107377077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: 3 prime UTR variant
orthologous variants: 62910142-C-T

107377263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: 3 prime UTR variant
orthologous variants: 62910332-T-C

107377353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: 3 prime UTR variant
orthologous variants: 62910422-G-T

107377417-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: 3 prime UTR variant
orthologous variants: 62910542-G-T

http://identifiers.org/hco/5/GRCh38#107377451-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#62910591-C-A

107377451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: 3 prime UTR variant
orthologous variants: 62910591-C-T

107378499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: 3 prime UTR variant
orthologous variants: 62911577-A-G

107378666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: 3 prime UTR variant
orthologous variants: 62911753-A-G

107378830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: 3 prime UTR variant
orthologous variants: 62911913-C-T

107379059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: 3 prime UTR variant
orthologous variants: 62912134-G-A

107379059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: 3 prime UTR variant
orthologous variants: 62912134-G-T

107379763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: 3 prime UTR variant
orthologous variants: 62912829-C-T

http://identifiers.org/hco/5/GRCh38#107379764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#62912830-C-A

107379764-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: 3 prime UTR variant
orthologous variants: 62912830-C-T

107380118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: 3 prime UTR variant
orthologous variants: 62913185-G-A

107380161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: 3 prime UTR variant
orthologous variants: 62913229-G-A

107380161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: 3 prime UTR variant
orthologous variants: 62913229-G-T

http://identifiers.org/hco/5/GRCh38#107380576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#62913633-C-A

107380757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: 3 prime UTR variant
orthologous variants: 62913832-G-A

107380757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: 3 prime UTR variant
orthologous variants: 62913832-G-T

107380866-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: 3 prime UTR variant
orthologous variants: 62913941-T-A

107380866-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: 3 prime UTR variant
orthologous variants: 62913941-T-C

107380898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: 3 prime UTR variant
orthologous variants: 62913973-T-C

http://identifiers.org/hco/5/GRCh38#107380900-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#62913975-A-C

107380901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: 3 prime UTR variant
orthologous variants: 62913976-C-T

107380919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: 3 prime UTR variant
orthologous variants: 62913994-G-A

107380919-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: 3 prime UTR variant
orthologous variants: 62913994-G-C

107380919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: 3 prime UTR variant
orthologous variants: 62913994-G-T

107381020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 62914092-G-A

107381118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 62914200-G-T

107381241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 62914323-G-A

107381609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62914690-A-G

107381726-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62914800-C-T

107381976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62915051-C-T

107382305-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62915381-A-T

107382711-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62915454-G-C

107382767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62915510-G-A

107383117-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62915854-T-G

107383147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62915885-G-A

107383337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62916050-C-T

107384074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62916842-T-C

107385321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62917844-G-A

107385366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62918443-T-C

http://identifiers.org/hco/5/GRCh38#107385885-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#62918917-C-A

107385935-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62918966-C-T

107385936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62918967-C-T

107385989-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62919016-G-C

107386099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62919125-G-A

107387068-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62920144-C-G

107387147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62920223-A-G

107387555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62920657-T-C

107387559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62920661-A-G

107387668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62920795-G-A

107387668-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62920795-G-T

107387752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 62920878-A-G

107387877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62921000-A-G

107387981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62921115-T-C

http://identifiers.org/hco/5/GRCh38#107388373-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#62921522-C-A

107388373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 62921522-C-T

107388838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, undefined
orthologous variants: 62921990-G-A

107388938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, undefined
orthologous variants: 62922081-C-T

107388969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, undefined
orthologous variants: 62922104-A-G

107389249-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62922373-A-G

107389371-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, undefined
orthologous variants: 62922500-C-T

107389393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, undefined
orthologous variants: 62922522-C-T

107389531-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62922626-T-G

107389584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62922678-A-G

107389630-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62922731-C-G

107389658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62922759-A-G

107389715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62922821-C-T

107389785-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62922890-C-T

107391844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62923290-T-C

107391880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62923321-G-A

107391887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62923328-G-A

107392264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62923700-G-T

107392283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62923719-T-C

107392283-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62923719-T-G

107392374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62923811-A-G

http://identifiers.org/hco/5/GRCh38#107392433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#62923856-C-A

107392433-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62923856-C-G

http://identifiers.org/hco/5/GRCh38#107392438-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#62923861-A-C

107392479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62923901-A-G

107392506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62923929-G-A

107392551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62923977-C-T

107392758-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62924111-T-G

107392876-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62924227-C-T

107393535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62924835-T-C

107393551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62924851-G-A

107393551-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62924851-G-T

107393686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62924971-G-A

107393698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62924987-T-C

107393769-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62925058-T-G

107393853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62925173-A-G

107393856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62925176-T-C

107393979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62925324-A-G

107394272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62925630-G-A

107394342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62925700-A-G

107394351-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62925705-T-C

107394538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62925895-A-G

107394614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62925975-G-A

107394624-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62925985-C-G

107394624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62925985-C-T

http://identifiers.org/hco/5/GRCh38#107394829-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#62926187-C-A

107394829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62926187-C-T

107394935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62926305-G-A

107394982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62926353-G-A

107396751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62927389-A-G

107396796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62927435-G-A

107396896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62927532-A-G

107396937-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62927573-G-C

107397663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62927794-A-G

107397765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62927884-T-C

107398534-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62928516-T-A

107399065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62928769-G-A

107399065-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62928769-G-C

107400357-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62930008-C-G

107400384-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62930035-C-G

107400384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62930035-C-T

107400466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62930112-C-T

107400576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62930250-G-A

http://identifiers.org/hco/5/GRCh38#107400633-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#62930307-A-C

107400633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62930307-A-G

107400638-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62930312-G-T

107400669-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62930343-G-C

107400779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62930416-T-C

107400846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62930467-G-A

107401201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62931034-G-A

107401364-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62931189-A-T

107401828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62931640-G-A

107401976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62931788-C-T

http://identifiers.org/hco/5/GRCh38#107402226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#62932089-C-A

107402226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62932089-C-T

http://identifiers.org/hco/5/GRCh38#107402374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#62932236-C-A

107402501-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62932358-A-T

107402855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62932694-C-T

107403191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62933025-T-C

107403324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62933160-G-A

107403371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62933210-G-A

107403371-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62933210-G-C

107403644-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62933472-T-A

107403704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62933532-T-C

107403776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62933597-A-G

107403919-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62933758-G-C

http://identifiers.org/hco/5/GRCh38#107404004-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#62933850-C-A

107404004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62933850-C-T

107404068-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62933914-T-G

107404198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62934042-G-A

107404738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62934581-C-T

107404910-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62934753-C-G

107404965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62934809-A-G

107405059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62934851-G-A

107405085-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62934879-A-G

http://identifiers.org/hco/5/GRCh38#107405424-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#62935438-A-C

107405424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62935438-A-G

107406805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: -C-T

http://identifiers.org/hco/5/GRCh38#107406920-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: -A-C

107407028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: -C-T

107407697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62939320-C-T

107407751-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62939356-T-C

107407775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62939382-C-T

http://identifiers.org/hco/5/GRCh38#107407835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#62939442-C-A

107408193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62940434-C-T

107408465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62940692-G-T

107408509-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62940736-C-G

107408512-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62940739-A-T

107408920-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62941126-T-C

107409041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62941192-A-G

107409064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62941215-G-T

107409092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62941243-T-C

107409231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62941372-G-A

107409231-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62941372-G-C

107409270-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62941419-G-C

107409288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62941437-G-A

107409288-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62941437-G-T

107410959-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62941555-T-G

107411070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62941667-A-G

107411298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62941891-C-T

107412990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62943586-T-C

107413108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62943707-T-C

107413684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62944249-T-C

107413703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62944275-G-A

http://identifiers.org/hco/5/GRCh38#107413821-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#62944596-C-A

http://identifiers.org/hco/5/GRCh38#107414168-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#62944901-C-A

