107490268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 43050390-G-A

107490268-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 43050390-G-C

107490268-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 43050390-G-T

107490283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 43050375-G-A

107490283-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 43050375-G-T

107490305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 43050368-G-A

107490305-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 43050368-G-T

107490728-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43049955-G-A

107490728-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43049955-G-T

http://identifiers.org/hco/6/GRCh38#107490733-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43049950-C-A

107490733-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43049950-C-G

107490733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43049950-C-T

107491111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43049560-C-T

http://identifiers.org/hco/6/GRCh38#107491425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43049257-C-A

http://identifiers.org/hco/6/GRCh38#107491748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43048931-C-A

107491748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43048931-C-T

107492048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43048614-A-G

107493039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43047651-T-C

107493800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43046915-G-A

107493800-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43046915-G-T

107494371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43046295-A-G

107495430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43045248-G-A

107495731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43044948-T-C

107496064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43044608-G-A

107496106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43044562-C-T

107496169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43044500-A-G

107496379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43044285-G-A

107496421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43044251-C-T

107496432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43044240-A-G

107496703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43043963-A-G

107497487-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43043168-A-T

http://identifiers.org/hco/6/GRCh38#107497638-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43042788-A-C

107497638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43042788-A-G

107497698-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43042738-T-C

107497790-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43042647-T-C

107498929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43041611-G-A

107499239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43040871-A-G

107499743-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43040290-G-T

107500165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43039798-G-A

107500424-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43039588-T-G

107500903-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43039183-T-C

107501504-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43038550-G-A

107501537-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43038514-A-G

107501549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43038502-C-T

107501602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43038452-G-A

107501602-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43038452-G-T

107502081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43038016-G-A

107502167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43037944-C-T

107502230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43037883-G-T

107502262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43037852-G-A

107502477-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43037659-A-G

107502567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43037575-A-G

107502580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43037562-G-A

http://identifiers.org/hco/6/GRCh38#107502614-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43037534-A-C

http://identifiers.org/hco/6/GRCh38#107503256-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43037225-C-A

http://identifiers.org/hco/6/GRCh38#107503262-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43037219-C-A

107503289-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43037193-T-C

107503549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43036941-G-A

107503596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43036899-G-A

107503634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43036861-A-G

107503714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 43036781-G-A

107503723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 43036772-G-A

107503724-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 43036771-A-T

107503801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43036694-G-A

107503863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43036632-G-A

107503868-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43036627-T-G

107504042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43035524-G-A

107504097-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43035474-A-G

107504330-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43035250-A-G

107504484-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43035129-G-A

107504484-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43035129-G-T

http://identifiers.org/hco/6/GRCh38#107504747-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43034883-C-A

107504747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43034883-C-T

http://identifiers.org/hco/6/GRCh38#107504760-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43034870-A-C

107505242-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43034436-C-G

107505244-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43034434-C-T

107505283-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43034397-T-A

http://identifiers.org/hco/6/GRCh38#107506096-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43034233-C-A

107506096-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43034233-C-G

107506130-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43034199-A-T

107506148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43034181-T-C

107506158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43034170-T-C

107506158-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43034170-T-G

107506200-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43034129-A-T

http://identifiers.org/hco/6/GRCh38#107506481-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43033845-C-A

107506481-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43033845-C-G

107506578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43033752-A-G

107506597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43033732-G-T

107507106-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43033546-T-G

107508041-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43033128-T-C

107508125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43033053-G-T

107508685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43032851-A-G

107508725-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43032810-C-G

107508766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43032769-C-T

http://identifiers.org/hco/6/GRCh38#107508956-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43032588-C-A

107511383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 43031625-T-C

107511404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43031604-G-A

107511404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43031604-G-T

http://identifiers.org/hco/6/GRCh38#107511521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43031494-C-A

107511666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43031360-G-A

107511666-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 43031360-G-T

107511852-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43031169-A-G

107511856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43031165-T-C

107511888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43031131-G-A

107511908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43031111-G-A

107512198-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43030836-A-G

107512612-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43030303-C-G

107512697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43030241-T-C

http://identifiers.org/hco/6/GRCh38#107513135-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43029839-A-C

107513378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43029593-C-T

107513732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43029170-A-G

107513747-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43029155-A-G

107513752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43029150-A-G

107513756-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43029103-T-A

http://identifiers.org/hco/6/GRCh38#107513906-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43028948-C-A

