93969632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 4055888-C-T

93969661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 4055911-C-T

93969935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4056168-C-T

93969994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4056224-C-T

93970290-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4056501-T-G

93970536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4056743-A-G

93970825-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4057002-G-C

93970825-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4057002-G-T

93971170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4057331-A-G

93971179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4057344-A-G

93971518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4057674-T-C

93971532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4057688-T-C

93971596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4057752-T-C

93971599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4057755-T-C

93971614-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4057770-T-A

93972045-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4058163-G-T

93972216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4058307-A-G

93972431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 4058512-G-T

93972534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 4058609-T-C

93972634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 4058702-C-T

93972752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4059469-G-T

93973328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4059981-C-T

93973447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4060077-A-G

93973546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4060171-A-G

93973567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4060184-A-G

93973608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4060225-C-T

93973639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4060262-C-T

http://identifiers.org/hco/7/GRCh38#93973695-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#4060310-C-A

93973758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4060495-A-G

93973872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4060678-A-G

93974506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4061309-A-G

93974770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4062716-T-C

93974775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4062721-G-A

93974846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4062788-T-C

93974890-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4062830-C-G

93975265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4063163-G-A

http://identifiers.org/hco/7/GRCh38#93975337-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#4063266-A-C

93975342-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4063271-T-A

93975370-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4063322-G-A

93975405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4063356-T-C

93975406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4063357-G-A

93975736-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4063686-G-C

http://identifiers.org/hco/7/GRCh38#93975811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#4063764-C-A

93975811-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4063764-C-G

93975822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4063775-A-G

93975919-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 4063856-T-A

93975919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 4063856-T-C

93975934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 4063891-A-G

93975938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 4063895-A-G

93975952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 4063909-T-C

93976001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 4063942-C-T

93976045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 4063973-T-C

93976045-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 4063973-T-G

http://identifiers.org/hco/7/GRCh38#93976082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#4064001-C-A

93976210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4064113-G-A

93976210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4064113-G-T

http://identifiers.org/hco/7/GRCh38#93976245-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#4064144-A-C

93976264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4064166-A-G

93976577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4064487-T-C

93983104-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4070455-T-G

93983166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4070516-T-C

93983211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4070559-G-T

http://identifiers.org/hco/7/GRCh38#93983324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#4070666-C-A

93983345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4070688-C-T

93983368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4070711-T-C

93983374-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4070717-T-A

http://identifiers.org/hco/7/GRCh38#93983431-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#4070773-A-C

93983832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4071214-C-T

93984094-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4071445-T-G

93984265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4071594-A-G

93984387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4071696-T-C

93984472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4071784-G-A

93984661-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4071965-T-G

93984830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4072131-G-A

93984992-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4072282-A-G

93985167-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4072462-T-G

93985252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4072531-A-G

93985334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4072610-T-C

93985385-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4072661-C-T

93985434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4072704-G-A

93986005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4073503-C-T

93986086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4073588-T-C

93986224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4073712-T-C

93986293-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4073772-T-G

93986363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4073842-C-T

93986501-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4073965-A-T

93986547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4074010-C-T

93986549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4074012-C-T

93987137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 4074217-C-T

93988097-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4074618-A-T

93988205-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4074725-A-G

93989876-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4075938-G-C

93989988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4076050-C-T

93990023-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4076089-T-A

93990263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4076291-C-T

93990371-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4076396-G-C

93993241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4076907-G-A

93993259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4076916-A-G

http://identifiers.org/hco/7/GRCh38#93993273-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#4076929-A-C

93993287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4076943-G-T

93993451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4077171-T-C

93993533-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4077258-A-T

http://identifiers.org/hco/7/GRCh38#93993548-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#4077273-C-A

93993548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4077273-C-T

http://identifiers.org/hco/7/GRCh38#93993606-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#4077328-C-A

93993826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4077511-T-C

93993826-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4077511-T-G

93993852-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4077535-T-C

93993852-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4077535-T-G

http://identifiers.org/hco/7/GRCh38#93993866-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#4077548-C-A

93993866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4077548-C-T

http://identifiers.org/hco/7/GRCh38#93994003-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#4077663-A-C

http://identifiers.org/hco/7/GRCh38#93994018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#4077689-C-A

93994018-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4077689-C-G

93994043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4077714-A-G

93994155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4077810-T-C

93994178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4077830-G-A

93994178-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4077830-G-T

http://identifiers.org/hco/7/GRCh38#93994219-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#4077870-A-C

http://identifiers.org/hco/7/GRCh38#93994274-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#4077925-A-C

93994274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4077925-A-G

93994473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4078115-T-C

93994483-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4078125-G-T

93994664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4078296-T-C

93994820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4078450-G-T

93995339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4078743-T-C

93995463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4078803-A-G

93995484-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4078810-C-G

93995484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4078810-C-T

93995546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4078860-C-T

93995556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4078870-C-T

93995599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4078913-A-G

93995961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4079250-T-C

93995972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4079260-G-A

93995972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4079260-G-T

93996065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4079357-C-T

93996244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4079940-G-T

93996349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4080045-T-C

93996403-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4080102-A-T

93996640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4080304-T-C

93997111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4080608-C-T

93997282-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4080768-T-G

http://identifiers.org/hco/7/GRCh38#93999044-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#4082364-C-A