107414190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62944923-C-T

107415661-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62946365-C-T

107415854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62946910-G-A

107415911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62946954-G-A

107416020-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62947063-C-T

http://identifiers.org/hco/5/GRCh38#107416146-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#62947176-A-C

107416146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62947176-A-G

107416838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62948073-G-A

107416838-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62948073-G-T

107416921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62948161-T-C

107416944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62948184-G-A

107416959-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62948199-T-G

107417186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62948423-T-C

107417186-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62948423-T-G

107417256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62948498-T-C

http://identifiers.org/hco/5/GRCh38#107417257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#62948499-C-A

107417452-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62948695-C-G

107417632-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62948876-G-T

http://identifiers.org/hco/5/GRCh38#107417977-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#62949227-C-A

107418481-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62949742-G-C

http://identifiers.org/hco/5/GRCh38#107418570-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#62949840-A-C

107418710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62949936-T-C

107418897-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62950126-G-C

107419374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62950645-C-T

http://identifiers.org/hco/5/GRCh38#107419441-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#62950712-C-A

http://identifiers.org/hco/5/GRCh38#107419485-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#62950762-C-A

107419485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62950762-C-T

107419982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62951214-C-T

107420040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62951270-A-G

107420088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62951319-A-G

107420440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62951824-C-T

107420720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62952166-T-C

107420902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62952365-C-T

107420979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62952442-G-A

107421414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62952848-T-C

107421458-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62952908-C-G

107421641-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62953090-G-A

107422757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62953971-G-A

107422846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62954013-G-A

107423207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62954340-G-A

107423221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62954360-C-T

107423229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62954368-A-G

107423235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62954374-G-A

http://identifiers.org/hco/5/GRCh38#107423301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#62954450-C-A

107423301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62954450-C-T

107423368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62954513-T-C

http://identifiers.org/hco/5/GRCh38#107423659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#62954758-C-A

107423659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62954758-C-T

107423841-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62954881-G-C

107423924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62954961-T-C

107424037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62955060-T-C

107424567-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62955163-C-G

107424631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62955228-T-C

107424796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62955387-C-T

107424797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62955388-G-A

107425309-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62955902-G-C

107425754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, undefined
orthologous variants: 62956350-T-C

107425835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, undefined
orthologous variants: 62956432-C-T

107426431-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62957025-T-G

107426448-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62957043-C-G

107426448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62957043-C-T

107426453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62957051-T-C

107426580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62957179-A-G

http://identifiers.org/hco/5/GRCh38#107426864-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#62957452-A-C

107426864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62957452-A-G

107426864-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62957452-A-T

107426916-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62957509-T-A

107426916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62957509-T-C

http://identifiers.org/hco/5/GRCh38#107426942-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#62957541-A-C

107426942-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62957541-A-T

107426965-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron variant
orthologous variants: 62957573-A-G

107426990-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62957598-A-G

http://identifiers.org/hco/5/GRCh38#107427032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#62957640-C-A

107427032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62957640-C-T

107427077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62957685-T-C

107427077-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62957685-T-G

107427129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62957737-G-A

107427129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62957737-G-T

107427139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 62957745-A-G

http://identifiers.org/hco/5/GRCh38#107427559-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#62958180-C-A

107427559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62958180-C-T

107427596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62958217-G-A

http://identifiers.org/hco/5/GRCh38#107427611-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#62958232-A-C

107427664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62958283-G-T

107428444-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62958362-T-A

107428512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62958428-G-A

107428591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62958506-G-A

107428759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62958706-T-C

107428788-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62958735-A-T

107429539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62959152-A-G

http://identifiers.org/hco/5/GRCh38#107430455-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#62959825-A-C

107430455-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62959825-A-T

107430541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62959905-A-G

107430551-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62959927-A-T

107430650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62960036-T-C

107430659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62960045-G-A

107430659-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62960045-G-C

107430711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62960095-G-T

107431037-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62960329-G-A

107431049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62960341-C-T

http://identifiers.org/hco/5/GRCh38#107431229-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#62960445-C-A

107431373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62960544-G-A

107431373-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62960544-G-T

107431462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62960621-T-C

107431511-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62960669-T-G

107431518-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62960673-T-C

107431679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62960801-G-A

107431903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62961022-T-C

107432208-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62961314-C-G

107432211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62961316-C-T

107432304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62961408-A-G

107432470-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62961583-A-T

107432655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62961751-C-T

http://identifiers.org/hco/5/GRCh38#107432743-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#62961844-A-C

107432743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62961844-A-G

107433244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62961927-C-T

107434064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62962619-G-A

http://identifiers.org/hco/5/GRCh38#107434272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#62962818-C-A

107434483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62963028-A-G

107434532-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62963077-G-T

107434955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62963489-A-G

107435061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62963596-C-T

107435108-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62963643-T-A

107435108-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62963643-T-C

107435150-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62963685-G-C

107435166-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62963715-T-C

107435166-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62963715-T-G

107435349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62963881-G-A

http://identifiers.org/hco/5/GRCh38#107435475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#62964012-C-A

107435478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62964015-G-A

107435482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62964019-A-G

107435493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62964030-G-A

http://identifiers.org/hco/5/GRCh38#107435559-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#62964089-C-A

107435955-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62964555-T-A

107435985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62964585-C-T

107436007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62964614-T-C

107436146-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62964745-C-G

107436366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62964960-G-A

107436749-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62965340-G-C

107436798-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62965389-A-T

107437056-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62965588-T-G

107437084-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62965631-T-A

107437084-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62965631-T-C

107437108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62965661-C-T

107437123-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62965676-G-T

http://identifiers.org/hco/5/GRCh38#107437169-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#62965739-A-C

107437171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62965741-T-C

107437240-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62965811-C-G

107437317-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62965879-G-C

http://identifiers.org/hco/5/GRCh38#107437471-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#62966033-A-C

107437771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62966256-T-C

107437879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62966453-T-C

http://identifiers.org/hco/5/GRCh38#107438116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#62966690-C-A

107438189-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62966763-G-A

107438713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62967246-A-G

107438981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62967478-G-A

107439217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62967724-G-A

107439294-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62967798-T-G

107439313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62967817-G-A

107439313-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62967817-G-C

107439324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62967828-C-T

107439369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62967868-G-A

107439369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62967868-G-T

107439461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62967941-A-G

107440289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62968761-A-G

107440576-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62969036-T-A

107440576-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62969036-T-G

107440586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62969046-G-A

107440701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62969161-C-T

107440808-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62969287-A-T

107440863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62969335-G-A

107440863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62969335-G-T

107440882-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62969349-T-A

107440882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62969349-T-C

107440981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62969448-A-G

107441017-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62969485-T-A

107441054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62969524-C-T

107441287-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62969751-T-G

107441458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62969870-T-C

107441467-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62969879-G-A

107441552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62969944-A-G

107441572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62969965-A-G

http://identifiers.org/hco/5/GRCh38#107441636-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#62970031-A-C

http://identifiers.org/hco/5/GRCh38#107441666-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#62970061-C-A

107441666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62970061-C-T

107441755-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62970150-C-G

107441772-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62970347-G-C

107441853-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62970440-T-C

107442089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62970810-T-C

107442222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62970952-G-A

107442244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62970974-C-T

107442253-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62970983-G-T

107442590-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62971339-G-C

107442590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62971339-G-T

107442722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62971475-G-A

107442908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62971662-G-T

107442924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62971679-G-A

107442924-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62971679-G-C

http://identifiers.org/hco/5/GRCh38#107442948-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#62971706-A-C