107513967-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 43028885-C-G

107513967-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 43028885-C-T

107514040-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43028823-T-C

107514078-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43028791-G-T

107514113-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43028757-G-A

107514235-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43028104-C-T

107514277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43028063-C-T

107514311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43028020-A-G

107514364-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 43027968-G-T

http://identifiers.org/hco/6/GRCh38#107514422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43027931-C-A

http://identifiers.org/hco/6/GRCh38#107514563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43027647-C-A

http://identifiers.org/hco/6/GRCh38#107515152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43023288-C-A

107515152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43023288-C-T

107516950-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43021880-C-G

107517783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43020968-A-G

107517904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43020809-A-G

107517970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43020761-A-G

107518054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43020677-A-G

107518510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43020039-A-G

107518538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43020011-A-G

107519828-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43018934-C-G

107520124-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43018611-C-G

107522002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43017819-C-T

107522206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43017641-G-A

107522212-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43017635-C-T

107522340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43017510-A-G

107522971-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43017258-G-A

107522988-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43017241-G-C

107523006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43017223-G-A

107524841-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43016513-C-G

107524841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43016513-C-T

107524920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43016432-A-G

107525181-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43016200-C-T

http://identifiers.org/hco/6/GRCh38#107525585-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43015487-A-C

107525592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43015480-T-C

107525625-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43015447-A-G

107526506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43014911-C-T

107526543-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43014875-C-T

107526606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43014797-T-C

107527149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43012879-T-C

107527215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43012813-T-C

http://identifiers.org/hco/6/GRCh38#107527389-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43012646-A-C

107528239-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43010958-T-G

107528332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43010869-G-A

107528578-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43010643-A-T

107529329-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43009136-G-C

http://identifiers.org/hco/6/GRCh38#107529358-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43009119-C-A

107529372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43009105-C-T

http://identifiers.org/hco/6/GRCh38#107529602-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43008880-C-A

107529602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 43008880-C-T

107529616-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43008866-G-C

107529616-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43008866-G-T

107529754-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43008741-T-C

107530204-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43008274-T-C

107530733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43007313-T-C

http://identifiers.org/hco/6/GRCh38#107531315-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43006806-A-C

107531316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43006805-A-G

107531377-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43006736-T-A

107531515-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43006614-A-G

107531698-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43006496-G-C

107531926-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43006266-A-G

107532364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43005089-A-G

107532471-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43004996-G-C

107532547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43004910-A-G

107532695-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43004753-G-A

107532763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43004654-A-G

http://identifiers.org/hco/6/GRCh38#107532785-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43004634-A-C

107532850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43004570-G-A

107533159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43004251-A-G

107533159-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43004251-A-T

107533196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43004235-G-A

107533196-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43004235-G-T

107533225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43004207-G-T

107533259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43004172-A-G

http://identifiers.org/hco/6/GRCh38#107533270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43004153-C-A

107533270-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43004153-C-G

107533348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43004036-G-A

107533348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43004036-G-T

http://identifiers.org/hco/6/GRCh38#107533704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#43003696-C-A

107534062-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43003393-C-T

107534332-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43003132-A-T

107534953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43002594-A-G

107535282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43002194-A-G

107536785-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43000368-T-G

107536925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 43000225-G-A

107537180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42999240-C-T

http://identifiers.org/hco/6/GRCh38#107537305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42999142-C-A

107537305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42999142-C-T

107537308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42999139-G-A

107537452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42998994-C-T

107537995-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42998806-C-G

107537995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42998806-C-T

107538007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42998794-A-G

107538008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42998793-T-C

107538044-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42998763-C-G

107538135-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42998675-C-G

107538191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42998596-A-G

107539188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42997618-T-C

107539238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42997575-C-T

107539929-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42996886-G-C

107540178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42996631-A-G

107540453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42996358-G-A

107540605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42996262-A-G

107540775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 42996025-T-C

107540829-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42995809-C-G

107540829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42995809-C-T

http://identifiers.org/hco/6/GRCh38#107541381-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42995277-A-C

107541460-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42995199-T-G

107541492-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42995139-A-G

107541493-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42995138-T-G

107541986-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42994658-G-A

http://identifiers.org/hco/6/GRCh38#107542212-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42994306-C-A

