67200743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: 3 prime UTR variant
orthologous variants: 63549329-C-T

67200755-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: 3 prime UTR variant
orthologous variants: 63549317-T-C

67200755-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: 3 prime UTR variant
orthologous variants: 63549317-T-G

67201057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: 3 prime UTR variant
orthologous variants: 63549145-G-A

67201148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: 3 prime UTR variant
orthologous variants: 63549057-T-C

http://identifiers.org/hco/15/GRCh38#67201224-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#63548966-A-C

67201224-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: 3 prime UTR variant
orthologous variants: 63548966-A-T

67201227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: 3 prime UTR variant
orthologous variants: 63548963-T-C

67201404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: 3 prime UTR variant
orthologous variants: 63548795-G-A

67201404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: 3 prime UTR variant
orthologous variants: 63548795-G-T

67201603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: 3 prime UTR variant
orthologous variants: 63548668-A-G

67201651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: 3 prime UTR variant
orthologous variants: 63548629-A-G

http://identifiers.org/hco/15/GRCh38#67201686-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#63548591-A-C

http://identifiers.org/hco/15/GRCh38#67201732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#63548548-C-A

67201733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63548547-A-G

67201826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63548519-G-A

67201826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63548519-G-T

67201891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63548450-A-G

67201915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63548426-T-C

67202014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63548357-G-A

67202014-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63548357-G-T

67202110-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63548274-T-C

http://identifiers.org/hco/15/GRCh38#67202160-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#63548219-C-A

67202160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63548219-C-T

67202367-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63548036-A-G

67202424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63547985-A-G

67202624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63547756-C-T

67202693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 63547695-G-T

67202852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63547533-A-G

http://identifiers.org/hco/15/GRCh38#67202885-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#63547500-A-C

http://identifiers.org/hco/15/GRCh38#67203032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#63547354-C-A

67203032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63547354-C-T

67203174-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63547227-T-G

http://identifiers.org/hco/15/GRCh38#67203225-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#63547167-C-A

67203251-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63547141-T-A

67203280-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63547112-A-G

67203408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63547006-T-C

67203515-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63546950-G-A

67203515-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63546950-G-C

67203515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63546950-G-T

67203585-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63546885-G-A

67203654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63546815-A-G

67203920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63546537-G-T

67203983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63546484-T-C

67203984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63546483-A-G

67204012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63546455-G-T

67204091-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63546377-T-A

67204278-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63546208-A-G

67204347-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63546152-A-G

67204348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63546151-A-G

67204487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63546066-C-T

67204548-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63546013-C-G

67204560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63546001-C-T

67204605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63545982-C-T

67204721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63545855-C-T

67205054-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63545185-G-T

67205262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63545023-T-C

67205285-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63545000-A-T

http://identifiers.org/hco/15/GRCh38#67205470-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#63544821-A-C

67205470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63544821-A-G

67208548-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63543777-A-G

67208548-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63543777-A-T

67208551-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63543774-G-A

67208581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 63543744-G-A

67208624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63543701-G-T

67208640-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63543685-C-G

67208640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63543685-C-T

67208690-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63543636-T-A

67208746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63543580-T-C

67208746-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63543580-T-G

http://identifiers.org/hco/15/GRCh38#67208779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#63543546-C-A

67208898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63543427-A-G

67209170-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63542954-A-T

67209323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63542793-G-A

67209323-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63542793-G-T

67209384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63542737-G-A

67209384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63542737-G-T

67209404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63542717-T-C

67209470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63542659-G-A

67211549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63541314-G-A

http://identifiers.org/hco/15/GRCh38#67211648-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#63541243-A-C

67212311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63541024-C-T

67212514-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63540811-A-G

67212573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63540602-A-G

67212574-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63540601-G-A

67212884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63540306-T-C

67212885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63540305-T-C

67215613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63538398-G-A

67215662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63538346-T-C

67215680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63538328-G-A

67215714-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63538294-A-G

67215785-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63538216-A-T

http://identifiers.org/hco/15/GRCh38#67216632-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#63537539-C-A

