22563737-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 136683958-G-T

22563758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136683937-G-A

22563761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136683934-G-A

http://identifiers.org/hco/1/GRCh38#22563837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136683895-C-A

22563837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 136683895-C-T

22564486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136683440-G-A

22564708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136683237-G-A

http://identifiers.org/hco/1/GRCh38#22564901-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136683081-C-A

22564901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136683081-C-T

22564947-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136683060-G-C

22565121-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136682923-G-A

22565123-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136682921-A-G

22565129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136682915-G-A

http://identifiers.org/hco/1/GRCh38#22565214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136682827-C-A

22565337-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136682713-G-C

22565411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136682624-G-A

22565426-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136682606-G-C

22565567-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136682476-G-T

22566027-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136682093-C-T

22566047-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136682072-T-A

22566361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136681830-A-G

22566441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136681751-G-T

22566624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136681601-G-A

22566624-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136681601-G-C

http://identifiers.org/hco/1/GRCh38#22566676-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136681550-C-A

22566676-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136681550-C-T

22566725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136681512-T-C

22566835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136681403-C-T

22566888-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136681325-G-T

22567616-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136680694-G-A

22567616-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136680694-G-C

22567617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136680693-G-A

22567617-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136680693-G-T

22567897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136680367-G-A

22568006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136680260-G-A

22568006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136680260-G-T

22568054-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136680230-G-C

22568206-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136680104-A-G

22568388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136679918-A-G

22568429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136679896-A-G

22568434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136679891-G-A

22568472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136679870-C-T

22568546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136679800-A-G

22568573-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136679777-C-G

22568673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136679666-C-T

22568883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136679494-T-C

22568924-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136679453-G-T

22569053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136679356-G-A

22569152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136679259-G-T

22569222-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136679191-A-G

22569250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136679177-T-C

22569267-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136679160-C-T

http://identifiers.org/hco/1/GRCh38#22569315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136679112-C-A

22569315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136679112-C-T

http://identifiers.org/hco/1/GRCh38#22569385-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136679061-C-A

http://identifiers.org/hco/1/GRCh38#22569386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136679060-C-A

22569407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136679044-G-A

22569599-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136678844-G-T

22572200-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136677763-C-G

22572200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136677763-C-T

22572255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136677713-G-A

22572338-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136677645-T-A

22572467-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136677565-C-G

22572715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136677348-G-A

22572750-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136677313-G-A

22572756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136677307-C-T

22572947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136677141-C-T

22572948-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136677140-C-G

22572955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136677133-G-A

22573223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136676898-C-T

22573227-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136676894-A-G

22573445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136676679-C-T

22573502-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136676622-G-T

22575419-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136674561-C-G

22575677-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136674323-G-T

22575698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136674136-G-A

22575820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136674011-G-A

22575937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136673881-C-T

22576076-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136673763-G-A

22576076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136673763-G-T

http://identifiers.org/hco/1/GRCh38#22576107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136673722-C-A

22576107-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136673722-C-G

22576157-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136673684-T-C

http://identifiers.org/hco/1/GRCh38#22576161-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136673680-C-A

22576161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136673680-C-T

22576262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136673579-A-G

22576271-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136673570-G-C

http://identifiers.org/hco/1/GRCh38#22576310-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136673531-C-A

22576310-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136673531-C-G

22576310-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136673531-C-T

22576328-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136673513-C-G

22576328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 136673513-C-T

22576394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136673447-G-A

22576394-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136673447-G-C

22576448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136673393-C-T

22576520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136673321-A-G

22576550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136673291-A-G

22576592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136673249-C-T

22576595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136673246-G-A

22576595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136673246-G-T

http://identifiers.org/hco/1/GRCh38#22576631-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136673210-C-A

22576631-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136673210-C-G

22576631-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 136673210-C-T

22576670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136673171-C-T

22576682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136673159-C-T

22576706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136673135-G-A

22576706-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136673135-G-C

22576715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136673126-G-A

22576730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136673111-T-C

22576891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136672950-C-T

22576905-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136672934-G-C

22576905-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136672934-G-T

22576933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136672895-G-T

22576963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136672870-T-C

22576963-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136672870-T-G

http://identifiers.org/hco/1/GRCh38#22576969-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136672864-C-A

22577148-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136672788-G-A

22577238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136672700-T-C

22577299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136672643-G-A

22577299-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136672643-G-C

22577305-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136672637-C-T

22577568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136672380-G-A

22577775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136672268-T-C

22577779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136672264-T-C

22577780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136672263-G-A

22577792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136672251-G-A

22577809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136672244-T-C

http://identifiers.org/hco/1/GRCh38#22577831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136672222-C-A

