66825634-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93725579-C-T

66825738-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93725683-A-G

66825808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93727365-G-A

http://identifiers.org/hco/13/GRCh38#66825933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#93727471-C-A

66825933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93727471-C-T

66825945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93727487-G-A

66826191-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93727701-T-C

66826258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93727768-T-C

66826258-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93727768-T-G

66826311-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93727811-T-A

66826311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93727811-T-C

66826311-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93727811-T-G

66826376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93727868-T-C

66826487-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93727981-A-T

http://identifiers.org/hco/13/GRCh38#66826494-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#93727988-C-A

66826494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93727988-C-T

66826515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93728013-A-G

66826515-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93728013-A-T

66826546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93728046-A-G

66826791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93728159-G-A

66826791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93728159-G-T

66826847-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93728217-A-T

66826860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93728226-C-T

66826874-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93728240-T-G

http://identifiers.org/hco/13/GRCh38#66827218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#93728577-C-A

66827218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93728577-C-T

http://identifiers.org/hco/13/GRCh38#66827315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#93728638-C-A

66827656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93729084-G-A

66827719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93729140-A-G

66827862-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93729276-G-C

66827875-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93729288-A-T

66828008-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93729411-T-G

66828107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93729504-G-A

66828242-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93730059-G-A

66828341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93730158-G-A

66828774-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93730607-T-C

66828819-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93730647-T-A

66829759-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93731116-T-A

66829772-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93731129-T-A

66829772-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93731129-T-C

66829774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93731131-G-A

66829774-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93731131-G-C

66829774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93731131-G-T

66829947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93731275-T-C

66830323-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93731617-C-G

66830461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93731751-T-C

66830508-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93731797-T-G

66830549-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93731835-T-G

66830638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93731921-A-G

66830822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93732048-G-A

66830839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93732065-G-T

66831104-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93732334-C-T

66831215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93732457-T-C

http://identifiers.org/hco/13/GRCh38#66831346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#93732583-C-A

66831525-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93732767-A-T

66831592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93732841-G-A

66831592-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93732841-G-C

66831827-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93733045-T-A

66831860-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93733078-T-C

66831955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93733184-G-A

66832005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93733236-G-A

66832082-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93733313-A-T

66832137-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93733376-A-G

66832137-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93733376-A-T

66832185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93733423-G-A

66832185-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93733423-G-C

66832232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93733476-T-C

66832232-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93733476-T-G

66832413-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93733653-T-A

66832450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93733687-C-T

66832513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93733723-T-C

66833968-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93734652-G-T

66834931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93736282-T-C

66835142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93736488-G-A

66835142-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93736488-G-C

http://identifiers.org/hco/13/GRCh38#66835356-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#93736701-A-C

66835623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93736971-T-C

http://identifiers.org/hco/13/GRCh38#66835935-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#93737282-A-C

66836100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93737455-G-A

66837379-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93740045-G-C

66837380-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93740046-T-A

66837419-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93740084-C-G

66837429-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93740094-C-G

66837463-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93740128-T-C

66837522-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93740231-T-G

66837560-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93740280-C-G

66837587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93740307-G-A

66837600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93740320-G-A

66837649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93740369-C-T

http://identifiers.org/hco/13/GRCh38#66838032-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#93740690-A-C

http://identifiers.org/hco/13/GRCh38#66838133-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#93740791-A-C

66838133-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93740791-A-G

66838191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93740842-C-T

66838295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93740960-G-A

66838590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93741555-T-C

66838673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93741637-G-A

66838673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93741637-G-T

66838779-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93741740-A-G

66838937-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93741895-T-C

http://identifiers.org/hco/13/GRCh38#66839350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#93742014-C-A

66839350-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93742014-C-G

66839354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93742018-C-T

66839460-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93742049-A-T

66839482-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93742071-G-A

66839757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93742310-C-T

66840080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93742738-C-T

66840100-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93742756-C-G

http://identifiers.org/hco/13/GRCh38#66840162-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#93742817-A-C

66840162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93742817-A-G

66840731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93743605-T-C

66840862-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93743736-C-T

66841060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93743936-G-A

66841060-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93743936-G-C

66841143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93744018-C-T

66841418-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93744312-T-C

66841540-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93744418-C-G

66841540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93744418-C-T

66841573-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93744439-T-C

66841630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93744495-T-C

66841782-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93744609-G-T

66842323-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93744783-C-T

66842433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93744894-T-C

http://identifiers.org/hco/13/GRCh38#66842586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#93745053-C-A

