104864543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 112687982-C-T

104864837-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 112688233-G-C

104864967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 112688363-G-T

104865031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 112688421-G-A

104865031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 112688421-G-T

104865046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 112688449-G-A

104865067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 112688462-G-A

104865080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 112688474-G-A

104865462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 112688795-C-T

104865583-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron_variant, undefined
orthologous variants: 112688895-G-A

104865583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron_variant, undefined
orthologous variants: 112688895-G-T

104865596-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: -C-G

104865612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112688914-G-A

104865655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112688967-G-A

http://identifiers.org/hco/14/GRCh38#104865666-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112688978-C-A

104865666-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112688978-C-T

104865670-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112688982-G-C

104865760-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron_variant, undefined
orthologous variants: 112689091-C-T

104865762-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron_variant, undefined
orthologous variants: -C-G

104865762-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron_variant, undefined
orthologous variants: -C-T

http://identifiers.org/hco/14/GRCh38#104865984-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112689339-A-C

104868299-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112690933-G-T

http://identifiers.org/hco/14/GRCh38#104868308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112690947-C-A

104868308-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112690947-C-G

104868308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112690947-C-T

104868346-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112690984-T-A

http://identifiers.org/hco/14/GRCh38#104868410-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112691043-C-A

http://identifiers.org/hco/14/GRCh38#104868689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112691248-C-A

104868700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 112691259-T-C

104868758-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 112691291-C-G

104869771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112692598-A-G

104869803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112692607-C-T

104869877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112692666-G-A

104869910-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112692697-C-G

104869971-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112692763-C-G

104869971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112692763-C-T

104870073-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112692818-C-T

104870145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112692868-C-T

http://identifiers.org/hco/14/GRCh38#104870147-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112692870-A-C

104870147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112692870-A-G

104870147-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112692870-A-T

104870215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112692927-A-G

104870223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112692935-G-A

104870366-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112693035-C-G

104870366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112693035-C-T

104870429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112693079-G-A

104870582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112693228-C-T

104870597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112693241-C-T

104870745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112693371-C-T

104870946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron_variant, undefined
orthologous variants: 112693574-T-C

104871237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112693767-G-A

104871349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112693854-G-A

http://identifiers.org/hco/14/GRCh38#104871352-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112693857-A-C

104871383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112693880-C-T

104871433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112693916-C-T

104871507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112693996-G-A

104871748-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112694218-G-T

104871984-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112694454-C-G

104872138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112694522-T-C

104872138-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112694522-T-G

104872167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112694536-G-A

104872247-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112694573-G-C

104872609-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112694839-G-C

104872717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112694926-G-A

104872837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112695038-G-A

104872839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112695040-G-A

104873107-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112695328-C-G

104873129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112695357-C-T

104873629-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112695823-G-C

104873679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112695868-C-T

104873799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112695968-C-T

http://identifiers.org/hco/14/GRCh38#104873910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112696028-C-A

104873910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112696028-C-T

http://identifiers.org/hco/14/GRCh38#104874424-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112696291-C-A

104874547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112696407-C-T

104874703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112696542-C-T

104874789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112696565-G-A

104874795-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112696571-C-T

104874829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112696590-C-T

104874951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112696704-T-C

104874987-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112696725-T-G

104875165-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112696873-C-G

104875377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112696991-C-T

104875542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112697122-T-C

104875748-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112697228-G-A

104875924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112697433-G-A

104875924-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112697433-G-T

104876000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112697550-A-G

104876021-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112697577-C-G

104876210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112697739-A-G

104876309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 112697838-C-T

104876391-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112697925-T-G

http://identifiers.org/hco/14/GRCh38#104877985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112698538-C-A

104877985-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112698538-C-T

http://identifiers.org/hco/14/GRCh38#104877990-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112698543-C-A

104877990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112698543-C-T

http://identifiers.org/hco/14/GRCh38#104878010-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112698560-C-A

104878010-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112698560-C-G

104878010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112698560-C-T

http://identifiers.org/hco/14/GRCh38#104878065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112698602-C-A

104878065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112698602-C-T

http://identifiers.org/hco/14/GRCh38#104878089-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112698623-A-C

104878089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112698623-A-G

104878089-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112698623-A-T

http://identifiers.org/hco/14/GRCh38#104878103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112698644-C-A

