http://identifiers.org/hco/15/GRCh38#80059200-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#84339526-A-C

80059238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: 84339486-T-C

80059313-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: 84339432-A-G

http://identifiers.org/hco/15/GRCh38#80059407-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#84339334-A-C

http://identifiers.org/hco/15/GRCh38#80059521-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#84339238-C-A

80059521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: 84339238-C-T

http://identifiers.org/hco/15/GRCh38#80059557-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#84339204-C-A

80059619-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 84339141-T-C

http://identifiers.org/hco/15/GRCh38#80059683-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#84339078-A-C

80059979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, undefined
orthologous variants: 84338866-G-A

80059979-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, undefined
orthologous variants: 84338866-G-C

http://identifiers.org/hco/15/GRCh38#80061019-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#84338402-A-C

80061096-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: 84338336-T-G

http://identifiers.org/hco/15/GRCh38#80061301-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#84337965-C-A

http://identifiers.org/hco/15/GRCh38#80061386-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#84337922-C-A

80061433-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: 84337877-A-T

http://identifiers.org/hco/15/GRCh38#80061452-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#84337857-C-A

80061452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: 84337857-C-T

80061472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: 84337837-T-C

80061493-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: 84337816-A-G

http://identifiers.org/hco/15/GRCh38#80061496-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#84337813-A-C

80062045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: 84337282-A-G

80062312-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: 84337021-T-G

80062553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: 84336846-G-A

80062938-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: 84336143-C-T

80063024-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: 84335971-G-A

80063040-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: 84335819-T-G

80063081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: 84335748-T-C

80063148-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: 84335679-T-C

80063277-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: 84335559-A-T

80064988-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: 84335324-C-G

80064988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: 84335324-C-T

80067455-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: 84333516-A-G

80067874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: 84333137-A-G

80069070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: 84332450-C-T

http://identifiers.org/hco/15/GRCh38#80069090-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#84332431-C-A

80069090-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: 84332431-C-T

80069274-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: 84332243-A-G

80069313-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: 84332205-T-A

80069313-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: 84332205-T-G

80069423-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: 84332101-G-A

80069473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: 84332042-G-T

80070246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: 84331370-A-G

80070478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: 84331136-T-C

80070668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: 84330869-G-A

80070668-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: 84330869-G-C

80070871-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: 84330496-T-A

80071499-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: 84329792-A-G

80071608-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: 84329698-G-A

http://identifiers.org/hco/15/GRCh38#80071707-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#84329524-A-C

80071743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: 84329487-A-G

80072258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: 84328899-G-A

80072778-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84328385-A-G

80072855-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84328313-T-C

80072954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84328215-G-A

80073081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84328104-A-G

80073224-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84327955-G-A

80073224-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84327955-G-T

http://identifiers.org/hco/15/GRCh38#80073239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#84327940-C-A

80073279-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 84327919-A-G

80073329-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 84327867-A-G

80073355-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84327841-A-G

80073386-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 84327811-A-G

80073425-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84327757-T-G

80073882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84327336-C-T

80074686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84326564-T-C

80074826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84326440-T-C

80074960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84326351-T-C

80074984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84326327-G-A

80075154-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84326127-T-A

80075542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84325684-A-G

80075630-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84325618-G-C

80075660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84325589-A-G

80075693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84325556-A-G

80075829-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84325344-G-A

80076074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84325129-C-T

80076115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84325093-C-T

80076236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84324939-A-G

80076378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84324822-A-G

80076398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84324803-C-T

http://identifiers.org/hco/15/GRCh38#80076710-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#84324507-A-C

80076803-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84324314-C-T

80077091-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84324023-G-C

http://identifiers.org/hco/15/GRCh38#80077133-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#84323981-A-C

80077212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84323893-A-G

80077685-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84323503-T-A

80082007-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84322767-C-T

80082152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84322581-A-G

80087353-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84321738-G-T

80087585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84321553-A-G

80087786-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84321350-T-G

80087815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84321340-C-T

80088112-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84321109-G-T

80088638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84320785-T-C

80088716-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84320722-G-T

80088958-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84320524-T-C

80089013-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84320464-G-C

80089125-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84320296-A-G

80089609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84320144-A-G

80089625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84320136-T-C

80089694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84320066-G-A

80089849-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84319931-G-C

80090210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84319527-G-A

80091390-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84315636-T-C

80091452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84315570-C-T

80091508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84315513-T-C

80093818-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84306763-G-C

80094066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84306540-G-A

80094773-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84305758-T-C

80094792-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84305721-C-G

80094792-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84305721-C-T

80094795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84305718-T-C

80095484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84304958-A-G

80095750-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84304731-T-C

80095838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84304641-T-C

80095976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84304512-A-G

80097732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84302920-T-C

80097793-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84302861-A-T

80097857-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84302794-A-G

80097986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84302664-C-T

80098095-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84302544-G-T

80098239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84302406-T-C

80098240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84302405-G-A

80098623-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84302044-T-G

80098675-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84301997-A-T

80098845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84301836-C-T

http://identifiers.org/hco/15/GRCh38#80098949-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#84301763-A-C

80099338-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84301446-G-A

80099338-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84301446-G-C

80100164-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 84301065-A-T

80100167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 84301062-C-T

80100213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84301022-A-G

80100237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84300996-A-G

80100364-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84300875-T-C

80100735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84300550-G-A

80100785-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84300505-T-A

80100839-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84300449-T-G

80102528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84299505-T-C

http://identifiers.org/hco/15/GRCh38#80104665-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#84298994-A-C