107542239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42994279-G-A

107542289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42994230-G-A

107542372-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42994150-G-T

107543032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42993595-G-A

107543231-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42993430-C-G

107543231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42993430-C-T

107543240-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42993415-C-G

107543339-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42992683-T-C

107543701-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42992380-T-G

107543706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42992375-C-T

107543814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42992267-C-T

107544178-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42991919-T-G

107544376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42991719-C-T

107544629-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42991382-A-T

107544655-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42991357-C-G

107544684-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42991315-T-C

107544684-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42991315-T-G

107544918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42990943-G-A

107545150-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42990705-G-A

107545150-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42990705-G-T

107545183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42990697-G-A

107545216-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42990664-C-G

107545216-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42990664-C-T

107545294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42990582-A-G

107545294-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42990582-A-T

107545552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42990361-T-C

107545729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42990185-G-A

107545783-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42990124-G-C

107546146-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42989755-C-T

107546478-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42989482-G-T

107546631-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42989357-T-G

107546809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42989206-A-G

107546809-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42989206-A-T

107546814-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42989201-A-T

107546973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42989054-G-A

107546973-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42989054-G-T

107546999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42989027-G-A

107547056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42988971-A-G

107547084-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42988947-C-T

107547280-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42988844-A-T

107547691-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42988485-A-T

107547827-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42988355-C-G

107547936-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42987897-T-A

107547936-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42987897-T-C

107548047-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42987791-G-C

107548049-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42987789-A-G

107548234-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42987632-A-T

107549445-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42987226-T-A

107549507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42987165-A-G

107549533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42987139-G-A

http://identifiers.org/hco/6/GRCh38#107549568-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42987113-C-A

http://identifiers.org/hco/6/GRCh38#107549576-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42987105-C-A

107549627-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42987069-A-T

107549656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42987040-G-A

107549656-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42987040-G-C

107549666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42987030-G-A

107549758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42986939-T-C

107549803-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42986894-A-G

107550203-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42986624-G-T

http://identifiers.org/hco/6/GRCh38#107550375-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42986464-A-C

107550446-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42986413-A-G

107550585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42986274-T-C

107550600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42986259-G-A

107550622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42986240-A-G

107550771-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42986111-C-T

107550772-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42986110-A-G

107550918-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42986005-C-T

107550993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42985933-G-A

107551022-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42985911-G-C

107551022-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42985911-G-T

107552059-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42984603-G-T

107552955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42983795-A-G

107552971-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42983779-G-C

107552971-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42983779-G-T

107554423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42983558-G-A

107554628-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42983358-G-C

107554653-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42983333-G-C

107554877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42983142-G-A

107555408-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42982606-T-G

107555610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42982387-T-C

107555773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42982224-G-A

107556069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42981938-A-G

http://identifiers.org/hco/6/GRCh38#107556358-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42981659-A-C

107556358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42981659-A-G

107556359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42981658-T-C

107556431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42981573-T-C

http://identifiers.org/hco/6/GRCh38#107556541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42981464-C-A

107556541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42981464-C-T

107556542-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42981463-G-A

107556718-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42981304-T-C

107556929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42981100-G-A

107557689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42980474-T-C

107557991-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42980236-T-G

107558144-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42980072-T-C

107559317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42979194-G-A

107559577-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42978928-T-A

107559577-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42978928-T-C

107559616-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42978904-G-C

107559687-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42978842-A-G

107559993-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42978525-G-T

107560299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42978214-G-A

107560338-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42978175-C-G

107560365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42978148-G-T

107560435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42978084-G-A

107560946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42977372-A-G

107561207-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42977143-A-T

107561348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42976885-G-A

http://identifiers.org/hco/6/GRCh38#107561393-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42976840-C-A

107561450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42976785-A-G

http://identifiers.org/hco/6/GRCh38#107561648-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42976599-A-C

107561648-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42976599-A-G

107561653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42976594-C-T

107561798-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42976449-T-C

107561881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42976366-T-C

107562665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42975897-A-G

107562709-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42975841-A-G

107562765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42975787-A-G

107562765-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42975787-A-T

107562791-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42975768-T-G

107563424-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42975051-A-G

107563424-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42975051-A-T

107563523-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42974763-G-A

107563589-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42974699-C-T

107563659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42974629-T-C

107563763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42974536-A-G

107563963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42974357-G-A

107563998-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42974322-G-T

107564016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42974304-G-A

http://identifiers.org/hco/6/GRCh38#107564115-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42974194-A-C

107564115-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42974194-A-T

http://identifiers.org/hco/6/GRCh38#107564518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42973785-C-A