104878103-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112698644-C-G

104878103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112698644-C-T

http://identifiers.org/hco/14/GRCh38#104878108-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112698646-C-A

104878108-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112698646-C-G

104878108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112698646-C-T

http://identifiers.org/hco/14/GRCh38#104878132-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112698667-A-C

http://identifiers.org/hco/14/GRCh38#104878298-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112698802-C-A

104878298-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112698802-C-T

104878359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112698850-A-G

http://identifiers.org/hco/14/GRCh38#104878387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112698874-C-A

104878387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112698874-C-T

http://identifiers.org/hco/14/GRCh38#104878393-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112698880-C-A

104878393-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112698880-C-T

104878396-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112698883-T-A

104878396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112698883-T-C

104878495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: synonymous variant
orthologous variants: 112698986-A-G

http://identifiers.org/hco/14/GRCh38#104878549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112699067-C-A

104878549-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112699067-C-G

104878578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112699097-A-G

http://identifiers.org/hco/14/GRCh38#104878582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112699101-C-A

104878582-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112699101-C-T

http://identifiers.org/hco/14/GRCh38#104878584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112699103-C-A

104878584-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112699103-C-G

104878584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112699103-C-T

104878636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112699141-A-G

104878675-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112699180-A-G

104879020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112699437-G-A

http://identifiers.org/hco/14/GRCh38#104880226-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112699769-A-C

104880325-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112699864-G-C

104880334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: synonymous variant
orthologous variants: 112699873-G-A

http://identifiers.org/hco/14/GRCh38#104880391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112699930-C-A

104880440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112699990-T-C

104880481-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112700014-G-T

104880484-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112700017-C-G

104880486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112700019-G-A

104880486-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112700019-G-T

http://identifiers.org/hco/14/GRCh38#104880562-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112700056-A-C

104880562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112700056-A-G

104880958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112700211-C-T

104880999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112700226-G-T

104881220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112700410-G-A

104881221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112700411-G-A

104881257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112700449-G-A

104881268-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112700451-C-T

104881524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112700692-A-G

104881559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112700727-C-T

104881931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112700954-G-A

104882014-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112701041-A-G

104882256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112701253-G-A

http://identifiers.org/hco/14/GRCh38#104882537-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112701462-A-C

104882537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112701462-A-G

104882611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112701499-C-T

104882621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112701509-A-G

http://identifiers.org/hco/14/GRCh38#104882630-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112701518-C-A

http://identifiers.org/hco/14/GRCh38#104882634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112701522-C-A

104882634-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112701522-C-G

104882634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112701522-C-T

104882681-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112701555-C-G

104882681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112701555-C-T

104882707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112701581-G-A

104882707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112701581-G-T

104882735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: synonymous variant
orthologous variants: 112701602-C-T

104882743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112701610-G-A

104882743-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112701610-G-T

104882748-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112701615-C-G

104882748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112701615-C-T

104882762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: synonymous variant
orthologous variants: 112701629-G-A

http://identifiers.org/hco/14/GRCh38#104882839-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112701706-C-A

104882839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 112701706-C-T

104882908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112701733-G-T

104882984-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112701737-G-T

104883009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112701763-G-A

104883009-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112701763-G-T

http://identifiers.org/hco/14/GRCh38#104883068-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112701819-A-C

104883068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112701819-A-G

104883068-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112701819-A-T

104883069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: synonymous variant
orthologous variants: 112701820-G-A

104883069-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112701820-G-T

http://identifiers.org/hco/14/GRCh38#104883072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112701823-C-A

104883083-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112701834-G-A

104883083-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112701834-G-C

104883083-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112701834-G-T

http://identifiers.org/hco/14/GRCh38#104883088-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112701839-C-A

104883088-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112701839-C-T

104883096-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112701847-G-T

http://identifiers.org/hco/14/GRCh38#104883108-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: stop gained
orthologous variants: http://identifiers.org/mco/12/GRCm39#112701859-C-A

104883108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: synonymous variant
orthologous variants: 112701859-C-T

http://identifiers.org/hco/14/GRCh38#104883110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: stop gained
orthologous variants: http://identifiers.org/mco/12/GRCm39#112701861-C-A

104883110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112701861-C-T

104883123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: synonymous variant
orthologous variants: 112701874-G-A

