107065645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32094702-T-C

107067171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32092799-T-C

http://identifiers.org/hco/7/GRCh38#107067212-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#32092787-C-A

http://identifiers.org/hco/7/GRCh38#107067222-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#32092777-C-A

107067222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32092777-C-T

107067296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32092709-A-G

107067302-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32092703-G-T

107067381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32092624-G-T

107067508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32092491-T-C

107067598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32092412-G-A

107067598-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32092412-G-C

107067732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32092277-A-G

107067998-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32090783-G-C

107068339-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32090422-A-T

107068354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32090415-G-A

http://identifiers.org/hco/7/GRCh38#107068408-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#32090364-C-A

http://identifiers.org/hco/7/GRCh38#107068419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#32090353-C-A

107068434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32090337-G-A

107068434-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32090337-G-C

107068434-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32090337-G-T

107068505-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32090214-T-G

107068733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32089994-G-A

107068800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32089949-G-A

107069409-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32089509-C-G

107069535-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32089374-G-T

107069574-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 32089323-A-G

http://identifiers.org/hco/7/GRCh38#107069575-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#32089322-C-A

107069575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 32089322-C-T

107069599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32089298-A-G

107069599-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32089298-A-T

107069649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32089263-G-A

107069649-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32089263-G-T

107069652-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32089260-T-G

http://identifiers.org/hco/7/GRCh38#107069663-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#32089249-C-A

107069836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32089106-A-G

107069838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32089104-G-A

107069838-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32089104-G-C

107069838-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32089104-G-T

107069860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32089094-T-C

107069865-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32089089-C-G

107069919-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32089033-G-C

107070028-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32088931-G-A

107070044-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32088915-G-T

http://identifiers.org/hco/7/GRCh38#107070126-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#32088813-C-A

107070186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32088754-T-C

107070307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 32088628-C-T

107070324-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 32088611-T-C

107070324-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 32088611-T-G

http://identifiers.org/hco/7/GRCh38#107070382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#32088557-C-A

107070382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32088557-C-T

107070710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32088267-C-T

107070822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32088237-A-G

107070973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32088116-T-C

107071097-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32087989-T-A

107072035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32087242-C-T

http://identifiers.org/hco/7/GRCh38#107072131-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#32087212-A-C

http://identifiers.org/hco/7/GRCh38#107072185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#32087167-C-A

107072208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32087144-G-A

http://identifiers.org/hco/7/GRCh38#107072293-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#32087091-A-C

107072312-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32087075-C-G

107072784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32086698-A-G

107072834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32086644-T-C

107072875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32086597-T-C

107072885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32086586-G-A

107072939-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32086544-T-G

107072994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32086499-A-G

107073347-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32085912-T-G

107073413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32085847-G-A

107073541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32085740-C-T

http://identifiers.org/hco/7/GRCh38#107075771-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#32085130-A-C

107075986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32084956-C-T

107076081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32084834-G-A

107076303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32084499-A-G

107076544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32084273-A-G

107076719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32084083-T-C

107076735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32084067-A-G

107076746-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32084056-A-T

107076772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32084028-A-G

107076772-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32084028-A-T

107079164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32083555-T-C

107079185-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32083534-C-G

107079185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32083534-C-T

107079349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32083361-A-G

107079402-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32083308-T-C

107079495-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32083223-G-T

107079499-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32083220-G-A

107079499-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32083220-G-T

107079518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 32083197-G-A

107079518-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 32083197-G-T

107079566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 32083155-G-A

107079656-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32083054-A-T

http://identifiers.org/hco/7/GRCh38#107079666-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#32083044-C-A

107079666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32083044-C-T

107079716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32082998-G-A

107079716-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 32082998-G-T

107079815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32082890-G-A

107080153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32077919-G-A

107080192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32077880-C-T

107080363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32077768-G-A

http://identifiers.org/hco/7/GRCh38#107080759-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#32077439-A-C

107081031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32077115-T-C

107081092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32077056-T-C

107081222-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32076930-G-C

107081222-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32076930-G-T

http://identifiers.org/hco/7/GRCh38#107081474-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#32076707-A-C

107081480-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32076701-G-C

107081532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32076636-A-G

107084038-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32074266-T-G

107084091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32073935-A-G

107084106-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32073923-C-G

107084114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32073915-C-T

107084320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32073717-T-C

107084382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32073659-T-C

107084496-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32073560-T-G

107084782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32073394-G-A

107084872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32073351-G-A

107084872-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32073351-G-C

107084878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32073348-G-A

http://identifiers.org/hco/7/GRCh38#107084900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#32073326-C-A

107085039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32073187-T-C

107086975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32069867-T-C

http://identifiers.org/hco/7/GRCh38#107090398-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#32066939-C-A

107090541-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32066801-G-C

http://identifiers.org/hco/7/GRCh38#107090563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#32066779-C-A

107090713-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32066687-T-A

107091036-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32066334-A-G

107091036-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32066334-A-T

107091122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32066012-T-C

107091230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32065897-T-C

107091270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32065854-A-G

107091535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32065697-T-C

107091588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32065658-A-G

107091593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32065653-T-C

http://identifiers.org/hco/7/GRCh38#107091642-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#32065564-A-C

