http://identifiers.org/hco/6/GRCh38#108848477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41894367-C-A

108848477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 41894367-C-T

108848544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 41894298-C-T

http://identifiers.org/hco/6/GRCh38#108848620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41894235-C-A

108848620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41894235-C-T

108848623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41894232-G-A

108848623-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41894232-G-T

http://identifiers.org/hco/6/GRCh38#108848648-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41894207-C-A

108848648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41894207-C-T

http://identifiers.org/hco/6/GRCh38#108848652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41894203-C-A

108848652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41894203-C-T

108848679-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41894176-T-A

108848679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41894176-T-C

108848689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41894166-A-G

108848694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41894161-G-A

108848695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41894160-A-G

108848832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41894013-C-T

108848878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41893970-T-C

108848881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41893967-T-C

108848881-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41893967-T-G

108848985-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41893874-T-A

http://identifiers.org/hco/6/GRCh38#108849168-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41893718-A-C

108849168-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41893718-A-G

108849667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41893351-T-C

108850017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41893040-T-C

108850325-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41892486-T-C

108850340-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41892471-C-G

108850340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41892471-C-T

108850480-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41892388-C-T

108850582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41892320-G-A

108850595-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41892307-A-T

108850688-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41892205-A-T

108850867-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41892050-A-G

108851043-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41891903-A-G

108851116-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41891826-T-G

108851159-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41891781-T-G

108851229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41891727-C-T

108851302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41891663-A-G

108851328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41891638-C-T

http://identifiers.org/hco/6/GRCh38#108852061-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41891235-A-C

108852331-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41890964-C-T

http://identifiers.org/hco/6/GRCh38#108852394-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41890760-A-C

108852395-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41890759-A-T

108852618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41890337-G-A

108852826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41890024-T-C

108853055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41889751-G-A

108853282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41889521-T-C

108853361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41889453-G-A

http://identifiers.org/hco/6/GRCh38#108853539-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41889245-C-A

108853559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41889186-G-A

108853577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41889168-A-G

108854073-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41888537-G-C

108854106-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41888504-T-G

108854133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41888106-A-G

http://identifiers.org/hco/6/GRCh38#108854140-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41888099-A-C

108854167-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41888078-T-A

108854167-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41888078-T-G

108854244-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 41888003-G-T

108854325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41887922-G-A

108854325-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41887922-G-T

108854401-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41887846-C-G

108855560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41887463-A-G

108855586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41887438-A-G

108855592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41887432-G-T

108855659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41887360-A-G

108855723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41887288-T-C

108855757-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41887265-G-A

108855757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41887265-G-T

108855830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41887216-A-G

108856238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41886809-T-C

108856337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41886719-A-G

108856855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41886404-T-C

108856866-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41886397-T-A

108856938-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41886349-T-C

108856961-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41886323-A-G

108857068-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41886211-T-A

108857248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41885986-G-A

http://identifiers.org/hco/6/GRCh38#108857419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41885807-C-A

108857584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41885636-C-T

http://identifiers.org/hco/6/GRCh38#108857627-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41885586-C-A

108857804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41885354-G-A

108858060-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41884845-T-C

108858060-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41884845-T-G

108858110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41884803-T-C

108858110-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41884803-T-G

108858134-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41884779-A-T

http://identifiers.org/hco/6/GRCh38#108858317-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41884613-A-C

http://identifiers.org/hco/6/GRCh38#108858328-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41884602-C-A

108858328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41884602-C-T

108858669-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41884291-C-G

108859501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41883507-C-T

http://identifiers.org/hco/6/GRCh38#108860322-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41882631-A-C