104883123-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112701874-G-T

104883126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: synonymous variant
orthologous variants: 112701877-C-T

http://identifiers.org/hco/14/GRCh38#104883172-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112701923-C-A

104883172-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112701923-C-G

104883172-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112701923-C-T

http://identifiers.org/hco/14/GRCh38#104883175-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112701926-C-A

104883175-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112701926-C-G

104883175-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112701926-C-T

104883185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112701936-C-T

104883186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: synonymous variant
orthologous variants: 112701937-G-A

104883186-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: synonymous variant
orthologous variants: 112701937-G-T

http://identifiers.org/hco/14/GRCh38#104883201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112701952-C-A

104883223-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112701974-G-A

104883223-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112701974-G-C

104883233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112701984-C-T

104883255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: synonymous variant
orthologous variants: 112702006-C-T

104883267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: synonymous variant
orthologous variants: 112702018-C-T

104883268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112702019-A-G

http://identifiers.org/hco/14/GRCh38#104883285-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: stop gained
orthologous variants: http://identifiers.org/mco/12/GRCm39#112702036-C-A

104883285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: synonymous variant
orthologous variants: 112702036-C-T

http://identifiers.org/hco/14/GRCh38#104883346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112702097-C-A

104883346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112702097-C-T

http://identifiers.org/hco/14/GRCh38#104883348-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112702099-C-A

104883348-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: synonymous variant
orthologous variants: 112702099-C-T

104883383-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112702134-C-G

104883383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112702134-C-T

104883384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: synonymous variant
orthologous variants: 112702135-G-A

104883384-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: synonymous variant
orthologous variants: 112702135-G-C

104883413-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112702164-T-G

104883450-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: synonymous variant
orthologous variants: 112702201-T-G

104883458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112702209-A-G

104883461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112702212-G-A

104883461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112702212-G-T

http://identifiers.org/hco/14/GRCh38#104883468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112702219-C-A

104883468-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112702219-C-G

104883468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: synonymous variant
orthologous variants: 112702219-C-T

104883523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112702273-G-A

104883523-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112702273-G-T

http://identifiers.org/hco/14/GRCh38#104883528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112702278-C-A

104883528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112702278-C-T

104883530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112702280-G-A

104883530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112702280-G-T

http://identifiers.org/hco/14/GRCh38#104883539-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112702289-C-A

104883539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112702289-C-T

http://identifiers.org/hco/14/GRCh38#104883598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112702341-C-A

104883598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112702341-C-T

104883696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112702453-G-A

104883696-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112702453-G-C

104883696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112702453-G-T

104883742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112702511-G-A

104883742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112702511-G-T

104883769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112702548-T-C

104883780-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112702559-G-T

104883859-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112702618-T-A

104883859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: synonymous variant
orthologous variants: 112702618-T-C

104883859-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112702618-T-G

http://identifiers.org/hco/14/GRCh38#104883865-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112702624-A-C

104883865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: synonymous variant
orthologous variants: 112702624-A-G

http://identifiers.org/hco/14/GRCh38#104883905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112702664-C-A

104883905-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112702664-C-T

104883967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: synonymous variant
orthologous variants: 112702726-G-A

104883967-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112702726-G-C

104884030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: synonymous variant
orthologous variants: 112702789-G-A

104884057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: synonymous variant
orthologous variants: 112702816-G-A

http://identifiers.org/hco/14/GRCh38#104884098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112702857-C-A

104884098-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112702857-C-G

104884098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112702857-C-T

http://identifiers.org/hco/14/GRCh38#104884271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112703024-C-A

104884271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112703024-C-T

104884319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112703072-G-A

104884319-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112703072-G-T

104884324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: synonymous variant
orthologous variants: 112703077-C-T

http://identifiers.org/hco/14/GRCh38#104884350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112703103-C-A

104884350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112703103-C-T

104884543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 112703296-C-T

104884610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112703362-G-A

104884610-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112703362-G-C

104884610-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112703362-G-T

104885301-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112703532-G-A

104885301-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112703532-G-C

104885301-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112703532-G-T

104885316-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112703545-T-G

104885323-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112703552-T-A

104885323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112703552-T-C

104885323-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112703552-T-G

104885325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112703554-G-A

104885325-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112703554-G-T

104885329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112703558-T-C

104885329-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112703558-T-G

104885557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112703780-G-A

104885557-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112703780-G-T

104885571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112703794-G-A

104885571-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112703794-G-C

104885571-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112703794-G-T

104885577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112703800-G-A

104885577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112703800-G-T

104885749-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112703870-C-G

104885749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112703870-C-T

104885774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112703879-A-G

http://identifiers.org/hco/14/GRCh38#104885964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112703945-C-A