107444530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62972997-T-C

107444795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62973462-T-C

107445549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62973897-G-A

107445549-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62973897-G-C

107445619-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62973966-G-C

107445820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62974165-C-T

107445901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62974241-A-G

107447235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62976108-C-T

107447269-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62976138-A-T

http://identifiers.org/hco/5/GRCh38#107447328-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#62976212-A-C

107447404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62976253-T-C

107447404-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62976253-T-G

107447434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62976283-T-C

107447471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62976320-A-G

107447708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62976566-G-A

107448244-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62976837-G-A

http://identifiers.org/hco/5/GRCh38#107448300-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#62976906-A-C

107448379-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62976985-T-G

107448527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62977134-G-A

107449361-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62978068-T-A

107449499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62978190-C-T

107449992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62978683-T-C

107450178-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62978861-G-C

107450549-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62979184-T-A

107450549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62979184-T-C

107450644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62979281-T-C

107451492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62980077-T-C

107451544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62980140-G-A

107451561-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62980157-T-A

107451561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62980157-T-C

http://identifiers.org/hco/5/GRCh38#107453069-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#62980481-C-A

107453070-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62980482-T-G

107453135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62980799-A-G

107453143-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62980807-A-G

107453194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62980856-A-G

107453233-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62981089-T-A

107453397-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62981204-G-A

107453456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62981259-T-C

107453536-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62981337-A-T

107453735-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62981541-T-C

107453756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62981566-G-A

107454017-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62981781-A-T

107454095-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62981852-T-A

107454121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62981878-C-T

107454275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62982028-G-A

107454396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62982133-T-C

107454411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62982148-C-T

107454536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62982259-C-T

http://identifiers.org/hco/5/GRCh38#107454641-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#62982353-A-C

107454777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62982479-G-A

107454777-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62982479-G-C

107455091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62982764-A-G

107455666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62983353-T-C

107456755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62984353-G-A

107456785-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62984385-A-T

107456806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62984406-G-A

107456886-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62984454-C-G

107456903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62984471-C-T

107457006-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62984566-C-G

107457009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62984569-G-T

107457088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62984629-A-G

107457211-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62984730-T-G

107458317-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62985586-T-G

107458334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62985603-C-T

http://identifiers.org/hco/5/GRCh38#107458570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#62985856-C-A

107458820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62986121-C-T

http://identifiers.org/hco/5/GRCh38#107459405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#62986499-C-A

107459432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62986516-G-A

107459443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62986526-G-A

http://identifiers.org/hco/5/GRCh38#107459649-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#62986724-C-A

107459649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62986724-C-T

107459771-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62986851-G-C

107459778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62986861-C-T

107459791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62986874-G-A

107459937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62986957-C-T

107459972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62986975-G-A

107459972-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62986975-G-C

107459988-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62986983-T-G

107460530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62987505-A-G

107461629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62988570-G-A

107462061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62988984-G-A

107462073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62988996-T-C

107462125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62989127-C-T

107462134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62989155-C-T

107462608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62989896-A-G

107462761-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62990117-A-G

107462960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62990310-T-C

107462960-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62990310-T-G

http://identifiers.org/hco/5/GRCh38#107463019-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#62990369-A-C

107463019-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62990369-A-T

107463539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62991165-T-C

http://identifiers.org/hco/5/GRCh38#107463583-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#62991251-C-A

107463584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62991252-T-C

107463585-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62991253-T-A

107463653-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62991336-T-G

107463699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62991395-G-A

107463948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62991621-T-C

107463989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62991657-G-A

107464138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62991810-G-A

http://identifiers.org/hco/5/GRCh38#107464150-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#62991822-C-A

107464324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62991949-G-A

107464447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62992070-G-A

107464559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62992157-A-G

107464684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62992285-C-T

107464704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62992305-G-A

107464704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62992305-G-T

http://identifiers.org/hco/5/GRCh38#107465003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#62992522-C-A

107465058-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62992577-T-A

http://identifiers.org/hco/5/GRCh38#107465087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#62992612-C-A

107465147-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62992672-C-G

107466244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62994368-C-T

107466245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62994369-G-A

107467503-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62995797-T-A

107467503-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62995797-T-C

107467745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62996023-T-C

107467777-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62996056-G-A

107467869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62996145-T-C

107467920-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62996182-G-C

107467926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62996188-G-A

107468229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62996491-A-G

107468247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62996546-G-A

107468267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62996566-A-G

http://identifiers.org/hco/5/GRCh38#107468462-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#62996752-A-C

107469048-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62997514-T-A

107469052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62997518-T-C

107469071-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62997537-G-C

107469087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62997553-A-G

107469384-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62998043-T-C

http://identifiers.org/hco/5/GRCh38#107469389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#62998048-C-A

107469405-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62998089-C-T

http://identifiers.org/hco/5/GRCh38#107469980-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#62999037-C-A

107469980-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62999037-C-G

107469980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62999037-C-T

107470128-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62999181-A-T

http://identifiers.org/hco/5/GRCh38#107470149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#62999203-C-A

107470167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62999222-C-T

107470254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62999316-G-A

107470259-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62999321-T-G

107470370-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -T-C

107470614-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62999660-T-A

107470718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 62999762-T-C

http://identifiers.org/hco/5/GRCh38#107471102-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63000045-A-C

http://identifiers.org/hco/5/GRCh38#107471236-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63000142-A-C

107471374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63000272-G-T

107471575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63000473-C-T

107471890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63001192-A-G

http://identifiers.org/hco/5/GRCh38#107471894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63001196-C-A

107471894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63001196-C-T

107471951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63001238-C-T

107472082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63001361-C-T

107472088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63001367-A-G

107472264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63001656-T-C

107472418-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63001769-T-A

107472629-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63001982-G-C

107472629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63001982-G-T

107472741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63002085-G-A

http://identifiers.org/hco/5/GRCh38#107472984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63002328-C-A

107473043-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63002384-T-G

107473047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63002391-G-A

107473266-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63002594-T-A

107474127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63004152-C-T

http://identifiers.org/hco/5/GRCh38#107474598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63004662-C-A

107474747-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63004818-T-A

107475290-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63005302-G-C

107475308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 63005320-A-G

107475468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63005480-A-G

107475506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63005515-A-G

107475702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63005717-T-C

http://identifiers.org/hco/5/GRCh38#107475986-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63006028-A-C

107476372-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63006104-G-A

107476675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63006425-C-T

107476905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 63006621-T-C

107477506-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63007110-A-G

107477759-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63007346-A-T

107477843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63007653-T-C

107478640-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63008469-A-G

107478883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63008714-A-G

107479120-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63008987-T-G

107479214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63009086-A-G

107479406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63009268-A-G

http://identifiers.org/hco/5/GRCh38#107479469-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63009321-A-C

107479623-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63009459-T-A

107479639-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63009475-T-A

107479703-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63009551-T-A

107480359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63009993-T-C

http://identifiers.org/hco/5/GRCh38#107480497-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63010078-A-C

107482759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63011103-C-T

http://identifiers.org/hco/5/GRCh38#107482777-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63011121-A-C

107482777-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63011121-A-T

107482786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63011131-T-C

107482893-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63011177-T-A

107482893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63011177-T-C

107482915-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63011199-C-G

107482915-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63011199-C-T

107483077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63011355-G-A

107483820-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63012139-G-C

107483840-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63012159-A-T

107484096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63012556-C-T

107484421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63012845-T-C

107484596-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63012987-G-C

http://identifiers.org/hco/5/GRCh38#107484907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63013261-C-A

107484907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63013261-C-T

http://identifiers.org/hco/5/GRCh38#107485606-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63013937-A-C