22577831-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136672222-C-T

http://identifiers.org/hco/1/GRCh38#22577855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136672198-C-A

22577855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136672198-C-T

22577858-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136672195-A-G

22582518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136670919-C-T

22582590-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136670849-A-G

22582590-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136670849-A-T

22582633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136670806-G-A

22582789-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136670681-C-T

22583131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136670333-A-G

22583235-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136670229-C-G

22583241-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136670223-C-T

22583414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136670055-C-T

22583665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136669730-G-A

22584384-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136669178-G-A

22584713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136668865-G-A

22584729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136668849-G-A

http://identifiers.org/hco/1/GRCh38#22584844-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136668811-A-C

22585192-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136668563-C-G

22585560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136668317-C-T

22585847-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136668115-C-G

22585870-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136668099-C-G

22585870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136668099-C-T

22585999-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136668020-C-G

22586355-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136667756-T-C

22586355-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136667756-T-G

22586393-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136667725-G-T

http://identifiers.org/hco/1/GRCh38#22586429-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136667700-C-A

22586429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136667700-C-T

http://identifiers.org/hco/1/GRCh38#22586475-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136667662-C-A

http://identifiers.org/hco/1/GRCh38#22586509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136667628-C-A

22586509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136667628-C-T

22586556-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 136667581-A-G

22586643-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 136667494-C-G

22586643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 136667494-C-T

22586713-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136667439-A-G

22587735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136667107-G-A

22588230-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136666655-G-C

22588334-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136666549-G-A

22588368-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136666525-A-G

22588527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 136666390-G-A

22588581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136666338-G-A

22588587-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136666332-T-G

22588790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136666212-G-A

22588790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136666212-G-T

22588791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136666211-G-A

22588844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136666203-G-A

22589119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136665928-T-C

22589236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 136665826-C-T

22589249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 136665813-C-T

22589263-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 136665799-G-C

22589388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 136665710-A-G

22589458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 136665638-T-C

22589485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 136665611-A-G

22589485-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 136665611-A-T

22589667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136665304-G-T

22589692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136665283-G-A

22589692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136665283-G-T

22589693-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136665282-G-T

22589706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136665269-T-C

22589706-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136665269-T-G

http://identifiers.org/hco/1/GRCh38#22589735-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136665247-C-A

22589735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136665247-C-T

http://identifiers.org/hco/1/GRCh38#22589880-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136665100-C-A

22590401-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136664704-C-T

22592389-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136664537-C-G

22592389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136664537-C-T

22592421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136664507-A-G

22592773-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136664134-C-G

22593167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136663863-G-A

22593201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136663832-G-A

22593214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136663819-A-G

22593222-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136663811-G-T

http://identifiers.org/hco/1/GRCh38#22593301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136663773-C-A

22593301-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136663773-C-T

http://identifiers.org/hco/1/GRCh38#22593539-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136663492-A-C

22593560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136663471-G-A

22593717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136663315-G-A

22593717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136663315-G-T

22593791-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136663257-T-A

22593792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136663256-G-A

22593792-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136663256-G-T

22593803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136663245-G-A

22593803-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136663245-G-C

22593803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136663245-G-T

22594657-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136662911-G-A

22594679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136662889-G-A

22594800-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136662791-T-C

22594955-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 136662629-C-T

http://identifiers.org/hco/1/GRCh38#22595121-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136662491-C-A

22595121-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136662491-C-G

22595121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136662491-C-T

22595122-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136662490-C-T

22595128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136662484-G-A

22595128-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 136662484-G-T

22595239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136662444-A-G

http://identifiers.org/hco/1/GRCh38#22595295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136662388-C-A

22595299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136662384-T-C

22595310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 136662373-A-G

22595324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: splice donor variant
orthologous variants: 136662359-G-A

22595324-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: splice donor variant
orthologous variants: 136662359-G-T

http://identifiers.org/hco/1/GRCh38#22595349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136662337-C-A

22595349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: 136662337-C-T

22595351-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: 136662336-G-A

http://identifiers.org/hco/1/GRCh38#22595373-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136662315-C-A

22595373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: 136662315-C-T

22595387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: 136662301-C-T

http://identifiers.org/hco/1/GRCh38#22595412-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136662279-C-A