104885964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112703945-C-T

http://identifiers.org/hco/14/GRCh38#104886169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112704140-C-A

104886169-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112704140-C-G

104886169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112704140-C-T

104886219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112704188-G-A

104886219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112704188-G-T

104886242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112704238-G-A

104886242-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112704238-G-C

104886242-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112704238-G-T

104886295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense_variant, synonymous_variant
orthologous variants: 112704293-G-A

104886295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112704293-G-T

http://identifiers.org/hco/14/GRCh38#104886603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112704577-C-A

104886603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense_variant, synonymous_variant
orthologous variants: 112704577-C-T

104886617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112704591-C-T

104886624-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense_variant, synonymous_variant
orthologous variants: 112704598-C-G

104886624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense_variant, synonymous_variant
orthologous variants: 112704598-C-T

104886663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense_variant, synonymous_variant
orthologous variants: 112704637-A-G

http://identifiers.org/hco/14/GRCh38#104886709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112704683-C-A

104886795-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 112704769-G-A

104886833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 112704819-G-A

104886833-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 112704819-G-C

104886833-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 112704819-G-T

104886909-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 112704895-G-A

104886909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 112704895-G-T

104886944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 112704930-G-A

104886944-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 112704930-G-C

104886944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 112704930-G-T

104886958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 112704944-T-C

http://identifiers.org/hco/14/GRCh38#104886968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112704954-C-A

104886973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 112704959-C-T

http://identifiers.org/hco/14/GRCh38#104886978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112704964-C-A

104886978-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 112704964-C-G

104887019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 112705005-G-A

104887026-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 112705012-C-G

104887044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 112705027-C-T

104887045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 112705028-G-A

104887045-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 112705028-G-C

104887045-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3_prime_UTR_variant, stop_gained
orthologous variants: 112705028-G-T

104887053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 112705036-G-A

104887054-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 112705037-G-A

104887068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 112705051-G-A

104887068-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 112705051-G-T

104887074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 112705057-G-A

104887091-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 112705074-C-G

104887103-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 112705086-A-G

104887116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 112705099-C-T

104887118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 112705101-G-A

104887119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 112705102-C-T

104887137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 112705120-T-C

104887138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 112705121-G-T

http://identifiers.org/hco/14/GRCh38#104887140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112705123-C-A

104887140-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 112705123-C-G

104887150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 112705133-C-T

104887179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: synonymous variant
orthologous variants: 112705162-G-A

104887179-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: synonymous variant
orthologous variants: 112705162-G-T

104887206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: synonymous variant
orthologous variants: 112705189-G-A

104887207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112705190-C-T

104887210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112705193-G-A

104887210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112705193-G-T

http://identifiers.org/hco/14/GRCh38#104887221-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112705204-C-A

104887221-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: synonymous variant
orthologous variants: 112705204-C-T

104887224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: synonymous variant
orthologous variants: 112705207-G-A

104887224-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: synonymous variant
orthologous variants: 112705207-G-C

104887224-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: synonymous variant
orthologous variants: 112705207-G-T

104887236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: synonymous variant
orthologous variants: 112705219-C-T

104887238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112705221-T-C

104887250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112705233-G-A

104887250-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112705233-G-T

104887257-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: synonymous variant
orthologous variants: 112705240-G-A

104887257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112705240-G-T

104887258-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112705241-T-A

104887281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: synonymous variant
orthologous variants: 112705264-A-G

http://identifiers.org/hco/14/GRCh38#104887282-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112705265-C-A

104887282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112705265-C-T

http://identifiers.org/hco/14/GRCh38#104887302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112705282-C-A

104887302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: synonymous variant
orthologous variants: 112705282-C-T

104887311-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112705291-G-T

http://identifiers.org/hco/14/GRCh38#104887312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112705292-C-A

104887312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112705292-C-T

104887461-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: synonymous variant
orthologous variants: 112705426-A-T

