http://identifiers.org/hco/4/GRCh38#75724707-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92285845-A-C

75724707-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: 5 prime UTR variant
orthologous variants: 92285845-A-G

http://identifiers.org/hco/4/GRCh38#75724747-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#92285885-C-A

75724747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 92285885-C-T

75724930-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92286045-G-C

http://identifiers.org/hco/4/GRCh38#75725110-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92286140-C-A

75725110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92286140-C-T

75725306-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92286259-A-T

75726744-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92287238-C-G

75726818-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92287312-A-G

75726985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92287456-A-G

75727081-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92287551-C-G

75727081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92287551-C-T

75727150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92287602-A-G

75727309-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92287764-A-T

75727370-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92287823-G-T

75727605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92287988-A-G

75728270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92289843-G-A

75728684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92289935-A-G

75729229-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92290173-T-A

75729229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92290173-T-C

75729705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92290252-A-G

75729861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92290400-A-G

75729897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92290436-T-C

http://identifiers.org/hco/4/GRCh38#75729904-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92290444-A-C

75730381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92291003-T-C

75730874-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92291948-C-T

75731206-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92292209-T-A

75731216-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92292214-A-G

75731234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92292232-A-G

75731789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92292525-A-G

75731794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92292530-G-A

75736922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92293786-A-G

75736954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92293817-A-G

75737073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92293924-A-G

75740608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92296264-C-T

75740672-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92296321-T-A

75740672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92296321-T-C

75740691-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92296340-T-C

75740705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92296354-G-A

75740722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92296373-A-G

75740835-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92296496-T-C

75740950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92296573-A-G

75740954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92296577-A-G

75740976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92296595-G-A

75746112-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92297163-G-C

75746112-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92297163-G-T

http://identifiers.org/hco/4/GRCh38#75746245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92297268-C-A

75746245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92297268-C-T

75746490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92297455-G-A

75746556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92297501-G-A

http://identifiers.org/hco/4/GRCh38#75746629-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92297566-C-A

75746651-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92297590-A-T

75746665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92297604-T-C

75746665-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92297604-T-G

75746759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92297707-G-A

75749117-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92298461-T-G

75749244-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92298567-A-G

75752178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92299909-T-C

75752253-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92300178-G-C

75752338-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92300265-T-A

http://identifiers.org/hco/4/GRCh38#75754386-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92301631-A-C

75754386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92301631-A-G

75755516-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: -G-T

75755583-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: -G-C

75755606-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: -C-T

75755849-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: -C-G

75756982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92305383-C-T

75757036-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92305429-G-T

75757374-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92306129-G-T

75757430-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92306195-T-A

75757430-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92306195-T-C

75757554-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: missense variant
orthologous variants: 92306320-T-A

75757554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: synonymous variant
orthologous variants: 92306320-T-C

75757602-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92306370-T-C

75757653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92306412-G-A

75757653-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92306412-G-T

75757783-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92306550-A-T

75757855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92307018-A-G

75757967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92307128-T-C

75758221-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92307378-T-C

75760371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92309147-T-C

75760437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92309213-G-T

75760461-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92309244-A-T

75764117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92311458-A-G

75764319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92311641-C-T

75769979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92313912-G-T

75770028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92313950-C-T

75770077-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92314007-A-T

75770239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 92314196-A-G

75770239-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 92314196-A-T

75770503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 92314454-G-A

75770503-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 92314454-G-T

75770559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92314510-G-A

75770663-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92314651-G-T

75770758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92314820-A-G

75770793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92314856-G-A

http://identifiers.org/hco/4/GRCh38#75770972-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92315030-C-A

75770999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92315049-G-A

75771002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92315052-T-C

75771170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92315219-A-G

75771186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92315237-T-C

http://identifiers.org/hco/4/GRCh38#75771191-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92315242-C-A

75771191-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92315242-C-G

75771191-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92315242-C-T

75771192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92315243-A-G

75771224-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92315270-T-G

http://identifiers.org/hco/4/GRCh38#75771432-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92315321-A-C