66842732-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93745166-C-T

66842782-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93745218-T-G

66842848-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93745277-G-A

66842943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93745370-G-A

66843122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93745547-T-C

http://identifiers.org/hco/13/GRCh38#66843124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#93745549-C-A

66843270-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93745700-C-G

66843270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93745700-C-T

66843355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93745770-T-C

66843589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93745967-A-G

66843589-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93745967-A-T

66843606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93745984-C-T

66843690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93746067-G-A

66843788-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93746161-T-A

66843799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93746172-G-T

66843809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93746182-G-A

66844015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93746363-T-C

66844037-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93746387-A-T

66844087-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93746450-G-C

66844106-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93746466-T-G

66844122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93746482-A-G

66846676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93747223-C-T

66846773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93747324-T-C

66846796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93747348-A-G

http://identifiers.org/hco/13/GRCh38#66846910-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#93747465-A-C

66847049-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93747618-C-T

66847111-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93747847-T-A

66848057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93748148-C-T

66848146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93748241-G-A

66848235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93748327-C-T

66848316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93748400-T-C

http://identifiers.org/hco/13/GRCh38#66849097-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#93749614-C-A

66849109-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93749626-T-C

66849664-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93749901-T-A

66849695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93749930-G-A

66849872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93750090-C-T

66849949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93750153-C-T

66849976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93750180-T-C

66850555-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93750678-A-T

66850587-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93750710-T-C

http://identifiers.org/hco/13/GRCh38#66851085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#93751207-C-A

66851085-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93751207-C-T

66851167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93751287-C-T

66851217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93751336-A-G

http://identifiers.org/hco/13/GRCh38#66851242-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#93751361-A-C

66851271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93751392-C-T

66851354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93751469-A-G

http://identifiers.org/hco/13/GRCh38#66851405-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#93751522-A-C

66853083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93752197-T-C

66853126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93752236-A-G

66853155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93752253-G-A

66854239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93753111-C-T

66854372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93753262-C-T

http://identifiers.org/hco/13/GRCh38#66854410-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#93753332-C-A

66854632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93753563-T-C

66854651-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93753581-T-C

http://identifiers.org/hco/13/GRCh38#66854691-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#93753617-C-A

66854889-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93753808-A-G

66854890-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93753809-T-C

66854909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93753831-T-C

66854938-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93753860-C-G

http://identifiers.org/hco/13/GRCh38#66855017-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#93753935-C-A

66855637-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93754618-A-G

66855883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93754884-A-G

66855883-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93754884-A-T

http://identifiers.org/hco/13/GRCh38#66855886-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#93754887-A-C

66855886-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93754887-A-G

66855985-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93754975-T-A

66855989-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93754979-T-A

http://identifiers.org/hco/13/GRCh38#66856403-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#93755388-A-C

66856416-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93755401-A-T

66856500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93755486-T-C

66856536-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93755517-T-C

66856699-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93755678-C-T

66856745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93755723-C-T

66856760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93755738-A-G

66856783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93755753-G-A

66857456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93757278-T-C

http://identifiers.org/hco/13/GRCh38#66857501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#93757315-C-A

66857501-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93757315-C-G

66857609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93757413-T-C

http://identifiers.org/hco/13/GRCh38#66857698-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#93757539-A-C

66857903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93757750-C-T

66857904-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93757751-C-G

66857957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93757803-C-T

66857990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93757839-C-T

66858095-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93757950-T-C

66858255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93758138-G-T

66858573-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93758438-C-T

http://identifiers.org/hco/13/GRCh38#66858592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#93758472-C-A

66859182-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93759023-G-T

66859247-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93759117-A-T

66859259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93759129-A-G

66859363-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93759233-T-C

66859369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93759239-C-T

66859440-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93759308-G-T

66859590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93759458-G-A

66859948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93759880-C-T

66859966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93759895-G-T

66860177-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93760082-G-C

66860323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93760201-G-A

66860781-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93760637-G-T

66860974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93760829-A-G

66861088-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93760943-G-A

66861156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93761012-C-T

66861179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93761035-A-G

66861184-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93761040-T-C

66861376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93761202-A-G

66861473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93761310-C-T

66861504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93761341-C-T

66861701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93761538-A-G

66861780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93761617-C-T

66861805-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93761642-T-A

66861895-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93761731-C-T

http://identifiers.org/hco/13/GRCh38#66862035-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#93761880-C-A

66862055-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93761982-T-C

66862136-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93762075-C-T

66862180-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93762142-T-C

66862305-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93762252-T-G

66862369-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93762312-A-G

66862381-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93762324-G-C

66864773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93763382-A-G

66864809-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93763416-G-A

66867178-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93765701-A-T

http://identifiers.org/hco/13/GRCh38#66867255-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#93765779-A-C