104887487-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112705452-C-G

104887487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112705452-C-T

104887489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112705454-G-A

104887489-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112705454-G-T

104887510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112705475-G-A

104887510-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112705475-G-T

104887530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: synonymous variant
orthologous variants: 112705495-T-C

104887567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112705532-A-G

http://identifiers.org/hco/14/GRCh38#104887568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112705533-C-A

104887568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112705533-C-T

104887571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112705536-G-A

104887571-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112705536-G-T

http://identifiers.org/hco/14/GRCh38#104887575-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112705540-C-A

104887575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: synonymous variant
orthologous variants: 112705540-C-T

http://identifiers.org/hco/14/GRCh38#104887578-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112705543-C-A

104887578-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112705543-C-G

104887578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: synonymous variant
orthologous variants: 112705543-C-T

http://identifiers.org/hco/14/GRCh38#104887586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112705551-C-A

104887586-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112705551-C-G

http://identifiers.org/hco/14/GRCh38#104887591-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112705556-C-A

104887591-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112705556-C-G

104887591-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112705556-C-T

104887602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: synonymous variant
orthologous variants: 112705567-A-G

104887613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112705578-G-A

104887613-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112705578-G-T

http://identifiers.org/hco/14/GRCh38#104887615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112705580-C-A

104887615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: synonymous variant
orthologous variants: 112705580-C-T

104887629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: synonymous variant
orthologous variants: 112705594-G-A

104887629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: synonymous variant
orthologous variants: 112705594-G-T

104887632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: synonymous variant
orthologous variants: 112705597-G-A

104887632-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: synonymous variant
orthologous variants: 112705597-G-C

104887632-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: synonymous variant
orthologous variants: 112705597-G-T

104887639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112705604-G-A

104887639-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112705604-G-C

104887639-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112705604-G-T

104887657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112705622-G-A

104887657-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112705622-G-T

104887670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112705635-G-A

104887670-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112705635-G-T

http://identifiers.org/hco/14/GRCh38#104887678-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112705643-C-A

104887680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: synonymous variant
orthologous variants: 112705645-G-A

104887680-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: synonymous variant
orthologous variants: 112705645-G-T

http://identifiers.org/hco/14/GRCh38#104887686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112705651-C-A

104887686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: synonymous variant
orthologous variants: 112705651-C-T

104887703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112705668-G-A

104887703-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112705668-G-C

104887703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112705668-G-T

104887707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: synonymous variant
orthologous variants: 112705672-A-G

104887715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112705680-A-G

http://identifiers.org/hco/14/GRCh38#104887759-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112705724-C-A

104887759-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112705724-C-G

104887759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112705724-C-T

104887766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112705731-G-A

104887766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112705731-G-T

104887814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112705779-G-A

104887814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112705779-G-T

104887827-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: synonymous variant
orthologous variants: 112705792-T-A

http://identifiers.org/hco/14/GRCh38#104887831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112705796-C-A

104887831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112705796-C-T

104887832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112705797-G-A

104887832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112705797-G-T

104887842-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112705807-G-T

http://identifiers.org/hco/14/GRCh38#104887914-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112705879-C-A

http://identifiers.org/hco/14/GRCh38#104887953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112705918-C-A

104887953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: synonymous variant
orthologous variants: 112705918-C-T

http://identifiers.org/hco/14/GRCh38#104887971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: stop gained
orthologous variants: http://identifiers.org/mco/12/GRCm39#112705936-C-A

104887971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: synonymous variant
orthologous variants: 112705936-C-T

104888125-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112706022-T-A

104888141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112706031-A-G

http://identifiers.org/hco/14/GRCh38#104888238-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112706109-C-A

104888347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112706187-C-T

104888454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112706283-A-G

104888703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112706532-C-T

104888712-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112706541-T-C

104888755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112706571-C-T

104888767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112706583-C-T

104888954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112706688-C-T

104889101-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112706818-G-A

104889285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112707024-G-A

104889374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112707078-G-A

104889374-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112707078-G-C

104889374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112707078-G-T

http://identifiers.org/hco/14/GRCh38#104889416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112707111-C-A

104889416-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112707111-C-G

104889520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron_variant, missense_variant
orthologous variants: 112707213-A-G