75771586-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92315467-C-T

75771643-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92315515-A-G

75773198-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92316445-A-T

75773373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92316623-A-G

75774148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92318060-A-G

75774217-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92318127-G-C

75774251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92318166-G-A

75774607-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92318463-T-C

75774607-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92318463-T-G

http://identifiers.org/hco/4/GRCh38#75777552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92320163-C-A

75777637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92320245-G-T

75777685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92320288-A-G

75777826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92320405-G-A

75777919-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92320500-T-C

75777965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92320541-C-T

75778001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92320577-A-G

75778055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92320625-A-G

http://identifiers.org/hco/4/GRCh38#75782446-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92321618-A-C

75782446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92321618-A-G

http://identifiers.org/hco/4/GRCh38#75782728-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92321833-A-C

75782855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: synonymous variant
orthologous variants: 92321960-A-G

75782855-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: synonymous variant
orthologous variants: 92321960-A-T

75782927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92322031-C-T

http://identifiers.org/hco/4/GRCh38#75782980-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92322080-A-C

75786247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92324469-A-G

75786315-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92324514-T-A

75786497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92324662-T-C

75786819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92324965-A-G

http://identifiers.org/hco/4/GRCh38#75786957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92325093-C-A

75786957-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92325093-C-G

75786957-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92325093-C-T

75786970-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92325106-T-G

75787299-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92325511-A-T

75787528-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92326805-T-A

75787552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92326831-T-C

75787634-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92326913-T-G

75787821-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92327429-T-A

75788145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92327736-C-T

75788159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92327750-A-G

75788159-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92327750-A-T

75790083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92328337-T-C

75790129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92328382-T-C

http://identifiers.org/hco/4/GRCh38#75790273-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92328524-A-C

75790294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92328538-A-G

75790326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92328595-A-G

75790488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92328962-T-C

75790495-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92328979-G-A

75790495-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92328979-G-C

http://identifiers.org/hco/4/GRCh38#75790498-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92328982-A-C

75790498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92328982-A-G

75790525-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92329075-A-G

http://identifiers.org/hco/4/GRCh38#75790528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92329078-C-A

75790528-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92329078-C-T

75790552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92329106-T-C

75790587-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92329152-C-T

75793727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: synonymous variant
orthologous variants: 92329794-T-C

75793790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: synonymous variant
orthologous variants: 92329857-G-A

75793790-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: synonymous variant
orthologous variants: 92329857-G-C

75793943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92330000-G-A

75794078-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92330124-T-C

75794106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92330150-C-T

75794420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92330422-G-A

75794511-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92330478-G-T

75794538-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92330502-C-T

75794574-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92330534-T-C

75794691-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92330680-C-T

75794783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92330867-C-T

75794951-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92331033-A-G

75795085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92331147-G-T

75795243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92331257-G-A

75795248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92331258-T-C

75796162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92332169-A-G

http://identifiers.org/hco/4/GRCh38#75796717-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92333304-C-A

http://identifiers.org/hco/4/GRCh38#75796914-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92333488-C-A

75796914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92333488-C-T

75797310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92333943-A-G

http://identifiers.org/hco/4/GRCh38#75797511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92334128-C-A

75797511-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92334128-C-G

75797511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92334128-C-T

http://identifiers.org/hco/4/GRCh38#75797553-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92334179-C-A

75797553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92334179-C-T

75799414-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92334890-T-G

75799456-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92334930-A-G

75799480-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92334953-A-T

75799487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92334960-T-C

75799562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92335035-A-G

75800513-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92335717-T-A

75800513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92335717-T-C

75800513-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92335717-T-G

http://identifiers.org/hco/4/GRCh38#75800610-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92335794-C-A

75800821-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92336006-G-T

75801017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92336200-C-T

75801104-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: synonymous variant
orthologous variants: 92337107-G-A

75801163-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: missense variant
orthologous variants: 92337166-A-G

75801230-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92337229-T-A

75801230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92337229-T-C

75801260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92337254-G-A

75801260-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92337254-G-T

75801270-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92337263-T-A

75801270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92337263-T-C

http://identifiers.org/hco/4/GRCh38#75801310-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92337304-C-A

http://identifiers.org/hco/4/GRCh38#75801315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92337309-C-A

