http://identifiers.org/hco/11/GRCh38#93661924-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#15268796-A-C

93662304-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15268567-A-T

93662575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15268321-A-G

93664872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15267562-T-C

93665405-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15267130-A-G

93665954-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15266393-A-G

93666116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15266269-A-G

http://identifiers.org/hco/11/GRCh38#93666917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15265808-C-A

93666917-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15265808-C-G

93667167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15265132-A-G

http://identifiers.org/hco/11/GRCh38#93667476-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15264516-A-C

93667563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15264434-A-G

93668009-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15264001-A-T

93668138-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15263872-G-T

93668166-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15263797-T-G

http://identifiers.org/hco/11/GRCh38#93668390-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15263498-C-A

http://identifiers.org/hco/11/GRCh38#93668830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15263087-C-A

93668830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: missense variant
orthologous variants: 15263087-C-T

93668943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15262974-A-G

93669254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15262748-G-A

93669556-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15262337-T-G

http://identifiers.org/hco/11/GRCh38#93669640-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15262235-C-A

93669640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15262235-C-T

93669734-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: missense variant
orthologous variants: 15262141-T-G

http://identifiers.org/hco/11/GRCh38#93669844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15262095-C-A

93669864-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15262080-T-G

http://identifiers.org/hco/11/GRCh38#93669865-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15262079-A-C

93669894-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15262057-T-A

93669894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15262057-T-C

93669894-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15262057-T-G

93669899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15262052-G-A

93669899-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15262052-G-T

93669945-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15262009-T-A

93669945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15262009-T-C

93670486-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15261576-T-C

93670677-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15261405-C-T

93670680-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15261402-A-T

93671662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15260600-G-A

93671726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15260536-T-C

93671767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15260493-G-A

93671979-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15260173-C-T

93671989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15260162-T-C

93672176-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15259959-A-T

93672206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15259929-C-T

93674763-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15259544-A-T

93675500-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15258395-T-G

93675532-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15258365-T-G

93675551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15258349-T-C

93675580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 15258321-G-A

93675580-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 15258321-G-T

93675677-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15258224-T-A

93675677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15258224-T-C

http://identifiers.org/hco/11/GRCh38#93675696-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15258202-C-A

93675696-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15258202-C-T

93675741-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15258157-A-G

93675741-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15258157-A-T

http://identifiers.org/hco/11/GRCh38#93675768-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15258130-A-C

93675768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15258130-A-G

93675772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15258126-G-A

93675772-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15258126-G-C

93675772-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15258126-G-T

93676243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15257440-C-T

93678103-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15256940-T-A

93679300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15255728-C-T

93679485-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 15255485-G-A

93679485-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 15255485-G-C

93679560-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 15255410-T-A

93679560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 15255410-T-C

93679560-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 15255410-T-G

93681948-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15254026-T-C

93682680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15253671-G-A

93683142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15253288-C-T

93683530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15252948-G-A

93683640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: missense variant
orthologous variants: 15252837-C-T

93683922-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15252316-T-A

93683940-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15252299-G-A

93683940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15252299-G-T

93684006-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: stop gained
orthologous variants: 15252233-T-A

93684264-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15251995-G-C

93684264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15251995-G-T

http://identifiers.org/hco/11/GRCh38#93684271-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15251988-C-A

93684271-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15251988-C-G

93684271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15251988-C-T

93684300-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15251960-T-A

93684310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15251950-G-A

93684310-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15251950-G-T

93685020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15251683-T-C

93685241-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15251318-C-G

93686780-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15250489-T-C

93686904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15250367-A-G

http://identifiers.org/hco/11/GRCh38#93686986-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#15250289-C-A

93687799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: missense variant
orthologous variants: 15249558-G-T

93687806-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: missense variant
orthologous variants: 15249551-C-G

93687806-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: missense variant
orthologous variants: 15249551-C-T

