179944938-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: 3 prime UTR variant
orthologous variants: 77726172-T-A

179945079-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: 3 prime UTR variant
orthologous variants: 77726308-T-A

179945079-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: 3 prime UTR variant
orthologous variants: 77726308-T-C

179945082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: 3 prime UTR variant
orthologous variants: 77726311-G-A

179945082-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: 3 prime UTR variant
orthologous variants: 77726311-G-T

179945091-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: 3 prime UTR variant
orthologous variants: 77726320-G-T

179945100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: 3 prime UTR variant
orthologous variants: 77726329-G-T

179945209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 77726431-T-C

179945225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 77726447-T-C

179945236-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 77726458-C-G

179945236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 77726458-C-T

179945388-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 77726610-C-G

179945405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 77726624-A-G

179945427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 77726646-A-G

179945498-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 77726708-T-C

179945501-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 77726711-T-A

179945525-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 77726735-C-G

179945789-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77726993-T-A

179945789-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77726993-T-G

179947140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77727627-T-C

179947291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77727752-T-C

http://identifiers.org/hco/2/GRCh38#179947712-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#77728143-A-C

179947808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77728243-G-A

179947900-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77728318-T-C

179947916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77728325-T-C

179950375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77734048-A-G

http://identifiers.org/hco/2/GRCh38#179950376-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#77734049-C-A

179950376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77734049-C-T

179950518-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron_variant, missense_variant
orthologous variants: 77734164-C-G

179950518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron_variant, missense_variant
orthologous variants: 77734164-C-T

179950548-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron_variant, missense_variant
orthologous variants: 77734197-C-T

179950555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 77734204-T-C

179950579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 77734228-A-G

179950603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 77734252-G-A

179950603-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 77734252-G-C

179951004-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77734639-T-C

179951012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77734647-A-G

179951069-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77734698-T-G

179951075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77734704-A-G

179951099-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77734721-A-T

179951214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77734797-C-T

179951243-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77734825-T-A

179951243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77734825-T-C

179951251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77734833-C-T

179951266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77734851-T-C

179951302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77734879-T-C

179951304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77734881-T-C

179951312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77734889-C-T

http://identifiers.org/hco/2/GRCh38#179952402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#77735630-C-A

179952402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77735630-C-T

179952442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77735669-G-A

179952442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77735669-G-T

179952452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77735682-T-C

179952452-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77735682-T-G

179952453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77735683-G-A

179952453-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77735683-G-C

179952453-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77735683-G-T

179952479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: synonymous variant
orthologous variants: 77735709-T-C

http://identifiers.org/hco/2/GRCh38#179952487-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#77735717-C-A

179952487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: missense variant
orthologous variants: 77735717-C-T

179952698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77735926-T-C

179952729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77735954-G-A

179952729-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77735954-G-T

179952796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77736031-G-T

179953062-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77736300-A-G

179954084-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77737289-G-T

179954163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77737384-G-A

179954163-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77737384-G-C

179954163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77737384-G-T

179954247-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: synonymous_variant, undefined
orthologous variants: 77737468-C-T

179954378-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77737606-A-T

http://identifiers.org/hco/2/GRCh38#179954481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#77737696-C-A

179954828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77738250-G-A

http://identifiers.org/hco/2/GRCh38#179954854-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#77738278-C-A

179954854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77738278-C-T

179955044-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77738499-A-G

179955071-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77738527-A-T

179955156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77738609-T-C

http://identifiers.org/hco/2/GRCh38#179955362-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#77738791-A-C

179955527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77738921-G-A

179956098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77739551-T-C

179956501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77739890-C-T

179956918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77740260-G-A

179956933-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77740275-A-G

179957510-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77740824-G-C

179957897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77741130-T-C

179958933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77741765-G-T

http://identifiers.org/hco/2/GRCh38#179958954-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#77741782-C-A

179958967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77741795-T-C

http://identifiers.org/hco/2/GRCh38#179958983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#77741811-C-A

179958983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77741811-C-T

http://identifiers.org/hco/2/GRCh38#179959262-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#77742055-A-C

