64914388-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 76812263-A-T

64914389-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 76812264-T-C

64914410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 76812285-G-A

64914410-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 76812285-G-C

64914411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 76812287-G-A

64914427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 5_prime_UTR_variant, missense_variant, undefined
orthologous variants: 76812306-T-C

http://identifiers.org/hco/14/GRCh38#64914477-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#76812355-C-A

64914477-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76812355-C-G

64914477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 76812355-C-T

64914598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76812461-G-A

64914598-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76812461-G-C

64914598-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76812461-G-T

64914604-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76812467-C-G

64914712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76812533-A-G

64914749-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76812568-T-G

64914779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76812593-C-T

64914853-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76812669-C-G

64918203-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76815988-A-T

64918260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76816045-G-A

64918438-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76816235-G-C

64918488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76816312-A-G

64918513-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76816331-C-G

64918647-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76816503-G-C

64918898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76816642-T-C

64918969-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76816688-A-T

64920240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76817397-C-T

64921768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76817991-A-G

http://identifiers.org/hco/14/GRCh38#64921883-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76818111-A-C

64921910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76818135-C-T

64921912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76818137-A-G

64921983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76818179-G-A

64921991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76818187-A-G

64922705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76818872-A-G

64922870-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76818972-A-T

64922954-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76819034-G-C

64922973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76819047-G-A

64923011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76819080-G-T

64923387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76819400-T-C

64923591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76819591-T-C

http://identifiers.org/hco/14/GRCh38#64923758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76819844-C-A

64923758-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76819844-C-G

64923758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76819844-C-T

64923812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76819877-A-G

64923812-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76819877-A-T

64923982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 76820023-A-G

64924119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 76820160-C-T

64924162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76820203-G-A

64924162-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76820203-G-T

64924448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76820567-G-A

64924453-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76820573-C-G

http://identifiers.org/hco/14/GRCh38#64924465-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76820585-C-A

64924465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 76820585-C-T

64924560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76820853-C-T

64924564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76820857-A-G

64924779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76821105-A-G

64924829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76821258-A-G

64925674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76822040-G-A

64925674-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76822040-G-C

64925674-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76822040-G-T

64925682-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76822048-G-T

http://identifiers.org/hco/14/GRCh38#64925689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76822055-C-A

64925689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76822055-C-T

64925746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76822157-A-G

64925836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76822214-G-A

64925883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76822249-T-C

64925883-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76822249-T-G

64925926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76822294-A-G

64925926-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76822294-A-T

64925946-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76822314-T-A

64925986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76822350-G-A

64925986-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76822350-G-C

64925986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76822350-G-T

64925994-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76822352-C-G

64926023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 76822381-T-C

64926047-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron_variant, missense_variant
orthologous variants: 76822405-T-G

64926164-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76822510-T-C

64926164-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76822510-T-G

64926654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76823176-G-A

64926679-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76823201-T-C

64926820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76823702-T-C

64926827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76823709-G-A

64927128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76823998-A-G

64927597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76825353-C-T

64927603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76825364-G-A

64928489-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76826034-G-C

64928586-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76826126-A-G

64928589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76826127-C-T

64928628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76826165-G-A

64928647-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76826184-A-T

64928651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76826188-G-A

64928651-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76826188-G-C

64928747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76826485-G-T

64928817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76826564-T-C

64928823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76826565-T-C

64928829-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76826571-T-C

64929842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76826609-G-A

64929861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76826628-G-A

64929924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76826673-A-G

http://identifiers.org/hco/14/GRCh38#64929927-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76826676-C-A

64929927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76826676-C-T

64929966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76826703-G-T

64930092-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76826786-A-G

http://identifiers.org/hco/14/GRCh38#64930140-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76826827-C-A

64930140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76826827-C-T

64930159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76826846-G-A

64930159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76826846-G-T

http://identifiers.org/hco/14/GRCh38#64930198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76826877-C-A

64930375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76827041-A-G

64930550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76827223-T-C

http://identifiers.org/hco/14/GRCh38#64930657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76827344-C-A

64930670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76827364-G-A

64930670-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76827364-G-T

http://identifiers.org/hco/14/GRCh38#64930684-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76827378-C-A

64930685-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76827379-A-T

64930711-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76827405-G-C

64930711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76827405-G-T

64930934-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76828138-T-G

64930954-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76828158-T-A

64930954-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76828158-T-C

64930970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76828172-C-T

http://identifiers.org/hco/14/GRCh38#64931015-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76828217-C-A

