37641840-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78785879-G-A

37641840-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78785879-G-T

37641891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78785929-A-G

37641943-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78785981-T-C

37641943-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78785981-T-G

37641944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78785982-G-A

37641944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78785982-G-T

37642160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78786317-G-A

http://identifiers.org/hco/22/GRCh38#37642190-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#78786347-C-A

37642190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78786347-C-T

http://identifiers.org/hco/22/GRCh38#37642205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#78786361-C-A

37642205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78786361-C-T

http://identifiers.org/hco/22/GRCh38#37642206-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#78786362-C-A

37642206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78786362-C-T

37642260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78786422-G-A

37642260-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78786422-G-T

37642263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78786425-T-C

37642263-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78786425-T-G

37642277-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78786439-T-A

37642277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78786439-T-C

37642346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78786501-A-G

37642346-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78786501-A-T

37642368-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78786527-T-G

37642397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78786556-G-A

37642397-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78786556-G-T

37642415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78786580-C-T

37642460-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78786629-G-T

http://identifiers.org/hco/22/GRCh38#37642482-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#78786651-C-A

37642482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78786651-C-T

37642510-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78786725-A-T

37642521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78786736-G-A

37642526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78786741-A-G

37642648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78786858-G-A

37642662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78786868-G-A

37642662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78786868-G-T

37642850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78787006-G-T

37642859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78787015-G-A

37642859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78787015-G-T

37642875-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78787034-A-G

37642886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78787045-T-C

37642982-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78787141-G-C

37643051-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78787208-G-A

http://identifiers.org/hco/22/GRCh38#37643084-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#78787245-A-C

37643085-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78787246-T-A

37643085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78787246-T-C

37643366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78787470-C-T

37643368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78787472-G-A

37643368-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78787472-G-C

37643439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78787545-T-C

37643439-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78787545-T-G

37643455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78787571-A-G

http://identifiers.org/hco/22/GRCh38#37643469-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#78787586-C-A

37643469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78787586-C-T

37643503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78787620-G-A

37643503-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78787620-G-C

37643533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78787643-G-T

http://identifiers.org/hco/22/GRCh38#37643559-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#78787669-C-A

37643801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78787910-G-A

37643801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78787910-G-T

37643802-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78787911-G-C

37643806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78787915-C-T

37643819-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78787921-A-T

37643831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78787933-G-A

37643886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78787984-G-T

37644047-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78788118-G-C

37644406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78788295-C-T

37644413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78788302-A-G

37644479-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78788366-G-T

http://identifiers.org/hco/22/GRCh38#37644493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#78788380-C-A

37644493-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78788380-C-G

37644493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78788380-C-T

37644610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78788443-G-A

37644610-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78788443-G-T

37644625-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78788458-T-A

37644687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78788520-T-C

37644712-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 78788545-C-T

http://identifiers.org/hco/22/GRCh38#37644827-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#78788622-A-C

37644862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 78788656-C-T

37644872-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 78788666-C-G

37644917-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78788711-G-A

37644923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78788717-A-G

37644930-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78788724-G-T

37644952-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78788746-G-C

37644973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78788767-G-A

37644983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78788777-A-G

37644986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78788780-A-G

http://identifiers.org/hco/22/GRCh38#37644987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#78788781-C-A

37645043-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78788867-A-T

37645050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78788874-A-G

37645088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78788943-T-C

37645100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78788956-G-A

37645100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78788956-G-T

37645126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78788991-G-A

37645126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78788991-G-T

37645134-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78789004-G-T

http://identifiers.org/hco/22/GRCh38#37645156-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#78789023-C-A

37645156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78789023-C-T

http://identifiers.org/hco/22/GRCh38#37645258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#78789131-C-A

37645258-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78789131-C-T

http://identifiers.org/hco/22/GRCh38#37645268-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#78789141-C-A

37645268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78789141-C-T

http://identifiers.org/hco/22/GRCh38#37645276-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#78789149-A-C

37645276-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78789149-A-G

37645276-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78789149-A-T

37645309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78789175-G-A

37645320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78789186-C-T

37645459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78789324-G-A

37645521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78789390-C-T

37645567-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78789425-A-T

http://identifiers.org/hco/22/GRCh38#37645737-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#78789577-A-C

37645738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78789578-A-G

http://identifiers.org/hco/22/GRCh38#37646620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#78789810-C-A

37646624-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78789814-G-C

37646624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78789814-G-T

http://identifiers.org/hco/22/GRCh38#37646643-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#78789833-A-C

37646643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78789833-A-G

37646661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78789851-T-C

37646661-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78789851-T-G

37646667-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78789860-C-T

http://identifiers.org/hco/22/GRCh38#37646674-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#78789867-C-A

http://identifiers.org/hco/22/GRCh38#37646791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#78789943-C-A

