http://identifiers.org/hco/11/GRCh38#64823430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6375621-C-A

64823430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: 3 prime UTR variant
orthologous variants: 6375621-C-T

http://identifiers.org/hco/11/GRCh38#64823603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6375442-C-A

64823734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: 3 prime UTR variant
orthologous variants: 6375315-G-T

http://identifiers.org/hco/11/GRCh38#64823791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6375252-C-A

64823806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: 3 prime UTR variant
orthologous variants: 6375237-T-C

64823829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: 3 prime UTR variant
orthologous variants: 6375214-T-C

64823865-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: 3 prime UTR variant
orthologous variants: 6375180-T-C

http://identifiers.org/hco/11/GRCh38#64823940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6375110-C-A

http://identifiers.org/hco/11/GRCh38#64824010-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6375044-A-C

64824010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: 3 prime UTR variant
orthologous variants: 6375044-A-G

64824375-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: 3 prime UTR variant
orthologous variants: 6374700-T-G

64824480-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 6374594-G-C

64824480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 6374594-G-T

64825209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron variant
orthologous variants: 6374408-G-A

64825411-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron variant
orthologous variants: 6374036-C-G

64825801-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron variant
orthologous variants: 6373740-C-G

64825857-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron variant
orthologous variants: 6373663-G-A

64826041-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron variant
orthologous variants: 6373320-T-G

64826114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron variant
orthologous variants: 6373165-C-T

64826436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron variant
orthologous variants: 6372942-A-G

64826625-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron variant
orthologous variants: 6372752-C-G

64826625-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron variant
orthologous variants: 6372752-C-T

64826628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron variant
orthologous variants: 6372749-G-T

64826643-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron variant
orthologous variants: 6372734-A-T

http://identifiers.org/hco/11/GRCh38#64826703-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, missense_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6372674-C-A

64826703-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, missense_variant, synonymous_variant
orthologous variants: 6372674-C-T

64827057-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: missense variant
orthologous variants: 6372392-T-G

http://identifiers.org/hco/11/GRCh38#64827067-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6372382-C-A

64827067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: missense variant
orthologous variants: 6372382-C-T

64827138-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: missense_variant, synonymous_variant
orthologous variants: 6372311-G-A

64827229-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron variant
orthologous variants: 6372224-A-G

64827287-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: missense_variant, synonymous_variant
orthologous variants: 6372166-T-G

http://identifiers.org/hco/11/GRCh38#64827320-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: missense_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6372133-A-C

64827377-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: missense_variant, synonymous_variant
orthologous variants: 6372076-G-A

64827377-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: missense_variant, synonymous_variant
orthologous variants: 6372076-G-C

64827517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron variant
orthologous variants: 6371949-A-G

64827517-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron variant
orthologous variants: 6371949-A-T

64827580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: missense_variant, synonymous_variant
orthologous variants: 6371886-A-G

64827740-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 6371728-G-A

64828329-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron variant
orthologous variants: 6371208-C-G

64828330-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron variant
orthologous variants: 6371207-C-G

64829485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: missense variant
orthologous variants: 6370856-G-A

64829527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: missense variant
orthologous variants: 6370814-G-A

64829527-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: missense variant
orthologous variants: 6370814-G-C

64829713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: missense variant
orthologous variants: 6370628-G-A

64829755-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: missense variant
orthologous variants: 6370586-A-G

64829786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: missense variant
orthologous variants: 6370555-G-A

64829914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: missense variant
orthologous variants: 6370427-T-C

64830305-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, missense_variant, synonymous_variant
orthologous variants: 6370060-C-G

64830305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, missense_variant, synonymous_variant
orthologous variants: 6370060-C-T

64830318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, missense_variant
orthologous variants: 6370057-C-T

64830429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 6369932-A-G

64830475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6369878-A-G

64830478-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6369875-T-A

64831061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6368974-T-C

64831205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6368839-G-A

64831513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6368594-G-A

64831579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6368528-G-A

64831659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 6368448-G-A

64831659-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6368448-G-C

64831659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6368448-G-T

64831768-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6368339-G-A

64831768-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6368339-G-T

http://identifiers.org/hco/11/GRCh38#64831858-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6368238-C-A

64831858-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6368238-C-T

64831863-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6368233-A-T

64832185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6367972-G-A

64832197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6367960-C-T

http://identifiers.org/hco/11/GRCh38#64832257-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6367907-A-C

64832401-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6367741-C-G

64832401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6367741-C-T

64832423-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6367718-C-T

64832595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6367551-G-A

64832767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6367380-G-A

http://identifiers.org/hco/11/GRCh38#64832787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6367362-C-A

64832792-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6367357-A-G

64832793-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6367356-T-A

64832793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6367356-T-C

64832793-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6367356-T-G

http://identifiers.org/hco/11/GRCh38#64832911-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6367237-C-A

64832911-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6367237-C-G

64832926-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 6367222-G-A

64832996-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6367153-T-C

64833036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6367130-G-A

64833100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6367072-A-G

64833112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6367062-G-A

64833112-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6367062-G-T

64833118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6367056-G-A

64833118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6367056-G-T

64833137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6367040-G-A

64833137-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6367040-G-T

http://identifiers.org/hco/11/GRCh38#64833149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6367028-C-A

64833149-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6367028-C-T

64833166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6367014-G-A

64833166-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6367014-G-T

64833219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6366974-G-A

64833219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6366974-G-T

64833220-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6366973-G-T

64833323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6366870-G-A

64833323-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6366870-G-C

64833323-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6366870-G-T

http://identifiers.org/hco/11/GRCh38#64833363-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6366823-A-C