107564646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42973652-A-G

107564690-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42973611-C-G

107565129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42973171-A-G

107565560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42972767-C-T

107565562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42972765-A-G

107565667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42972566-G-A

107566074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42972080-A-G

107566083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42972071-T-C

107566118-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42972040-G-C

107566150-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42972009-C-G

107566150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42972009-C-T

107566158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42972001-T-C

107566197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42971962-C-T

107566922-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42971577-G-T

107566968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42971534-A-G

107566987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42971515-T-C

107568417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42970937-G-A

107568417-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42970937-G-T

107568589-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42970766-C-G

107568674-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42970684-G-A

107568686-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42970674-A-G

107568964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42970417-G-A

107569200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42970178-C-T

107569254-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42970117-T-G

107569417-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42969948-G-C

http://identifiers.org/hco/6/GRCh38#107569893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42969482-C-A

107569893-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42969482-C-G

107569893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42969482-C-T

107570092-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42969295-T-A

107570092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42969295-T-C

107570259-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42969125-A-G

107570298-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42969094-G-A

http://identifiers.org/hco/6/GRCh38#107570379-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42969028-C-A

107570485-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42968946-T-G

107570762-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42968866-G-C

107570763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42968865-G-A

107570817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42968811-G-A

107570943-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42968708-C-G

107570943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42968708-C-T

107571694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42967920-G-A

107571694-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42967920-G-T

107571784-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42967830-G-A

107572068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42967550-C-T

107572609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42967102-T-C

107572975-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42966731-T-C

107573072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42966418-A-G

107573074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42966416-T-C

107573123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42966315-A-G

107573320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42966120-G-T

107573387-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42966057-T-G

107573862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42965339-T-C

107573902-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42965299-A-T

107574251-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42964546-T-C

http://identifiers.org/hco/6/GRCh38#107574703-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42964158-C-A

107574737-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42964137-G-C

107574780-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42964118-C-G

107574842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42964050-C-T

http://identifiers.org/hco/6/GRCh38#107574861-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42964032-C-A

107574997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42963891-G-A

107575089-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42963820-G-C

107575389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42963589-G-T

107576026-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42963090-C-G

107576158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42962959-C-T

107576362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42962727-A-G

107576366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42962723-A-G

107576824-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42961822-C-G

107576907-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42961763-A-G

107577041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42961590-C-T

107577467-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42961181-T-G

107577532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42961115-A-G

107577677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42960968-C-T

107578121-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42960842-A-T

107578202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42960772-G-A

http://identifiers.org/hco/6/GRCh38#107578445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42960594-C-A

107579166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42959891-C-T

107579279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42959754-T-C

107579504-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42959548-A-G

107579661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42959422-G-A

107579662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42959421-T-C

107579834-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42959242-A-G

107580023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42959043-T-C

107580097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42958966-G-A

107580196-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42958869-A-G

107580359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42958791-T-C

107580505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42957767-G-A

107580526-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42957747-A-G

107580857-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42957449-A-T

107581100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42957274-G-A

107581121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42957253-C-T

107581213-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42957231-G-C

http://identifiers.org/hco/6/GRCh38#107581393-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42957070-A-C

107581393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42957070-A-G

107581407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42957056-G-A

107581432-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42957031-A-G

107581637-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42956833-C-G

107581813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42956709-C-T

107581843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42956680-A-G

107581844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42956679-C-T

107581894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42956629-G-A

107581987-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42956441-C-G

107581987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42956441-C-T

107582371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42956004-G-A

107582397-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42955982-G-C

http://identifiers.org/hco/6/GRCh38#107582531-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42954856-A-C

107582531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42954856-A-G

107583018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42954366-A-G

107583018-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42954366-A-T

107584143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42953798-G-A

107585435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42952385-T-C

107585791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42952029-A-G

107585917-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42951902-C-G

107586239-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42951577-G-T

107587537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42950227-G-A

107587986-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42949783-A-G

107588358-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42949416-T-A

107588785-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42948993-G-A

107588785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42948993-G-T

107589250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42948554-C-T

107589729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42948034-A-G

107590240-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42947501-T-C

http://identifiers.org/hco/6/GRCh38#107590941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42946771-C-A

107590941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42946771-C-T

107591042-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42946682-A-G

107591486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42946323-A-G

107591524-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42946284-A-T

107591534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42946274-T-C

107591840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42945984-A-G

107591853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42945971-A-G

http://identifiers.org/hco/6/GRCh38#107592591-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42942409-A-C

107592612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42942390-G-A

107592953-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42942061-C-G

107593143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42941897-T-C

http://identifiers.org/hco/6/GRCh38#107593170-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42941870-A-C