108860516-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41882389-G-A

108860528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41882377-G-A

108861147-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41881947-T-C

108861264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41881855-G-T

108863460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41881300-A-G

108863637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41881126-G-A

108863719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41881049-C-T

108863846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41880908-G-T

108864002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41880751-A-G

108864024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41880739-T-C

108864088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41880673-T-C

108864213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41880544-G-A

108864221-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41880536-G-C

108864418-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41880500-T-G

108864817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41880232-A-G

108864845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41880204-A-G

108866183-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41878384-C-T

108866200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41878367-G-A

108866575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41878039-A-G

108866599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41878024-A-G

108866691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41877940-G-A

108867131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41877572-A-G

108867136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41877567-T-C

http://identifiers.org/hco/6/GRCh38#108868754-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41876554-C-A

108868754-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41876554-C-G

108868754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41876554-C-T

108868780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41876534-G-A

108868788-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41876526-A-T

108868836-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41876480-C-G

108868837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41876479-C-T

108868978-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: 5_prime_UTR_variant, coding_sequence_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41876341-C-G

108868978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: 5_prime_UTR_variant, coding_sequence_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41876341-C-T

http://identifiers.org/hco/6/GRCh38#108869019-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41876301-A-C

http://identifiers.org/hco/6/GRCh38#108869061-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41876262-C-A

108869061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41876262-C-T

http://identifiers.org/hco/6/GRCh38#108869087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41876233-C-A

108869087-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41876233-C-G

108869140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41876179-A-G

108869747-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41875688-G-C

108869856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41875587-A-G

108869920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41875529-A-G

108869922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41875527-T-C

108870119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41875349-T-C

108870142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41875326-C-T

108870352-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41875139-A-G

108870354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41875137-G-A

108870414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41875086-C-T

108870584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41875020-G-A

108870833-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41874878-C-G

108870959-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41874759-G-C

108870965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41874753-G-A

108871121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41874618-C-T

108871271-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41874493-T-A

http://identifiers.org/hco/6/GRCh38#108872168-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41873734-C-A

108872182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41873720-G-A

108872182-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41873720-G-C

108872470-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41873491-C-G

108872669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41873312-A-G

108872669-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41873312-A-T

108872892-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41873091-C-T

108872971-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41872963-C-G

108873354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41872602-G-A

108873408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41872547-C-T

108873467-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41872493-C-G

108873483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41872098-C-T

108873738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41871892-G-A

108873772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41871859-C-T

108873935-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41871770-A-G

108874017-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41871715-T-A

108874102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41871622-C-T

108874648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41870871-C-T

108875171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41870383-C-T

108875237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41870322-G-A

108875302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41870250-A-G

108875418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41870171-C-T

108875859-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41869496-T-C

108876122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41869245-A-G

108876134-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41869231-A-T

108876154-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41869211-G-A

108876170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41869195-C-T

108876176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: missense_variant, non_coding_transcript_exon_variant, start_lost
orthologous variants: 41869189-T-C

http://identifiers.org/hco/6/GRCh38#108876188-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41869177-C-A

108876188-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41869177-C-G

108876188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41869177-C-T

108876268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41869100-G-A

108876277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41869091-G-T

108876303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41869065-A-G

108876304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41869064-A-G

http://identifiers.org/hco/6/GRCh38#108876400-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41868975-A-C

108876419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41868960-T-C

108876698-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41868688-A-G

108876703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41868683-C-T

108876715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41868672-T-C

108877142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41868304-A-G

108877607-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41867822-T-G

http://identifiers.org/hco/6/GRCh38#108877608-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41867821-A-C

108878377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41867082-G-A

108878449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41867005-C-T

108878451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41867003-G-T

108878558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41866883-A-G

http://identifiers.org/hco/6/GRCh38#108878699-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41866776-A-C

108879597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41866596-T-C

108879622-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41866571-G-C

108879674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41866536-A-G

http://identifiers.org/hco/6/GRCh38#108879934-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41866212-C-A

108879943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 41866203-G-A

108879943-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 41866203-G-T

108879976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41866170-A-G

108879999-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41866147-T-G

108880087-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41865980-G-A

108880087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41865980-G-T

108880131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41865899-A-G

http://identifiers.org/hco/6/GRCh38#108880246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41865761-C-A