104889861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112707539-G-A

104889861-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112707539-G-T

104891063-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112707834-A-G

104891105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112707869-G-A

104891140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112707899-C-T

104891527-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112708253-G-C

104891575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112708293-G-A

104891753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112708433-T-C

104891770-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112708453-C-G

104891770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112708453-C-T

104891798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112708483-C-T

104891817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112708497-G-A

104892342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112708841-G-T

104892458-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112708952-C-G

104892609-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112709100-A-T

104892843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112709218-G-A

104892843-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112709218-G-T

104892850-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112709227-A-T

104892898-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112709282-G-C

104892899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112709283-G-A

104892899-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112709283-G-C

104892899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112709283-G-T

104892908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112709298-G-A

104892971-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 112709382-T-A

104892971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 112709382-T-C

104893063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: synonymous variant
orthologous variants: 112709474-G-A

104893063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: synonymous variant
orthologous variants: 112709474-G-T

104893074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112709485-A-G

104893088-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112709499-A-G

http://identifiers.org/hco/14/GRCh38#104893104-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112709515-C-A

104893104-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112709515-C-G

104893104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112709515-C-T

104893390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112709691-G-A

104893390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112709691-G-T

http://identifiers.org/hco/14/GRCh38#104893434-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112709748-C-A

104893445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112709759-G-A

104893445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112709759-G-T

104893567-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: synonymous variant
orthologous variants: 112709881-G-T

104893570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: synonymous variant
orthologous variants: 112709884-G-A

104893570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: synonymous variant
orthologous variants: 112709884-G-T

104893579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: synonymous variant
orthologous variants: 112709893-G-A

104893591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: synonymous variant
orthologous variants: 112709905-G-A

104893622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112709936-G-A

104893624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: synonymous variant
orthologous variants: 112709938-G-A

104893624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112709938-G-T

104893634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112709948-G-A

104893634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112709948-G-T

104893645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: synonymous variant
orthologous variants: 112709959-G-A

104893645-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: synonymous variant
orthologous variants: 112709959-G-T

104893647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112709961-G-A

104893647-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense variant
orthologous variants: 112709961-G-T

104893688-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112710003-C-G

104893688-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112710003-C-T

104893689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112710004-G-A

104893826-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: synonymous variant
orthologous variants: 112710169-A-G

104893826-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: synonymous variant
orthologous variants: 112710169-A-T

104893855-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron variant
orthologous variants: 112710198-T-G

http://identifiers.org/hco/14/GRCh38#104894093-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112710355-C-A

104894093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 112710355-C-T

http://identifiers.org/hco/14/GRCh38#104894101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112710363-C-A

104894101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 112710363-C-T

104894111-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 112710371-T-A

104894111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 112710371-T-C

104894111-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 112710371-T-G

104894148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 112710398-A-G

104894150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 112710400-G-T

104894396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112710634-G-A

104894396-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112710634-G-C

104894396-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112710634-G-T

104894403-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112710641-T-A

104894404-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112710642-T-G

104894405-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112710643-G-C

104894410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112710650-G-A

http://identifiers.org/hco/14/GRCh38#104894411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112710651-C-A

104894411-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112710651-C-G

104894411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112710651-C-T

104894412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112710652-C-T

http://identifiers.org/hco/14/GRCh38#104894414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112710654-C-A

104894414-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112710654-C-G

104894414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112710654-C-T

104894420-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112710663-A-G

104894425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112710678-G-A

104894425-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112710678-G-C

104894428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112710681-T-C

104894440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112710710-G-A

104894440-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112710710-G-T

http://identifiers.org/hco/14/GRCh38#104894441-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112710711-C-A

104894441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112710711-C-T

104894451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112710721-T-C

104894457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112710741-A-G

104894473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112710757-G-A

http://identifiers.org/hco/14/GRCh38#104894477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112710761-C-A

104894477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112710761-C-T

104894478-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112710762-G-A

104894492-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112710882-G-A

104894492-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112710882-G-C

104894497-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112710887-T-A

104894497-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112710887-T-G

http://identifiers.org/hco/14/GRCh38#104894690-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112711077-A-C

104894690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 112711077-A-G

http://identifiers.org/hco/14/GRCh38#104894724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112711112-C-A

