65872839-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94116909-G-C

65872909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94116976-G-T

65873000-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94117025-T-C

65873094-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94117124-T-C

65873236-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94117234-G-T

65873416-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94117365-A-T

65873442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94117394-G-T

65873564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94117496-C-T

65873565-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94117497-T-C

65873663-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94117591-C-G

65878869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94119437-T-C

65878891-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94119459-T-C

65878905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94119473-T-C

65878913-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94119481-G-A

65878974-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94119529-G-A

http://identifiers.org/hco/3/GRCh38#65879295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#94119817-C-A

65879295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94119817-C-T

65879323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94119851-G-A

65881929-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94122473-C-G

65882092-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94122682-G-T

65882946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94123523-A-G

65883485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94124531-T-C

65883663-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94124789-T-A

65883688-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94124814-T-G

65883698-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94124824-C-T

http://identifiers.org/hco/3/GRCh38#65883709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#94124835-C-A

65883709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94124835-C-T

65883719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94124843-T-C

65883723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94124847-C-T

65883870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94124984-T-C

65883907-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94125019-T-G

http://identifiers.org/hco/3/GRCh38#65883961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#94125073-C-A

65883961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94125073-C-T

65884392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94125437-C-T

65884404-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94125449-T-G

65884477-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94125506-G-C

65884477-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94125506-G-T

65885996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94126511-G-A

65886224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94126733-T-C

65886255-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94126765-T-C

65886589-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94127061-C-G

65886798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94127219-G-A

65886940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94127341-C-T

http://identifiers.org/hco/3/GRCh38#65886962-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#94127364-C-A

65886962-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94127364-C-G

65886990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94127389-T-C

65887026-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94127424-T-A

65887341-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94128754-T-A

http://identifiers.org/hco/3/GRCh38#65887376-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#94128793-C-A

65887376-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94128793-C-T

65887395-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94128809-A-G

65887407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94128821-G-A

65887491-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94128893-T-C

http://identifiers.org/hco/3/GRCh38#65888184-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#94129837-C-A

65888297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94129930-A-G

http://identifiers.org/hco/3/GRCh38#65888308-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#94129940-A-C

65888356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94129988-A-G

65888578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94130166-G-A

65888733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94130342-C-T

65888931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94130548-C-T

http://identifiers.org/hco/3/GRCh38#65889248-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#94130798-A-C

http://identifiers.org/hco/3/GRCh38#65889257-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#94130807-A-C

65890524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94131857-T-C

65891344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94133137-T-C

65891398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94133190-G-A

65891412-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94133204-C-G

65891449-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94133239-A-T

65891645-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94133398-T-C

65891685-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94133440-G-T

65891988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94133508-T-C

65892059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94133573-C-T

65892272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94133772-G-A

65892275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94133775-C-T

65892289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94133789-G-A

65892379-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94133837-T-G

65892543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94133945-G-A

65892820-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94134026-C-G

65892887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 94134091-G-A

65892913-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 94134117-A-T

65893213-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94134363-T-C

http://identifiers.org/hco/3/GRCh38#65894563-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#94135007-A-C

65894810-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94135222-A-G

65894850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 94135262-T-C

65894863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 94135274-T-C

65895017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94135430-G-A

65895017-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94135430-G-T

65895020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94135433-G-A

http://identifiers.org/hco/3/GRCh38#65895335-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#94135719-C-A

65895335-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94135719-C-T

65895719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94136117-G-A

65895952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94136327-A-G

65896098-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94136459-G-C

65896294-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94136618-T-A

http://identifiers.org/hco/3/GRCh38#65896295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#94136619-C-A

65896360-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94136679-T-A

65896360-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94136679-T-G

65896362-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94136681-T-C

65896484-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94136821-C-G

65896802-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94136969-T-C

65896803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94136970-T-C

http://identifiers.org/hco/3/GRCh38#65898133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#94137407-C-A

65898133-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94137407-C-G

65898133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94137407-C-T

65898167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94137443-C-T

65898255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94137519-C-T

65898306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94137586-G-T

65898308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94137588-G-A

65898655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94137834-A-G

65899558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 94138352-A-G

65899975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94138746-C-T

http://identifiers.org/hco/3/GRCh38#65900093-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#94138856-A-C

