http://identifiers.org/hco/3/GRCh38#72888051-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100681649-C-A

72888051-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100681649-C-T

72888068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100681669-T-C

http://identifiers.org/hco/3/GRCh38#72888214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100681794-C-A

72888214-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100681794-C-G

72888214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 100681794-C-T

http://identifiers.org/hco/3/GRCh38#72888295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#100681866-C-A

72888295-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 100681866-C-G

72888295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: missense_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 100681866-C-T

72888335-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 100681909-G-A

72888335-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 100681909-G-T

72888485-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 100682062-T-A

72888485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 100682062-T-C

72888485-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 100682062-T-G

http://identifiers.org/hco/3/GRCh38#72888579-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100682158-A-C

72888579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100682158-A-G

72888579-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100682158-A-T

72888596-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100682175-G-C

72888596-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100682175-G-T

72888752-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100682306-C-T

72888854-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100682405-A-T

http://identifiers.org/hco/3/GRCh38#72888985-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#100682533-A-C

72889097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100682643-G-A

72889127-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100682671-C-T

72889197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100682730-A-G

72889233-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100682766-G-A

72889255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100682821-G-A

72889603-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100683278-G-T

72889664-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100683376-T-C

72889836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100683517-A-G

72890544-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100684094-G-C

72890584-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100684128-C-T

72890729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100684290-G-A

http://identifiers.org/hco/3/GRCh38#72890861-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100684416-A-C

72890861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100684416-A-G

http://identifiers.org/hco/3/GRCh38#72890939-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#100684503-A-C

72890939-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100684503-A-G

72891321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100684867-G-A

http://identifiers.org/hco/3/GRCh38#72891752-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100685302-A-C

72891936-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100685495-A-T

72891955-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100685514-G-T

72892177-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100686066-C-T

72892199-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100686087-A-T

72892210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100686098-T-C

72892230-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100686118-T-A

72892252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100686120-G-A

72892753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100686804-A-G

72892820-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100686871-G-A

http://identifiers.org/hco/3/GRCh38#72893905-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100690120-A-C

72893957-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100690172-G-A

http://identifiers.org/hco/3/GRCh38#72894156-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100690318-C-A

72894172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100690334-T-C

72894350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100690932-G-A

72894367-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100690953-G-C

72894367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100690953-G-T

72894417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100691045-T-C

72894431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100691055-T-C

http://identifiers.org/hco/3/GRCh38#72895185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100691136-C-A

72895282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100691201-C-T

72895369-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100691268-C-G

http://identifiers.org/hco/3/GRCh38#72895513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100691415-C-A

72895513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100691415-C-T

72895616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100691502-T-C

72895739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100691608-T-C

72895912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100692250-A-G

72895975-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100692312-A-G

72896074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100692411-G-A

72896074-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100692411-G-C

72896226-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100692540-C-G

72896227-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100692541-T-C

72896505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100692658-A-G

72897383-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100693875-G-T

72897458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100693958-A-G

http://identifiers.org/hco/3/GRCh38#72897500-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100694011-A-C

72897500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100694011-A-G

72897635-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100694133-G-T

http://identifiers.org/hco/3/GRCh38#72897681-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100694171-A-C

72897691-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100694181-C-G

72897733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100694222-G-A

72897894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100694397-G-A

72897894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100694397-G-T

72897897-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100694400-C-T

72898025-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100694709-A-T

72898053-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100694730-T-A

72898129-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100694806-A-G

72898208-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100695874-G-C

72898249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100695914-C-T

72898509-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100696195-A-G

72898509-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100696195-A-T

72898538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100696218-A-G

72898556-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100696239-G-A

http://identifiers.org/hco/3/GRCh38#72898626-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100696279-C-A

72898626-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100696279-C-T

72899164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100697106-A-G

72899459-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100697400-T-C

72899588-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100697526-A-G

72899813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100698103-C-T

72903702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -G-A

http://identifiers.org/hco/3/GRCh38#72903713-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: -A-C

72904118-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100702446-G-T

72904147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100702475-G-A

72904310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100702613-G-A

72904380-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100702683-T-G

72906872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100708684-C-T

72906948-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100708763-A-G

72907932-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100709703-T-C

72908304-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100710076-T-G

72908319-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100710091-A-T

72908344-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 100710119-T-C

72908447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 100710219-A-G

72908547-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 100710319-G-C

http://identifiers.org/hco/3/GRCh38#72908635-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100710416-A-C