179959356-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77742134-G-C

179959356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77742134-G-T

179962250-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77743878-T-A

http://identifiers.org/hco/2/GRCh38#179963163-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#77744890-C-A

179963189-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77744917-T-C

179963705-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77745079-A-G

179963711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77745085-T-C

179963731-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron_variant, undefined
orthologous variants: 77745100-T-A

179963922-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77745274-C-T

179964062-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77745404-G-C

179964102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77745445-A-G

179964218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77745531-T-C

179964233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77745545-C-T

179964301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77745608-A-G

179964443-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77745756-T-A

179964443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77745756-T-C

http://identifiers.org/hco/2/GRCh38#179964497-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#77745809-C-A

179964497-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77745809-C-G

179964497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77745809-C-T

179964700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77746005-G-T

http://identifiers.org/hco/2/GRCh38#179964701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#77746006-C-A

http://identifiers.org/hco/2/GRCh38#179964707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#77746012-C-A

179964707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77746012-C-T

http://identifiers.org/hco/2/GRCh38#179964736-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#77746038-A-C

179964736-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77746038-A-T

179964747-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77746048-T-A

179964747-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77746048-T-C

179964759-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77746060-T-A

http://identifiers.org/hco/2/GRCh38#179965100-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#77746459-C-A

179965757-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77747289-T-G

179965772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77747309-G-A

179965772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77747309-G-T

179965824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77747356-T-C

179965894-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: synonymous variant
orthologous variants: 77747419-T-G

179965906-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: synonymous variant
orthologous variants: 77747431-T-C

179966048-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77747576-A-T

http://identifiers.org/hco/2/GRCh38#179966106-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#77747612-A-C

179967311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77748709-T-C

179967403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77748796-A-G

179967465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77748858-A-G

179967940-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77749301-A-T

http://identifiers.org/hco/2/GRCh38#179967956-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#77749317-A-C

http://identifiers.org/hco/2/GRCh38#179968531-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#77749870-A-C

179968905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77749933-T-C

179969249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77750269-G-A

179969250-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77750270-G-A

179969250-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77750270-G-C

179969254-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77750274-A-T

179969805-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77750582-T-G

179969913-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77750661-T-A

179970230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77750927-T-C

179970230-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77750927-T-G

179970382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77751058-C-T

179970425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77751097-T-C

179970442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77751113-T-C

179970490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77751151-A-G

179970581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77751243-G-A

179970581-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77751243-G-C

179970581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77751243-G-T

179970593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77751257-T-C

179970593-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77751257-T-G

179970831-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: synonymous variant
orthologous variants: 77751492-A-G

http://identifiers.org/hco/2/GRCh38#179971035-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#77751848-C-A

179971038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: synonymous variant
orthologous variants: 77751851-G-A

179971038-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: synonymous variant
orthologous variants: 77751851-G-C

179971142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77751957-A-G

http://identifiers.org/hco/2/GRCh38#179971169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#77751982-C-A

179971169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77751982-C-T

179971173-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77751986-A-T

179972020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77752857-T-C

179973138-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77754429-A-G

http://identifiers.org/hco/2/GRCh38#179973141-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#77754432-C-A

179973141-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77754432-C-G

179973141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77754432-C-T

179973160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77754451-G-A

179973160-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77754451-G-T

http://identifiers.org/hco/2/GRCh38#179973168-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#77754459-C-A

179973168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77754459-C-T

179973500-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77754738-T-G

http://identifiers.org/hco/2/GRCh38#179973513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#77754752-C-A

179973513-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77754752-C-G

179973513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77754752-C-T

179973745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: synonymous variant
orthologous variants: 77754942-A-G

http://identifiers.org/hco/2/GRCh38#179973813-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#77755010-A-C

179973813-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77755010-A-T

http://identifiers.org/hco/2/GRCh38#179973917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#77755102-C-A

179973917-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77755102-C-G

179974023-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77755205-A-T

179975750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77756218-T-C

179975839-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77756266-C-T

179976218-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77756485-G-C

179976644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77756833-T-C

179976806-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77756987-T-C

179977803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77757191-A-G

179977866-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77757242-T-A

179977943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77757319-G-A

http://identifiers.org/hco/2/GRCh38#179979295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#77758105-C-A