67216642-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63537529-A-T

67216750-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63537433-T-A

67216816-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63537360-T-C

67216890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63537298-T-C

67217530-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63536592-G-C

67218312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63536237-C-T

67218762-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63535900-T-G

67218851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63535813-A-G

67218889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63535777-G-A

67218889-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63535777-G-C

67218900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63535766-T-C

67219266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63535470-T-C

67219292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63535451-T-C

67220167-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63534225-T-C

67220319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63534087-G-A

67220377-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63534035-G-T

67220531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63533907-T-C

67221400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63532915-G-A

67223909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63532354-T-C

67223913-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63532350-A-T

67224068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63532230-A-G

http://identifiers.org/hco/15/GRCh38#67224119-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#63532181-A-C

67224434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63531941-C-T

67224769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63531802-T-C

67225032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63531677-T-C

67225065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63531647-G-A

67225079-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63531637-A-T

67225104-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63531611-G-C

67225121-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63531594-T-C

http://identifiers.org/hco/15/GRCh38#67227649-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#63529795-C-A

67227688-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63529761-A-G

http://identifiers.org/hco/15/GRCh38#67228325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#63528723-C-A

67228325-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63528723-C-G

67229602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63528608-G-A

67229695-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63528521-G-C

http://identifiers.org/hco/15/GRCh38#67230211-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#63528352-C-A

67230465-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63528162-C-G

67230465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63528162-C-T

67230503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63528124-C-T

67230607-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63528029-T-G

http://identifiers.org/hco/15/GRCh38#67230622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#63528010-C-A

67230650-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63527982-A-G

67230738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63527909-T-C

67230905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63527766-T-C

67231381-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63527267-T-A

67231381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63527267-T-C

67231554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63527120-T-C

67231567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63527110-A-G

67231704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63526985-G-T

67231720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63526975-T-C

67231768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63526924-A-G

67231768-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63526924-A-T

http://identifiers.org/hco/15/GRCh38#67231793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#63526529-C-A

67231793-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63526529-C-G

67231793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63526529-C-T

67232332-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63526302-T-C

67232335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63526299-T-C

67232360-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63526261-A-T

67232367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63526254-T-C

http://identifiers.org/hco/15/GRCh38#67232383-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#63526238-C-A

67235465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63525574-G-A

http://identifiers.org/hco/15/GRCh38#67235871-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#63524985-C-A

67235871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63524985-C-T

67235873-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63524983-G-C

67235873-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63524983-G-T

67235893-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63524960-G-C

67235893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63524960-G-T

67235954-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63524899-T-A

67235987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63524869-T-C

67236082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63524774-C-T

67236090-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63524766-T-A

67236090-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63524766-T-C

http://identifiers.org/hco/15/GRCh38#67236161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#63524721-C-A

67236161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63524721-C-T

http://identifiers.org/hco/15/GRCh38#67236265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#63524604-C-A

67236313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63524534-G-T

67236470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63524302-G-A

67236852-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63523934-G-C

67236852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63523934-G-T

67236854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63523932-G-A

67236854-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63523932-G-C

67236854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63523932-G-T

http://identifiers.org/hco/15/GRCh38#67236884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#63523903-C-A

67236884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63523903-C-T

67236941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63523839-A-G

67237383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63523350-T-C

67237453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63523287-A-G

67238976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63521678-T-C

67239001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63521648-G-A

67239001-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63521648-G-C

67239018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63521634-A-G

67239156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63521530-C-T

http://identifiers.org/hco/15/GRCh38#67239999-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#63520921-C-A