72908637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100710418-C-T

72908661-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100710442-A-G

72908661-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100710442-A-T

http://identifiers.org/hco/3/GRCh38#72908670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100710451-C-A

72909366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100711087-G-A

72909438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100711165-C-T

72909458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100711177-G-A

72909558-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100711260-A-T

72909621-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100711319-C-T

72909801-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100711469-G-C

72921706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100726860-G-A

72921706-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100726860-G-T

72921897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100727048-G-A

72921903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100727054-C-T

72921970-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100727131-C-G

72921970-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100727131-C-T

72922077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100727233-G-A

72922092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100727248-T-C

http://identifiers.org/hco/3/GRCh38#72922115-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100727271-A-C

http://identifiers.org/hco/3/GRCh38#72922135-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100727291-A-C

72922135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100727291-A-G

72922156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100727312-T-C

72922164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100727320-A-G

http://identifiers.org/hco/3/GRCh38#72922419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100727574-C-A

72922419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100727574-C-T

http://identifiers.org/hco/3/GRCh38#72922424-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100727579-C-A

72922424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100727579-C-T

72922483-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100727637-G-T

72922570-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100727720-G-T

72922572-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100727722-G-C

72922705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100727824-C-T

72922771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100727881-T-C

72924968-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100736241-T-G

72924972-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100736245-G-A

http://identifiers.org/hco/3/GRCh38#72925042-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100736313-C-A

72925042-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100736313-C-T

72925129-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100736391-C-T

72925172-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100736434-T-C

72925489-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100736655-A-G

72925489-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100736655-A-T

72925513-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100736694-G-C

72925534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100736715-T-C

72925682-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100736864-A-G

72925759-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100736941-T-A

72925904-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100737093-T-C

72925914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100737103-C-T

72926144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100737313-A-G

72926285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100738062-A-G

72926378-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100738327-C-T

72926411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100738359-G-A

72926458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100738407-A-G

72926506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100738452-G-A

72926513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100738459-A-G

72926606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100738714-T-C

72926702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100738802-A-G

72926725-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100738825-C-G

72926725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100738825-C-T

72926733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100738833-T-C

72926855-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100738953-T-A

72927271-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100740481-T-A

http://identifiers.org/hco/3/GRCh38#72927701-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100740901-C-A

72927701-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100740901-C-G

72927706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100740906-A-G

72927738-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100740937-G-A

72938502-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100744766-C-G

72938565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100744842-G-A

http://identifiers.org/hco/3/GRCh38#72938569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#100744846-C-A

72938745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100745005-C-T

72938841-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100745098-A-G

72938855-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100745112-A-G

72939005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100745255-G-T

72939108-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100745384-C-G

72939109-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100745385-C-T

http://identifiers.org/hco/3/GRCh38#72939146-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100745418-A-C

72940264-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100746275-T-C

72940318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100746384-C-T

72940326-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100746392-T-G

72940406-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100746476-A-G

72941207-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100747702-A-G

72941243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100747738-G-A

http://identifiers.org/hco/3/GRCh38#72941348-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100747803-C-A

72944957-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100751412-G-C

72944988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100751443-C-T

72945011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100751452-C-T

72945374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100751994-A-G

http://identifiers.org/hco/3/GRCh38#72950722-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100753487-A-C

72950830-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100753591-G-T

72950882-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100753898-G-A

72950953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100753941-G-A

72951175-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100754137-A-G

72951951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100758193-C-T

72952021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100758272-G-T

72952022-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100758273-A-T

72952270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100758467-G-A

72952307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100758504-G-A

72952824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100759006-C-T

http://identifiers.org/hco/3/GRCh38#72952954-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100759126-C-A

72952954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100759126-C-T

72954759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100759757-T-C

http://identifiers.org/hco/3/GRCh38#72954872-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100759874-A-C

http://identifiers.org/hco/3/GRCh38#72954966-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100759974-C-A

72954996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100759999-G-A

72954996-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100759999-G-T

72954999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100760002-G-A

72954999-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100760002-G-C

72954999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100760002-G-T

http://identifiers.org/hco/3/GRCh38#72955004-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100760007-A-C

