48636761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 108729877-G-A

48636761-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 108729877-G-T

48636769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 108729870-G-A

48636769-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 108729870-G-T

48637254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 108729429-A-G

48637254-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 108729429-A-T

48637775-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 108728924-G-T

http://identifiers.org/hco/3/GRCh38#48637805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108728895-C-A

48637805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 108728895-C-T

http://identifiers.org/hco/3/GRCh38#48637842-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108728861-A-C

48637842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 108728861-A-G

http://identifiers.org/hco/3/GRCh38#48637861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108728842-C-A

http://identifiers.org/hco/3/GRCh38#48637903-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108728810-C-A

48637903-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 108728810-C-G

48637903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 108728810-C-T

48638270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108728458-A-G

48638292-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108728454-T-A

48638292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108728454-T-C

48638293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108728453-G-T

http://identifiers.org/hco/3/GRCh38#48638347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108728447-C-A

48638347-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108728447-C-T

48638377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108728417-A-G

48638843-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108727990-G-A

48639213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108727421-A-G

http://identifiers.org/hco/3/GRCh38#48639258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108727403-C-A

48639577-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108726770-A-G

48639606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108726741-A-G

48639707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108726639-G-A

48639713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108726633-G-A

48639887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108726471-C-T

48640013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108726345-A-G

48640109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108726249-G-T

48640289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108726069-G-A

48640289-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108726069-G-T

48640431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108725921-C-T

48640460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108725892-A-G

48640493-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108725859-C-G

http://identifiers.org/hco/3/GRCh38#48640540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108725812-C-A

48640540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 108725812-C-T

48640590-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108725762-T-G

48640669-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108725703-T-G

48640809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108725595-G-A

48640812-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108725593-G-T

48640813-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108725592-G-T

http://identifiers.org/hco/3/GRCh38#48640920-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108725486-C-A

48640920-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108725486-C-G

48640923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108725482-G-A

http://identifiers.org/hco/3/GRCh38#48640961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108725423-C-A

48641055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108725274-T-C

48641116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108725161-G-A

48641116-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108725161-G-T

http://identifiers.org/hco/3/GRCh38#48641117-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108725153-C-A

48641117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108725153-C-T

48641121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108725149-C-T

48641133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108725137-G-A

48641133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108725137-G-T

http://identifiers.org/hco/3/GRCh38#48641198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108725063-C-A

48641244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108725022-A-G

http://identifiers.org/hco/3/GRCh38#48641258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108725008-C-A

48641464-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108724802-G-C

48642020-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108723895-G-C

48642027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108723888-A-G

48642091-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108723820-G-A

48642091-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108723820-G-T

48642093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108723818-T-C

48642209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108723770-G-A

48642209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108723770-G-T

48642212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108723767-T-C

48642313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108723671-G-A

48642313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108723671-G-T

48642360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 108723624-G-A

48642419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 108723565-G-A

48642419-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 108723565-G-C

http://identifiers.org/hco/3/GRCh38#48642483-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108723503-C-A

48642483-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108723503-C-G

48642483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108723503-C-T

48642538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108723429-T-C

http://identifiers.org/hco/3/GRCh38#48642544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108723423-C-A

http://identifiers.org/hco/3/GRCh38#48642568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108723392-C-A

48642568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108723392-C-T

48642613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 108723350-A-G

48642907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108723084-G-A

48642912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108723079-C-T

http://identifiers.org/hco/3/GRCh38#48642958-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108723031-C-A

48643098-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108722842-G-T

48643129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108722805-G-A

48643288-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108722633-T-A

48643288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108722633-T-C

48643288-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108722633-T-G

48643321-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108722601-G-T

48643423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108722492-G-A

48643423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108722492-G-T

48643488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 108722432-T-C

http://identifiers.org/hco/3/GRCh38#48643732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108722187-C-A

http://identifiers.org/hco/3/GRCh38#48643743-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108722176-C-A

48643743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 108722176-C-T

http://identifiers.org/hco/3/GRCh38#48643946-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108721995-C-A

48643946-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108721995-C-T

48643962-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108721981-G-C

48643962-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108721981-G-T

48643981-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108721962-G-T

http://identifiers.org/hco/3/GRCh38#48643999-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108721945-C-A

48643999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108721945-C-T

48644033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108721918-A-G

48644042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108721909-T-C

http://identifiers.org/hco/3/GRCh38#48644058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108721893-C-A

48644058-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108721893-C-T

48644240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 108721715-C-T

48644243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 108721712-T-C

48644336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108721615-G-A

48644336-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108721615-G-C

48644336-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108721615-G-T

48644348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108721603-G-A

http://identifiers.org/hco/3/GRCh38#48644356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108721595-C-A

48644356-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108721595-C-G

48644356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108721595-C-T

http://identifiers.org/hco/3/GRCh38#48644416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108721515-C-A

