143577359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81422204-A-G

http://identifiers.org/hco/4/GRCh38#143577394-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#81422175-C-A

http://identifiers.org/hco/4/GRCh38#143577415-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#81422156-C-A

143577429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81422146-G-T

143577460-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81422115-A-G

143577460-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81422115-A-T

http://identifiers.org/hco/4/GRCh38#143577497-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#81422094-C-A

143577511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 81422080-T-C

143577664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81421942-T-C

143577698-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 81421908-T-A

143577698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 81421908-T-C

143577781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81421825-C-T

http://identifiers.org/hco/4/GRCh38#143578055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#81421589-C-A

143578055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81421589-C-T

143578283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81421418-A-G

143578560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81421140-A-G

143579670-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81419809-G-C

143579753-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81419724-C-G

143579753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81419724-C-T

143580040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81419430-A-G

143580041-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81419429-C-G

143585503-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81418179-G-A

143585503-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81418179-G-C

143585745-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81417547-G-T

http://identifiers.org/hco/4/GRCh38#143585751-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#81417541-C-A

143585751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81417541-C-T

http://identifiers.org/hco/4/GRCh38#143585784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#81417508-C-A

http://identifiers.org/hco/4/GRCh38#143585808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#81417484-C-A

143585904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81417388-G-T

http://identifiers.org/hco/4/GRCh38#143585913-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#81417379-C-A

143585913-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81417379-C-G

143585913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81417379-C-T

http://identifiers.org/hco/4/GRCh38#143585975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#81417317-C-A

143585975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81417317-C-T

143585986-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 81417306-G-T

http://identifiers.org/hco/4/GRCh38#143586070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#81417216-C-A

http://identifiers.org/hco/4/GRCh38#143586091-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#81417197-C-A

143586116-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81417172-T-A

143586116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81417172-T-C

143586280-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81416824-T-C

143586678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81416518-C-T

143586862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81416264-A-G

http://identifiers.org/hco/4/GRCh38#143586897-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#81416137-C-A

143586950-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81416072-A-T

143587172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81415800-G-A

143587425-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81415531-G-C

143587426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81415530-G-A

http://identifiers.org/hco/4/GRCh38#143587675-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#81415173-C-A

143587712-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81415141-A-G

143587869-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81414996-C-T

143587903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 81414952-G-A

143587928-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81414927-C-G

143611291-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81413730-C-T

143611341-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 81413680-C-T

143611530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 81413488-A-G

143611555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81413473-G-A

143611567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81413461-A-G

143611575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81413453-C-T

143611742-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81410737-A-G

143617049-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81401388-G-A

143617285-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81401150-A-T

143617529-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81400983-T-A

143620309-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81396581-G-A

http://identifiers.org/hco/4/GRCh38#143620523-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#81396422-A-C

143620728-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81396256-A-T

143620776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81396227-C-T

http://identifiers.org/hco/4/GRCh38#143620848-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#81396156-C-A

143620848-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81396156-C-G

http://identifiers.org/hco/4/GRCh38#143620872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#81396126-C-A

143620905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81396088-A-G

143620907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81396086-G-T

143620913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81396080-T-C

143620928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81396065-T-C

143620939-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81396049-A-G

143620939-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81396049-A-T

143621017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81395976-G-A

143621057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81395936-A-G

143621190-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81395803-C-G

143621190-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81395803-C-T

143621228-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81395763-T-C

143621292-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81395698-A-G

143624122-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81395584-A-G

http://identifiers.org/hco/4/GRCh38#143624130-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#81395576-A-C

143624230-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81395476-C-T

143624384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81395324-A-G

http://identifiers.org/hco/4/GRCh38#143624468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#81395239-C-A

143624468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81395239-C-T

143624486-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81395222-C-T

143624541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81395098-G-A

http://identifiers.org/hco/4/GRCh38#143624726-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#81394811-A-C

143624754-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81394790-G-A

143625997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81394161-G-A

143626000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81394158-A-G

143626070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81394090-C-T

143626113-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81394043-G-T

143627062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81393096-G-A

143627091-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81393067-C-T

143627539-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81390213-T-G

143627542-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81390210-T-C

143627543-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81390209-T-C

143627563-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81390190-G-T

143627570-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81390183-T-A

143627570-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81390183-T-C

143627644-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 81390113-T-A

http://identifiers.org/hco/4/GRCh38#143627683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#81390074-C-A