67239999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63520921-C-T

67240064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63520847-G-A

67240064-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63520847-G-C

67240420-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63520546-A-T

67241135-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63519920-A-T

67241185-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63519861-G-T

67241337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 63519752-C-T

67241516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63519430-T-C

67241746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 63519023-A-G

67241817-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63518960-A-G

67241820-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63518957-G-T

67241870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63518932-C-T

67241930-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63518866-A-T

67242002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63518806-C-T

67242006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63518802-G-A

67242045-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63518764-G-A

67242111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63518699-C-T

67242818-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 63518377-G-T

67243193-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63518011-A-T

67243504-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63517470-G-C

67243621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63517367-T-C

http://identifiers.org/hco/15/GRCh38#67243737-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#63517252-A-C

67246020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63516730-G-A

http://identifiers.org/hco/15/GRCh38#67247389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#63516471-C-A

67247389-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63516471-C-G

67247608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63516297-C-T

67247835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63516079-T-C

http://identifiers.org/hco/15/GRCh38#67247985-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#63515967-C-A

67248560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63515485-T-C

67248686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63515414-C-T

http://identifiers.org/hco/15/GRCh38#67249665-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#63514478-A-C

67249711-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63514435-A-T

67249812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63514312-T-C

67249840-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63514286-T-C

67250698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63513583-C-T

67250710-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63513571-T-C

67251226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63513286-G-A

67251226-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63513286-G-C

67251230-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63513282-G-C

67251234-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63513278-G-C

67251238-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63513274-G-C

67252162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63512569-T-C

67252162-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63512569-T-G

67252210-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63512517-C-G

67252210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63512517-C-T

67252766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63511742-T-C

67252855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 63511657-T-C

http://identifiers.org/hco/15/GRCh38#67254240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#63510292-C-A

67254271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63510263-A-G

67254271-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63510263-A-T

67254453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63510151-G-A

67254453-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63510151-G-C

67254453-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63510151-G-T

67254465-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63510139-G-T

67254508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63510096-C-T

http://identifiers.org/hco/15/GRCh38#67254525-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#63510085-C-A

http://identifiers.org/hco/15/GRCh38#67254531-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#63510079-A-C

67254531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63510079-A-G

http://identifiers.org/hco/15/GRCh38#67254544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#63510066-C-A

67254544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 63510066-C-T

67254591-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63510019-G-A

67254591-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63510019-G-C

67254591-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63510019-G-T

67254609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63510001-G-A

67254609-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63510001-G-C

67254609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63510001-G-T

67254615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63509995-G-A

67254615-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63509995-G-C

67254615-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 63509995-G-T

http://identifiers.org/hco/15/GRCh38#67254657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#63509955-C-A

67254657-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63509955-C-G

67254657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 63509955-C-T

67254691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron variant
orthologous variants: 63509921-C-T

http://identifiers.org/hco/15/GRCh38#67254695-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#63509917-C-A

67254695-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron variant
orthologous variants: 63509917-C-T

67254697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron variant
orthologous variants: 63509915-G-A

67254726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron variant
orthologous variants: 63509887-G-A

67254726-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron variant
orthologous variants: 63509887-G-T

http://identifiers.org/hco/15/GRCh38#67254755-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#63509851-C-A

67254755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron variant
orthologous variants: 63509851-C-T

http://identifiers.org/hco/15/GRCh38#67254773-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#63509825-C-A

http://identifiers.org/hco/15/GRCh38#67254790-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#63509808-C-A

67254821-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 63509776-G-C

67254821-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 63509776-G-T

http://identifiers.org/hco/15/GRCh38#67254833-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#63509761-C-A

http://identifiers.org/hco/15/GRCh38#67254856-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#63509740-A-C

67254856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 63509740-A-G

http://identifiers.org/hco/15/GRCh38#67254877-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#63509721-A-C

67254877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 63509721-A-G

67254890-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 63509708-C-G

http://identifiers.org/hco/15/GRCh38#67255191-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#63509396-C-A

67255197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25662
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 63509387-A-G