64931028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76828230-T-C

64931053-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76828255-A-G

64931604-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76828464-G-T

64931687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76828556-T-C

64932020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76829469-A-G

64932087-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76829536-G-T

64932092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76829541-T-C

64932128-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76829577-C-G

64932212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 76829661-A-G

64932241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76829687-A-G

64932249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76829695-G-A

64932269-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76829715-G-T

http://identifiers.org/hco/14/GRCh38#64932279-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76829725-C-A

64932530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76830160-A-G

http://identifiers.org/hco/14/GRCh38#64932533-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76830164-A-C

64932533-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76830164-A-G

64932533-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76830164-A-T

64932631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76830246-G-A

64932631-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76830246-G-C

64932631-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76830246-G-T

http://identifiers.org/hco/14/GRCh38#64932655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76830352-C-A

64932655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76830352-C-T

64932805-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76830613-T-A

64932805-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76830613-T-G

64932811-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76830621-G-T

http://identifiers.org/hco/14/GRCh38#64932817-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76830627-A-C

http://identifiers.org/hco/14/GRCh38#64932818-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76830628-A-C

64932818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76830628-A-G

64932820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76830656-C-T

64932982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76830823-A-G

64933087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76830875-A-G

64933114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76830900-A-G

64933130-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76830913-T-C

64933151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76830923-T-C

64933157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76830929-A-G

64933192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76830963-A-G

64933243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76831009-G-A

64933243-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76831009-G-C

64933243-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76831009-G-T

64933306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76831057-G-T

http://identifiers.org/hco/14/GRCh38#64933322-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76831073-C-A

64933322-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76831073-C-T

64933334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76831083-G-A

64933334-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76831083-G-C

http://identifiers.org/hco/14/GRCh38#64933339-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76831088-C-A

64933339-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76831088-C-T

64933531-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76831269-T-C

64933540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76831282-G-A

64933540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76831282-G-T

64933542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76831284-A-G

64933542-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76831284-A-T

64933617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76831358-T-C

http://identifiers.org/hco/14/GRCh38#64933626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76831367-C-A

64933715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76831452-G-A

64933731-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76831472-G-C

64933755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76831483-G-A

64933779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76831503-A-G

64934402-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76831657-A-T

http://identifiers.org/hco/14/GRCh38#64934414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76831669-C-A

64934440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76831695-T-C

64934467-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76831722-G-T

64934529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76831785-T-C

64934533-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76831789-A-T

64934545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76831799-A-G

64934588-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76831822-T-C

64934616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76831850-G-T

64934772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76831998-T-C

64934778-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76832004-G-A

64934778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76832004-G-T

64934783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76832009-A-G

64934944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76832166-A-G

64934944-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76832166-A-T

64934956-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76832178-A-G

64934965-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76832187-T-A

64934995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76832222-T-C

64935006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76832241-C-T

64936182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76836711-T-C

64936337-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76836845-A-G

64936990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76837132-C-T

64937051-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76837184-A-G

64937235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76837328-C-T

http://identifiers.org/hco/14/GRCh38#64937417-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76837496-C-A

64937485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76837584-T-C

64937826-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76837909-C-T

64938180-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76838143-G-A

64938293-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76838279-T-C

64938332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76838311-G-A

64938425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76838317-C-T

64938557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76838382-C-T

64938802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76838558-G-A

64938931-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76838693-G-T

64938947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76838707-G-A

64938975-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76838727-C-G

64938975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76838727-C-T

http://identifiers.org/hco/14/GRCh38#64939011-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76838763-C-A

64939135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76838884-A-G

http://identifiers.org/hco/14/GRCh38#64939139-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76838888-C-A

http://identifiers.org/hco/14/GRCh38#64939163-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#76839116-A-C

64939163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76839116-A-G

64939206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76839158-C-T

64939299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76839253-T-C

64939299-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76839253-T-G

64939300-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76839254-T-G

64939314-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76839265-G-C

64939314-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76839265-G-T

http://identifiers.org/hco/14/GRCh38#64939342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#76839293-C-A

64939342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76839293-C-T

64939343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76839294-A-G

64939344-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76839295-G-T

64939378-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76839313-T-A

64939379-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76839314-G-T

http://identifiers.org/hco/14/GRCh38#64939385-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#76839320-A-C

64939408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76839343-T-C

64939436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76839371-G-A

64939471-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76839407-T-A

64939471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76839407-T-C

64939518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 76839454-G-A

64939550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76839486-G-A

64939566-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 76839502-G-T

64939578-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 76839514-C-G

64939578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 76839514-C-T

http://identifiers.org/hco/14/GRCh38#64939599-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#76839535-A-C