143627694-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81390063-T-C

143627927-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81389883-G-T

http://identifiers.org/hco/4/GRCh38#143630371-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#81388136-A-C

143630418-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81388107-T-A

143630501-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81388026-A-G

143630603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81387923-C-T

143630855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81387712-A-G

143636506-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81386985-G-T

143636880-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81384923-T-G

143639747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81384753-A-G

http://identifiers.org/hco/4/GRCh38#143639982-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#81384532-C-A

http://identifiers.org/hco/4/GRCh38#143639983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#81384531-C-A

143640164-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81384376-G-C

143640370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81384201-A-G

143640385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81384186-A-G

143640818-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81383997-A-T

143641078-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81383565-C-G

143652980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81383055-T-C

143652998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81383044-G-A

143653000-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81383042-A-G

143653256-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81382765-T-G

143653297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81382735-G-A

143653358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81382666-A-G

143653384-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81382639-C-T

http://identifiers.org/hco/4/GRCh38#143653613-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#81381818-A-C

143653686-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81381750-C-G

143653804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81381647-G-A

143653997-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81381444-T-A

143654835-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81379192-G-A

143654835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81379192-G-T

143654934-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81379106-A-T

143655154-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81378951-T-G

http://identifiers.org/hco/4/GRCh38#143670129-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#81362042-A-C

143670143-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81362028-G-C

http://identifiers.org/hco/4/GRCh38#143670532-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#81361519-A-C

143679988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81359755-T-C

143680233-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81355876-T-G

http://identifiers.org/hco/4/GRCh38#143680427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#81355679-C-A

143680427-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81355679-C-T

143680461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81355276-T-C

143681577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81351555-C-T

http://identifiers.org/hco/4/GRCh38#143681643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#81351491-C-A

143681854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81351313-G-A

143682058-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81351156-A-T

143682126-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81351063-G-C

143690114-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81350662-G-C

143690205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81350585-G-A

143690246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81350529-C-T

143690341-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81350463-A-T

143690503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81350300-A-G

http://identifiers.org/hco/4/GRCh38#143690538-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#81350265-C-A

143690818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81348930-G-A

143691946-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81347073-T-C

143691949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81347070-T-C

143692003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81347017-A-G

143692225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81346873-G-A

http://identifiers.org/hco/4/GRCh38#143692245-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#81346856-A-C

http://identifiers.org/hco/4/GRCh38#143692517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#81346601-C-A

143692517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81346601-C-T

http://identifiers.org/hco/4/GRCh38#143693113-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, stop_gained
orthologous variants: http://identifiers.org/mco/8/GRCm39#81344924-C-A

143693113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 81344924-C-T

143693133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81344904-T-C

143693141-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 81344896-G-A

143693141-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81344896-G-T

http://identifiers.org/hco/4/GRCh38#143693152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#81344885-C-A

143693152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81344885-C-T

http://identifiers.org/hco/4/GRCh38#143693183-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#81344851-C-A

http://identifiers.org/hco/4/GRCh38#143693240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#81344793-C-A

143693240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81344793-C-T

http://identifiers.org/hco/4/GRCh38#143693267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#81344768-C-A

143693267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81344768-C-T

143694225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81344381-G-A

143694319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81344290-G-A

http://identifiers.org/hco/4/GRCh38#143694511-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#81344096-C-A

143694788-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81343668-T-C

143694824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81343632-C-T

143694870-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81343567-G-C

143695061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81343235-T-C

143695061-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81343235-T-G

143695076-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81343220-C-G

http://identifiers.org/hco/4/GRCh38#143695300-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#81343051-A-C

143695392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81342953-A-G

143695392-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81342953-A-T

http://identifiers.org/hco/4/GRCh38#143695435-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#81342923-A-C

143695435-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81342923-A-T

143695436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81342922-G-A

143695436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 81342922-G-T

143695534-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 81342818-G-T

143695538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81342814-A-G

143695596-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81342756-C-G

143695596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81342756-C-T

http://identifiers.org/hco/4/GRCh38#143695622-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#81342730-C-A