65900175-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94138953-C-G

65900230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94139009-G-A

65900281-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94139060-A-G

65900281-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94139060-A-T

65900338-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94139198-A-G

65900764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94140069-G-A

65900814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94140122-A-G

65900905-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94140191-G-A

http://identifiers.org/hco/3/GRCh38#65901016-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#94140245-A-C

65901035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94140248-C-T

http://identifiers.org/hco/3/GRCh38#65901279-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#94140484-A-C

65901698-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94140898-G-A

65901698-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94140898-G-T

65901832-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94141026-T-G

http://identifiers.org/hco/3/GRCh38#65901881-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#94141078-A-C

65901881-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94141078-A-G

65901922-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94141114-A-T

http://identifiers.org/hco/3/GRCh38#65901964-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#94141159-C-A

65901964-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94141159-C-G

65901964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94141159-C-T

65902071-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94141326-T-C

http://identifiers.org/hco/3/GRCh38#65902509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#94141693-C-A

65902509-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94141693-C-G

65902509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94141693-C-T

http://identifiers.org/hco/3/GRCh38#65902523-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#94141707-C-A

65902539-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94141723-A-G

65902551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94141734-A-G

65902552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94141735-G-A

65902552-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94141735-G-C

65902552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94141735-G-T

http://identifiers.org/hco/3/GRCh38#65902647-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#94141832-C-A

65902925-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94142085-T-A

65902925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94142085-T-C

65904018-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94142541-A-G

65904370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94142855-C-T

65904396-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94142879-G-A

65904443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94142926-T-C

65904455-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94142938-C-G

65911885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94145036-A-G

http://identifiers.org/hco/3/GRCh38#65912216-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#94145387-A-C

http://identifiers.org/hco/3/GRCh38#65912236-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#94145407-C-A

65912254-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94145425-A-T

65912387-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94145551-G-A

65912460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94145601-C-T

http://identifiers.org/hco/3/GRCh38#65912707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#94145839-C-A

65914145-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94146660-A-G

65914196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94146711-T-C

65914216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94146731-G-A

65914216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94146731-G-T

65914256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94146772-G-A

65914256-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94146772-G-C

http://identifiers.org/hco/3/GRCh38#65914267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#94146786-C-A

65914320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94146839-C-T

65914526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94147015-C-T

65914603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94147077-C-T

65914605-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94147079-A-G

65914853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94147389-G-A

65914877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94147410-G-A

65915036-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94147852-T-C

http://identifiers.org/hco/3/GRCh38#65915062-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#94147877-A-C

65915079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94147894-C-T

65915105-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94147920-G-A

65915337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94148151-C-T

65915348-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94148161-C-G

65915367-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94148180-C-G

65915759-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94148561-A-G

65915947-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94148783-A-G

65917235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94151206-A-G

http://identifiers.org/hco/3/GRCh38#65917238-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#94151209-C-A

65917312-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94151282-G-T

65917503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94151464-A-G

65917750-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94151561-A-T

http://identifiers.org/hco/3/GRCh38#65917838-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#94151626-A-C

65917867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94151654-T-C

65918033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94151813-G-A

65918039-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94151819-A-G

http://identifiers.org/hco/3/GRCh38#65918159-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#94151939-A-C

65918342-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94152124-A-T

http://identifiers.org/hco/3/GRCh38#65918943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#94152442-C-A

65918947-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94152450-C-G

65918947-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94152450-C-T

http://identifiers.org/hco/3/GRCh38#65918971-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#94152590-C-A

http://identifiers.org/hco/3/GRCh38#65919187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#94152786-C-A

65919187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94152786-C-T

65920597-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94154389-T-G

65921094-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94154580-G-C

65921190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94154659-T-C

65924138-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94155429-A-T

65924216-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94155507-A-T

65924230-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94155521-T-A

65924722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94156740-C-T

http://identifiers.org/hco/3/GRCh38#65925444-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#94157986-C-A

65925444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94157986-C-T

http://identifiers.org/hco/3/GRCh38#65925495-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#94158030-A-C