80104665-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84298994-A-G

80104675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84298984-G-A

80104830-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84297493-T-C

http://identifiers.org/hco/15/GRCh38#80104982-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#84297368-C-A

80104982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84297368-C-T

80105071-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84297278-G-T

http://identifiers.org/hco/15/GRCh38#80105114-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#84297230-A-C

80105125-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84297219-T-G

80105609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84296525-G-A

80105609-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84296525-G-C

80105611-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84296523-C-T

80105789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 84296341-T-C

80106810-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84295236-T-A

80106811-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84295235-T-G

80108211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84293883-A-G

http://identifiers.org/hco/15/GRCh38#80108349-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#84293730-A-C

80108447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84293589-C-T

80112869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84291118-G-A

80112962-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84291006-A-G

80113295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84290028-C-T

80113473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84289868-T-C

80114305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84289316-T-C

80114425-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84289201-T-A

http://identifiers.org/hco/15/GRCh38#80115125-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#84288464-A-C

80115190-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84288408-G-C

80115348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84288285-T-C

80115505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84288126-C-T

80115566-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84288053-A-G

http://identifiers.org/hco/15/GRCh38#80115619-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#84287980-C-A

80116048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84287551-C-T

80116083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84287514-T-C

80116284-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84287385-C-G

80116284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84287385-C-T

80116285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84287384-G-A

80116285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84287384-G-T

80116290-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84287379-A-G

80116354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84287289-T-C

80116444-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84287199-C-G

80116444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84287199-C-T

80118749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84285371-A-G

80119171-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84284629-C-T

80119560-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84284274-T-C

80119578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84284255-G-T

80119602-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84284238-C-T

80119615-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84284227-T-C

80119801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84284050-G-A

80120000-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84283910-G-C

80120118-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84283809-T-C

http://identifiers.org/hco/15/GRCh38#80120272-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#84283670-A-C

80120272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84283670-A-G

http://identifiers.org/hco/15/GRCh38#80120584-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#84283377-C-A

80121770-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 84283141-G-T

80121786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 84283125-G-A

80122779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 84281883-C-T

http://identifiers.org/hco/15/GRCh38#80122847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#84281814-C-A

80122847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84281814-C-T

http://identifiers.org/hco/15/GRCh38#80122921-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#84281739-C-A

80122921-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84281739-C-T

80122977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84281673-T-C

80123003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84281650-A-G

80123090-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: 84281580-G-A

80123090-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: 84281580-G-T

80123117-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: 84281553-T-C

80123225-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: 84281464-C-G

80123267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: 84281413-A-G

80123293-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: 84281400-C-T

80123336-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: 84281360-C-G

80123336-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: 84281360-C-T

http://identifiers.org/hco/15/GRCh38#80123342-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#84281354-A-C

80123413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: 84281303-C-T

80124413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: 84280504-A-G

80124546-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: 84280405-C-G

80124682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: 84280299-A-G

80124794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: 84273957-C-T

80124864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: 84273882-G-A

80124875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: 84273871-T-C

80124891-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: 84273591-A-T

80125162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: 84273358-T-C

80125162-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: 84273358-T-G

http://identifiers.org/hco/15/GRCh38#80125189-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#84273331-A-C

80125647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: 84272924-A-G

80125647-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: 84272924-A-T

80125819-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: 84272618-C-G

80125821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: 84272616-A-G

80126210-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: 84272168-G-A

80126262-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: 84272111-T-A

80126277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: 84272097-G-A

80126410-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: 84271970-G-C

80126519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: 84271852-G-A

http://identifiers.org/hco/15/GRCh38#80126641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#84271758-C-A

80126641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: 84271758-C-T

80126673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: 84271727-G-A

80128723-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: 84269467-T-C

80128898-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: 84269310-C-G

80128932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: 84269277-T-C

80129036-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: 84269167-G-A

80129226-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: 84268935-G-A

80129528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: 84268682-G-A

80129528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: 84268682-G-T

80129583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron variant
orthologous variants: 84268629-A-G

80129600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84268617-T-C

80129634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84268584-G-A

80129634-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84268584-G-T

http://identifiers.org/hco/15/GRCh38#80129999-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#84268308-C-A

80130038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84268275-G-A

80130038-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84268275-G-T

80130039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84268274-G-A

http://identifiers.org/hco/15/GRCh38#80130331-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#84268046-C-A

80130412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84267975-G-T

80130490-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84267920-T-C

80130586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84267826-G-A

http://identifiers.org/hco/15/GRCh38#80130795-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#84267499-C-A

80130795-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84267499-C-G

80130798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84267496-C-T

80131054-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 84267315-A-T

80131322-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 84267027-T-A

80131408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 84266944-T-C

80131427-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 84266925-T-A

80131522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84266865-A-G

http://identifiers.org/hco/15/GRCh38#80131545-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/7/GRCm39#84266842-C-A

80131545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84266842-C-T

80131569-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84266818-T-C

80131619-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84266767-G-T

80131667-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84266726-G-A

80131667-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84266726-G-T

80131697-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84266702-A-G

80131834-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84266583-T-C

80131905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84266509-G-A

80136639-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84265956-G-A

80136805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84265806-G-A

80136822-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84265789-A-G

80136822-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84265789-A-T

80136927-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84265690-C-T

80136989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84265641-C-T

80137422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84265238-G-A

80137432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84265229-T-C

80137456-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84265197-G-A

80137470-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 84265184-C-G

80137671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30164
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 84264982-A-G