75801315-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92337309-C-G

75801316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92337310-A-G

75801684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92338948-C-T

75801808-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92338980-A-G

75802218-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92339074-T-A

75802469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92339253-T-C

75803985-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92340432-A-T

75804027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92340478-A-G

75804027-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92340478-A-T

75804064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92340499-A-G

75804067-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92340507-A-G

75804096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92340535-A-G

http://identifiers.org/hco/4/GRCh38#75804143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92340581-C-A

75804220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: synonymous variant
orthologous variants: 92340658-A-G

75804340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92340747-A-G

http://identifiers.org/hco/4/GRCh38#75804375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92340779-C-A

75804375-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92340779-C-G

75804863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92341637-G-A

http://identifiers.org/hco/4/GRCh38#75804921-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92341694-C-A

75804921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92341694-C-T

75805066-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 92341798-T-A

75805066-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 92341798-T-C

75805201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 92341932-A-G

http://identifiers.org/hco/4/GRCh38#75805225-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92341956-A-C

http://identifiers.org/hco/4/GRCh38#75806346-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92343072-C-A

75806346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92343072-C-T

75806384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92343110-G-A

75806384-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92343110-G-T

75806387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92343113-A-G

75806569-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: synonymous variant
orthologous variants: 92343290-A-G

75806632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92343316-G-A

75806632-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92343316-G-C

75806632-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92343316-G-T

75806671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92343358-G-A

http://identifiers.org/hco/4/GRCh38#75806677-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92343364-A-C

75806677-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92343364-A-G

75808190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92345486-G-A

75808205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92345501-G-A

75808374-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92345641-T-C

75808385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92345649-A-G

75808567-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92345805-C-T

75808594-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92345830-T-C

75808594-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92345830-T-G

75808667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92345915-G-A

75808729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92345977-G-T

75808766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92346030-G-T

75808772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92346036-G-T

75809089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92346330-G-A

75809089-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92346330-G-T

75809098-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92346339-G-T

http://identifiers.org/hco/4/GRCh38#75809116-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92346355-C-A

75809374-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92346705-T-G

75809669-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92347054-G-C

75810179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92347450-T-C

75810232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92347492-A-G

http://identifiers.org/hco/4/GRCh38#75810293-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92347554-C-A

75810293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92347554-C-T

75810357-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92347613-A-G

75810424-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 92347668-A-T

75810512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: synonymous variant
orthologous variants: 92347756-A-G

75810668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92347872-T-C

75811492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92348071-A-G

75811563-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92348156-T-G

75811613-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92348257-A-G

75811621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92348265-C-T

75811853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92348509-G-T

75812210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: synonymous variant
orthologous variants: 92349044-G-A

75812210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: synonymous variant
orthologous variants: 92349044-G-T

75812509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92349323-A-G

75812633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: intron variant
orthologous variants: 92349436-A-G

75813265-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: missense variant
orthologous variants: 92349769-A-T

75813308-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: 3 prime UTR variant
orthologous variants: 92349807-T-G

http://identifiers.org/hco/4/GRCh38#75813507-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92349992-C-A

75813507-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: 3 prime UTR variant
orthologous variants: 92349992-C-G

75813611-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: 3 prime UTR variant
orthologous variants: 92350095-T-G

75813636-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: 3 prime UTR variant
orthologous variants: 92350119-A-G

75813642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: 3 prime UTR variant
orthologous variants: 92350125-A-G

75813779-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: 3 prime UTR variant
orthologous variants: 92350247-T-A

75813786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: 3 prime UTR variant
orthologous variants: 92350252-C-T

http://identifiers.org/hco/4/GRCh38#75813787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#92350253-C-A

75813787-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: 3 prime UTR variant
orthologous variants: 92350253-C-G

75813836-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: 3 prime UTR variant
orthologous variants: 92350302-T-G

75813857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: 3 prime UTR variant
orthologous variants: 92350321-A-G

75813911-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: 3 prime UTR variant
orthologous variants: 92350363-T-C

75813922-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: 3 prime UTR variant
orthologous variants: 92350374-T-C

75813940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: 3 prime UTR variant
orthologous variants: 92350388-A-G

75813977-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: 3 prime UTR variant
orthologous variants: 92350424-A-G

75814252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30904
most severe consequence: 3 prime UTR variant
orthologous variants: 92350699-A-G