37646791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78789943-C-T

http://identifiers.org/hco/22/GRCh38#37646797-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#78789949-C-A

37646797-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78789949-C-G

37646797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78789949-C-T

http://identifiers.org/hco/22/GRCh38#37646892-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#78790045-C-A

37646892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78790045-C-T

http://identifiers.org/hco/22/GRCh38#37646904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#78790057-C-A

37646904-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78790057-C-G

37646904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78790057-C-T

37646957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78790113-G-A

37646957-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78790113-G-T

37646975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78790134-G-A

37646975-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78790134-G-C

37646975-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78790134-G-T

37646998-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78790157-A-T

37647364-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78790555-G-A

http://identifiers.org/hco/22/GRCh38#37647365-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#78790556-A-C

37647369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78790560-A-G

37647381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78790565-G-A

37647386-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78790570-A-T

37647421-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78790609-G-A

37647450-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78790632-G-T

37647491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78790673-G-A

37647491-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78790673-G-T

http://identifiers.org/hco/22/GRCh38#37647528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#78790711-C-A

http://identifiers.org/hco/22/GRCh38#37647535-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#78790718-C-A

37647535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78790718-C-T

37647539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78790722-T-C

37648106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78791248-G-A

http://identifiers.org/hco/22/GRCh38#37648216-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#78791328-C-A

37648222-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78791334-T-A

37648223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78791335-G-T

37648280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78791376-T-C

37648281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78791377-G-A

37648281-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78791377-G-T

http://identifiers.org/hco/22/GRCh38#37648334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#78791429-C-A

37648334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 78791429-C-T

37648362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 78791457-G-A

37648362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 78791457-G-T

37648483-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78791562-A-T

http://identifiers.org/hco/22/GRCh38#37649791-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#78791860-A-C

37649791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78791860-A-G

37649791-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78791860-A-T

http://identifiers.org/hco/22/GRCh38#37649854-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#78791921-C-A

http://identifiers.org/hco/22/GRCh38#37649861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#78791928-C-A

37649880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78791947-C-T

37650002-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78792080-A-T

http://identifiers.org/hco/22/GRCh38#37650012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#78792090-C-A

37650012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78792090-C-T

37650032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78792100-G-A

37650135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78792143-G-A

37650147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 78792156-C-T

37650275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78792300-C-T

37650282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78792307-G-T

37650351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78792383-T-C

37650491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78792504-G-A

37650531-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78792542-T-G

37650535-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 78792546-T-A

37650671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 78792682-C-T

37650672-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 78792683-G-A

37650672-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 78792683-G-C

37650672-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 78792683-G-T

37650876-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78792831-G-A

37650876-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78792831-G-T

37650917-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78792858-G-T

37653851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78794277-A-G

37653888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78794314-G-A

37653913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78794331-G-A

37653913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78794331-G-T

37653916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78794334-G-A

37653916-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78794334-G-T

37653989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78794402-T-C

37653989-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78794402-T-G

37654013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78794424-G-A

37654013-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78794424-G-T

37654089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78794497-G-A

37654089-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78794497-G-C

37654500-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78794902-G-A

http://identifiers.org/hco/22/GRCh38#37655162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#78795439-C-A

37655162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78795439-C-T

37655183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78795455-G-A

37655183-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78795455-G-C

37655183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78795455-G-T

37655213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78795487-T-C

37655213-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78795487-T-G

http://identifiers.org/hco/22/GRCh38#37655231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#78795501-C-A

37655231-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78795501-C-G

37655231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78795501-C-T

37655233-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78795503-T-C

37655234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78795504-G-A

37655234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78795504-G-T

http://identifiers.org/hco/22/GRCh38#37655363-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#78795630-C-A

37655363-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78795630-C-G

37655363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78795630-C-T

http://identifiers.org/hco/22/GRCh38#37655365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#78795632-C-A

37655365-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78795632-C-G

37655365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78795632-C-T

37655416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78795683-G-A

37655416-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78795683-G-T

37655444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78795711-G-A

37655444-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78795711-G-C

37655444-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78795711-G-T

37655445-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78795712-T-A

37655445-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78795712-T-C

37655445-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78795712-T-G

37655596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78795827-G-T

http://identifiers.org/hco/22/GRCh38#37655698-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#78795928-C-A

37655698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78795928-C-T

37656039-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 78796248-C-G

37656074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78796278-G-A

http://identifiers.org/hco/22/GRCh38#37656113-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#78796317-C-A

37656113-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 78796317-C-G

http://identifiers.org/hco/22/GRCh38#37656133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#78796337-C-A

37656133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78796337-C-T

37656595-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78796705-A-T

37656608-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78796717-C-G

37658100-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 78797614-T-G

37658291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: non coding transcript exon variant
orthologous variants: 78797814-G-A

37658291-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40525
most severe consequence: non coding transcript exon variant
orthologous variants: 78797814-G-T