114128016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 43643929-G-A

114128063-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 43643882-C-G

114128414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 43643519-A-G

114128555-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 43643368-G-A

114128555-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 43643368-G-T

114128575-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 43643348-T-A

114128575-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 43643348-T-G

114128591-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 43643335-G-C

114128591-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 43643335-G-T

114128621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 43643306-T-C

114128755-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 43643161-G-A

114128755-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 43643161-G-T

114128978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43642946-A-G

http://identifiers.org/hco/3/GRCh38#114129004-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#43642922-C-A

114129004-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43642922-C-T

114129015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43642911-G-A

114129015-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43642911-G-T

114129019-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43642907-G-A

114129047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43642884-T-C

114129551-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43642622-A-G

114129700-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43642514-G-C

114129700-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43642514-G-T

114131052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43641975-A-G

http://identifiers.org/hco/3/GRCh38#114131053-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#43641974-C-A

http://identifiers.org/hco/3/GRCh38#114131077-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#43641957-C-A

114131077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43641957-C-T

114131155-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 43641886-C-T

114131414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43641630-A-G

114131414-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43641630-A-T

114131420-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43641624-G-T

114133497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43640237-A-G

114133511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43640223-G-A

http://identifiers.org/hco/3/GRCh38#114133681-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#43640080-A-C

114133681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43640080-A-G

114133719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43640045-T-C

114133769-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43639996-C-T

114136266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43639629-A-G

114136642-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43639296-G-A

114136656-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43639282-G-T

114136871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43639062-C-T

114137183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43638752-G-A

114137412-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43638511-T-C

114138847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43638100-C-T

114139047-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43637945-G-C

114139296-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43637707-G-T

114139348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43637658-T-C

114139534-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 43637489-T-G

http://identifiers.org/hco/3/GRCh38#114139746-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#43637285-A-C

114139746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43637285-A-G

114139845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43637201-A-G

114139877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43637170-T-C

114140082-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43636960-G-A

114140327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43636636-T-C

114140327-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43636636-T-G

114140340-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43636532-C-G

114140890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43636010-G-A

114141435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43635792-G-A

114141604-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43635500-G-A

114142424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43635022-G-A

114142714-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43634758-G-A

114143237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43634243-T-C

114143604-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43633322-A-G

114144059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43632893-T-C

114144094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43632860-G-A

114144186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43632765-C-T

114144332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43632646-G-A

114144416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43632559-G-A

114144498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43632123-A-G

114144760-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43631850-T-C

114144989-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43630218-T-C

114145188-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43630024-G-A

114145440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43629785-A-G

114146772-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43628462-G-A

114147102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43628173-T-C

http://identifiers.org/hco/3/GRCh38#114147343-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#43627952-C-A

114147343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43627952-C-T

114147488-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, synonymous_variant
orthologous variants: 43627808-G-A

http://identifiers.org/hco/3/GRCh38#114147656-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#43627565-A-C

114147730-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43627520-C-G

114147730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43627520-C-T

114148117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43627057-G-A

114149068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43626049-C-T

http://identifiers.org/hco/3/GRCh38#114149456-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#43625523-A-C

114149832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43625151-G-A

114149910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43625067-C-T

114150006-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43624989-A-G

114150381-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43624661-A-G

114150593-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43624477-G-T

114150628-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43624450-A-G

114150799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43624268-C-T

114150828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43624249-G-A

114151074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43624044-T-C

114151234-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43623926-A-G

http://identifiers.org/hco/3/GRCh38#114151754-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#43623177-A-C

114151764-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43623164-A-G

114152081-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43622909-T-A

114152885-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43622322-G-C

114153015-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43622264-A-G

http://identifiers.org/hco/3/GRCh38#114153055-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#43622224-C-A

114153410-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43621925-C-T

114153669-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43621744-T-G

114154329-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43621025-G-C

114154906-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43620502-G-C

114155256-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43620106-A-G

114155299-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43620063-A-G

114155704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43619689-C-T

114155745-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43619626-G-A

114155755-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43619616-C-G

114159355-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43611474-C-T

http://identifiers.org/hco/3/GRCh38#114159634-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#43611191-A-C