72955004-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100760007-A-T

http://identifiers.org/hco/3/GRCh38#72955010-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100760011-C-A

72955010-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100760011-C-G

72955010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100760011-C-T

72955035-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100760036-G-A

72955035-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100760036-G-T

72955099-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 100760071-T-A

72955130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 100760102-C-T

72955160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 100760132-T-C

72955251-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 100760223-T-G

72955382-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100760506-G-T

http://identifiers.org/hco/3/GRCh38#72955396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100760520-C-A

72955396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100760520-C-T

72955418-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100760554-G-T

72955428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100760564-A-G

72955428-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100760564-A-T

72955495-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100760619-A-T

72955497-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100760621-T-C

72955497-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100760621-T-G

72955579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100760694-A-G

72955736-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100760847-G-T

72955947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100761042-G-A

72957009-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100763991-T-G

72957116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100764091-T-C

72957288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 100764231-G-A

72957373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100764316-G-A

72957388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100764330-G-A

http://identifiers.org/hco/3/GRCh38#72957424-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#100764366-C-A

72957424-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100764366-C-T

72957435-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100764377-T-A

72957487-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100764424-G-A

72957487-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100764424-G-T

72957524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100764459-G-A

72957550-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100764484-G-A

72957572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100764506-A-G

72957610-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100764545-T-C

72957631-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100764566-G-A

72957844-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100764710-T-C

72958291-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100765265-T-C

72960388-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100768475-A-G

72960396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100768479-T-C

72960412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100768484-T-C

72960978-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100769199-C-G

72961043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100769263-C-T

72961144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100769372-C-T

72961185-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100769412-G-A

72961444-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100770157-G-T

72961782-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100770402-C-G

72961875-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100770477-T-C

72962067-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100770670-C-G

72962293-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100771258-G-A

72962293-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100771258-G-T

http://identifiers.org/hco/3/GRCh38#72966365-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100773784-A-C

72966365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100773784-A-G

72966365-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100773784-A-T

72967316-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100774852-A-T

72967473-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100774991-G-A

72967473-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100774991-G-C

72967473-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100774991-G-T

http://identifiers.org/hco/3/GRCh38#72967487-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100775005-C-A

72967487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100775005-C-T

http://identifiers.org/hco/3/GRCh38#72967501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100775019-C-A

72967501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100775019-C-T

http://identifiers.org/hco/3/GRCh38#72967518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#100775034-C-A

72967518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100775034-C-T

72967530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100775046-T-C

72967756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100775262-A-G

72970972-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100777564-G-C

72971373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100777934-A-G

72971552-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100778124-G-A

72971973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100778604-G-A

72972493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100779109-C-T

72972497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100779113-C-T

72972665-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100779272-G-A

72972665-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100779272-G-C

72973220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100779413-A-G

72973292-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100779486-G-A

72973292-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100779486-G-T

72973448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100779652-A-G

72973526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100779695-T-C

72973642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100779805-G-A

72974251-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100780217-C-G

72974284-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100780245-C-G

72974390-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100780474-T-A

72974399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100780483-C-T

72974470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100780794-T-C

http://identifiers.org/hco/3/GRCh38#72974522-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100780832-A-C

72974553-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100780845-G-C

72974968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100781470-A-G

72974968-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100781470-A-T

http://identifiers.org/hco/3/GRCh38#72975087-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100781589-A-C

72975087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 100781589-A-G

72975136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 100781638-G-A

72975136-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 100781638-G-T

72975187-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100781665-G-A

72975208-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100781685-T-C

http://identifiers.org/hco/3/GRCh38#72975217-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100781692-C-A

72975221-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100781696-G-T

http://identifiers.org/hco/3/GRCh38#72975261-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100781744-A-C

72975261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100781744-A-G

http://identifiers.org/hco/3/GRCh38#72975617-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100782495-C-A

72975617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100782495-C-T

72975682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100782560-C-T

72975695-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100782573-C-G

http://identifiers.org/hco/3/GRCh38#72975736-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100782620-C-A

72975760-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100782644-G-C

72975804-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100782687-A-G

72975808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100782691-G-A

72975808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100782691-G-T

72975900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100782773-G-A

72975900-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100782773-G-T

72976243-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100782780-A-G

72976416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 100782935-C-T

72976421-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 100782940-G-T

72976574-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100783734-G-T

72976602-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100783762-T-G

72976630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100783791-G-T

72976728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100783899-T-C

http://identifiers.org/hco/3/GRCh38#72976737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100783908-C-A