107485666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63013997-G-A

107485765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63014399-C-T

107485766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63014400-G-A

107485822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63014455-C-T

107485849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63014482-A-G

107485851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63014484-T-C

107485999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63014626-C-T

107486008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63014635-A-G

107486011-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63014638-A-T

http://identifiers.org/hco/5/GRCh38#107486054-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63014680-C-A

107486054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63014680-C-T

107486110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63014732-G-A

http://identifiers.org/hco/5/GRCh38#107486228-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63014855-C-A

107486327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63015002-G-A

107486328-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63015003-G-T

107486521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63015170-A-G

107486531-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63015189-G-C

107486718-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63015373-C-G

107487269-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63015879-G-T

107487289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63015899-C-T

http://identifiers.org/hco/5/GRCh38#107487367-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63015981-C-A

107487367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63015981-C-T

107487375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63015989-A-G

107487380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63015994-T-C

107487523-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63016121-G-C

107487740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63016347-C-T

107487746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63016353-C-T

107487783-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63016390-G-T

107487921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63016525-C-T

http://identifiers.org/hco/5/GRCh38#107488060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63016661-C-A

107488396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63016953-G-A

107488460-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63017014-T-A

107489169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63017316-C-T

107489713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63017617-T-C

107490095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63018171-C-T

107490180-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63018255-G-T

107490225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63018299-T-C

http://identifiers.org/hco/5/GRCh38#107490389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63018322-C-A

107491120-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63018994-A-G

107491148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63019022-C-T

107491193-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63019076-A-G

107492346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63019939-T-C

107493147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63020418-C-T

107493148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63020419-T-C

107493180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63020451-T-C

107493403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63020662-C-T

http://identifiers.org/hco/5/GRCh38#107493696-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63020917-A-C

107493696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63020917-A-G

107493738-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63020952-C-T

107495680-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63021701-G-C

107495804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63021797-A-G

107496387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63022035-T-C

107496751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63022154-C-T

107496844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63022241-C-T

107496863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63022260-T-C

107496913-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63022310-G-C

107497158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63022553-T-C

107497321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63022715-C-T

http://identifiers.org/hco/5/GRCh38#107497389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63022783-C-A

107497570-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63022936-T-G

107497814-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63023130-A-T

107497916-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63023146-T-G

107498244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63023227-C-T

107498260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63023242-A-G

107498590-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63023573-C-T

http://identifiers.org/hco/5/GRCh38#107498866-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63023808-C-A

107498866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63023808-C-T

107499089-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63024027-C-T

107499437-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63024395-A-T

107499715-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63024650-G-T

107499823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63024768-A-G

107499944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63024889-T-C

107500001-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63024930-C-G

107500271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63025213-T-C

107500282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63025224-T-C

107500308-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63025256-C-G

107500308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63025256-C-T

107500309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63025257-G-A

107501229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63026041-C-T

107501414-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63026222-A-T

http://identifiers.org/hco/5/GRCh38#107501483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63026281-C-A

107501701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63026952-C-T

107501715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63026971-T-C

107501880-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63027244-A-G

107502149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63027522-T-C

107502159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63027532-G-T

107502251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63027626-A-G

107502355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63027740-C-T

107502389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63027775-C-T

107502592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63027984-G-A

107502652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63028032-G-A

107502689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63028069-T-C

107503061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63028443-G-A

107503261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63028594-A-G

http://identifiers.org/hco/5/GRCh38#107503440-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63028708-A-C

107503562-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63028832-T-A

107503695-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63029021-G-T

107504062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63029786-A-G

107504101-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63029813-C-G

107504101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63029813-C-T

107504185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63029894-A-G

107504439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63030170-T-C

107504834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63030858-T-C

107505487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63031479-T-C

107505575-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63031566-C-G

107505868-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63031722-G-A

107505894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63031749-T-C

http://identifiers.org/hco/5/GRCh38#107506001-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63031831-C-A

http://identifiers.org/hco/5/GRCh38#107506131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63031963-C-A

107506131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63031963-C-T

http://identifiers.org/hco/5/GRCh38#107506142-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63031973-C-A

107506207-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63032026-T-C

107506210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63032029-T-C

107506271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63032090-G-A

107506271-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63032090-G-T

107507648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63032761-G-A

107508066-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63033145-T-A

107508369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63033441-A-G

http://identifiers.org/hco/5/GRCh38#107508799-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63033794-C-A

http://identifiers.org/hco/5/GRCh38#107508899-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63033913-A-C

107508913-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63033927-T-G

107508922-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63033932-T-G

107509199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63034178-A-G

107509199-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63034178-A-T

107509220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63034199-T-C

107511961-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63035432-C-G

107511961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63035432-C-T

107512170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63035643-A-G

107512267-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63035740-A-T

107512311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63035784-C-T

107512451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63035870-T-C

107512638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63036068-T-C

107512693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63036123-A-G

107512716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63036146-G-A

107513643-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63037041-T-G

107514000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63037389-G-A

107514254-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63037629-T-A

107514254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63037629-T-C

http://identifiers.org/hco/5/GRCh38#107514738-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63038080-A-C

107515748-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63038554-T-A

107515748-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63038554-T-C

107515855-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63038949-C-G

107515872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63038966-C-T

107516379-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63039130-A-T

107516737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 63039557-C-T

107516882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63039703-C-T

107516902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63039722-T-C

107517079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63039878-T-C

107517183-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63039973-G-C

107517226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63040015-G-A

107517716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63040509-T-C

107517760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63040550-A-G

107518527-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63041339-C-G

107518648-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63041477-T-C

107518945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63041836-G-A

107519040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63041932-T-C

107519165-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63042057-T-G

http://identifiers.org/hco/5/GRCh38#107519216-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63042101-C-A

107519216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63042101-C-T

http://identifiers.org/hco/5/GRCh38#107519226-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63042111-A-C

107519312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63042183-T-C

http://identifiers.org/hco/5/GRCh38#107519541-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63042418-A-C

107519786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63042727-A-G

107520016-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63043008-C-G

107520295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 63043289-T-C

107520420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63043412-C-T

107520722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63043627-G-A

107520742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63043647-G-A

107520742-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63043647-G-C

107520742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63043647-G-T

107520754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63043659-C-T

107520785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63043693-G-A

107520834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63043737-T-C

107520918-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63043820-A-T

107523317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63046993-T-C

107523382-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63047061-T-C

107523636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63047308-G-A

107523741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63047414-T-C

107523867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63047606-G-A

http://identifiers.org/hco/5/GRCh38#107524014-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63047839-A-C

107524128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63047952-A-G

107524144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63047968-T-C

107524158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63047983-G-A

107524161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63047986-C-T

107524192-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63048017-G-T

107524228-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63048054-T-G

107526252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63048441-T-C

107526385-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63048549-T-G

107526484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63048637-C-T

107526493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63048646-G-A

107526605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63048757-T-C

107526779-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63048939-G-A

107526845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63048975-A-G

107526956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63049075-G-A

107528609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63049667-G-A

107528731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63049787-C-T

http://identifiers.org/hco/5/GRCh38#107528840-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63049907-A-C

107528840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63049907-A-G

107528843-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63049910-T-A

107529129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63050214-G-A

107529193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63050282-G-A

107529340-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63050383-G-A

107529340-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63050383-G-C

107529418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63050470-T-C

107529482-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63050533-G-C

107529532-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63050583-T-C

107529560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63050610-A-G

107529748-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63050767-C-G

107529807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63050820-C-T

107530265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63051532-T-C

107530512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63052173-C-T

107530549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63052216-G-A

107530614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63052345-T-C

107530822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63052565-T-C

107531318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63053038-G-A

107531355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63053074-T-C

http://identifiers.org/hco/5/GRCh38#107531685-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63053338-C-A