114159634-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43611191-A-G

114159692-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43611136-A-T

114159871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 43610955-G-A

114159871-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 43610955-G-T

http://identifiers.org/hco/3/GRCh38#114159968-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#43610853-C-A

114159968-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43610853-C-T

114160148-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43610674-G-T

114160591-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43610415-G-C

114160876-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43610134-A-T

114161028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43609987-T-C

114161392-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43609552-G-T

114161663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43609284-G-A

114161825-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43609128-G-T

114162267-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43608170-T-C

114162307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43608130-C-T

114162359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43608046-A-G

114162595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43607831-G-A

114163188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43606296-T-C

114163767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43605026-C-T

http://identifiers.org/hco/3/GRCh38#114165682-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#43596793-A-C

114166861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43595458-A-G

114167074-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43595272-C-T

114167600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43594186-G-A

114167604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43594182-C-T

114167693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43594093-C-T

114167753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43594046-G-A

114167779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43594012-T-C

114167841-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43593933-G-C

114168105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43593702-A-G

http://identifiers.org/hco/3/GRCh38#114168430-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#43593222-C-A

114168430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43593222-C-T

114168488-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43593176-T-C

114168525-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43593144-C-G

114168525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43593144-C-T

114168624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43593021-G-T

114168717-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43592919-G-T

http://identifiers.org/hco/3/GRCh38#114168735-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#43592901-C-A

114168889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43592745-G-A

114169005-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43592633-A-G

114169022-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43592629-T-C

114169026-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43592625-A-T

114169400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43592353-A-G

114169419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43592323-C-T

114169682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43592115-G-A

114169997-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43584355-A-T

http://identifiers.org/hco/3/GRCh38#114170472-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#43584077-C-A

114170472-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43584077-C-T

114170522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43584033-C-T

114170528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43584027-G-T

114170611-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43583945-T-G

114170615-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43583944-G-T

114171005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43583558-G-A

114171462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43583091-C-T

114171485-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43583068-A-G

http://identifiers.org/hco/3/GRCh38#114171587-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#43582988-C-A

114171714-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43582881-T-A

114171895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 43582700-G-A

114171952-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 43582643-G-A

114171952-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 43582643-G-C

114171952-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 43582643-G-T

http://identifiers.org/hco/3/GRCh38#114172009-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#43582586-C-A

114172009-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 43582586-C-T

114172266-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43582339-T-A

114172347-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43582254-G-A

114172697-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43581943-C-T

114173474-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43579925-G-T

114173591-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43579826-G-T

114173613-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43579804-G-A

114173672-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43579700-G-T

114173805-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43579535-C-G

114173954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43579390-C-T

114174009-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43579328-T-G

114174214-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43579123-A-G

114174482-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43578861-G-T

114174607-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43578735-A-T

114174871-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43578455-G-A

114175316-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43578053-T-A

114175514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43578640-G-T

114175745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43578861-C-T

114175821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43577700-A-G

114175836-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43577685-A-G

114175887-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43577631-G-A

114175887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43577631-G-T

http://identifiers.org/hco/3/GRCh38#114176002-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#43577519-A-C

114176002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 43577519-A-G

114176054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 43577467-T-C

114176743-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43576399-A-G

114177034-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43576129-T-A

114177332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43575850-G-A

114177441-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43575731-A-T

114178252-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43574984-T-C

114178349-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 43574887-T-C

114178729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 43574558-C-T

114178736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 43574551-A-G

http://identifiers.org/hco/3/GRCh38#114178800-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#43574474-C-A

114178960-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 43574310-G-C

114179613-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: intron variant
orthologous variants: 43573651-C-T

114179633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: intron variant
orthologous variants: 43573631-T-C

114179713-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: intron variant
orthologous variants: 43573552-T-C

