http://identifiers.org/hco/7/GRCh38#103175135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24430898-C-A

103175135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24430898-C-T

103175152-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24430915-T-C

103175154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24430920-T-C

103175363-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24469435-A-T

103175369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24469441-A-G

103175465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24469528-A-G

103175469-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24469532-T-A

103175469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24469532-T-C

103175522-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24469588-A-T

http://identifiers.org/hco/7/GRCh38#103175543-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24469609-C-A

103175543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24469609-C-T

http://identifiers.org/hco/7/GRCh38#103175550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24469619-C-A

103175727-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24469764-C-T

103175923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24469964-G-A

103175924-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24469965-G-T

http://identifiers.org/hco/7/GRCh38#103176150-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24470113-C-A

103176298-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24470243-A-G

103182656-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24491031-T-C

103182919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24491311-T-C

103182953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24491346-T-C

103183148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24491504-A-G

103183453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24491823-T-C

103183844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24492188-T-C

103183957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24492381-T-C

http://identifiers.org/hco/7/GRCh38#103183973-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24492397-A-C

103184070-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24492494-T-C

http://identifiers.org/hco/7/GRCh38#103184097-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24492521-A-C

103184097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24492521-A-G

103184327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24492730-A-G

http://identifiers.org/hco/7/GRCh38#103184444-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24492833-A-C

103184447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24492836-A-G

103184570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24492960-C-T

103184806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24493221-A-G

103184810-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24493225-T-G

103184997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24493487-C-T

103185305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24493955-T-C

103185335-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24493983-T-G

103185342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24493990-G-A

103185342-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24493990-G-C

103185342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24493990-G-T

103185362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24494010-G-A

103185362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24494010-G-T

http://identifiers.org/hco/7/GRCh38#103185376-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24494019-C-A

103185376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24494019-C-T

103185530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24494176-G-A

103185530-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24494176-G-C

103185530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24494176-G-T

103185671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24494316-T-C

103186236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24494865-G-A

103186329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24494991-T-C

103186435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24495117-T-C

103195330-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24495673-T-C

http://identifiers.org/hco/7/GRCh38#103195384-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24495727-A-C

http://identifiers.org/hco/7/GRCh38#103195417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24495751-C-A

103195705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24496036-G-A

103195795-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24496117-C-G

103197033-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24496658-T-C

103197039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24496664-A-G

103197039-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24496664-A-T

http://identifiers.org/hco/7/GRCh38#103197119-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24496738-C-A

103197322-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24496938-T-A

103197322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24496938-T-C

103197373-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24496983-T-C

103197417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24497026-A-G

103197463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24497082-C-T

http://identifiers.org/hco/7/GRCh38#103198513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24498261-C-A

103198549-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24498297-A-G

103198653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24498394-A-G

103198678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24498419-A-G

103198682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24498423-A-G

103198688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24498429-T-C

http://identifiers.org/hco/7/GRCh38#103198726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24498467-C-A

103209959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24528376-A-G

103209980-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24528413-A-T

http://identifiers.org/hco/7/GRCh38#103209989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24528422-C-A

103209989-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24528422-C-G

103210102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24528579-T-C

103210345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24528814-G-A

103210345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24528814-G-T

103210747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24529198-A-G

103210747-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24529198-A-T

103211333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24529655-T-C

103211462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24529770-T-C

103211519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24529820-C-T

http://identifiers.org/hco/7/GRCh38#103211626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24529923-C-A

103211657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24529949-T-C

http://identifiers.org/hco/7/GRCh38#103211728-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24530021-A-C

103211814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24530079-G-A

103212087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24530327-G-A

103212087-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24530327-G-C

103212087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24530327-G-T

http://identifiers.org/hco/7/GRCh38#103212111-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24530356-A-C

103212111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24530356-A-G

103212282-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24530526-A-T

103212844-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24538566-T-A

103212978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24538677-A-G

103212988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24538686-A-G

103214025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24539470-G-A

103214025-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24539470-G-T

103214073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24539518-T-C

103214157-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24539595-G-A

103214157-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24539595-G-C

103214157-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24539595-G-T

103214191-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24539634-G-A

103214191-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24539634-G-T

103214223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24539666-A-G

103214242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24539682-A-G

http://identifiers.org/hco/7/GRCh38#103214401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24541022-C-A

103214579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24541198-C-T

103214691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24541276-C-T

103214693-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24541278-C-G

103214955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24541472-C-T

http://identifiers.org/hco/7/GRCh38#103215732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24541953-C-A