108880246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41865761-C-T

108880266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41865741-G-A

108880266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41865741-G-T

108880267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41865740-G-A

108880267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41865740-G-T

108880330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41865696-A-G

http://identifiers.org/hco/6/GRCh38#108880387-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41865629-C-A

108880462-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41865555-T-G

108883553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41863126-A-G

http://identifiers.org/hco/6/GRCh38#108883554-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41863125-A-C

108883683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41863001-T-C

108883951-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41862697-A-T

http://identifiers.org/hco/6/GRCh38#108884093-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41862556-C-A

108884093-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41862556-C-G

108885830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41862288-C-T

108885925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41862186-T-C

108885927-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41862184-T-A

108885953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41862158-C-T

108886753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41861698-T-C

108887364-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41861418-G-C

108887778-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41861029-A-T

108887815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41860992-T-C

108887955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41860858-A-G

108888055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41860762-A-G

108888087-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41860735-T-C

108888193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41860668-G-A

108888447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41860441-T-C

108888498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41860391-G-A

108888660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41860169-C-T

108888677-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41860155-G-C

108888698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41860134-G-A

108892309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41857763-G-A

108894561-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41856497-T-C

108896111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41855138-T-C

108896387-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41854862-G-C

108896719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41854576-G-A

108896721-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41854574-G-T

108896907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41854077-C-T

108896955-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41854022-T-A

108897436-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41853364-T-C

108897525-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41853273-A-T

108898691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41852564-T-C

108899046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41852155-A-G

108899558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41851579-G-T

http://identifiers.org/hco/6/GRCh38#108899573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41851565-C-A

108899577-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41851561-G-T

http://identifiers.org/hco/6/GRCh38#108899867-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41851300-C-A

108899903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41851263-T-C

http://identifiers.org/hco/6/GRCh38#108899953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41851213-C-A

108899968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41851192-T-C

108901080-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41850471-T-A

108901775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41849847-A-G

108902208-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41849363-G-C

108902557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41849050-T-C

http://identifiers.org/hco/6/GRCh38#108902568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41849039-C-A

108902718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41848885-G-A

108902759-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41848847-T-G

108902764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41848842-A-G

http://identifiers.org/hco/6/GRCh38#108902787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41848819-C-A

108902787-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41848819-C-G

108902814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41848792-A-G

108904105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41847315-G-A

108904360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41847064-T-C

108904514-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41846910-A-T

http://identifiers.org/hco/6/GRCh38#108904516-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41846908-A-C

http://identifiers.org/hco/6/GRCh38#108904544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41846882-C-A

108904544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41846882-C-T

108905403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41846694-A-G

108905954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41845966-G-A

108905973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41845948-G-A

108905973-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41845948-G-C

108905973-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41845948-G-T

108908216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41844175-G-A

108908280-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41844101-C-G

http://identifiers.org/hco/6/GRCh38#108909274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41843708-C-A

108909434-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41843402-A-G

108909434-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41843402-A-T

http://identifiers.org/hco/6/GRCh38#108910868-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41842832-C-A

108910868-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41842832-C-T

108910873-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41842822-A-G

108910908-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41842788-A-G

108910908-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41842788-A-T

108910927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41842769-A-G

108910928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 41842768-T-C

108910958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 41842738-G-A

108910958-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41842738-G-C

108910958-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41842738-G-T

108910968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41842728-A-G

http://identifiers.org/hco/6/GRCh38#108911011-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41842685-A-C

108911011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41842685-A-G

108911029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41842668-G-A

108911029-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41842668-G-T

108911045-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41842652-A-T

108911064-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41842632-G-T

108911073-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41842623-T-G

108911089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41842603-G-A

108911089-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41842603-G-T

108911103-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41842590-T-A

108912188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41839977-T-C

108912194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41839971-A-G

108912404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41839787-G-T

http://identifiers.org/hco/6/GRCh38#108912499-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41839692-A-C