22595412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: 136662279-C-T

22595413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: 136662278-G-A

22595413-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: 136662278-G-T

22595423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: 136662268-G-A

22595423-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: 136662268-G-T

22595424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: 136662267-G-A

22595424-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: 136662267-G-T

http://identifiers.org/hco/1/GRCh38#22595425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136662266-C-A

22595425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: 136662266-C-T

22595428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: 136662263-G-A

22595428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: 136662263-G-T

http://identifiers.org/hco/1/GRCh38#22595447-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136662257-A-C

http://identifiers.org/hco/1/GRCh38#22595449-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136662255-C-A

22595449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: 136662255-C-T

22595901-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: 136662065-G-A

22596035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: 136661967-T-C

22596073-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: 136661942-T-G

22596076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: 136661939-C-T

22596090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: 136661926-G-A

http://identifiers.org/hco/1/GRCh38#22596098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136661918-C-A

22596098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 136661918-C-T

22596178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: 136661825-G-A

22596178-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: 136661825-G-C

22596219-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: 136661814-G-A

22596219-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: 136661814-G-C

22596239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: 136661794-G-A

22596239-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: 136661794-G-T

22596294-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: 136661759-A-G

http://identifiers.org/hco/1/GRCh38#22596320-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136661728-C-A

22596320-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: 136661728-C-G

22596320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: 136661728-C-T

22596427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: 136661650-G-A

22596430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: 136661635-G-A

22596433-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: 136661632-G-A

22596433-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: 136661632-G-C

22596511-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: 136661554-C-T

http://identifiers.org/hco/1/GRCh38#22596736-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136661473-A-C

22597111-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: 136661300-G-T

22597141-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: 136661273-G-C

22597141-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: 136661273-G-T

22597185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: 136661224-T-C

http://identifiers.org/hco/1/GRCh38#22597252-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136661177-A-C

22597252-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: 136661177-A-G

22597252-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: 136661177-A-T

http://identifiers.org/hco/1/GRCh38#22597275-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136661155-C-A

22597275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: 136661155-C-T

22597473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: missense variant
orthologous variants: 136660955-T-C

22597491-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: 136660937-T-G

http://identifiers.org/hco/1/GRCh38#22597549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136660876-C-A

22597549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: 136660876-C-T

22597638-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: 136660815-T-A

22597723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: missense variant
orthologous variants: 136660740-C-T

22597750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: missense variant
orthologous variants: 136660713-C-T

http://identifiers.org/hco/1/GRCh38#22597765-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136660698-A-C

22597840-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: missense variant
orthologous variants: 136660623-C-T

http://identifiers.org/hco/1/GRCh38#22597883-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136660580-C-A

22597883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: 136660580-C-T

22597904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: 136660560-C-T

22598020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: 136660458-G-A

22598020-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: 136660458-G-T

22598031-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: 136660447-A-G

22598195-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: missense variant
orthologous variants: 136660302-C-G

22598331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: 136660172-G-A

22598331-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: 136660172-G-T

22598349-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: 136660154-G-A

22598415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: 136660103-C-T

22598434-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: 136660084-C-G

22598721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: 136659898-G-A

22598721-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: 136659898-G-T

22598752-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: 136659869-A-G

22598812-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: 136659830-G-T

22598961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: missense variant
orthologous variants: 136659674-G-A

http://identifiers.org/hco/1/GRCh38#22599065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136659571-C-A

22599065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: 136659571-C-T

22600667-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: missense variant
orthologous variants: 136659344-A-G

22600724-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: missense variant
orthologous variants: 136659287-G-T

22600766-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: missense variant
orthologous variants: 136659245-C-G

http://identifiers.org/hco/1/GRCh38#22600784-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136659227-C-A

22600784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: missense variant
orthologous variants: 136659227-C-T

22600799-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: missense variant
orthologous variants: 136659212-A-G

22600826-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: 136659185-T-G

22600847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: 136659167-A-G

http://identifiers.org/hco/1/GRCh38#22600853-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136659155-A-C

22600853-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: 136659155-A-G

22600882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: 136659133-C-T

22601054-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: missense variant
orthologous variants: 136658959-C-T

22601114-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: 136658910-T-G

22601115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: 136658909-G-T

22601126-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: 136658905-G-T

http://identifiers.org/hco/1/GRCh38#22601142-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136658894-C-A

22601142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: 136658894-C-T

22601160-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: 136658875-C-T

22601172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: 136658863-G-A

22601172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: 136658863-G-T

22601319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: missense variant
orthologous variants: 136658759-G-A