107593289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42941758-G-A

107593394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42941632-G-A

107593641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42941433-T-C

107593803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42941226-T-C

107593877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42941040-T-C

107593894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42941023-T-C

107593970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42940949-A-G

107594106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42940853-C-T

107594163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42940798-G-A

107594197-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42940766-T-A

107594461-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42940501-T-C

107594651-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42940193-G-A

107594651-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42940193-G-T

107594720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42940128-C-T

107594925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42939923-T-C

107595018-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42939844-G-A

107595122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42939759-C-T

http://identifiers.org/hco/6/GRCh38#107595301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42939427-C-A

107595671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42938746-A-G

107595879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42938494-A-G

107596027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42938270-A-G

107596037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42938260-T-C

107596187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42938108-G-A

107596187-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42938108-G-T

107596287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42937952-G-T

107596443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42937799-T-C

107596571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42937617-G-A

107596571-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42937617-G-C

107596583-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42937605-A-T

107596888-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42937338-G-A

107597107-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42937159-G-C

107597461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42937019-A-G

107597721-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42936763-A-T

107597762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42936722-A-G

107597798-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42936691-G-C

107597798-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42936691-G-T

107598285-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42936097-T-G

107598291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42936091-T-C

107598407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42935964-G-A

107598706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42935699-G-A

107598706-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42935699-G-T

107598709-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42935696-T-G

107598773-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42935648-G-T

107599032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42935398-G-A

107599127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42935291-C-T

107599291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42935124-A-G

107599315-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42935112-A-T

http://identifiers.org/hco/6/GRCh38#107599545-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42934638-A-C

107599545-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42934638-A-T

107599611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42934573-A-G

107599649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42934529-C-T

107600229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42933866-T-C

107600807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42933236-A-G

107600877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42933166-A-G

107600983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, undefined
orthologous variants: 42932844-T-C

107600984-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, undefined
orthologous variants: 42932843-A-G

107601092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, undefined
orthologous variants: 42932568-G-A

107601170-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, undefined
orthologous variants: 42932490-G-C

107601209-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42932453-G-A

http://identifiers.org/hco/6/GRCh38#107601433-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42932235-A-C

107602151-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42931112-C-G

107602276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42931011-G-A

107602465-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42930845-T-C

107602516-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42930794-A-G

107602523-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42930787-C-T

107602524-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42930786-C-G

107602524-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42930786-C-T

107602528-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42930782-T-A

107602528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42930782-T-C

107602529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42930781-G-A

107602537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42930773-G-A

107602537-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42930773-G-T

107602595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42930730-G-A

107602595-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42930730-G-C

http://identifiers.org/hco/6/GRCh38#107602962-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42930369-C-A

107603001-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42930326-T-G

http://identifiers.org/hco/6/GRCh38#107603052-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#42930275-A-C

107603242-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42930089-T-C

http://identifiers.org/hco/6/GRCh38#107603249-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42930082-A-C

107603560-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42929752-A-G

107603561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42929751-C-T

107603626-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42929690-C-G

107603671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42929646-G-A

107603855-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42929506-G-C

107603988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42929374-C-T

107604349-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42929013-A-T

107604361-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42929002-C-T

107604840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42928517-A-G

107604962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42928394-T-C

http://identifiers.org/hco/6/GRCh38#107605062-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42928295-A-C

107605363-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42925700-G-A

107606710-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42924390-C-T

107607018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42924258-A-G

107607089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42924206-G-A

107608137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42923272-G-A

107608620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42922549-C-T

107608628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42922541-C-T

107608881-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42922369-T-C

107609247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42921568-A-G

http://identifiers.org/hco/6/GRCh38#107609847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42920909-C-A

107609947-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42920808-T-C

107610241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42920554-C-T

107610314-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42920479-G-A

107610379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42920426-C-T

107610538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42920283-G-A

107610616-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42920209-C-G

107610753-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42920030-T-A

107610777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42919998-T-C

107611041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42919756-G-T

107611531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42919259-C-T

107611966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42918839-A-G

http://identifiers.org/hco/6/GRCh38#107612124-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42918692-A-C

107612287-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42918517-G-C

107612329-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42918461-T-A

107612349-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42918439-C-G

107613012-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42917757-T-C

107613106-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42917664-T-G

http://identifiers.org/hco/6/GRCh38#107613145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42917639-C-A