108912516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 41839675-A-G

108912518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41839673-G-A

108912648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41839553-C-T

108912675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41839527-T-C

http://identifiers.org/hco/6/GRCh38#108912796-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41839425-C-A

108913315-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41838528-A-G

108913570-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41838266-A-G

108913633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41838204-C-T

108914778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41835496-A-G

108920396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41835294-T-C

108920914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41834865-G-A

108920969-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41834780-C-G

108920987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41834762-G-A

http://identifiers.org/hco/6/GRCh38#108921171-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41834456-A-C

108921171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41834456-A-G

http://identifiers.org/hco/6/GRCh38#108921205-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41834422-C-A

108921356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41834167-A-G

108921486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41834059-A-G

108921522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 41834022-A-G

108921524-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 41834020-T-G

108921685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 41833859-T-C

http://identifiers.org/hco/6/GRCh38#108921702-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41833842-A-C

108921794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41833749-T-C

108921858-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41833697-G-A

108921858-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41833697-G-T

108921923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41833625-G-A

108921936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41833612-C-T

108922006-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41833524-G-C

http://identifiers.org/hco/6/GRCh38#108922268-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41833202-A-C

108922268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41833202-A-G

108922268-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41833202-A-T

108922424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41833052-C-T

108922841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41832756-C-T

108922928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41832652-T-C

108922975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 41832613-A-G

108923023-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41832573-T-A

108923050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 41832546-G-T

108923075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41832517-A-G

108923084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41832484-A-G

108925646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41831296-T-C

108925716-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41831231-T-G

108925847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41831107-A-G

108925906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41830944-G-A

108926044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41830804-A-G

108928073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41827754-A-G

108928121-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41827707-T-A

108928224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41827604-G-A

108928224-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41827604-G-T

108936850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41824039-T-C

http://identifiers.org/hco/6/GRCh38#108936907-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41823982-A-C

http://identifiers.org/hco/6/GRCh38#108936916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41823973-C-A

108936916-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41823973-C-G

108936916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41823973-C-T

108936955-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41823934-T-C

http://identifiers.org/hco/6/GRCh38#108936987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: http://identifiers.org/mco/10/GRCm39#41823902-C-A

108936987-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 41823902-C-G

108936987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41823902-C-T

http://identifiers.org/hco/6/GRCh38#108937041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41823845-C-A

108937041-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41823845-C-G

108937122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41823760-A-G

108937122-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41823760-A-T

108937129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41823753-G-A

http://identifiers.org/hco/6/GRCh38#108937130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41823752-C-A

108937130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41823752-C-T

108937491-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41823435-G-C

108940072-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41820634-C-G

108942136-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41817532-T-C

108942140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41817528-C-T

108942536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41817139-G-A

108942691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41816995-T-C

108942702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41816984-A-G

108942989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 41813446-G-A

http://identifiers.org/hco/6/GRCh38#108943201-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41813260-C-A

108944529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41812209-G-A

http://identifiers.org/hco/6/GRCh38#108945252-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41811560-A-C

108945253-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41811559-G-C

108945651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41811135-G-A

108945863-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41810929-G-C

108945945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41810848-G-A

108946002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41810791-A-G

108946091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41810680-G-A

108946091-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41810680-G-T

108946855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41809888-T-C

108947039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41809738-A-G

108947315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41809426-T-C

108947826-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41808972-T-A

108947826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41808972-T-C

108947829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41808969-G-A

108947830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41808968-A-G

108948236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41808411-G-A

108948799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 41807918-G-T

108949268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41807659-G-A

108949421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41807098-G-T

108949612-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41806908-T-G

108949692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41806850-G-A

108951706-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 41804832-C-G

108951723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41804816-C-T

108951724-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41804815-G-A

108951724-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41804815-G-C

108951813-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41804730-C-G

108952075-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41804522-C-G

108952075-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41804522-C-T

108952386-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41803690-C-T

108952619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41803507-C-T

108952736-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41803364-T-C

http://identifiers.org/hco/6/GRCh38#108952916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41803218-C-A