64833363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 6366823-A-G

64833442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6366744-G-A

64833442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6366744-G-T

http://identifiers.org/hco/11/GRCh38#64833561-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6366643-C-A

64833561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6366643-C-T

64833720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6366499-G-A

64833967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 6366237-G-A

64833983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 6366221-A-G

64834061-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6366142-T-A

http://identifiers.org/hco/11/GRCh38#64834079-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6366136-C-A

64834104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6366119-C-T

http://identifiers.org/hco/11/GRCh38#64834193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6366043-C-A

64834193-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6366043-C-G

64834193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6366043-C-T

64834212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6366024-G-A

64834212-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6366024-G-C

64834212-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6366024-G-T

64834219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6366016-G-A

64834219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6366016-G-T

64834230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6366005-G-T

http://identifiers.org/hco/11/GRCh38#64834236-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6365999-C-A

64834236-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6365999-C-G

64834236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6365999-C-T

64834245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6365990-A-G

64834245-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6365990-A-T

http://identifiers.org/hco/11/GRCh38#64834269-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6365977-C-A

64834269-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6365977-C-T

http://identifiers.org/hco/11/GRCh38#64834412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6365832-C-A

64834412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6365832-C-T

64834613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6365630-T-C

64834616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6365627-G-A

64834616-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6365627-G-C

64834616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6365627-G-T

http://identifiers.org/hco/11/GRCh38#64834659-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6365571-A-C

64834659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6365571-A-G

http://identifiers.org/hco/11/GRCh38#64834708-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6365522-C-A

64834854-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6365309-G-T

64835036-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6365135-C-G

64835096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6365075-G-A

64835096-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 6365075-G-T

64835170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6365003-G-A

64835197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6364960-C-T

64835224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6364921-C-T

64835244-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6364901-T-A

64835313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6364836-C-T

64835315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6364834-G-A

64835597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 6364548-T-C

64835633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6364512-G-A

64835740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6364416-C-T

64835814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6364350-G-A

64835872-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6364291-G-T

64836008-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6364174-C-T

64836009-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6364173-T-C

http://identifiers.org/hco/11/GRCh38#64836039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6364148-C-A

64836238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6363977-T-C

64836344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6363881-G-T

64836354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6363867-T-C

64836449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6363801-T-C

64836563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6363685-T-C

64836565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6363677-G-A

64836565-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6363677-G-C

64836601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6363640-T-C

64836654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6363601-A-G

64836654-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6363601-A-T

http://identifiers.org/hco/11/GRCh38#64836779-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6363483-C-A

64836779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 6363483-C-T

64836801-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 6363461-G-C

64836950-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6363316-C-G

64836950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 6363316-C-T

64837000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6363266-A-G

64837295-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6363033-T-G

64837354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6362938-G-A

64837778-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6362466-C-T

64838069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6362239-A-G

64838152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6362156-G-A

64838152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6362156-G-T

64838190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6362121-G-A

64838190-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6362121-G-T

http://identifiers.org/hco/11/GRCh38#64838217-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6362095-A-C

64838217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6362095-A-G

64838217-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6362095-A-T

http://identifiers.org/hco/11/GRCh38#64838580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6361662-C-A

64838640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6361612-C-T

64838694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6361558-G-A

http://identifiers.org/hco/11/GRCh38#64838709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6361543-C-A

64838709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6361543-C-T

http://identifiers.org/hco/11/GRCh38#64838805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6361447-C-A

64838805-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6361447-C-G

64838805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6361447-C-T

http://identifiers.org/hco/11/GRCh38#64838956-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6361306-A-C

64838984-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6361279-T-G

64838990-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6361273-G-T

http://identifiers.org/hco/11/GRCh38#64839384-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6360971-C-A

http://identifiers.org/hco/11/GRCh38#64839447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6360945-C-A

64839447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6360945-C-T

64839619-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6360781-G-C

64839619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6360781-G-T

64839637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6360765-G-A

64839637-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6360765-G-C

64839637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6360765-G-T

64839651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6360748-G-A

64839651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6360748-G-T

http://identifiers.org/hco/11/GRCh38#64839669-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6360728-C-A

64839866-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6360533-C-T

64839867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6360532-G-A

64840306-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6360203-G-A

64840345-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6360163-G-T

64840488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6359925-T-C

http://identifiers.org/hco/11/GRCh38#64840711-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6359692-C-A

64840739-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6359668-G-T

64841489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6359524-T-C

http://identifiers.org/hco/11/GRCh38#64841601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6359448-C-A

64841662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 6359398-C-T

64841782-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6359274-T-A

64842161-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6358952-G-C

64843141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6357970-C-T

64843169-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6357942-G-A

http://identifiers.org/hco/11/GRCh38#64843251-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6357862-C-A

http://identifiers.org/hco/11/GRCh38#64843554-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#6357557-A-C

64844261-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6357044-G-C

64844324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6356990-G-A

64844324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6356990-G-T

64844343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6356972-G-A

64844343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6356972-G-T

http://identifiers.org/hco/11/GRCh38#64844379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#6356938-C-A

64844379-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6356938-C-G

64844379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6356938-C-T

64844380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6356937-G-A

64844380-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6356937-G-C

http://identifiers.org/hco/11/GRCh38#64844529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/19/GRCm39#6356784-C-A

64844529-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 6356784-C-T

64844625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6356690-T-C

64844629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6356686-G-A

64844629-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6356686-G-C

64844629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6356686-G-T

http://identifiers.org/hco/11/GRCh38#64844633-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6356682-C-A

64844633-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6356682-C-G

64844633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6356682-C-T

http://identifiers.org/hco/11/GRCh38#64844637-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6356678-C-A

64844637-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6356678-C-G

64844637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29829
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6356678-C-T