66867469-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93765999-A-G

66868079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93767398-G-A

66868198-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93767516-T-A

66868232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93767546-A-G

66868232-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93767546-A-T

66868341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93767654-G-A

66868360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93767673-A-G

66868374-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93767689-A-T

66868513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93767834-G-A

66868655-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93767972-T-A

66868725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93768041-T-C

http://identifiers.org/hco/13/GRCh38#66868750-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#93768066-A-C

66868912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93768211-C-T

66868938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93768237-A-G

http://identifiers.org/hco/13/GRCh38#66869385-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#93768698-C-A

66869420-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93768732-T-C

66869653-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93768963-T-A

66869750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93769042-C-T

66869899-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93769178-G-C

66875076-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93771983-T-C

66875076-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93771983-T-G

66875337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93772314-C-T

66875526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93772502-C-T

http://identifiers.org/hco/13/GRCh38#66875749-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#93772725-C-A

66875759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93772735-T-C

66875807-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93772782-C-T

http://identifiers.org/hco/13/GRCh38#66875850-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#93772827-A-C

66876208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93773184-A-G

66876277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93773276-G-A

66876415-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93773390-T-A

66876419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93773394-G-A

66876443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93773418-G-A

66876664-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93773604-A-T

66877057-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93773991-T-A

66877057-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93773991-T-C

66877400-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93774172-A-T

66877528-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93774278-C-G

66877894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93774646-C-T

66878033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93774785-A-G

http://identifiers.org/hco/13/GRCh38#66878719-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#93775109-A-C

66878879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93775265-A-G

66881685-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93775579-T-C

66881710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93775604-A-G

66881715-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93775609-T-C

66882033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93776906-A-G

66882057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93776929-G-T

66882061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93776933-T-C

66882163-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93777049-C-G

66882527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93777366-T-C

66882535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93777374-C-T

66882582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93777422-T-C

66882861-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93777687-T-A

66882861-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93777687-T-C

66882861-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93777687-T-G

66882916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93777742-T-C

http://identifiers.org/hco/13/GRCh38#66883016-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#93777845-A-C

66883466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93778497-C-T

66883610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93778638-T-C

66884207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93778913-G-A

66884463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93779167-C-T

66884538-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93779231-A-T

66884542-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93779235-G-C

66884706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93779397-T-C

http://identifiers.org/hco/13/GRCh38#66885951-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#93780586-C-A

http://identifiers.org/hco/13/GRCh38#66886048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#93780689-C-A

66886048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 93780689-C-T

66886153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93780795-T-C

66886300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93781008-G-A

66886324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93781031-A-G

66886328-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93781035-A-G

66886344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93781051-C-T

66886547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93781256-A-G

http://identifiers.org/hco/13/GRCh38#66886896-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#93781597-C-A

66887138-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93781781-T-A

66887229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93781871-T-C

66887250-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93781891-T-A

66887250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93781891-T-C

66887257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93781898-T-C

66887314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93781954-G-A

66887750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93782349-T-C

66887885-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93782483-C-G

66888118-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93782722-G-A

66888592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93782808-G-A

66888636-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93782848-G-A

66888742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93782936-G-A

66888968-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93783170-G-C

http://identifiers.org/hco/13/GRCh38#66889259-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#93783462-A-C

66889338-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93783543-G-T

http://identifiers.org/hco/13/GRCh38#66889457-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#93783661-A-C

66889457-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93783661-A-T

66889581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93783780-T-C

66889931-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93784126-T-C

66889933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93784128-T-C

66890114-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93784295-A-T

66890356-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93784532-T-G

http://identifiers.org/hco/13/GRCh38#66890380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#93784556-C-A

66890504-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93784726-G-T

66890533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93784796-T-C

66890580-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93784845-T-G

66890889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93785151-C-T

66891241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93785412-G-T

66891376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93785608-A-G

http://identifiers.org/hco/13/GRCh38#66891442-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#93785674-A-C

66893024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93788616-A-G

66893347-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93789087-C-G

66893933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93789617-G-T

66894175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93789831-A-G

66894472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93790086-C-T

66894636-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93790190-T-A

66894681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93790245-T-C

66895294-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93790774-C-T

66895769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93791210-T-C

http://identifiers.org/hco/13/GRCh38#66895884-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#93791325-C-A