93691017-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15248436-A-G

93691517-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15248098-G-C

93691523-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15248092-T-C

93691593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15248022-T-C

93691669-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15247950-A-G

93691893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15247752-T-C

93691957-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 15247683-T-A

93691957-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 15247683-T-C

93692032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 15247608-T-C

93692138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 15247537-T-C

http://identifiers.org/hco/11/GRCh38#93696425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15246857-C-A

93696559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15246736-G-A

93696559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15246736-G-T

93696725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 15246556-G-A

93696725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: 5_prime_UTR_variant, stop_gained
orthologous variants: 15246556-G-T

93696756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 15246525-C-T

93696786-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 15246495-A-T

93696790-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 15246491-T-A

93696806-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 15246475-T-A

93696818-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 15246463-G-C

http://identifiers.org/hco/11/GRCh38#93696833-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15246448-A-C

93696833-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 15246448-A-G

93696843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 15246438-A-G

93696843-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 15246438-A-T

93696877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 15246404-T-C

93697263-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron_variant, missense_variant
orthologous variants: 15246030-C-G

93697549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 15245765-G-A

93697562-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron_variant, missense_variant
orthologous variants: 15245752-G-A

93697571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron_variant, missense_variant
orthologous variants: 15245743-G-A

93697588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 15245726-A-G

93697619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron_variant, missense_variant
orthologous variants: 15245695-G-A

93697619-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron_variant, missense_variant
orthologous variants: 15245695-G-C

93697751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron_variant, stop_gained
orthologous variants: 15245584-C-T

93697757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron_variant, missense_variant
orthologous variants: 15245578-A-G

93697865-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron_variant, missense_variant
orthologous variants: 15245470-A-G

93697936-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 15245399-A-T

93698096-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron_variant, missense_variant
orthologous variants: 15245239-G-A

93698096-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron_variant, stop_gained
orthologous variants: 15245239-G-T

93698125-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 15245210-T-A

93698134-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 15245201-G-A

93698182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 15245153-G-A

93698205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron_variant, missense_variant
orthologous variants: 15245130-G-A

93698248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 15245090-A-G

93698362-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 15245000-T-A

93698362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 15245000-T-C

93698363-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron_variant, missense_variant
orthologous variants: 15244999-A-G

93698438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron_variant, missense_variant
orthologous variants: 15244924-A-G

93698543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron_variant, missense_variant
orthologous variants: 15244819-G-A

93698543-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron_variant, missense_variant
orthologous variants: 15244819-G-C

93698549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron_variant, missense_variant
orthologous variants: 15244813-G-A

93698549-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron_variant, stop_gained
orthologous variants: 15244813-G-T

93698554-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 15244808-T-A

http://identifiers.org/hco/11/GRCh38#93698563-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15244799-C-A

93698563-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron_variant, missense_variant
orthologous variants: 15244799-C-G

93698563-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 15244799-C-T

93698581-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron_variant, missense_variant
orthologous variants: 15244781-C-G

93698674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 15244688-A-G

93698777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron_variant, missense_variant
orthologous variants: 15244585-T-C

93698840-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron_variant, missense_variant
orthologous variants: 15244522-A-G

93698944-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 15244418-C-T

http://identifiers.org/hco/11/GRCh38#93699105-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15244269-C-A

93699105-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 15244269-C-G

93699109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 15244265-A-G

http://identifiers.org/hco/11/GRCh38#93699144-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15244230-A-C

93699144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 15244230-A-G

93699281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 15244096-A-G

93699565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 15243815-T-C

http://identifiers.org/hco/11/GRCh38#93699659-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15243733-C-A

93699659-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant
orthologous variants: 15243733-C-G

93700144-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: 5_prime_UTR_variant, intron_variant, synonymous_variant
orthologous variants: 15243272-G-A

http://identifiers.org/hco/11/GRCh38#93700236-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15243182-A-C

