41208516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 81549067-G-A

41209684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 81551347-A-G

41209737-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 81551401-C-G

41209737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 81551401-C-T

41209878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 81551542-G-A

41209878-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 81551542-G-C

41209878-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 81551542-G-T

41211091-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81552027-G-T

41211123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81552058-C-T

41213766-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 81552722-C-G

41213787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 81552740-G-T

http://identifiers.org/hco/22/GRCh38#41214124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#81553060-C-A

41214124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 81553060-C-T

41214147-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 81553083-T-A

http://identifiers.org/hco/22/GRCh38#41216097-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#81554286-C-A

41216097-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81554286-C-G

41216097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81554286-C-T

http://identifiers.org/hco/22/GRCh38#41216103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#81554292-C-A

41216103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81554292-C-T

41216135-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 81554324-C-G

41216135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 81554324-C-T

41216323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81554487-G-A

41216323-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81554487-G-T

http://identifiers.org/hco/22/GRCh38#41216413-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#81554539-C-A

http://identifiers.org/hco/22/GRCh38#41216552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#81554668-C-A

41216562-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81554678-A-T

41216789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81554819-G-A

41216867-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81554965-C-G

41216867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81554965-C-T

41216908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81555049-T-C

41216915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81555056-C-T

41217057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 81555188-G-A

41217057-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 81555188-G-C

41217057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 81555188-G-T

41217059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 81555190-G-T

http://identifiers.org/hco/22/GRCh38#41217240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#81555386-C-A

41217240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 81555386-C-T

41217759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 81557923-T-C

41217787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 81557943-G-A

41217787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 81557943-G-T

41217936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 81558056-A-G

41218552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 81559307-A-G

41218583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 81559338-A-G

http://identifiers.org/hco/22/GRCh38#41219010-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#81559397-A-C

41219010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 81559397-A-G

41219010-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 81559397-A-T

http://identifiers.org/hco/22/GRCh38#41219031-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#81559414-A-C

41219031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 81559414-A-G

41219031-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 81559414-A-T

41219081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 81559453-G-A

41219081-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 81559453-G-T

41219318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 81559639-G-T

41219346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 81559667-G-A

41219346-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 81559667-G-T

41219355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 81559676-G-A

41219355-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 81559676-G-T

http://identifiers.org/hco/22/GRCh38#41219583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#81559884-C-A

41219583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81559884-C-T

41219649-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81559947-T-A

41219649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81559947-T-C

41219649-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81559947-T-G

41219652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81559950-A-G

http://identifiers.org/hco/22/GRCh38#41219677-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#81559975-C-A

http://identifiers.org/hco/22/GRCh38#41219682-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#81559980-A-C

41219905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81560197-G-A

41219905-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81560197-G-T

41220678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81560393-G-A

41220678-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81560393-G-C

41220678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81560393-G-T

http://identifiers.org/hco/22/GRCh38#41220682-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#81560397-A-C

41220682-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81560397-A-T

http://identifiers.org/hco/22/GRCh38#41220692-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#81560407-C-A

41220692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81560407-C-T

41220694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81560409-G-A

41220694-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81560409-G-C

41220694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81560409-G-T

http://identifiers.org/hco/22/GRCh38#41220695-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#81560410-C-A

41220695-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81560410-C-G

41220695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81560410-C-T

41220716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81560441-C-T

41220727-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 81560452-C-G

41220891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81560616-T-C

http://identifiers.org/hco/22/GRCh38#41220909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#81560634-C-A

41220909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81560634-C-T

41221185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81561012-T-C

41221185-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81561012-T-G

http://identifiers.org/hco/22/GRCh38#41221257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#81561084-C-A

41221257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 81561084-C-T

41221299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81561125-G-A

41221299-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81561125-G-C

41221299-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81561125-G-T

41221324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81561153-G-A

41221332-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81561161-A-G

41221355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81561196-C-T

http://identifiers.org/hco/22/GRCh38#41221409-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#81561277-C-A

41221409-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81561277-C-T

http://identifiers.org/hco/22/GRCh38#41221502-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#81561375-C-A

41221502-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81561375-C-G

41221502-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81561375-C-T

http://identifiers.org/hco/22/GRCh38#41221512-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#81561384-C-A

41221512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81561384-C-T

http://identifiers.org/hco/22/GRCh38#41221516-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#81561388-C-A