48644416-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108721515-C-G

48644416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108721515-C-T

48644445-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108721490-G-C

48644445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108721490-G-T

48644538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108721376-G-A

48644584-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108721335-G-A

48644584-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108721335-G-T

48644595-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108721324-T-C

48644608-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108721313-C-G

48644617-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108721304-T-A

48644617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108721304-T-C

48644834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 108721116-G-A

48644932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108721022-A-G

48644946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108721003-G-A

48644946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108721003-G-T

48644997-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108720948-C-T

48645288-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108720658-T-A

48645288-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108720658-T-C

http://identifiers.org/hco/3/GRCh38#48645302-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108720644-C-A

48645334-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108720608-C-G

48645334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108720608-C-T

48645403-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108720536-G-C

http://identifiers.org/hco/3/GRCh38#48645710-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108720230-C-A

48645710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108720230-C-T

http://identifiers.org/hco/3/GRCh38#48645812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108720127-C-A

48645812-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: missense variant
orthologous variants: 108720127-C-T

48646277-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108719670-G-C

48646305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108719647-T-C

48646305-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108719647-T-G

http://identifiers.org/hco/3/GRCh38#48646355-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108719601-A-C

48646355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108719601-A-G

48646355-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108719601-A-T

http://identifiers.org/hco/3/GRCh38#48646408-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108719547-C-A

http://identifiers.org/hco/3/GRCh38#48646581-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108719267-C-A

48646581-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108719267-C-G

48646793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: missense variant
orthologous variants: 108719020-G-A

48646838-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: missense variant
orthologous variants: 108718975-A-G

http://identifiers.org/hco/3/GRCh38#48646950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108718857-C-A

48646950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108718857-C-T

http://identifiers.org/hco/3/GRCh38#48647009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108718797-C-A

48647009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108718797-C-T

48647045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108718760-A-G

48647045-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108718760-A-T

48647683-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108718728-T-A

48647683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108718728-T-C

48647683-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108718728-T-G

48647687-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108718724-G-A

48647689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108718722-G-A

48647689-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108718722-G-C

48647807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108718579-G-T

48647863-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: synonymous variant
orthologous variants: 108718522-G-T

48648031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108718354-G-T

48648061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108718324-C-T

http://identifiers.org/hco/3/GRCh38#48648090-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108718294-C-A

http://identifiers.org/hco/3/GRCh38#48648092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108718292-C-A

48648092-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108718292-C-G

48648093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108718291-A-G

http://identifiers.org/hco/3/GRCh38#48648096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108718288-C-A

48648154-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108718232-G-C

48648154-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108718232-G-T

48648162-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108718224-T-A

48648162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108718224-T-C

48648228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108718179-C-T

48648268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 108718145-A-G

48648483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108717930-T-C

48648519-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108717894-A-G

http://identifiers.org/hco/3/GRCh38#48648710-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108717706-C-A

48648710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108717706-C-T

48649105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108717309-G-A

48649105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108717309-G-T

48649152-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: missense variant
orthologous variants: 108717260-G-C

48649194-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: missense variant
orthologous variants: 108717218-T-C

http://identifiers.org/hco/3/GRCh38#48649257-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108717155-C-A

48649257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108717155-C-T

48649741-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108716487-T-C

48649994-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108716277-A-G

48650029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108716239-G-A

48650341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108715878-G-A

48650341-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108715878-G-T

http://identifiers.org/hco/3/GRCh38#48650655-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108715588-A-C

48650655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108715588-A-G

48650728-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108715514-A-G

48650728-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108715514-A-T

48651317-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108714921-T-C

48651549-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108714684-C-G

http://identifiers.org/hco/3/GRCh38#48651842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108714392-C-A

48651880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: missense variant
orthologous variants: 108714357-G-A

48652147-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108714103-A-T

http://identifiers.org/hco/3/GRCh38#48652189-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108714065-C-A

48652189-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108714065-C-T

48652198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108714057-G-A

48652198-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108714057-G-C

48652198-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108714057-G-T

48652294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108713963-G-A

48652294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108713963-G-T

48652624-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108713657-T-A

48652624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108713657-T-C

48652926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108713267-G-A

48652926-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108713267-G-T

48653096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: missense variant
orthologous variants: 108713074-C-T

48653232-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108712945-G-T

48653266-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108712911-G-T

48653316-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108712863-C-T

48653335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108712850-G-A

48653335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108712850-G-T

48653479-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108712723-A-G

48653493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108712709-G-T

48653515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108712688-T-C

48653525-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108712678-G-A

48653525-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108712678-G-T

http://identifiers.org/hco/3/GRCh38#48653631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108712575-C-A

48653631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: synonymous variant
orthologous variants: 108712575-C-T

48653683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: missense variant
orthologous variants: 108712523-G-A

48653743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: stop gained
orthologous variants: 108712463-C-T

48653861-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108712340-C-G

48653861-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108712340-C-T

48653943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: missense variant
orthologous variants: 108712258-G-A