72976745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100783916-T-C

72976850-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100784043-C-G

72976850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100784043-C-T

http://identifiers.org/hco/3/GRCh38#72976874-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100784072-A-C

72976874-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100784072-A-G

72977036-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron variant
orthologous variants: 100784187-G-T

72977150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron variant
orthologous variants: 100784261-C-T

72977231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron variant
orthologous variants: 100784323-A-G

72977324-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron variant
orthologous variants: 100784394-T-G

72977438-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, undefined
orthologous variants: 100784464-T-C

72977538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron variant
orthologous variants: 100784558-G-A

72977608-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron variant
orthologous variants: 100784613-T-G

72978089-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron variant
orthologous variants: 100785175-G-A

72978581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron variant
orthologous variants: 100785671-G-A

72978727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron variant
orthologous variants: 100785799-G-A

72978860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron variant
orthologous variants: 100785922-G-A

72978860-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron variant
orthologous variants: 100785922-G-C

72978990-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron variant
orthologous variants: 100786769-G-T

http://identifiers.org/hco/3/GRCh38#72979120-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100786878-A-C

http://identifiers.org/hco/3/GRCh38#72980166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100787125-C-A

72980190-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron variant
orthologous variants: 100787151-T-A

72980443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron variant
orthologous variants: 100787377-T-C

http://identifiers.org/hco/3/GRCh38#72981048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100787696-C-A

72981048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron variant
orthologous variants: 100787696-C-T

72981389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron variant
orthologous variants: 100787984-G-A

72983195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron variant
orthologous variants: 100788465-T-C

72985732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron variant
orthologous variants: 100796098-A-G

http://identifiers.org/hco/3/GRCh38#72985844-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100796259-C-A

72985914-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron variant
orthologous variants: 100796383-A-T

72986079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron variant
orthologous variants: 100796549-G-A

72986155-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron variant
orthologous variants: 100796626-T-G

72986269-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron variant
orthologous variants: 100796734-G-C

http://identifiers.org/hco/3/GRCh38#72987549-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100799647-C-A

72987571-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron variant
orthologous variants: 100799665-T-A

http://identifiers.org/hco/3/GRCh38#72987681-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100799746-C-A

72987723-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron variant
orthologous variants: 100799784-A-G

72987985-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron variant
orthologous variants: 100800021-T-G

72990279-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron variant
orthologous variants: -G-T

72991598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron variant
orthologous variants: 100806221-C-T

72991769-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron variant
orthologous variants: 100806377-G-C

72991776-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron variant
orthologous variants: 100806384-C-T

72993653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100808219-G-A

http://identifiers.org/hco/3/GRCh38#72993757-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100808319-A-C

72993775-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100808337-A-G

72993865-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100808428-G-C

72993865-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 100808428-G-T

72994505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100809063-T-C

72994609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100809159-T-C

http://identifiers.org/hco/3/GRCh38#72994794-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/6/GRCm39#100809316-C-A

72994794-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100809316-C-G

72994851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100809369-T-C

72996673-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100810477-G-T

http://identifiers.org/hco/3/GRCh38#72996674-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#100810478-C-A

72996674-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100810478-C-G

72996674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100810478-C-T

72996679-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100810483-G-C

72996679-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100810483-G-T

72996692-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 100810496-C-T

http://identifiers.org/hco/3/GRCh38#72996757-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#100810546-A-C

72996757-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100810546-A-G

72996757-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100810546-A-T

http://identifiers.org/hco/3/GRCh38#72997055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/6/GRCm39#100810862-C-A

72997055-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 100810862-C-G

72997055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 100810862-C-T

72997073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant, undefined
orthologous variants: 100810880-T-C

72997163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 100810899-G-A

72997163-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 100810899-G-C

72997163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 100810899-G-T

72997251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100810954-C-T

72997637-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100811145-T-G

72997689-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100811205-C-G

72997689-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100811205-C-T

72997704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100811223-G-A

72997928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100811403-A-G

72997971-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100811463-T-G

72998041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33383
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 100811634-A-G