65925559-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94158076-T-C

65925632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94158152-T-C

65925650-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94158166-A-T

65925681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94158193-T-C

65926108-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94158684-T-A

65927921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94159436-G-A

65927939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94159454-T-C

65927992-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94159507-C-G

65927992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94159507-C-T

65928160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94159656-T-C

65928202-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94160400-T-A

65928208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94160406-C-T

65928268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94160468-G-A

65928285-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94160485-G-C

65928362-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94160559-G-T

65928460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94160651-C-T

65928674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94160864-C-T

65928814-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94161003-G-A

65928882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94161066-T-C

65928918-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94161102-T-G

65928994-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94161174-G-T

http://identifiers.org/hco/3/GRCh38#65929178-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#94161182-C-A

65929212-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94161220-G-A

65929820-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94161636-C-G

65929820-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94161636-C-T

65929841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94161657-T-C

65929852-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94161668-G-C

65932824-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94161792-G-A

65933048-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94162021-G-C

65933138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94162081-T-C

65933226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94162151-T-C

65937422-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94164164-T-G

65937498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94164233-A-G

http://identifiers.org/hco/3/GRCh38#65937542-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#94164273-A-C

65937560-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94164293-C-T

65937586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94164316-G-A

65938898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94166575-A-G

65939037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94166705-C-T

65939226-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94166899-T-A

65939399-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94167079-T-A

65939557-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94167225-T-C

65939718-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94167365-G-A

65939874-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94167500-T-C

65940074-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94167671-G-C

65940093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94167696-C-T

65940205-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94167860-G-A

65940221-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94167876-G-C

65940221-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94167876-G-T

65940461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94168094-G-A

65940627-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94168238-G-C

65940632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94168251-T-C

65940647-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94168266-T-C

65940678-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94168297-T-C

http://identifiers.org/hco/3/GRCh38#65943817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#94169898-C-A

65943817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94169898-C-T

65943850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94169930-G-A

65943938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94170006-G-A

65944000-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94170083-T-A

65944777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94170478-T-C

65944819-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94170520-G-C

65944845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94170545-G-A

65944845-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94170545-G-T

65944945-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94170729-G-C

65944960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94170744-A-G

65944982-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94170763-T-A

65944982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94170763-T-C

65944994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94170775-C-T

65944995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94170776-G-A

65945001-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94170777-C-T

65945099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94170867-C-T

65945119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94170887-G-A

65945198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94170973-G-A

65946381-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94172549-G-C

65946381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94172549-G-T

65946422-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94172590-T-A

65946458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94172623-T-C

65946460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94172625-C-T

65946461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94172626-G-A

65946461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94172626-G-T

65946482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94172647-C-T

65946492-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94172657-G-C

65946496-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94172661-G-C

http://identifiers.org/hco/3/GRCh38#65946544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#94172708-C-A

65946544-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94172708-C-G

65946610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94172753-A-G

65946662-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94172795-A-G

65946742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94172881-G-A

65947031-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94173187-C-G

65947031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94173187-C-T

65947188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94173337-G-A

65948457-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94174600-A-T

65948471-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94174614-G-T

65948616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94174738-T-C

65948670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94174788-C-T

http://identifiers.org/hco/3/GRCh38#65948720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#94174835-C-A

65948720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94174835-C-T

65948750-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94174856-C-G

65948847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94174959-C-T

65948890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94174991-A-G

65948895-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94174998-T-C

65949181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94175317-T-C

65949295-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94175469-T-C

65949521-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94176446-G-A

65952030-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94179901-G-C

65952083-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94179945-C-T

65952298-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 94180138-T-C

http://identifiers.org/hco/3/GRCh38#65952313-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#94180153-A-C

65952380-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 94180218-A-T

65952480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 94180326-T-C

65952942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94180456-G-A

65953249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94180701-G-A

65953444-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 94180876-C-G

65953554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 94180995-T-C

65953670-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94181112-G-A

65953951-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94181367-T-A

65953951-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94181367-T-G

65954014-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94181429-G-C

65954417-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94181792-T-A

65954417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 94181792-T-C

http://identifiers.org/hco/3/GRCh38#65954440-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#94181799-C-A

http://identifiers.org/hco/3/GRCh38#65954533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#94181872-C-A

65954536-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 42436
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 94181875-G-T