107531685-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63053338-C-G

107531729-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63053382-T-C

107532023-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63053680-G-T

107532438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63054100-C-T

107532782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63054436-C-T

107532963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63054656-T-C

107533096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63054786-C-T

107533217-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63054907-T-G

107533923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63055610-C-T

107534117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63055804-T-C

107534297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63055989-A-G

http://identifiers.org/hco/5/GRCh38#107534356-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63056048-A-C

107534511-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63056196-C-G

107534604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63056311-G-A

107534618-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63056326-T-A

http://identifiers.org/hco/5/GRCh38#107534667-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63056374-A-C

107534720-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63056427-A-G

107534899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63056591-A-G

107535007-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63056710-A-T

107535166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63056871-C-T

107535437-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63057186-T-G

107535459-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63057209-T-A

107535459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63057209-T-C

107536137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63057845-G-A

107536225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63057935-G-T

107536386-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63058072-G-C

107536484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63058176-A-G

107536525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63058209-A-G

107536813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63058476-A-G

107538068-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63060062-T-A

107538079-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63060073-G-T

107538106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63060100-T-C

107538162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63060149-T-C

107538164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63060151-C-T

http://identifiers.org/hco/5/GRCh38#107538441-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63060414-A-C

107538759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63060728-C-T

http://identifiers.org/hco/5/GRCh38#107538775-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63060744-A-C

107538869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63060829-T-C

107538959-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63060919-C-T

107539152-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63061117-A-T

107539536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63061414-G-A

107539782-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63061586-T-A

107539947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 63061726-G-A

107540125-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63061879-G-C

107540213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63061965-T-C

107540355-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63062104-G-T

107540439-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63062189-C-G

107540439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63062189-C-T

107540564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 63062313-A-G

107540605-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63062345-T-C

107540650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63062388-C-T

107541164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63062613-A-G

107541288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63062715-T-C

107541319-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63062747-C-G

107541549-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63063024-T-C

107541568-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63063039-G-C

107541653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63063119-C-T

107541752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63063210-G-A

107542019-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63063533-T-C

107542290-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63063811-T-A

107542290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63063811-T-C

107542706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63064257-C-T

107542888-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63064409-T-C

107542972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63064471-T-C

107543430-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63064877-G-C

107543625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63065077-T-C

107543630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63065087-T-C

107543770-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63065179-G-A

107543941-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63065364-G-C

107543960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63065383-G-A

107543960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63065383-G-T

107544104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63065539-T-C

107544824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63066397-T-C

107545033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63066562-A-G

107545045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63066573-A-G

107545431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63066902-G-A

107545431-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63066902-G-T

107545505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63066951-T-C

107545522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63066969-G-A

107545646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63067094-T-C

107545656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63067105-C-T

107545657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63067106-G-A

107545657-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63067106-G-T

107545675-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63067124-C-T

107545732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63067181-T-C

107545820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63067267-G-A

107546154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63067623-G-A

107546159-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63067628-T-A

107546250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63067716-C-T

107546251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63067717-G-A

http://identifiers.org/hco/5/GRCh38#107546346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63067813-C-A

107546524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63067983-G-A

107546846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 63068315-T-C

107547040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63068509-C-T

107547147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63068612-T-C

http://identifiers.org/hco/5/GRCh38#107547355-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63068786-C-A

107547380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63068804-C-T

107547461-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63068893-C-G

107547661-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63069284-G-C

107547730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63069350-T-C

http://identifiers.org/hco/5/GRCh38#107547764-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63069384-A-C

107547918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63069737-T-C

107547943-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63069763-G-T

107548017-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63069848-C-G

107548032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63069863-T-C

http://identifiers.org/hco/5/GRCh38#107548050-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63069881-C-A

107548071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63069903-A-G

107548083-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63069915-C-G

http://identifiers.org/hco/5/GRCh38#107548118-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63069945-A-C

107548200-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63070028-A-G

107548203-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63070031-C-G

107548203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63070031-C-T

107548288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63070097-T-C

107548377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63070187-C-T

107548476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63070475-A-G

107548730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63070700-G-A

107548790-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63070757-T-G

107551961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63070968-T-C

107551967-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63070974-T-A

107552174-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63071182-T-G

107552239-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63071235-A-T

http://identifiers.org/hco/5/GRCh38#107552290-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63071288-A-C

107552486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63071444-G-T

107552501-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63071458-C-G

107552689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63071635-T-C

107552704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63071650-C-T

107553382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63072287-C-T

107553418-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63072321-G-C

http://identifiers.org/hco/5/GRCh38#107553525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63072403-C-A

http://identifiers.org/hco/5/GRCh38#107553556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63072433-C-A

107553556-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63072433-C-T

107553603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63072474-G-A

107553923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63072950-C-T

107554985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63073971-T-C

107555117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63074103-A-G

107555145-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63074130-A-T

107555374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63074358-T-C

107555407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63074393-C-T

107555417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63074403-G-A

107555430-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63074408-T-G

107555533-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63074511-C-T

107555662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63074639-T-C

107555695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63074672-T-C

107555698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63074675-T-C

107555826-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63074818-C-G

107555854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63074846-A-G

107555877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63074869-G-A

107555882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63074874-C-T

107556045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63075020-A-G

107556063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63075038-T-C

107556170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63075130-G-A

107556170-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63075130-G-C

107557065-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63075467-G-C

107557065-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63075467-G-T

107557101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63075500-A-G

107557175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63075608-G-A

107557264-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 63075695-G-C

http://identifiers.org/hco/5/GRCh38#107557379-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63075810-A-C

107557404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 63075836-T-C

107557592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 63076248-T-C

107557635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63076291-A-G

107557666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63076313-A-G

107557666-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63076313-A-T

http://identifiers.org/hco/5/GRCh38#107557802-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63076458-C-A

107558083-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63076703-A-T

107558539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63077061-T-C

107558540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63077062-C-T

107559024-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63077531-C-T

107559065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63077569-T-C

107559357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63077898-G-A

107559722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63078368-T-C

107559764-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63078410-T-C

107559849-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63078546-G-C

107560629-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63079692-T-C

107560764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63079810-G-A

107560772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63079818-C-T

107561090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63080117-G-A

107561361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63080326-A-G

107561703-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63080404-A-T

107561879-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63080586-T-C

http://identifiers.org/hco/5/GRCh38#107562211-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63080943-A-C

107562404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63081123-T-C

107562516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63081423-G-A

107562537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63081448-G-A

107562541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63081452-A-G

107562553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63081464-C-T

http://identifiers.org/hco/5/GRCh38#107562572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63081483-C-A

http://identifiers.org/hco/5/GRCh38#107562642-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63081548-A-C

107562642-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63081548-A-T

107562655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63081583-A-G

107562749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63081680-T-C

107562819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63081752-G-A

http://identifiers.org/hco/5/GRCh38#107563035-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63081970-C-A

107563035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63081970-C-T

107563262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63082193-G-A

107563262-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63082193-G-C

107563327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63082250-T-C

107563844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63082823-C-T

107563852-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63082831-C-G

http://identifiers.org/hco/5/GRCh38#107563984-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63082938-C-A

107563984-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63082938-C-T

107564062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63083014-T-C

107564403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63083355-G-A

http://identifiers.org/hco/5/GRCh38#107564435-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63083383-A-C