107091642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32065564-A-G

107091799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32065355-G-A

107091799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32065355-G-T

107092048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32065125-C-T

107092108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32065067-G-A

107092474-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32064519-T-C

107092528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32064465-T-C

107092670-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32064334-A-G

107109721-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32058081-T-A

107109757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32058043-T-C

107109788-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32058009-T-A

107112499-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32056885-T-G

107112510-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32056874-C-G

107112510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32056874-C-T

107113123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32056279-C-T

107113595-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32054799-A-G

107113659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32054066-C-T

107113833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32053914-G-T

107113903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32053844-A-G

107114067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32053596-G-T

107114244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32053420-T-C

107114812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32053244-G-A

http://identifiers.org/hco/7/GRCh38#107114836-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#32053220-C-A

107115096-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32052948-C-G

107115096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32052948-C-T

http://identifiers.org/hco/7/GRCh38#107115110-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#32052934-A-C

107115127-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32052916-G-T

107115139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32052904-G-A

107115172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32052813-G-T

107115244-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32052741-T-G

http://identifiers.org/hco/7/GRCh38#107115326-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#32052663-C-A

107115326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32052663-C-T

107115350-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32052638-A-T

107115353-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32052635-T-G

107116850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32049697-C-T

107117097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32049620-A-G

107117249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32049486-G-A

107117457-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32049273-C-T

107118060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32048696-G-A

107118135-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32048623-G-A

107118135-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32048623-G-T

107118225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 32048543-A-G

107118252-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32048518-T-A

107118282-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32048488-G-A

http://identifiers.org/hco/7/GRCh38#107118343-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#32048458-A-C

107118343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32048458-A-G

107118800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32047935-C-T

107118823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32047916-T-C

107118874-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32047871-T-A

107118890-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32047855-G-T

107118924-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32047832-C-G

107119234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32047522-A-G

http://identifiers.org/hco/7/GRCh38#107119340-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#32047446-C-A

107119340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32047446-C-T

107119435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32047359-C-T

http://identifiers.org/hco/7/GRCh38#107119719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#32047077-C-A

107119784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32047012-C-T

107119926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32046874-G-A

107120145-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32046736-A-T

107120582-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32046333-T-G

107120602-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32046312-G-C

http://identifiers.org/hco/7/GRCh38#107120605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#32046309-C-A

107120744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32046174-A-G

http://identifiers.org/hco/7/GRCh38#107120800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#32046050-C-A

http://identifiers.org/hco/7/GRCh38#107120865-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#32045971-C-A

107120918-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32045931-G-C

107120984-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32045858-T-A

107121812-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32045094-G-T

http://identifiers.org/hco/7/GRCh38#107121823-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#32045083-C-A

107121823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32045083-C-T

107121918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32043815-A-G

107121921-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32043812-A-G

107121924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32043809-T-C

107122039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32043712-G-A

107122062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32043686-A-G

107122227-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32043475-T-G

107122231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32043471-G-A

107122402-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32043309-T-A

107122405-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32043306-A-T

http://identifiers.org/hco/7/GRCh38#107122499-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#32043241-A-C

107122499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32043241-A-G

107122562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32043175-A-G

107122609-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32043100-C-G

107123055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32042601-A-G

http://identifiers.org/hco/7/GRCh38#107123083-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#32042569-C-A

107123416-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32042303-G-T

107123541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32042002-A-G

107123590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32041958-A-G

107123936-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32041221-A-G

http://identifiers.org/hco/7/GRCh38#107124101-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#32041074-A-C

107124296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32040888-T-C

107124401-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32040798-G-A

107124805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32040334-G-T

107127006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32039102-A-G

107127043-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32039065-C-G

107127181-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32038920-T-G

107127390-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32038747-A-G

107127390-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32038747-A-T

107127671-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32038414-A-T

107127754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32038329-T-C

107127754-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32038329-T-G

107127800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32038284-A-G

http://identifiers.org/hco/7/GRCh38#107128063-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#32038089-A-C

107128064-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32038088-G-C

107128064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32038088-G-T

107128097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32038054-G-A

107128097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32038054-G-T

107128129-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32038028-T-A

107128388-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32037811-T-A

107128388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32037811-T-C

107128389-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32037810-A-G

107128389-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32037810-A-T

107128391-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32037808-G-T

http://identifiers.org/hco/7/GRCh38#107128392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#32037807-C-A

107128394-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32037803-G-C

http://identifiers.org/hco/7/GRCh38#107128834-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#32037348-A-C

107128834-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32037348-A-T

107129052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32037169-T-C

107129132-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32037090-T-A

107129173-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32037040-A-G

107129434-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32036801-G-C

107129495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32036738-A-G

107130950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32035759-A-G

107131000-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32035709-A-T

107132355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32034680-C-T

107132443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32034607-G-A

107132508-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32034542-C-G

107132575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32034498-A-G

107132712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32034360-A-G

107132750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32034322-A-G

107133067-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32034003-T-C

107133067-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32034003-T-G

107133145-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 32033926-A-T

107133659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32033376-A-G

107133678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32033360-A-G

107133681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 40472
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 32033357-A-G