108952916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41803218-C-T

http://identifiers.org/hco/6/GRCh38#108952921-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41803213-C-A

108952921-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41803213-C-G

108952921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41803213-C-T

108952968-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41803166-T-A

108952984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41803142-G-A

108953210-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41802919-A-G

108953235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41802910-C-T

http://identifiers.org/hco/6/GRCh38#108953288-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41802857-C-A

108953288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41802857-C-T

108953290-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41802855-G-A

108953290-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41802855-G-C

108953290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41802855-G-T

108953310-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41802835-C-G

108953310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41802835-C-T

108953359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 41802786-C-T

108953426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41802758-G-A

108953426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41802758-G-T

108953428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41802756-T-C

108953428-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41802756-T-G

108953453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41802744-G-A

108961237-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41800764-G-A

108961241-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41800760-T-G

108961416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41800595-G-A

108961592-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41800507-T-G

108961615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41800484-T-C

108961641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41800458-A-G

108961939-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41800202-A-G

108962060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 41799809-G-A

108963572-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41799299-C-G

108963572-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41799299-C-T

108963688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41799192-G-A

108964002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41798893-G-A

108964002-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41798893-G-T

http://identifiers.org/hco/6/GRCh38#108964138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41798734-C-A

108964138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41798734-C-T

108964156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41798716-T-C

108964195-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41798677-T-A

108964195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41798677-T-C

108964260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41798612-A-G

108964277-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 41798595-G-C

108964319-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 41798553-T-G

108964386-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41798499-T-C

108964926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 41798333-A-G

http://identifiers.org/hco/6/GRCh38#108965119-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41798137-C-A

http://identifiers.org/hco/6/GRCh38#108965291-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41797983-A-C

http://identifiers.org/hco/6/GRCh38#108965350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41797922-C-A

108965350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron variant
orthologous variants: 41797922-C-T

108966672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron variant
orthologous variants: 41796717-A-G

http://identifiers.org/hco/6/GRCh38#108966896-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41796515-A-C

http://identifiers.org/hco/6/GRCh38#108966899-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41796512-C-A

108966902-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron variant
orthologous variants: 41796509-T-G

108967052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron variant
orthologous variants: 41796430-T-C

http://identifiers.org/hco/6/GRCh38#108967133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#41796403-C-A

108972688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron variant
orthologous variants: 41794087-G-A

108973154-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron variant
orthologous variants: 41793399-C-T

108973245-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron variant
orthologous variants: 41793325-T-C

108973245-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron variant
orthologous variants: 41793325-T-G

108973329-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron variant
orthologous variants: 41793246-T-C

108973425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 41793145-A-G

108973476-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 41793094-C-G

108973513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: 3_prime_UTR_variant, intron_variant, undefined
orthologous variants: 41793057-A-G

http://identifiers.org/hco/6/GRCh38#108973605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41792964-C-A

108973685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 41792884-G-A

108973718-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 41792856-T-A

108973766-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 41792817-T-A

108973819-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 41792764-G-A

108973819-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 41792764-G-T

108973917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 41792673-A-G

http://identifiers.org/hco/6/GRCh38#108974498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41790961-C-A

108974829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron variant
orthologous variants: 41790597-C-T

108974872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: intron variant
orthologous variants: 41790535-C-T

108986713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 41784144-T-C

108987282-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 41783617-G-T

108987324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 41783572-A-G

108987340-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 41783556-A-T

http://identifiers.org/hco/6/GRCh38#108987361-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#41783535-C-A

108987361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 23045
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 41783535-C-T