107564435-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63083383-A-G

107564474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63083428-G-A

107564480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63083434-G-A

107564480-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63083434-G-C

107564637-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63083585-T-A

107564637-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63083585-T-G

107564652-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63083604-G-A

107564652-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63083604-G-T

107564684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63083648-C-T

107564975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63083930-G-A

107565117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63084072-C-T

107565314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63084235-G-A

107565314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63084235-G-T

107565654-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63084564-C-G

107565654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63084564-C-T

107565671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63084579-T-C

107565780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63084656-G-A

107565856-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63084835-G-T

107565862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63084841-G-A

107565953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63084934-C-T

107566171-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63085145-G-A

107566175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63085149-C-T

107566176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63085150-G-A

107566206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63085180-G-A

107566632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63085602-T-C

107566679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63085661-T-C

107566773-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63085775-G-T

107566825-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63085827-T-C

107566872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63085874-A-G

107566906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63085908-T-C

107567044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63086061-T-C

107567118-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63086138-G-C

107567118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63086138-G-T

107567299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63086318-A-G

107567483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63086499-A-G

107567626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63086636-C-T

107568757-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63087648-C-G

107568962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63087831-T-C

107569932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63088944-A-G

107570062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63089055-C-T

107570299-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63089288-C-G

107570445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63089435-A-G

107570560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63089550-C-T

107570612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63089602-C-T

107570620-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63089610-G-T

107570638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63089628-A-G

107570638-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63089628-A-T

107570839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63089832-C-T

107570888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63089882-G-A

107571064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63090050-A-G

107571064-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63090050-A-T

107571158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63090127-G-A

107571173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63090142-G-A

107571236-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63090194-G-C

107571431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63090392-A-G

107571582-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63090514-G-T

107571751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63090666-G-T

107571866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63090782-C-T

http://identifiers.org/hco/5/GRCh38#107572281-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/17/GRCm39#63091180-A-C

107572281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 63091180-A-G

107572576-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63091464-A-G

107572688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63091578-C-T

107572835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63091740-G-A

107572936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63091849-G-A

107573113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63092009-A-G

107573333-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63092229-T-A

107573540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63092452-T-C

107573540-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63092452-T-G

107573624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63092538-C-T

107573751-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63092637-G-A

107573898-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63092781-C-T

107574032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63092923-T-C

107574266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63093061-G-T

http://identifiers.org/hco/5/GRCh38#107574272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63093067-C-A

107574272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63093067-C-T

107574279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63093074-G-A

http://identifiers.org/hco/5/GRCh38#107574355-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63093172-C-A

107575104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63093934-G-A

107575104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63093934-G-T

107575154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63093987-A-G

http://identifiers.org/hco/5/GRCh38#107575340-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63094142-A-C

107575755-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63094531-C-G

107575755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63094531-C-T

107576266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63095046-A-G

http://identifiers.org/hco/5/GRCh38#107576301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63095081-C-A

107576501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63095282-G-A

107576664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63095443-T-C

107576732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63095507-T-C

107576846-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63095599-T-G

107576933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63095682-A-G

107576989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63095737-A-G

107577106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63095858-A-G

107577342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63096090-T-C

107577828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63096542-C-T

107578008-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63096730-A-T

107578022-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63096744-C-G

107578052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63096774-G-A

http://identifiers.org/hco/5/GRCh38#107578304-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63097032-A-C

107578544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63097233-G-A

107579015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63097841-C-T

107579016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63097842-A-G

107579036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63097862-G-A

107579082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63097913-G-A

107579082-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63097913-G-T

http://identifiers.org/hco/5/GRCh38#107579486-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63098279-C-A

107579486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63098279-C-T

107579615-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63098411-A-T

107579638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63098438-C-T

107579644-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63098444-G-T

107579675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63098470-G-A

107579675-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63098470-G-C

107579682-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63098477-T-A

107579727-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63098519-G-T

107579991-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63098655-C-T

107580143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63098777-T-C

http://identifiers.org/hco/5/GRCh38#107580145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63098779-C-A

107580195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63098829-T-C

107580313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63098946-G-T

http://identifiers.org/hco/5/GRCh38#107580505-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63099083-A-C

107580505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63099083-A-G

107580535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63099106-T-C

http://identifiers.org/hco/5/GRCh38#107580538-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63099109-C-A

107580578-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63099132-C-G

http://identifiers.org/hco/5/GRCh38#107580654-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63099164-C-A

107580654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63099164-C-T

107580730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63099174-A-G

107580734-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63099178-A-G

107580736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63099180-A-G

107580869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63099300-T-C

107580943-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63099405-G-T

http://identifiers.org/hco/5/GRCh38#107581014-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63099473-A-C

107581243-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63099694-G-C

107581467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63099924-C-T

107581713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63100159-G-A

107582419-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63101704-T-G

107582468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63101740-A-G

107582731-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63102060-T-A

107582734-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63102063-G-A

http://identifiers.org/hco/5/GRCh38#107582752-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63102146-A-C

http://identifiers.org/hco/5/GRCh38#107582777-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63102186-A-C

107582945-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63102350-G-T

107582965-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63102370-G-C

107583107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63102505-T-C

107583202-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63102598-T-G

107583209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63102605-G-A

107583564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63102929-A-G

107583565-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63102930-G-C

107583818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63103131-G-A

107584203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63103487-C-T

107584336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63103619-G-A

107584369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63103652-G-T

107584424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63103718-A-G

107584473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63103762-C-T

107584695-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63103984-T-A

107584773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63104037-A-G

107584940-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63104203-T-C

107585013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63104262-A-G

107585320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63104577-C-T

107585339-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63104598-G-C

107585516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63104907-G-A

107585590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63104978-G-T

107585694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63105089-T-C

107585937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63105329-T-C

107586031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63105423-C-T

107586184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63105587-A-G

107586322-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63105827-C-G

107586322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63105827-C-T

107586371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63105874-T-C

107586520-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63106024-A-T

107586583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63106073-C-T

107586807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63106472-G-T

107586992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63106657-T-C

107587054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63106710-T-C

107587365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63106971-G-T

107587452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63107050-T-C

107587988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63107275-C-T

107588458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63107850-G-A

107588458-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63107850-G-C

107588473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63107865-G-A

107588473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63107865-G-T

107588489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63107881-A-G

107588551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63107943-T-C

107588573-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63107965-G-T

107588791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63108192-C-T

http://identifiers.org/hco/5/GRCh38#107588976-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63108381-C-A

107589128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63108513-G-A

107589473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63108877-T-C

107589834-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63109211-T-A

107589870-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63109246-G-A

107589991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63109379-A-G

107590172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63109761-T-C

107590207-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63109796-A-T

107590342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63109917-T-C

107590812-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63110074-T-A

http://identifiers.org/hco/5/GRCh38#107590887-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63110153-C-A

107591195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63110513-C-T

107591312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63110636-C-T

107591352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63110673-A-G

107592697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63111990-C-T

107592777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63112061-T-C

107592809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63112096-C-T

107592815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63112102-T-C

107592826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63112112-C-T

107592882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63112165-G-A

107593152-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63112442-G-C

http://identifiers.org/hco/5/GRCh38#107593293-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63112553-A-C

http://identifiers.org/hco/5/GRCh38#107593467-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63112717-C-A

107593569-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63112838-T-G

107593957-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63113180-G-C

107594124-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63113545-C-G

107594257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63113657-C-T

107594475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63113867-A-G

107594562-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63113963-A-T

107594881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63114291-G-A

107595425-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63114829-T-G

107595825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63115609-G-A

107596060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63115824-A-G

http://identifiers.org/hco/5/GRCh38#107596303-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63116104-A-C

107596455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63116350-A-G

107596629-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63116536-T-G

107596723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63116635-T-C

107596894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63116811-G-A

107596985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63116886-C-T

107597055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63116956-C-T

http://identifiers.org/hco/5/GRCh38#107597059-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63116960-C-A