93700258-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15243161-A-G

93700258-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15243161-A-T

93700898-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15242908-G-C

93702359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15242297-G-T

93702377-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15242279-A-G

93702381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15242278-G-A

93702381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15242278-G-T

http://identifiers.org/hco/11/GRCh38#93702412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15242250-C-A

93702412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15242250-C-T

http://identifiers.org/hco/11/GRCh38#93702434-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15242228-C-A

93702434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15242228-C-T

93702582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: synonymous variant
orthologous variants: 15242100-G-A

93702608-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: missense variant
orthologous variants: 15242077-C-T

93707212-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15238770-A-T

93707369-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15238644-G-A

93721168-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15238178-C-G

93721168-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15238178-C-T

http://identifiers.org/hco/11/GRCh38#93721234-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15238112-C-A

93721306-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 15238047-T-C

http://identifiers.org/hco/11/GRCh38#93721378-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15237969-C-A

93721378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: missense variant
orthologous variants: 15237969-C-T

93721417-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15237930-G-T

93721438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15237913-G-A

93721444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15237907-T-C

http://identifiers.org/hco/11/GRCh38#93721537-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15237838-A-C

93721574-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 15237801-C-G

http://identifiers.org/hco/11/GRCh38#93721656-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15237710-C-A

http://identifiers.org/hco/11/GRCh38#93721657-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15237709-A-C

93721657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 15237709-A-G

93721657-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 15237709-A-T

93721688-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 15237677-G-A

93721699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 15237666-T-C

http://identifiers.org/hco/11/GRCh38#93721877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15237547-C-A

93721877-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15237547-C-G

93721877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15237547-C-T

http://identifiers.org/hco/11/GRCh38#93722127-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15237298-C-A

93722127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15237298-C-T

93723199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 15236891-G-A

93723241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: missense variant
orthologous variants: 15236849-A-G

93723247-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: missense variant
orthologous variants: 15236843-A-G

93723247-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: missense variant
orthologous variants: 15236843-A-T

93723341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15236753-A-G

http://identifiers.org/hco/11/GRCh38#93723343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15236751-C-A

93723343-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15236751-C-G

93723343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15236751-C-T

93723372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: 15236731-T-C

93723497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 15236614-T-C

93723497-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 15236614-T-G

93724201-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 15235621-A-T

http://identifiers.org/hco/11/GRCh38#93725573-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15235077-C-A

http://identifiers.org/hco/11/GRCh38#93725684-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15234974-A-C

93725684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 15234974-A-G

93725705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 15234953-G-A

http://identifiers.org/hco/11/GRCh38#93725730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15234935-C-A

http://identifiers.org/hco/11/GRCh38#93725735-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: missense_variant, start_lost
orthologous variants: http://identifiers.org/mco/9/GRCm39#15234929-A-C

http://identifiers.org/hco/11/GRCh38#93725867-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#15234830-C-A

93726708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 15234583-C-T

93727041-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 15234315-G-A

93727041-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 15234315-G-C

93727041-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 15234315-G-T

93727128-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 15234243-A-G

93727366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 15234020-G-A

93727366-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 15234020-G-T

93727475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 15233950-A-G

93728783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 15229248-G-A

93729504-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 15228994-T-A

93729504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 15228994-T-C

93729867-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 15228536-C-G

93729884-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: missense variant
orthologous variants: 15228519-C-G

93729884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: missense variant
orthologous variants: 15228519-C-T

93729886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: synonymous variant
orthologous variants: 15228517-T-C

93729947-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: missense variant
orthologous variants: 15228466-C-G

93729947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: synonymous variant
orthologous variants: 15228466-C-T

http://identifiers.org/hco/11/GRCh38#93729955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: 3_prime_UTR_variant, missense_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#15228458-C-A

93729955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: 3_prime_UTR_variant, synonymous_variant, undefined
orthologous variants: 15228458-C-T

93730282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 15228281-A-G

93730331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29366
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 15228238-T-C