179979332-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77758141-T-A

179979496-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77758303-A-G

179979501-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77758308-T-C

179979587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77758371-G-A

179979838-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77758650-C-T

179979892-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77758695-T-A

179981535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77759389-T-C

179981614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77759467-G-A

179981614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77759467-G-T

http://identifiers.org/hco/2/GRCh38#179981653-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#77759507-C-A

179981683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77759536-T-C

179981686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77759539-A-G

179981747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77759595-C-T

179981862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: synonymous variant
orthologous variants: 77759710-A-G

179981987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: stop gained
orthologous variants: 77759832-G-A

179981987-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: synonymous variant
orthologous variants: 77759832-G-T

179982061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77759899-G-A

179982061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77759899-G-T

http://identifiers.org/hco/2/GRCh38#179982062-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#77759900-C-A

179982062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77759900-C-T

179982146-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77759962-A-G

179982147-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77759963-G-C

http://identifiers.org/hco/2/GRCh38#179982180-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#77759995-C-A

179982180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77759995-C-T

179982286-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77760077-T-A

179982286-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77760077-T-G

179982495-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77760258-T-C

179982657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77760404-C-T

179984036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77760863-T-C

179984178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77761003-G-A

179986239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77761140-C-T

179986240-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77761141-A-T

179986301-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77761197-C-G

179986335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77761222-G-A

http://identifiers.org/hco/2/GRCh38#179986362-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#77761250-C-A

179986602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77761482-A-G

179986618-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77761499-G-C

179986618-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77761499-G-T

179986673-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77761757-G-C

179986673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77761757-G-T

179986677-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77761761-G-C

179986677-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77761761-G-T

http://identifiers.org/hco/2/GRCh38#179986735-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#77761819-A-C

179986735-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: missense variant
orthologous variants: 77761819-A-G

179986812-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 77761896-T-A

179986812-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 77761896-T-C

179986838-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77761920-T-A

179986993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77762069-C-T

179987178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77762216-G-A

179987290-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77762306-T-A

179987290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77762306-T-C

http://identifiers.org/hco/2/GRCh38#179987395-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#77762396-A-C

179990305-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77763847-T-A

179990505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77764057-A-G

http://identifiers.org/hco/2/GRCh38#179991074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#77764529-C-A

179991841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77765081-T-C

179992518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77765685-C-T

179992535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77765696-C-T

179993038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77766173-C-T

179993049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77766184-G-T

http://identifiers.org/hco/2/GRCh38#179993393-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#77767005-A-C

179993393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: 5 prime UTR variant
orthologous variants: 77767005-A-G

179993395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: 5 prime UTR variant
orthologous variants: 77767007-A-G

http://identifiers.org/hco/2/GRCh38#179993412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#77767024-C-A

179993626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77767245-C-T

179993701-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77767307-A-T

179994020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77767566-G-A

http://identifiers.org/hco/2/GRCh38#179994051-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#77767597-A-C

179994286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77768099-G-A

179994311-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77768124-G-C

179998628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77769313-A-G

179998783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77769441-G-A

179998825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77769470-C-T

179998873-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77769513-T-C

179999084-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77769700-G-A

179999084-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77769700-G-T

179999207-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77769827-C-T

179999262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77769884-T-C

179999262-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77769884-T-G

179999274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77769896-A-G

http://identifiers.org/hco/2/GRCh38#179999427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#77770049-C-A

179999580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77770206-T-C

179999580-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77770206-T-G

180000686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77770683-T-C

180000688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77770685-T-C

180000807-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77770819-G-A

180001474-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77771068-G-A

180001740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77771280-T-C

180002630-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77772961-T-C

180002743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77773057-C-T

180003407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77774107-T-C

http://identifiers.org/hco/2/GRCh38#180003840-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#77774507-C-A

180003840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77774507-C-T

180003913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: intron variant
orthologous variants: 77774630-T-C

http://identifiers.org/hco/2/GRCh38#180007025-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#77776449-C-A

180007046-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 77776470-G-T

180007136-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29322
most severe consequence: 5 prime UTR variant
orthologous variants: 77776551-A-G