107597060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63116961-A-G

107597288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63117213-C-T

107597362-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63117287-T-G

107597426-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63117351-A-T

107597432-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63117357-C-T

107597472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63117425-G-A

107597547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63117501-G-A

107597631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63117598-A-G

107597700-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63117667-G-A

107598076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63118028-T-C

107598098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63118050-T-C

107598282-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63118212-G-C

107598579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63118921-C-T

107598633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63118985-G-A

107599228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63119555-G-A

107599359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63119694-T-C

107599708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63120054-C-T

http://identifiers.org/hco/5/GRCh38#107599884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63120238-C-A

http://identifiers.org/hco/5/GRCh38#107600488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63120814-C-A

107600488-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63120814-C-G

107601251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63121920-A-G

107601410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63122064-G-A

107601461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63122149-C-T

107601734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63122476-T-C

107601874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63122596-T-C

107601986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63122709-C-T

107602040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63122762-G-A

107602040-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63122762-G-C

107602040-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63122762-G-T

107602265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63122988-A-G

http://identifiers.org/hco/5/GRCh38#107602536-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63123244-A-C

107602992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63123664-G-A

107603335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63123956-A-G

107603354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63123975-T-C

107603585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63124166-G-A

107603615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63124195-A-G

107603677-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63124257-G-T

107603781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63124362-T-C

http://identifiers.org/hco/5/GRCh38#107603889-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63124470-A-C

107604485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63124892-G-A

107604665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63125031-C-T

107604709-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63125081-G-C

107605315-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63125694-C-G

http://identifiers.org/hco/5/GRCh38#107605408-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63125797-A-C

107605571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63125959-C-T

107605572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63125960-G-A

107605572-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63125960-G-C

107605958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63126366-T-C

107606198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63126617-G-A

107606263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63126680-A-G

107606264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63126681-T-C

107606535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63126954-T-C

107606580-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63127032-C-G

107606580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63127032-C-T

107606584-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63127036-G-C

107606602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63127054-A-G

http://identifiers.org/hco/5/GRCh38#107606604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63127056-C-A

107606604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63127056-C-T

107606614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63127066-A-G

107606747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63127201-G-A

107606747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63127201-G-T

107606880-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63127324-C-T

107606953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63127387-T-C

107607308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63127671-C-T

107607341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63127700-G-A

107607363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63127722-G-A

107607483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63127825-C-T

107607524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63127867-G-T

107607863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63128227-C-T

107608084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63128442-G-A

107608133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63128486-G-T

107608476-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63128825-G-A

107608561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63128911-G-A

107608657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63128985-T-C

107608757-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63129067-G-C

107608993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63129274-C-T

107609286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63129543-G-A

107609287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63129544-C-T

107609288-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63129545-A-T

107609361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63129618-T-C

107609404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63129667-C-T

http://identifiers.org/hco/5/GRCh38#107609416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63129679-C-A

107609416-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63129679-C-G

107609416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63129679-C-T

107609889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63130218-A-G

107610356-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63130681-C-G

107610356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63130681-C-T

107610509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63130867-C-T

107610539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63130897-A-G

107610635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63130994-A-G

107610715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63131072-G-A

107610715-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63131072-G-C

107611129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 63131479-G-A

107611173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63131523-T-C

107611266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63131649-A-G

107611442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63131825-G-A

107611496-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63131891-G-A

107611659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63132268-G-A

107611659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63132268-G-T

http://identifiers.org/hco/5/GRCh38#107611913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63132511-C-A

107611924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63132522-C-T

107612255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63132853-A-G

107612438-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63133023-T-A

107612568-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63133174-T-C

107612713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63133305-A-G

107612844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63133434-T-C

107612866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63133456-C-T

107613449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63134068-C-T

107613695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63134338-C-T

107614159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63134803-C-T

107614952-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63135548-A-T

107615269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63135861-A-G

107615468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63136068-C-T

107615641-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63136241-G-C

107615797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63136443-C-T

107615911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63136553-T-C

107616007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63136642-G-A

107616050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63136685-T-C

http://identifiers.org/hco/5/GRCh38#107616334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63136961-C-A

107616334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63136961-C-T

107616519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63137149-T-C

107616658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63137314-C-T

107616662-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63137318-A-T

107616781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63137446-C-T

107616810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63137465-T-C

107617039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63137696-T-C

107617059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63137717-A-G

107617209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63137861-T-C

107617285-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63138015-C-G

107617397-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63138119-T-G

107617417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63138138-T-C

http://identifiers.org/hco/5/GRCh38#107617589-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63138268-A-C

http://identifiers.org/hco/5/GRCh38#107618311-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63138852-A-C

107618395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63138937-A-G

107618819-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63139364-T-C

107619349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63139570-T-C

107619413-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63139647-G-C

107619979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63139898-G-A

107620080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63139983-G-A

107620881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63140782-G-A

107621142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63140975-C-T

107621145-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63140978-T-C

107621189-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63141021-T-G

107621277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63141093-G-T

107621287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63141102-C-T

107621321-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63141137-A-T

107621659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63141447-G-A

http://identifiers.org/hco/5/GRCh38#107622098-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63142261-A-C

107622317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63142484-C-T

107622615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63143205-G-A

107622687-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63143276-T-G

107622714-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63143303-C-T

107623232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63143480-C-T

http://identifiers.org/hco/5/GRCh38#107623377-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63143697-A-C

107623759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63144091-G-A

107623959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63144283-T-C

107623959-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63144283-T-G

107624019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63144343-A-G

107624060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63144377-T-C

107624266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63144566-A-G

107625124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63145639-G-A

107625149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63145665-C-T

107625244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63145923-G-T

107625246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63145925-C-T

107626065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63146768-G-A

107626809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63147131-G-T

107626874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63147203-T-C

107626929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63147258-T-C

107626977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63147316-A-G

107627003-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63147338-G-A

107627051-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63147371-G-T

107627077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63147393-T-C

107627826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63147801-A-G

107628045-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63147999-C-T

107628150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63148114-C-T

107628167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63148128-A-G

107628646-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63148625-A-T

107628902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63148884-G-A

107631470-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63149545-A-T

107631521-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63149609-A-T

107631625-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63149724-T-G

107631637-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63149736-T-C

http://identifiers.org/hco/5/GRCh38#107631657-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63149756-A-C

107631720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63149821-T-C

107631768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63149865-A-G

http://identifiers.org/hco/5/GRCh38#107631858-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63149955-A-C

107631925-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 63150011-A-T

107632059-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 63150106-G-A

107632191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63150180-C-T

107632262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63150229-C-T

107632558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63150528-C-T

107632573-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63150550-C-G

107632578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63150555-C-T

107632589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63150588-T-C

107633379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63151425-G-A

107633394-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63151440-C-G

107633394-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63151440-C-T

107633399-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63151445-T-A

107633399-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63151445-T-C

107633716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63151768-T-C

107633816-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63151881-C-G

107634161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63152150-C-T

107634227-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63152211-A-T

107634660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63152376-C-T

107634926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63152656-T-C

107635037-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63152764-T-A

107635282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63153028-G-T

107635341-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63153087-C-G

107635365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63153111-C-T

107635435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63153179-C-T

107635510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63153257-G-T

107635521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63153267-C-T

107636130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63153818-A-G

107636171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63153870-T-C

107636325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63154036-T-C

107636502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63154213-G-T

http://identifiers.org/hco/5/GRCh38#107636707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63154439-C-A

http://identifiers.org/hco/5/GRCh38#107636885-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63154597-C-A