103215762-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24541980-T-A

103215793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24542010-T-C

103216292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24542326-T-C

103216292-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24542326-T-G

103216466-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24542498-G-T

103216614-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24542626-T-A

103216614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24542626-T-C

103216675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24542697-T-C

http://identifiers.org/hco/7/GRCh38#103216743-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24542765-C-A

103224050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24554899-C-T

103225114-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: non coding transcript exon variant
orthologous variants: 24555017-G-T

103225179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24555076-A-G

103225179-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24555076-A-T

103225249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24555121-T-C

http://identifiers.org/hco/7/GRCh38#103225262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24555134-C-A

103225290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24555159-T-C

103225381-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24555252-C-T

103233881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: non coding transcript exon variant
orthologous variants: 24556439-T-C

103233916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24556473-G-A

103233916-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24556473-G-T

103234395-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24557165-T-G

http://identifiers.org/hco/7/GRCh38#103234553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24557510-C-A

103234561-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24557517-G-C

103234744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24557696-A-G

103234745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24557697-G-A

103234745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24557697-G-T

http://identifiers.org/hco/7/GRCh38#103234793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24557747-C-A

103234793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24557747-C-T

103234978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24557936-C-T

103234995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24557953-C-T

103235038-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24557995-T-G

103235053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24558010-T-C

103236443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24569253-T-C

103237965-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24570068-T-C

103237992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24570094-T-C

103237992-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24570094-T-G

103238191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24570306-C-T

103238732-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24570508-A-T

103238753-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24570529-C-G

103238753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24570529-C-T

103238771-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24570552-G-C

http://identifiers.org/hco/7/GRCh38#103238931-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24570679-C-A

103238993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24570726-G-A

http://identifiers.org/hco/7/GRCh38#103239018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24570749-C-A

103239777-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24571261-A-G

103239879-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24571412-G-T

103239950-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24571528-A-T

103240516-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24571975-A-T

103240525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24571985-A-G

103240525-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24571985-A-T

103240723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24572185-G-A

103240723-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24572185-G-C

103240723-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24572185-G-T

103240777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24572239-G-A

103240777-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24572239-G-T

103240842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24572298-T-C

103240991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24572418-G-T

103241036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24572464-T-C

103241036-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24572464-T-G

103241060-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24572486-C-G

103241081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24572501-T-C

103241449-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24572951-C-G

103241549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24573048-G-A

http://identifiers.org/hco/7/GRCh38#103241767-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24573124-A-C

103241964-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24573153-T-C

103242093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24573264-G-A

103242199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24573365-A-G

http://identifiers.org/hco/7/GRCh38#103242214-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24573382-A-C

103242299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24573454-G-A

103242412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24573788-T-C

103242445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24573842-G-A

103242576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24574032-C-T

103242713-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24574148-T-G

103242751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24574186-C-T

103242845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24574275-A-G

103242845-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24574275-A-T

103242922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24574346-T-C

103242922-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24574346-T-G

103243001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: non coding transcript exon variant
orthologous variants: 24574423-G-A

103243001-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: non coding transcript exon variant
orthologous variants: 24574423-G-T

http://identifiers.org/hco/7/GRCh38#103243069-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24574484-A-C

103243069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24574484-A-G

103243069-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24574484-A-T

103243070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24574485-G-A

103243070-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24574485-G-C

103243070-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24574485-G-T

http://identifiers.org/hco/7/GRCh38#103243120-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24574532-C-A

103243120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24574532-C-T

http://identifiers.org/hco/7/GRCh38#103243152-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24574564-A-C

103254102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24577763-C-T

103254343-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24577998-T-A

http://identifiers.org/hco/7/GRCh38#103254705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24578146-C-A

103254705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24578146-C-T

103254743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24578184-A-G

103254829-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: non coding transcript exon variant
orthologous variants: 24578252-T-A

103254865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: non coding transcript exon variant
orthologous variants: 24578288-A-G

103254966-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24578371-T-C

103255111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24578487-C-T

103255315-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24578656-T-A

103255315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24578656-T-C

103255377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24578717-T-C

103255447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24578809-G-A

103255872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24579140-C-T

http://identifiers.org/hco/7/GRCh38#103255917-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24579181-A-C

103255928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24579192-A-G

103256024-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24579242-T-A

103256024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24579242-T-C

103256117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24579308-C-T

103256163-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24579351-C-T

103256168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24579356-C-T

103256339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24579537-C-T

103256340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24579538-A-G

103256403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24579556-G-A

103256541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24579656-G-A

103256686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24579804-C-T

103256851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24579980-T-C

103257327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24580343-G-A

http://identifiers.org/hco/7/GRCh38#103257378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24580385-C-A