104894724-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 112711112-C-G

104894724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112711112-C-T

104894811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 112711199-G-A

http://identifiers.org/hco/14/GRCh38#104895134-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112711509-C-A

104895134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3 prime UTR variant
orthologous variants: 112711509-C-T

http://identifiers.org/hco/14/GRCh38#104895139-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112711514-C-A

104895139-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3 prime UTR variant
orthologous variants: 112711514-C-T

http://identifiers.org/hco/14/GRCh38#104895147-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112711522-C-A

104895147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3 prime UTR variant
orthologous variants: 112711522-C-T

http://identifiers.org/hco/14/GRCh38#104895203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112711564-C-A

104895203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3 prime UTR variant
orthologous variants: 112711564-C-T

http://identifiers.org/hco/14/GRCh38#104895351-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112711717-C-A

104895351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3 prime UTR variant
orthologous variants: 112711717-C-T

104895422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3 prime UTR variant
orthologous variants: 112711786-T-C

104895425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3 prime UTR variant
orthologous variants: 112711789-G-A

104895425-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3 prime UTR variant
orthologous variants: 112711789-G-C

104895425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3 prime UTR variant
orthologous variants: 112711789-G-T

104895455-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3 prime UTR variant
orthologous variants: 112711820-T-A

104895455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3 prime UTR variant
orthologous variants: 112711820-T-C

104895540-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3 prime UTR variant
orthologous variants: 112711919-T-A

104895566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3 prime UTR variant
orthologous variants: 112711946-G-A

104895566-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3 prime UTR variant
orthologous variants: 112711946-G-T

104895593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3 prime UTR variant
orthologous variants: 112711974-G-A

104895593-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3 prime UTR variant
orthologous variants: 112711974-G-C

104895593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3 prime UTR variant
orthologous variants: 112711974-G-T

104895747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3 prime UTR variant
orthologous variants: 112712017-T-C

104895792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3 prime UTR variant
orthologous variants: 112712053-G-A

104895792-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3 prime UTR variant
orthologous variants: 112712053-G-C

104895859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3 prime UTR variant
orthologous variants: 112712117-G-T

104895897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3 prime UTR variant
orthologous variants: 112712158-G-A

104895897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3 prime UTR variant
orthologous variants: 112712158-G-T

104895918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3 prime UTR variant
orthologous variants: 112712210-A-G

104895923-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3 prime UTR variant
orthologous variants: 112712215-G-T

104895996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3 prime UTR variant
orthologous variants: 112712294-G-A

104895996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3 prime UTR variant
orthologous variants: 112712294-G-T

104896055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3 prime UTR variant
orthologous variants: 112712343-T-C

104896070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3 prime UTR variant
orthologous variants: 112712358-G-A

104896070-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3 prime UTR variant
orthologous variants: 112712358-G-C

104896070-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3 prime UTR variant
orthologous variants: 112712358-G-T

104896130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3 prime UTR variant
orthologous variants: 112712408-G-T

104896165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3 prime UTR variant
orthologous variants: 112712443-G-A

104896165-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3 prime UTR variant
orthologous variants: 112712443-G-T

http://identifiers.org/hco/14/GRCh38#104896182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112712460-C-A

104896182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3 prime UTR variant
orthologous variants: 112712460-C-T

104896211-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3 prime UTR variant
orthologous variants: 112712488-T-C

104896225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3 prime UTR variant
orthologous variants: 112712506-G-A

104896225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3 prime UTR variant
orthologous variants: 112712506-G-T

104896277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3 prime UTR variant
orthologous variants: 112712555-G-T

104896323-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3 prime UTR variant
orthologous variants: 112712599-G-C

104896323-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3 prime UTR variant
orthologous variants: 112712599-G-T

http://identifiers.org/hco/14/GRCh38#104896378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112712656-C-A

104896378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3 prime UTR variant
orthologous variants: 112712656-C-T

http://identifiers.org/hco/14/GRCh38#104896430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#112712703-C-A

104896430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3 prime UTR variant
orthologous variants: 112712703-C-T

104896512-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3 prime UTR variant
orthologous variants: 112712785-G-A

104896512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3 prime UTR variant
orthologous variants: 112712785-G-T

104896600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3 prime UTR variant
orthologous variants: 112712871-G-A

104896642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20362
most severe consequence: 3 prime UTR variant
orthologous variants: 112712913-G-A