48653943-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: missense variant
orthologous variants: 108712258-G-C

48653943-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: stop gained
orthologous variants: 108712258-G-T

48654038-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108712164-A-G

48654046-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108712156-G-C

48654046-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108712156-G-T

http://identifiers.org/hco/3/GRCh38#48654098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108712104-C-A

48654099-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108712103-A-G

48654114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108712088-T-C

48654159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108712052-T-C

48654256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108711945-C-T

48654263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108711937-T-C

48654263-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108711937-T-G

48654534-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108711667-T-A

48654534-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108711667-T-G

48654642-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108711577-T-C

48654773-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108711431-G-T

48654832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108711373-G-A

http://identifiers.org/hco/3/GRCh38#48654894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108711300-C-A

48654894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108711300-C-T

48654950-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108711283-G-T

http://identifiers.org/hco/3/GRCh38#48654959-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108711274-A-C

http://identifiers.org/hco/3/GRCh38#48655530-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108710707-C-A

48655530-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108710707-C-T

48655774-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: missense variant
orthologous variants: 108710439-T-A

48655948-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108710284-G-A

48655948-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108710284-G-T

48656031-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108710226-G-A

48656031-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108710226-G-T

48656146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: missense variant
orthologous variants: 108710104-G-A

48656146-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: missense variant
orthologous variants: 108710104-G-C

48656146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: missense variant
orthologous variants: 108710104-G-T

http://identifiers.org/hco/3/GRCh38#48656170-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108710080-C-A

48656170-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: missense variant
orthologous variants: 108710080-C-T

http://identifiers.org/hco/3/GRCh38#48656176-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108710074-C-A

48656176-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: missense variant
orthologous variants: 108710074-C-G

48656176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: missense variant
orthologous variants: 108710074-C-T

48656233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: missense variant
orthologous variants: 108710017-G-A

48656233-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: missense variant
orthologous variants: 108710017-G-T

48656293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: missense variant
orthologous variants: 108709957-G-A

48656293-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: missense variant
orthologous variants: 108709957-G-C

http://identifiers.org/hco/3/GRCh38#48656538-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108709720-C-A

48656538-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108709720-C-G

48656538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108709720-C-T

48656609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron_variant, undefined
orthologous variants: 108709599-G-A

http://identifiers.org/hco/3/GRCh38#48656633-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108709575-C-A

48656633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108709575-C-T

http://identifiers.org/hco/3/GRCh38#48656840-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108709383-C-A

48656840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: synonymous variant
orthologous variants: 108709383-C-T

48656904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: missense variant
orthologous variants: 108709319-G-A

48656904-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: missense variant
orthologous variants: 108709319-G-C

48656904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: stop gained
orthologous variants: 108709319-G-T

http://identifiers.org/hco/3/GRCh38#48657341-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108708882-C-A

48657341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: synonymous variant
orthologous variants: 108708882-C-T

http://identifiers.org/hco/3/GRCh38#48657356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108708867-C-A

48657356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 108708867-C-T

http://identifiers.org/hco/3/GRCh38#48657470-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108708763-C-A

48657488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108708744-A-G

48658212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108707804-G-A

48658212-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108707804-G-C

48658491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108707570-C-T

48658497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108707564-A-G

48658752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108707325-A-G

48658752-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108707325-A-T

48658853-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108707271-T-A

48658874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: intron variant
orthologous variants: 108707250-C-T

48659293-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: synonymous variant
orthologous variants: 108706831-C-G

48659711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: missense variant
orthologous variants: 108706413-G-A

48659723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: missense variant
orthologous variants: 108706401-G-A

48659837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: missense variant
orthologous variants: 108706287-G-A

48660128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: missense variant
orthologous variants: 108705996-C-T

48660611-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: missense variant
orthologous variants: 108705513-G-A

48660997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: synonymous variant
orthologous variants: 108705127-G-A

48660997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: missense variant
orthologous variants: 108705127-G-T

48661082-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: missense variant
orthologous variants: 108705042-T-A

48661082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: missense variant
orthologous variants: 108705042-T-C

48661716-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: missense_variant, undefined
orthologous variants: 108704408-C-G

48661758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: missense_variant, undefined
orthologous variants: 108704366-G-A

48661758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: missense_variant, undefined
orthologous variants: 108704366-G-T

48661769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: missense_variant, undefined
orthologous variants: 108704355-T-C

48661769-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: missense_variant, undefined
orthologous variants: 108704355-T-G

48661969-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: synonymous_variant, undefined
orthologous variants: 108704167-T-G

48662114-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: missense_variant, undefined
orthologous variants: 108704022-T-C

48662435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: missense variant
orthologous variants: 108703713-G-A

http://identifiers.org/hco/3/GRCh38#48662772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#108703377-C-A

48662772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3230
most severe consequence: 5 prime UTR variant
orthologous variants: 108703377-C-T