114179721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: intron variant
orthologous variants: 43573544-C-T

114179817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: intron variant
orthologous variants: 43573451-G-T

114179854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: intron variant
orthologous variants: 43573419-T-C

114179967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: intron variant
orthologous variants: 43573307-A-G

114180417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: intron variant
orthologous variants: 43572077-G-A

http://identifiers.org/hco/3/GRCh38#114180756-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#43571775-C-A

114180830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: intron variant
orthologous variants: 43571699-A-G

114182256-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: intron variant
orthologous variants: 43569689-G-C

114182561-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: intron variant
orthologous variants: 43569387-A-T

114182634-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: intron variant
orthologous variants: 43569316-C-G

114186955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: intron variant
orthologous variants: 43558705-G-A

114187050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: intron variant
orthologous variants: 43558611-A-G

114187050-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: intron variant
orthologous variants: 43558611-A-T

114187531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: intron variant
orthologous variants: 43557429-A-G

114187651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: intron variant
orthologous variants: 43557315-A-G

114187763-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: intron variant
orthologous variants: 43557196-C-G

114188819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: intron variant
orthologous variants: 43554528-C-T

114189421-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: intron variant
orthologous variants: 43553971-C-T

114189446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: intron variant
orthologous variants: 43553946-G-A

114189465-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: intron variant
orthologous variants: 43553927-T-G

114189529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: intron variant
orthologous variants: 43553864-T-C

114189748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: intron variant
orthologous variants: 43553683-A-G

http://identifiers.org/hco/3/GRCh38#114189782-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#43553644-C-A

114189782-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: intron variant
orthologous variants: 43553644-C-G

114189820-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: intron variant
orthologous variants: 43553607-C-G

114190280-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: intron variant
orthologous variants: 43553110-T-A

114190398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: intron variant
orthologous variants: 43552997-G-A

http://identifiers.org/hco/3/GRCh38#114190518-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#43552955-A-C

114190934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: intron variant
orthologous variants: 43552543-A-G

114191177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: intron variant
orthologous variants: 43552373-A-G

114191371-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: intron variant
orthologous variants: 43552159-G-A

114191507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: intron variant
orthologous variants: 43552011-G-T

114191640-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: intron variant
orthologous variants: 43551897-G-A

114191654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: intron variant
orthologous variants: 43551883-A-G

114192021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: intron variant
orthologous variants: 43551540-G-A

114192226-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: intron variant
orthologous variants: 43551348-G-T

114192372-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: intron variant
orthologous variants: 43551190-T-C

114192393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: intron variant
orthologous variants: 43551157-T-C

http://identifiers.org/hco/3/GRCh38#114193457-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#43550140-A-C

114193484-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: intron variant
orthologous variants: 43550115-A-G

114193531-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: intron variant
orthologous variants: 43550072-A-G

http://identifiers.org/hco/3/GRCh38#114193532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#43550071-C-A

114193562-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: intron variant
orthologous variants: 43550042-A-G

114193566-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: intron variant
orthologous variants: 43550041-T-C

114194696-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: intron variant
orthologous variants: 43548714-A-T

http://identifiers.org/hco/3/GRCh38#114194748-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/16/GRCm39#43548668-C-A

114194748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: intron variant
orthologous variants: 43548668-C-T

114195091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: intron variant
orthologous variants: 43548304-A-G

114195105-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: intron variant
orthologous variants: 43548288-G-T

114195150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: intron variant
orthologous variants: 43548175-A-G

114195189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: intron variant
orthologous variants: 43548136-A-G

114195371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: intron variant
orthologous variants: 43547952-T-C

114195419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: intron variant
orthologous variants: 43547908-G-A

114195531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: intron variant
orthologous variants: 43547791-C-T

114195552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: intron variant
orthologous variants: 43547770-T-C

114195619-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: intron variant
orthologous variants: 43547722-G-A

114196080-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3024
most severe consequence: intron variant
orthologous variants: 43547270-G-T