143695622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81342730-C-T

143695650-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81342702-T-C

143695701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81342651-G-A

143695701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81342651-G-T

143695759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 81342593-G-A

143695793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81342559-G-A

143695902-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81342450-G-A

143695902-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81342450-G-C

143695902-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81342450-G-T

143695941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81342411-C-T

143696024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81342328-T-C

143696165-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81342187-T-A

143696165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81342187-T-C

143696336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81342013-T-C

143696336-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81342013-T-G

143696337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81342012-T-C

143696398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 81341951-G-A

143696398-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81341951-G-C

143696408-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81341941-T-A

143696408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81341941-T-C

143696437-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 81341912-G-A

143696511-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81341841-G-C

143696526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81341826-G-A

143696549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81341803-G-A

143696603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81341749-A-G

143696616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81341736-G-A

143696650-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 81341702-G-C

143696650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 81341702-G-T

143696734-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 81341618-C-G

143696749-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 81341603-C-G

143696782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 81341570-T-C

143696783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81341569-A-G

143696792-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81341560-A-T

143697028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 81341324-A-G

143697098-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81341254-T-C

143697234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81341118-G-A

143697234-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81341118-G-T

143697445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 81340907-G-A

143697448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 81340904-C-T

143697515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81340837-T-C

143697516-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81340836-C-G

143697518-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81340834-A-G

http://identifiers.org/hco/4/GRCh38#143697538-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#81340814-C-A

143697538-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81340814-C-G

http://identifiers.org/hco/4/GRCh38#143697744-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#81340608-C-A

143697985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 81340373-G-A

143697985-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81340373-G-C

143697985-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81340373-G-T

143698047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 81340311-A-G

143698171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 81340187-T-C

143698285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 81340073-T-C

143698501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 81339854-C-T

143698590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81339765-G-T

143698634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81339721-T-C

143698688-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81339670-T-C

143698726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81339632-T-C

143698755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81339603-C-T

143698886-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 81339472-C-T

http://identifiers.org/hco/4/GRCh38#143699094-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#81339264-C-A

143699094-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81339264-C-G

143699094-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81339264-C-T

143699102-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81339256-T-A

143699102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81339256-T-C

143699102-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81339256-T-G

http://identifiers.org/hco/4/GRCh38#143699106-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#81339252-C-A

143699106-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81339252-C-G

143699106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81339252-C-T

http://identifiers.org/hco/4/GRCh38#143699114-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#81339244-A-C

143699114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81339244-A-G

143699243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81339115-T-C

143699243-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81339115-T-G

143699333-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 81339025-G-T

143699345-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81339013-A-G

143699374-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 81338984-C-G

143699385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 81338973-G-A

143699385-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81338973-G-C

143699505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81338853-G-T

143699601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81338757-G-T

143699624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81338734-G-T

143699627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81338731-G-T

143699629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 81338729-G-A

143699639-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81338719-A-G

143699654-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81338704-T-G

143699732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81338626-A-G

http://identifiers.org/hco/4/GRCh38#143699746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#81338612-C-A

143699746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81338612-C-T

143699757-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81338601-G-T

143699834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81338524-G-A

143699900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 81338458-G-A

143699900-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 81338458-G-C

143699921-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81338434-T-A

143699986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 81338369-C-T

143700040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 81338315-T-C

143700125-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: 81338251-C-T

143700162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81338214-G-A

143700162-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81338214-G-T

http://identifiers.org/hco/4/GRCh38#143700183-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#81338193-A-C

143700183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81338193-A-G

143700312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81338064-G-T

143700473-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81337906-C-G

http://identifiers.org/hco/4/GRCh38#143700519-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/8/GRCm39#81337860-C-A

http://identifiers.org/hco/4/GRCh38#143700580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/8/GRCm39#81337799-C-A

143700580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 81337799-C-T

143700593-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81337786-G-A

143700593-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81337786-G-C

143700593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81337786-G-T

143700615-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 81337767-A-G

143700654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81337728-G-A

143700654-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25172
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 81337728-G-T