41224001-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81566102-T-A

41224012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 81566113-C-T

41224112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 81566213-G-A

41224137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 81566238-C-T

41224205-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 81566306-C-T

41224276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81566377-G-A

41224276-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81566377-G-C

41224276-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81566377-G-T

41224327-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81566427-T-A

41224327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81566427-T-C

41224370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81566470-G-T

41224461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81566552-T-C

41224612-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81566663-G-T

41224892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81567070-C-T

41224939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81567126-G-A

41224961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 81567148-T-C

41224999-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 81567186-T-G

41225097-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81567275-C-T

41225109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81567288-G-T

41225113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81567292-G-A

41225113-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81567292-G-C

41225113-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81567292-G-T

41225115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81567294-G-T

http://identifiers.org/hco/22/GRCh38#41225151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#81567325-C-A

41225151-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81567325-C-T

41225156-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81567330-G-A

41225156-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81567330-G-C

41225156-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81567330-G-T

41225159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81567333-A-G

http://identifiers.org/hco/22/GRCh38#41225182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#81567343-C-A

41225188-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81567348-T-A

http://identifiers.org/hco/22/GRCh38#41225198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#81567363-C-A

41225215-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81567378-G-A

41225215-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81567378-G-T

41225325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81567471-G-A

41225350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81567496-G-A

41225409-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81567545-G-A

41225409-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81567545-G-T

41225497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81567600-C-T

41225596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81567700-G-A

http://identifiers.org/hco/22/GRCh38#41225612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#81567716-C-A

41225705-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81567800-G-T

http://identifiers.org/hco/22/GRCh38#41225733-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#81567819-C-A

41225733-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81567819-C-G

41225742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81567828-A-G

41225835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 81568085-G-A

41225835-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 81568085-G-C

41225835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 81568085-G-T

41226406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81568284-G-A

41226509-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81568379-G-T

41226510-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81568380-T-A

41226510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81568380-T-C

41226520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81568390-A-G

41226536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81568399-G-A

41226536-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81568399-G-C

41226536-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81568399-G-T

41226539-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81568402-G-C

41226612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81568468-A-G

41226669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 81568509-G-A

41226770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81568601-G-A

41226771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81568602-G-A

http://identifiers.org/hco/22/GRCh38#41226782-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#81568613-C-A

41226782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81568613-C-T

http://identifiers.org/hco/22/GRCh38#41226795-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#81568619-C-A

41226795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81568619-C-T

41226807-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81568631-T-A

41226808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81568632-G-A

http://identifiers.org/hco/22/GRCh38#41226862-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#81568688-C-A

41226950-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81568787-T-C

41226950-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81568787-T-G

http://identifiers.org/hco/22/GRCh38#41226967-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#81568804-C-A

41226967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81568804-C-T

http://identifiers.org/hco/22/GRCh38#41226987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#81568821-C-A

41226987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81568821-C-T

41226999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81568833-T-C

http://identifiers.org/hco/22/GRCh38#41227001-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#81568835-C-A

41227001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81568835-C-T

41227022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81568851-G-A

41227022-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81568851-G-T

41227027-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81568856-G-C

41227027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81568856-G-T

41227028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81568857-G-A

41227028-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81568857-G-T

41227172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 81568998-G-A

41227172-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 81568998-G-C

http://identifiers.org/hco/22/GRCh38#41227181-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#81569007-A-C

41227181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 81569007-A-G

41227211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 81569037-T-C

41227226-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 81569052-C-G

41227226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 81569052-C-T

http://identifiers.org/hco/22/GRCh38#41227292-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#81569118-C-A

41227292-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 81569118-C-G

41227292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 81569118-C-T

41227349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 81569178-G-A

41227349-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 81569178-G-C

41227349-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 81569178-G-T

http://identifiers.org/hco/22/GRCh38#41227352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#81569181-C-A

41227368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 81569197-T-C

http://identifiers.org/hco/22/GRCh38#41227381-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#81569210-C-A

41227381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 81569210-C-T

41227397-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 81569232-G-T

41227407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 81569239-G-A

41227407-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 81569239-G-T

41227418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 81569250-T-C

41227466-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 81569297-T-C

http://identifiers.org/hco/22/GRCh38#41227471-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#81569302-C-A

http://identifiers.org/hco/22/GRCh38#41227487-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#81569316-C-A

41227487-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 81569316-C-G

41227510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 81569335-G-A

http://identifiers.org/hco/22/GRCh38#41227540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#81569365-C-A

41227540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 81569365-C-T

http://identifiers.org/hco/22/GRCh38#41227603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#81569418-C-A

41227603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 81569418-C-T

41227614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 81569429-G-T

41227688-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 81569486-T-A

41227732-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 81569517-G-T

41227829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 81569607-A-G

41227879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81569657-G-A

http://identifiers.org/hco/22/GRCh38#41227881-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#81569659-A-C

41227897-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81569675-T-A

41227899-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40847
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81569677-G-C