22601319-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: missense variant
orthologous variants: 136658759-G-T

22601346-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: missense variant
orthologous variants: 136658732-G-A

22601346-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: missense variant
orthologous variants: 136658732-G-T

22601409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: missense variant
orthologous variants: 136658669-T-C

http://identifiers.org/hco/1/GRCh38#22601445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136658633-C-A

22601445-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: missense variant
orthologous variants: 136658633-C-G

22601445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: synonymous variant
orthologous variants: 136658633-C-T

22601490-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: 136658586-G-A

22601490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: intron variant
orthologous variants: 136658586-G-T

22601935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: 3 prime UTR variant
orthologous variants: 136658221-G-A

22601935-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: 3 prime UTR variant
orthologous variants: 136658221-G-T

22601974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: 3 prime UTR variant
orthologous variants: 136658176-C-T

http://identifiers.org/hco/1/GRCh38#22602014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136658137-C-A

22602050-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: 3 prime UTR variant
orthologous variants: 136658101-G-A

22602050-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: 3 prime UTR variant
orthologous variants: 136658101-G-T

22602058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: 3 prime UTR variant
orthologous variants: 136658093-G-A

22602058-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: 3 prime UTR variant
orthologous variants: 136658093-G-T

22602075-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: 3 prime UTR variant
orthologous variants: 136658065-T-C

22602112-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: 3 prime UTR variant
orthologous variants: 136658028-T-C

http://identifiers.org/hco/1/GRCh38#22602131-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136658009-C-A

22602165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: 3 prime UTR variant
orthologous variants: 136657974-A-G

22602166-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: 3 prime UTR variant
orthologous variants: 136657973-G-T

22602235-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: 3 prime UTR variant
orthologous variants: 136657903-G-T

22602254-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: 3 prime UTR variant
orthologous variants: 136657876-A-G

22602347-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: 3 prime UTR variant
orthologous variants: 136657805-T-G

22602366-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: 3 prime UTR variant
orthologous variants: 136657786-A-G

22602366-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: 3 prime UTR variant
orthologous variants: 136657786-A-T

22602378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: 3 prime UTR variant
orthologous variants: 136657778-G-A

22602378-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: 3 prime UTR variant
orthologous variants: 136657778-G-T

22602393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: 3 prime UTR variant
orthologous variants: 136657763-A-G

22602393-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: 3 prime UTR variant
orthologous variants: 136657763-A-T

22602463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: 3 prime UTR variant
orthologous variants: 136657688-G-A

22602463-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: 3 prime UTR variant
orthologous variants: 136657688-G-T

22602475-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: 3 prime UTR variant
orthologous variants: 136657676-T-A

22602475-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: 3 prime UTR variant
orthologous variants: 136657676-T-C

22602545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: 3 prime UTR variant
orthologous variants: 136657609-A-G

22602566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: 3 prime UTR variant
orthologous variants: 136657588-G-A

22602594-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: 3 prime UTR variant
orthologous variants: 136657571-T-A

22602720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: 3 prime UTR variant
orthologous variants: 136657489-G-A

22602720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: 3 prime UTR variant
orthologous variants: 136657489-G-T

http://identifiers.org/hco/1/GRCh38#22602770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136657448-C-A

22602820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: 3 prime UTR variant
orthologous variants: 136657406-T-C

22602896-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: 3 prime UTR variant
orthologous variants: 136657328-G-T

http://identifiers.org/hco/1/GRCh38#22602929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136657297-C-A

http://identifiers.org/hco/1/GRCh38#22603058-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136657165-C-A

22603067-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: 3 prime UTR variant
orthologous variants: 136657156-G-T

22603095-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: 3 prime UTR variant
orthologous variants: 136657136-G-T

22603108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: 3 prime UTR variant
orthologous variants: 136657123-G-A

22603108-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: 3 prime UTR variant
orthologous variants: 136657123-G-T

22603134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: 3 prime UTR variant
orthologous variants: 136657115-C-T

22603147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: 3 prime UTR variant
orthologous variants: 136657102-G-A

22603147-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: 3 prime UTR variant
orthologous variants: 136657102-G-T

http://identifiers.org/hco/1/GRCh38#22603200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#136657056-C-A

22603200-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: 3 prime UTR variant
orthologous variants: 136657056-C-G

22603200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: 3 prime UTR variant
orthologous variants: 136657056-C-T

22603364-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3391
most severe consequence: 3 prime UTR variant
orthologous variants: 136656893-A-G