103257428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24580438-A-G

http://identifiers.org/hco/7/GRCh38#103257470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24580450-C-A

103257497-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24580477-T-G

http://identifiers.org/hco/7/GRCh38#103257527-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24580509-A-C

103257547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24580527-A-G

103257547-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24580527-A-T

103257569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24580552-G-A

103257569-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24580552-G-C

103257569-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24580552-G-T

103257572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24580555-T-C

http://identifiers.org/hco/7/GRCh38#103257574-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24580557-C-A

103257574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24580557-C-T

http://identifiers.org/hco/7/GRCh38#103257581-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24580564-C-A

http://identifiers.org/hco/7/GRCh38#103257742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24580723-C-A

103257742-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24580723-C-G

103257742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24580723-C-T

103271486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24591758-T-C

103271521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24591793-A-G

http://identifiers.org/hco/7/GRCh38#103271596-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24591842-C-A

103271596-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24591842-C-G

103271596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24591842-C-T

103271643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24591890-C-T

http://identifiers.org/hco/7/GRCh38#103271645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24591892-C-A

103271837-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24592074-A-G

103271867-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 24592104-T-A

103271867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 24592104-T-C

103271867-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 24592104-T-G

103271905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24592134-G-A

103271905-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24592134-G-T

http://identifiers.org/hco/7/GRCh38#103271997-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24592231-C-A

103272123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24592319-G-A

103272183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24592379-T-C

103272327-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24592500-A-G

103272428-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24592576-C-T

103272445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24592593-C-T

103272615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24592772-G-A

103272779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24593109-T-C

103273058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24593359-C-T

103274059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24593619-T-C

103275494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24601308-G-A

103275494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24601308-G-T

http://identifiers.org/hco/7/GRCh38#103275691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24601502-C-A

103275691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24601502-C-T

http://identifiers.org/hco/7/GRCh38#103275702-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24601513-C-A

103275702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24601513-C-T

103276156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24601876-T-C

103276193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24601911-C-T

103276301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24602018-G-A

103276301-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24602018-G-C

103276678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24602355-T-C

103277038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24602797-G-A

103277044-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24602803-G-A

103277044-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24602803-G-C

103277061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24602818-G-A

103277349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24603021-C-T

103277473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24603108-A-G

103277495-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24603130-G-T

http://identifiers.org/hco/7/GRCh38#103277501-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24603136-A-C

103277501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24603136-A-G

103277561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24603197-G-A

103277561-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24603197-G-T

103277657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24603297-G-A

103277657-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24603297-G-C

103277657-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24603297-G-T

103277664-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24603304-T-A

103277677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24603317-T-C

103277748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24603377-A-G

103277778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24603406-T-C

103277938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24603557-T-C

103278069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24603699-G-A

http://identifiers.org/hco/7/GRCh38#103278157-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#24603788-A-C

103278158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24603789-G-A

103278158-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24603789-G-C

103278551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24604142-T-C

103278921-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24604481-T-G

103279141-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 24605057-T-C

103279922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24607169-G-A

103279922-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24607169-G-C

103279922-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24607169-G-T

103279988-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24607238-G-C

103279988-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24607238-G-T

103279997-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24607247-C-G

103279997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24607247-C-T

103280012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 24607262-G-T

103280015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 24607265-G-A

103280015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 24607265-G-T

http://identifiers.org/hco/7/GRCh38#103280035-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#24607285-C-A

103280035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 24607285-C-T

http://identifiers.org/hco/7/GRCh38#103280045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#24607295-C-A

103280045-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 24607295-C-G

103280117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 24607406-T-C

103280124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 24607418-G-A

103280124-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 24607418-G-T

http://identifiers.org/hco/7/GRCh38#103280157-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#24607472-C-A

103280162-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: non coding transcript exon variant
orthologous variants: 24607486-T-A

103280162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: non coding transcript exon variant
orthologous variants: 24607486-T-C

103280162-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: non coding transcript exon variant
orthologous variants: 24607486-T-G

103280164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: non coding transcript exon variant
orthologous variants: 24607488-G-A

103280217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 24607528-G-A

103280217-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 24607528-G-T

103280308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 24607590-G-A

103280308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 21764
most severe consequence: non_coding_transcript_exon_variant, undefined
orthologous variants: 24607590-G-T