93999044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4082364-C-T

93999130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4082418-A-G

93999148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4082436-A-G

93999160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4082448-A-G

http://identifiers.org/hco/7/GRCh38#93999230-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#4082518-A-C

93999236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 4082524-A-G

93999245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 4082533-A-G

93999245-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 4082533-A-T

93999264-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 4082552-T-G

93999319-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4082607-T-A

93999319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4082607-T-C

93999326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4082620-A-G

93999337-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4082631-T-G

93999353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4082646-G-A

93999353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4082646-G-T

93999384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4082678-G-A

93999384-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4082678-G-C

93999384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4082678-G-T

93999393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4082687-A-G

93999408-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4082702-T-A

93999408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4082702-T-C

93999408-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4082702-T-G

93999522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4082802-A-G

93999535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4082815-G-A

93999535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4082815-G-T

http://identifiers.org/hco/7/GRCh38#93999635-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#4082914-C-A

http://identifiers.org/hco/7/GRCh38#93999654-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#4082930-C-A

93999688-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4082966-G-C

93999688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4082966-G-T

93999728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4083003-G-A

93999748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4083028-T-C

93999824-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4083106-G-C

93999832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4083114-A-G

93999842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4083124-G-A

http://identifiers.org/hco/7/GRCh38#93999920-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#4083200-C-A

93999987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4083270-T-C

94000031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4083309-G-A

94000455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4083415-A-G

94000487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4083446-T-C

94000514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4083465-G-T

94000586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4083539-C-T

http://identifiers.org/hco/7/GRCh38#94001054-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#4083886-C-A

http://identifiers.org/hco/7/GRCh38#94001148-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#4083975-A-C

94001186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4084011-C-T

94001191-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4084016-C-G

94001214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4084039-G-A

94001214-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4084039-G-C

94001242-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4084064-T-A

94001242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4084064-T-C

94001483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4084259-A-G

94001526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4084298-G-A

94001889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4084571-C-T

94002031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4084696-C-T

http://identifiers.org/hco/7/GRCh38#94002060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#4084724-C-A

94002101-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4084776-T-G

94002287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4084943-C-T

http://identifiers.org/hco/7/GRCh38#94002415-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#4085037-C-A

94002439-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4085061-T-A

94002591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4085148-C-T

94002729-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4085283-G-C

94002730-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4085284-A-T

94002749-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4085300-G-A

94002782-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4085336-T-G

94002797-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4085378-T-G

94002840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4085421-T-C

94002842-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4085423-T-A

94002945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4085503-T-C

94002954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4085512-C-T

94003181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4085726-T-C

94003206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4085821-C-T

94003250-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4085895-A-G

94003489-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4086179-T-A

94003489-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4086179-T-G

94003561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4086194-C-T

94004042-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4086630-G-T

http://identifiers.org/hco/7/GRCh38#94004268-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#4086838-A-C

http://identifiers.org/hco/7/GRCh38#94004315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#4086883-C-A

94004315-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 4086883-C-G

94004315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 4086883-C-T

http://identifiers.org/hco/7/GRCh38#94004392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#4086960-C-A

94004392-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4086960-C-G

94004392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4086960-C-T

http://identifiers.org/hco/7/GRCh38#94004451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#4087020-C-A

94004451-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4087020-C-G

94004451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4087020-C-T

http://identifiers.org/hco/7/GRCh38#94004493-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#4087064-C-A

94004493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4087064-C-T

http://identifiers.org/hco/7/GRCh38#94004500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#4087071-C-A

94004500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 4087071-C-T

http://identifiers.org/hco/7/GRCh38#94008033-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4087880-A-C

http://identifiers.org/hco/7/GRCh38#94008096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4087934-C-A

94008128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4087965-C-T

http://identifiers.org/hco/7/GRCh38#94008159-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4087996-C-A

94008194-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4088027-T-A

94008194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4088027-T-C

http://identifiers.org/hco/7/GRCh38#94008458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4088252-C-A

94008458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4088252-C-T

94008547-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4088357-C-G

94008547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4088357-C-T

94008866-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4088767-T-A

94008872-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4088773-G-C

http://identifiers.org/hco/7/GRCh38#94008884-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4088785-A-C

94009021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4088867-A-G

94009079-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4088944-T-A

94009079-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4088944-T-G

94009242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4089081-C-T

94009343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4089178-T-C

94010242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4102595-C-T

94010266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4102635-T-C

http://identifiers.org/hco/7/GRCh38#94010459-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4102828-C-A

94010459-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4102828-C-T

94010680-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4102971-A-T

94010935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 4103090-A-G

http://identifiers.org/hco/7/GRCh38#94011065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#4103226-C-A

94011111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4103268-A-G

94011111-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40690
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 4103268-A-T