T-C

124940081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59144300-G-A

124940389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59144591-T-C

124940459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59144661-A-G

124940716-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59144894-C-G

124941307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59146488-T-C

124941404-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59146584-A-T

124941438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59146618-T-C

http://identifiers.org/hco/8/GRCh38#124941513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59146688-C-A

124941513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59146688-C-T

124941555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 59146734-T-C

124941556-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59146735-G-T

124941618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59146793-G-T

124941623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59146798-G-A

124941679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59146855-T-C

124941681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59146857-A-G

124941681-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59146857-A-T

124941874-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59147036-C-G

124942595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59150366-G-T

124942699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59150423-G-A

124942871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59150671-G-A

124942871-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59150671-G-T

124942949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59150757-C-T

124943126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59150936-A-G

http://identifiers.org/hco/8/GRCh38#124943197-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59151008-C-A

http://identifiers.org/hco/8/GRCh38#124943338-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59151149-C-A

124943338-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59151149-C-G

124943480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59151246-C-T

124943488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59151254-G-A

124943662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59151430-G-A

124943662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59151430-G-T

124943679-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59151447-G-T

http://identifiers.org/hco/8/GRCh38#124943721-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59151481-A-C

124943721-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59151481-A-G

124943721-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59151481-A-T

124943727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59151487-T-C

124943779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59151549-A-G

http://identifiers.org/hco/8/GRCh38#124943807-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59151577-C-A

http://identifiers.org/hco/8/GRCh38#124943956-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59151721-A-C

124944093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59151839-A-G

http://identifiers.org/hco/8/GRCh38#124944095-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59151841-C-A

124944101-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59151854-T-C

124944126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59151879-G-T

124944169-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59151921-G-T

http://identifiers.org/hco/8/GRCh38#124944207-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59151953-C-A

http://identifiers.org/hco/8/GRCh38#124944218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59151964-C-A

124944218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59151964-C-T

124944269-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59152011-T-A

124944269-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59152011-T-C

124944270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59152012-G-T

124944276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59152027-G-A

124944515-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59152210-T-G

124945052-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 59153061-G-T

http://identifiers.org/hco/8/GRCh38#124945152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59153139-C-A

124945152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59153139-C-T

124946191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59155176-A-G

124946374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59155325-A-G

124952286-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59157122-G-T

124952334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59157170-T-C

124952336-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59157172-G-C

124953830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59157928-A-G

http://identifiers.org/hco/8/GRCh38#124953945-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#59158019-C-A

124954110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59158185-C-T

124954208-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59158387-T-A

124954208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 59158387-T-C

124954537-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 59158918-C-T

124957821-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59160250-T-A

124957864-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59160276-T-C

http://identifiers.org/hco/8/GRCh38#124961651-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#59163492-C-A

124961651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 59163492-C-T

124961800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27226
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 59163619-T-C