107613412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42917391-T-C

107613491-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42917266-G-C

107614009-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42916427-A-T

107614404-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42916321-T-C

107614605-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42916148-A-T

107614761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42916006-C-T

107614852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42915922-G-A

107614963-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42915814-C-T

107615181-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42915000-G-C

107615193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42914988-C-T

107615245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42914941-A-G

107615539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42914662-C-T

107615578-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42914623-T-G

107616056-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42914393-A-G

107616124-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42914334-C-G

107616402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42914079-A-G

107616432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42914051-T-C

107616766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42913743-A-G

107616906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42913644-C-T

107617055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42913505-G-A

107617315-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42913214-T-G

107617769-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42912771-T-C

107618169-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42912688-G-C

107618290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42912541-G-T

107618307-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42912520-G-C

107618320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42912505-C-T

107618358-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42912432-T-G

107618373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42912417-A-G

http://identifiers.org/hco/6/GRCh38#107618499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42912312-C-A

107618499-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42912312-C-G

http://identifiers.org/hco/6/GRCh38#107618562-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42912252-A-C

107618689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42912129-C-T

107618815-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, undefined
orthologous variants: 42912007-G-A

107618822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, undefined
orthologous variants: 42912000-G-A

107618872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, undefined
orthologous variants: 42911950-T-C

107618891-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42911931-A-G

107619081-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42911737-G-A

107619313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42911524-G-A

107619353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42911494-G-A

107619353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42911494-G-T

107619371-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42911470-G-T

107619393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42911449-T-C

107619540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42911322-T-C

107620408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42910880-A-G

107620408-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42910880-A-T

107620562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42910773-G-A

107620562-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42910773-G-C

107620747-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42910612-C-T

107621004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42910401-A-G

http://identifiers.org/hco/6/GRCh38#107621008-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42910397-C-A

107621008-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42910397-C-G

107621222-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42910201-T-G

107621508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42909953-C-T

107621867-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42909602-G-T

107621924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42909545-C-T

107621925-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42909544-A-T

107622355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42909136-A-G

107622431-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42908886-A-G

107622581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42908739-G-A

107622628-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42908712-G-T

107622661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42908690-A-G

http://identifiers.org/hco/6/GRCh38#107622944-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42908420-C-A

107622944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42908420-C-T

107623005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42908359-C-T

107623800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42907897-G-A

107623836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42907861-G-A

107623993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42907732-G-A

http://identifiers.org/hco/6/GRCh38#107626234-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42906295-A-C

107626236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42906293-C-T

107626378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42906139-A-G

107626519-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42906024-C-T

107626601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42905967-A-G

107626630-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42905938-A-G

107626710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42905849-G-A

107626715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42905844-G-A

107626728-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42905832-G-C

107627504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42904790-C-T

107627509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42904785-G-A

107627509-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42904785-G-C

107627560-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42904747-C-G

107627560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42904747-C-T

107627805-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42904593-A-G

107627811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42904587-G-A

107627811-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42904587-G-T

107627884-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42904518-T-G

107627913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42904512-C-T

107628142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42904307-G-A

107628335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42904126-C-T

http://identifiers.org/hco/6/GRCh38#107628758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#42903820-C-A

107628883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, undefined
orthologous variants: 42903726-G-A

107629784-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42902857-C-G

http://identifiers.org/hco/6/GRCh38#107629907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42902752-C-A

107629907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42902752-C-T

107629989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, undefined
orthologous variants: 42902672-T-C

http://identifiers.org/hco/6/GRCh38#107630845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42901916-C-A

107631052-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42901733-G-A

107631199-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42901559-C-G

107631199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42901559-C-T

107631200-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42901558-C-G

107631248-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42901509-A-T

107631349-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42901405-G-C

107631524-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42901103-A-G

107631737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42900738-C-T

107631766-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42900712-T-C

107631848-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42900653-A-G

107631969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42900536-C-T

107631970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42900535-A-G

107631993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42900512-C-T

107632358-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42900162-T-A

107632499-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42900022-T-G

107632756-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42899765-T-C

107633093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42899433-G-A

107633154-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42899372-T-C

107633383-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42899042-A-G

107633383-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42899042-A-T

107633763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: missense variant
orthologous variants: 42898663-G-A

107633784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: missense variant
orthologous variants: 42898642-C-T

107633859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: missense variant
orthologous variants: 42898567-A-G

107633859-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: missense variant
orthologous variants: 42898567-A-T

107633917-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: missense variant
orthologous variants: 42898509-C-G