107638839-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63155781-T-C

107638864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63155801-G-A

107638912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63155849-T-C

107638913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63155850-A-G

107639155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63156164-C-T

107639242-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63156256-A-G

107639422-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63156425-C-G

107639608-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63156600-T-C

107639687-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63156675-G-C

107640227-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63157231-A-T

107640230-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63157234-G-C

107640329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63157335-T-C

107640337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63157343-G-A

107640378-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63157388-A-T

107640525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63157527-T-C

107641570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63158091-G-A

107641634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63158144-T-C

http://identifiers.org/hco/5/GRCh38#107642248-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63158699-A-C

107642248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63158699-A-G

107642325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63158775-T-C

107642421-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63158886-T-A

107642430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63158895-G-A

107642430-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63158895-G-T

107642490-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63158944-T-A

107642490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63158944-T-C

107642664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63159078-T-C

107642785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63159187-G-A

http://identifiers.org/hco/5/GRCh38#107642956-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63159323-C-A

107642956-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63159323-C-G

107643281-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63160104-T-G

107643607-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63160416-G-A

107643607-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63160416-G-T

http://identifiers.org/hco/5/GRCh38#107643718-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63160523-A-C

107644021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63160797-A-G

http://identifiers.org/hco/5/GRCh38#107644345-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63161117-A-C

107644447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63161213-G-A

107644447-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63161213-G-T

107644607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63161332-T-C

http://identifiers.org/hco/5/GRCh38#107644650-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63161375-A-C

http://identifiers.org/hco/5/GRCh38#107644665-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63161390-C-A

107645367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63161621-C-T

107645905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63162120-T-C

107645905-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63162120-T-G

107645986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63162204-C-T

107646552-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63163311-A-G

107646557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63163316-T-C

107646557-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63163316-T-G

107646560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63163319-A-G

107646729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63163522-G-T

107646746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63163539-T-C

107646766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63163566-T-C

http://identifiers.org/hco/5/GRCh38#107646786-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63163586-A-C

107646914-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63163705-G-T

107646967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63163739-G-T

107647027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63163798-G-A

107647030-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63163802-T-A

107647030-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63163802-T-C

107647255-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63163987-G-C

107647725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63164427-C-T

107647850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63164532-C-T

107647947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63164632-A-G

107648015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63164699-T-C

107648226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63164925-T-C

107648237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63164936-T-C

107648309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63165004-G-A

107648328-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63165029-T-C

107648334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63165035-T-C

107648346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63165050-A-G

107648710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63165450-C-T

http://identifiers.org/hco/5/GRCh38#107649019-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63165705-A-C

107649134-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63165821-T-C

107649279-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63165981-T-A

107649353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63166045-T-C

107649502-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63166181-A-T

http://identifiers.org/hco/5/GRCh38#107649542-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63166205-C-A

107649542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63166205-C-T

107649765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63166398-G-A

107650104-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63166709-G-C

107650137-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63166742-C-T

107650387-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63166952-T-G

http://identifiers.org/hco/5/GRCh38#107650585-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63167233-C-A

107650585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63167233-C-T

107650616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63167260-G-T

107650668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63167309-T-C

107650794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63167409-C-T

107651219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63167763-T-C

http://identifiers.org/hco/5/GRCh38#107651312-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63167861-A-C

107651337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63167886-C-T

http://identifiers.org/hco/5/GRCh38#107651408-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63167957-A-C

107651565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63168117-A-G

http://identifiers.org/hco/5/GRCh38#107652406-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63168890-C-A

107652645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63169083-T-C

107652976-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63169418-C-T

107653016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63169458-A-G

107653284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63169721-T-C

107653823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63170269-G-A

107653831-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63170277-T-G

107653886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63170330-G-A

107653952-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63170395-T-C

107654188-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63170627-G-C

107654997-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63171888-T-C

http://identifiers.org/hco/5/GRCh38#107655041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63171929-C-A

107655061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63171948-G-A

107655167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63172029-C-T

107655439-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63172488-G-A

107655452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63172498-T-C

http://identifiers.org/hco/5/GRCh38#107655553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63172586-C-A

107655553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63172586-C-T

107655749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63172767-C-T

107656134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63173138-G-A

107656800-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63173879-C-T

107657003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63174304-A-G

107657193-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63174552-T-C

107657334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63174738-A-G

107657408-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63174809-T-G

107657486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63174888-G-A

107657804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63175338-G-A

107657818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63175351-A-G

107658034-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63175606-C-G

107658205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63175771-T-C

107658280-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63175888-T-A

107658544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63176151-A-G

107658608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63176220-A-G

107658708-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63176329-T-G

107658924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63176527-C-T

107658929-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63176532-G-C

107658988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63176589-T-C

107659009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63176608-T-C

107659087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63176686-G-A

107659227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63176860-A-G

107659398-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63177061-A-G

107659537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63177219-T-C

107659565-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63177241-A-T

http://identifiers.org/hco/5/GRCh38#107659683-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63177324-A-C

107659846-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63177476-G-A

107659891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63177517-A-G

107659938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63177581-G-A

107660077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63177698-T-C

107660318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63177895-G-A

107660318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63177895-G-T

107660319-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63177896-G-T

107660613-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63178187-G-C

107660613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63178187-G-T

107660668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63178238-A-G

107660848-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63178427-T-C

http://identifiers.org/hco/5/GRCh38#107661106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63178686-C-A

107661114-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63178693-T-A

http://identifiers.org/hco/5/GRCh38#107661180-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63178749-A-C

107661236-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63178812-A-T

107661264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63178841-G-A

http://identifiers.org/hco/5/GRCh38#107661322-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63178903-A-C

107661342-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63178924-A-T

107661395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63178975-G-A

107661407-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63178987-G-C

107661472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63179055-C-T

107661590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63179171-G-A

http://identifiers.org/hco/5/GRCh38#107662275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63179883-C-A

107662391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63179994-C-T

107662572-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63180179-T-A

107662572-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63180179-T-G

107662680-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63180329-G-C

107662722-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63180374-A-T

107662759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63180411-G-A

107663087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63180711-G-A

107663087-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63180711-G-C

107663110-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63180732-G-A

107663128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63180750-T-C

107663177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63180796-G-A

107663224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63180847-G-A

107663224-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63180847-G-T

107663235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63180864-C-T

107663252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63180878-G-A

107663451-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63181060-C-T

107663743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63181338-G-A

http://identifiers.org/hco/5/GRCh38#107663989-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63181585-A-C

107664015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63181611-C-T

107664052-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63181653-T-G

107664308-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63181928-T-G

107664383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63182008-G-A

107664578-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63182213-T-C

107664866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63182507-G-A

107665450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63183098-A-G

107665616-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63183232-G-C

107665972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63183575-C-T

107665989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63183592-C-T

107666141-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63183768-T-A

http://identifiers.org/hco/5/GRCh38#107666273-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63183900-C-A

107666273-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63183900-C-G

107666319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63183941-G-A

107666319-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63183941-G-C

107666331-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63183953-G-C

107666870-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63184432-G-C

107667104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63184633-T-C

107667349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63184873-A-G

107667681-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63185197-A-T

107668525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63186038-T-C

107669175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63186647-G-A

107669448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63186889-G-A

107669746-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

107669787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63187225-G-A

107669787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63187225-G-T

http://identifiers.org/hco/5/GRCh38#107670003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63187488-C-A

107670003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63187488-C-T

107670201-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63187704-T-C

107670293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 63187798-C-T

107670349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63187854-T-C

http://identifiers.org/hco/5/GRCh38#107670378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63187883-C-A

107670378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63187883-C-T

107670390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63187895-G-T

107670439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 63187946-A-G

http://identifiers.org/hco/5/GRCh38#107670708-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/17/GRCm39#63188218-C-A

107670708-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63188218-C-G

107670708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3225
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63188218-C-T