66895902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93791343-C-T

66895904-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93791345-G-A

66896143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93791584-G-A

66896422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93791852-G-A

66896590-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93791947-G-A

66897031-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93792296-A-T

66897179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93792430-G-A

66897179-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93792430-G-T

66897187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93792438-G-A

http://identifiers.org/hco/13/GRCh38#66897348-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#93792558-A-C

66898731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93792742-A-G

66898740-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93792760-T-G

http://identifiers.org/hco/13/GRCh38#66898744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#93792763-C-A

66898862-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93792851-G-A

66898956-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93792929-G-T

66899360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93793337-G-A

66899632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93793714-G-A

66899736-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93793819-T-A

66899893-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93793984-G-A

66899893-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93793984-G-T

66899901-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93793992-A-G

66900007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93794108-C-T

66900046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93794147-G-A

66900080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93794188-A-G

66900097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93794208-T-C

66900253-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93794356-C-T

http://identifiers.org/hco/13/GRCh38#66900365-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#93794441-A-C

66900463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93794522-A-G

66901026-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93795055-A-G

http://identifiers.org/hco/13/GRCh38#66901049-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#93795078-C-A

66901356-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93795464-T-A

66901410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93795529-C-T

66901751-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93795819-T-A

66902119-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93796576-G-C

66902161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93796614-A-G

66902209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93796665-A-G

66902215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93796671-A-G

66902605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93797082-C-T

http://identifiers.org/hco/13/GRCh38#66902886-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#93797314-C-A

66902971-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93797382-A-G

66903001-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93797412-G-A

66903031-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93797446-T-A

66903031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93797446-T-C

66903064-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93797478-T-G

66903105-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93797516-C-T

66903219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93797633-T-C

66903263-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93797674-T-C

http://identifiers.org/hco/13/GRCh38#66903303-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#93797712-C-A

66903319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93797728-T-C

66903324-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93797733-C-T

http://identifiers.org/hco/13/GRCh38#66903352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#93797756-C-A

66903429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93797837-G-A

66903429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93797837-G-T

66903488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93797897-T-C

66903492-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93797901-T-A

66903492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93797901-T-C

66903500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93797908-A-G

66903552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93797960-G-A

66903552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 93797960-G-T

66903651-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93798059-G-C

66903664-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93798072-G-A

66903664-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93798072-G-C

66903664-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93798072-G-T

http://identifiers.org/hco/13/GRCh38#66903687-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#93798095-C-A

66903687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93798095-C-T

66904240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93798253-G-A

66904251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93798265-T-C

66904259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93798282-A-G

66904274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93798297-A-G

66904329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93798353-C-T

66904435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93798465-T-C

66904857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93798651-T-C

66904866-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93798660-A-G

66904923-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93798711-T-A

66904923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93798711-T-C

http://identifiers.org/hco/13/GRCh38#66905424-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#93799216-A-C

66905462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93799254-T-C

66905462-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93799254-T-G

66906217-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93799551-G-C

66906575-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93799920-G-A

66906619-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93799964-C-T

66906628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93799973-G-A

66906739-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93800085-G-A

http://identifiers.org/hco/13/GRCh38#66906786-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#93800130-A-C

66907301-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93800312-T-C

66907302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93800313-G-A

66907554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93800561-T-C

66907881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93800887-A-G

66907972-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93800973-A-T

66908142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93801216-T-C

http://identifiers.org/hco/13/GRCh38#66908244-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#93801314-A-C

66908304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93801356-A-G

66908374-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93801422-C-T

66909853-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93804545-C-T

66910013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93804709-A-G

66910024-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93804720-T-G

66910055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93804765-C-T

66910072-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93804790-G-C

66910145-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93804858-C-G

66910403-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93805126-T-G

66910412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93805135-G-A

66910412-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93805135-G-C

66910594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93805303-G-A

66910670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93805377-T-C

66910849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93805553-C-T

66910904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93805607-T-C

66911042-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93805751-A-T

66911141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93805849-A-G

66911422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93806126-T-C

66911462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93806160-T-C

66911743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93806436-C-T

66911890-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93806572-G-T

66912197-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93806881-T-A

66912257-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93806941-C-T

66912352-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93807047-C-G

66912926-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93807449-T-C

66912938-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93807461-T-G

66913230-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93807747-G-C

66913292-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93807791-T-A

66913724-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93807944-A-T

66913811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93807993-A-G

66914178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93808308-T-C

66914614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93809017-T-C

66914616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93809019-T-C

http://identifiers.org/hco/13/GRCh38#66914747-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#93809197-A-C

66914841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 93809297-A-G

66915008-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 93809437-T-A

66915008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 39896
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 93809437-T-C