107633917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: missense variant
orthologous variants: 42898509-C-T

http://identifiers.org/hco/6/GRCh38#107633931-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42898495-C-A

107633931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: missense variant
orthologous variants: 42898495-C-T

http://identifiers.org/hco/6/GRCh38#107634138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42898288-C-A

107634159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: missense variant
orthologous variants: 42898267-G-A

107634159-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: missense variant
orthologous variants: 42898267-G-C

107634159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: missense variant
orthologous variants: 42898267-G-T

http://identifiers.org/hco/6/GRCh38#107634231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42898195-C-A

107634231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: missense variant
orthologous variants: 42898195-C-T

http://identifiers.org/hco/6/GRCh38#107634318-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42898108-C-A

107634318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: missense variant
orthologous variants: 42898108-C-T

http://identifiers.org/hco/6/GRCh38#107634336-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42898090-A-C

107634549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: missense variant
orthologous variants: 42897877-G-A

107634549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: missense variant
orthologous variants: 42897877-G-T

http://identifiers.org/hco/6/GRCh38#107634588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42897838-C-A

107634588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: synonymous variant
orthologous variants: 42897838-C-T

107634594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: missense variant
orthologous variants: 42897832-C-T

107634615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: missense variant
orthologous variants: 42897811-T-C

http://identifiers.org/hco/6/GRCh38#107634636-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42897790-C-A

107634636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: missense variant
orthologous variants: 42897790-C-T

107634649-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: missense variant
orthologous variants: 42897777-C-G

107634649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: missense variant
orthologous variants: 42897777-C-T

http://identifiers.org/hco/6/GRCh38#107634687-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42897745-C-A

107634687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: missense variant
orthologous variants: 42897745-C-T

http://identifiers.org/hco/6/GRCh38#107634741-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42897700-C-A

107634741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: missense variant
orthologous variants: 42897700-C-T

http://identifiers.org/hco/6/GRCh38#107634772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: missense_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#42897669-C-A

107634772-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: missense_variant, undefined
orthologous variants: 42897669-C-T

107634778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: missense_variant, undefined
orthologous variants: 42897663-T-C

107634778-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: missense_variant, undefined
orthologous variants: 42897663-T-G

http://identifiers.org/hco/6/GRCh38#107634867-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: missense_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#42897574-C-A

107634867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: missense_variant, undefined
orthologous variants: 42897574-C-T

107634963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: missense variant
orthologous variants: 42897478-G-A

107634969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: missense variant
orthologous variants: 42897472-G-A

107634990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 42897451-G-A

http://identifiers.org/hco/6/GRCh38#107635113-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42897340-C-A

http://identifiers.org/hco/6/GRCh38#107635386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42897067-C-A

107635404-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 42897049-C-G

107635404-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 42897049-C-T

107635516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42896930-T-C

107635527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42896919-G-A

107635527-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42896919-G-T

107635533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42896914-G-A

107635533-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42896914-G-T

107635571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42896884-G-A

107635571-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42896884-G-C

107635571-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42896884-G-T

107635573-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42896882-G-T

107635622-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42896832-C-T

107635721-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42896737-T-C

http://identifiers.org/hco/6/GRCh38#107636171-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42896453-C-A

107636171-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42896453-C-G

107636171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 42896453-C-T

http://identifiers.org/hco/6/GRCh38#107636280-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42896368-C-A

107636280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42896368-C-T

107636289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42896360-G-A

107636289-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42896360-G-T

http://identifiers.org/hco/6/GRCh38#107636303-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42896352-A-C

107636303-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42896352-A-G

107636303-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 42896352-A-T

107636514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42896176-G-A

107636770-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42895919-C-G

107636770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42895919-C-T

http://identifiers.org/hco/6/GRCh38#107637202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42895564-C-A

http://identifiers.org/hco/6/GRCh38#107637227-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42895545-A-C

107637227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42895545-A-G

107637429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42895403-G-T

107637486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42895349-G-A

107637761-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42895119-C-T

http://identifiers.org/hco/6/GRCh38#107637844-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42895041-A-C

107637968-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42894906-A-T

107637972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42894902-G-A

107640037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42893496-C-T

107640241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42893304-T-C

107640312-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42893253-G-A

107640520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42893055-A-G

107640520-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42893055-A-T

107640711-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42892883-A-G

107640883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 42892717-G-A

107640966-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 42892714-A-G

107641019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 42892666-C-T

107641398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 42892273-C-T

107641421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 42892250-C-T

http://identifiers.org/hco/6/GRCh38#107641562-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42892123-C-A