64939599-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 76839535-A-G

64939621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76839557-C-T

http://identifiers.org/hco/14/GRCh38#64939624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#76839560-C-A

64939624-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76839560-C-G

64939624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76839560-C-T

64939629-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 76839565-A-G

64939656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 76839592-G-A

64939677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 76839613-A-G

64939728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 76839664-G-A

64939728-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76839664-G-C

64939728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76839664-G-T

64939773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 76839709-C-T

64939791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 76839727-A-G

64939897-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76839828-A-G

64939935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76839862-G-T

http://identifiers.org/hco/14/GRCh38#64940306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#76840538-C-A

64940306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76840538-C-T

http://identifiers.org/hco/14/GRCh38#64941499-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#76840696-A-C

http://identifiers.org/hco/14/GRCh38#64941588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#76840783-C-A

64941588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76840783-C-T

http://identifiers.org/hco/14/GRCh38#64941651-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#76840846-C-A

64941657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76840852-G-A

64941657-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76840852-G-T

64941732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76840927-T-C

64941771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76840963-T-C

64941817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76841012-G-T

64941943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76841116-C-T

64942118-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76841294-G-C

64942309-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76841746-C-G

http://identifiers.org/hco/14/GRCh38#64942327-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#76841762-A-C

http://identifiers.org/hco/14/GRCh38#64942382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#76841818-C-A

64942382-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76841818-C-G

64942382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76841818-C-T

64942391-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76841827-A-T

http://identifiers.org/hco/14/GRCh38#64942440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#76841872-C-A

http://identifiers.org/hco/14/GRCh38#64942448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#76841875-C-A

64942456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76841883-G-A

64942456-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 76841883-G-T

64942648-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76842071-G-A

http://identifiers.org/hco/14/GRCh38#64942652-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/12/GRCm39#76842075-C-A

64942652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 76842075-C-T

64942687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 76842110-T-C

64942700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 76842123-A-G

64942786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76842205-G-A

64942786-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76842205-G-C

http://identifiers.org/hco/14/GRCh38#64942835-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76842251-A-C

64942835-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76842251-A-G

http://identifiers.org/hco/14/GRCh38#64942862-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76842278-C-A

64942862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76842278-C-T

64942887-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76842304-T-A

http://identifiers.org/hco/14/GRCh38#64943155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76842574-C-A

64943155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76842574-C-T

http://identifiers.org/hco/14/GRCh38#64943178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76842591-C-A

64943178-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76842591-C-G

64943178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron variant
orthologous variants: 76842591-C-T

64943315-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron_variant, missense_variant
orthologous variants: 76842634-C-G

64943315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: intron_variant, missense_variant, synonymous_variant
orthologous variants: 76842634-C-T

64943325-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 76842644-G-T

64943409-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 76842707-T-A

http://identifiers.org/hco/14/GRCh38#64943437-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76842735-C-A

64943475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76842773-G-A

64943475-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76842773-G-T

64943495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76842793-T-C

64943495-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76842793-T-G

http://identifiers.org/hco/14/GRCh38#64943497-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76842795-C-A

64943497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76842795-C-T

http://identifiers.org/hco/14/GRCh38#64943500-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76842798-C-A

64943500-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76842798-C-T

64943529-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76842825-T-A

64943529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76842825-T-C

http://identifiers.org/hco/14/GRCh38#64943606-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76842901-C-A

64943606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76842901-C-T

64943690-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76842990-T-A

64943690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76842990-T-C

64943691-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76842991-G-A

64943734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76843034-G-T

http://identifiers.org/hco/14/GRCh38#64943754-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76843054-C-A

64943754-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76843054-C-G

64943800-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76843093-A-G

http://identifiers.org/hco/14/GRCh38#64943809-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76843102-C-A

http://identifiers.org/hco/14/GRCh38#64943849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76843160-C-A

64943849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76843160-C-T

64943862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76843173-T-C

64944000-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76843269-G-A

64944015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76843281-G-A

64944015-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76843281-G-C

64944015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76843281-G-T

http://identifiers.org/hco/14/GRCh38#64944029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/12/GRCm39#76843295-C-A

64944029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76843295-C-T

64944111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76843363-C-T

64944243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76843494-G-A

64944259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76843511-G-A

64944259-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76843511-G-T

64944265-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76843517-A-G

64944271-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76843523-A-G

64944411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76843665-T-C

64944411-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76843665-T-G

64944538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76843753-A-G

64944565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76843780-A-G

64944565-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20099
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 76843780-A-T