107641810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 42891866-G-A

107641818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 42891858-G-A

107641818-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 42891858-G-T

http://identifiers.org/hco/6/GRCh38#107641983-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42891698-A-C

107641992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 42891695-G-A

107642208-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 42891504-A-G

107642255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 42891446-A-G

107642258-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 42891443-G-C

107642503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 42891077-A-G

107642522-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 42891050-G-C

107642522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 42891050-G-T

107642990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 42890663-C-T

107643989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42890007-G-A

107644374-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42889910-G-A

107644447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42889837-T-C

107644458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42889814-T-C

107644490-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42889786-A-G

107644515-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42889762-T-A

107644562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42889715-T-C

107645083-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42889186-C-G

107645200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42888847-T-C

107645589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42888474-G-A

107645659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42888408-C-T

107645673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42888398-G-A

107645677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42888396-G-A

107645814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42888283-G-A

http://identifiers.org/hco/6/GRCh38#107646082-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42888042-A-C

107646286-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42887877-C-G

http://identifiers.org/hco/6/GRCh38#107646399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42887762-C-A

107646509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42887621-C-T

107646592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42887531-C-T

107646641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42887472-A-G

107646668-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42887445-C-G

107646668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42887445-C-T

107647048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42887179-G-A

107647149-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42887098-C-G

107647219-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42887024-A-T

107647624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42886705-T-C

107654080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42883633-A-G

107654239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42883502-A-G

107654302-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42883491-G-C

107654631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42883180-G-A

107655875-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42882313-T-A

107657400-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42880942-G-A

107657651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42880805-C-T

107657895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42880734-G-A

107657895-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42880734-G-C

http://identifiers.org/hco/6/GRCh38#107658070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#42880560-C-A

http://identifiers.org/hco/6/GRCh38#107658129-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#42880506-C-A

107658129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, undefined
orthologous variants: 42880506-C-T

http://identifiers.org/hco/6/GRCh38#107658145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#42880491-C-A

107658145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron_variant, undefined
orthologous variants: 42880491-C-T

107658161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42880470-G-A

107658161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42880470-G-T

107658162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42880469-G-A

107658162-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: intron variant
orthologous variants: 42880469-G-T

http://identifiers.org/hco/6/GRCh38#107658334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42880279-C-A

107658334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: 3 prime UTR variant
orthologous variants: 42880279-C-T

http://identifiers.org/hco/6/GRCh38#107658384-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42880230-C-A

107658507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: 3 prime UTR variant
orthologous variants: 42880096-C-T

http://identifiers.org/hco/6/GRCh38#107658563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42880043-C-A

107658563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: 3 prime UTR variant
orthologous variants: 42880043-C-T

http://identifiers.org/hco/6/GRCh38#107658694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42879905-C-A

107658740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: 3 prime UTR variant
orthologous variants: 42879856-A-G

107658999-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: 3 prime UTR variant
orthologous variants: 42879596-T-C

http://identifiers.org/hco/6/GRCh38#107659511-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42879092-A-C

107659513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: 3 prime UTR variant
orthologous variants: 42879090-A-G

107659513-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: 3 prime UTR variant
orthologous variants: 42879090-A-T

107659953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: 3 prime UTR variant
orthologous variants: 42878666-A-G

107660061-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: 3 prime UTR variant
orthologous variants: 42878537-G-C

107660061-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: 3 prime UTR variant
orthologous variants: 42878537-G-T

107660175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: 3 prime UTR variant
orthologous variants: 42878451-T-C

107660260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: 3 prime UTR variant
orthologous variants: 42878374-A-G

107660336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: 3 prime UTR variant
orthologous variants: 42878292-C-T

107660532-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: 3 prime UTR variant
orthologous variants: 42878143-G-C

107660536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: 3 prime UTR variant
orthologous variants: 42878139-C-T

107660783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: 3 prime UTR variant
orthologous variants: 42877889-A-G

107660791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: 3 prime UTR variant
orthologous variants: 42877881-G-A

107660911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: 3 prime UTR variant
orthologous variants: 42877761-G-A

107660914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: 3 prime UTR variant
orthologous variants: 42877758-C-T

107660945-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: 3 prime UTR variant
orthologous variants: 42877727-G-C

107661069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: 3 prime UTR variant
orthologous variants: 42877588-T-C

107661264-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29256
most severe consequence: 3 prime UTR variant
orthologous variants: 42877389-C-G