64039217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106285554-C-T

64039611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106285939-G-T

64039688-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106286014-G-T

http://identifiers.org/hco/17/GRCh38#64039880-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106286203-C-A

64040078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106286387-G-A

64040501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106286733-G-A

64040501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106286733-G-T

http://identifiers.org/hco/17/GRCh38#64040550-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106286780-C-A

64040654-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106286877-A-G

64040656-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106286879-C-T

64040684-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106286894-G-T

64040695-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106286905-T-C

64040732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106286932-A-G

http://identifiers.org/hco/17/GRCh38#64041633-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106287277-C-A

64041640-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106287284-C-G

64041649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106287298-T-C

64041678-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106287338-C-G

64041678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106287338-C-T

64041685-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106287345-T-A

http://identifiers.org/hco/17/GRCh38#64041900-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106287548-C-A

http://identifiers.org/hco/17/GRCh38#64041909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106287557-C-A

64042012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106287648-C-T

http://identifiers.org/hco/17/GRCh38#64042041-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106287674-C-A

64042041-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106287674-C-T

64042043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106287676-G-A

64042043-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106287676-G-T

http://identifiers.org/hco/17/GRCh38#64042082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106287698-C-A

64042082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106287698-C-T

64042118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106287729-A-G

64042118-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106287729-A-T

64042290-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106287803-T-A

64042290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106287803-T-C

64042448-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106287946-G-C

64042452-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106287950-A-G

64042526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106288001-G-A

64042526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106288001-G-T

http://identifiers.org/hco/17/GRCh38#64042653-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106288137-C-A

64042802-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106288256-C-T

64042823-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106288277-G-C

http://identifiers.org/hco/17/GRCh38#64042854-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106288303-C-A

64042970-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106288420-G-T

http://identifiers.org/hco/17/GRCh38#64043010-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106288459-C-A

64043015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106288467-C-T

64043025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106288477-C-T

64043048-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106288500-C-T

64043065-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106288517-T-C

http://identifiers.org/hco/17/GRCh38#64043332-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106288757-C-A

64043332-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106288757-C-T

64043508-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106288891-T-A

64043508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106288891-T-C

http://identifiers.org/hco/17/GRCh38#64043517-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106288893-C-A

64043517-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106288893-C-G

64043517-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106288893-C-T

64043567-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106288941-T-C

64043603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106288978-A-G

64043629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106289001-C-T

http://identifiers.org/hco/17/GRCh38#64043694-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106289074-C-A

64043695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106289075-A-G

64043796-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106289178-A-G

64043796-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106289178-A-T

64043808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106289189-G-A

64043808-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106289189-G-C

64043808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106289189-G-T

http://identifiers.org/hco/17/GRCh38#64043821-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106289203-C-A

64043821-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106289203-C-G

64043822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106289204-T-C

64043954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106289335-G-A

64043954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106289335-G-T

64044117-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106289497-A-T

64044177-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106289557-A-G

http://identifiers.org/hco/17/GRCh38#64044736-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106290495-C-A

64044736-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106290495-C-T

64044742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106290501-G-T

64044783-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106290531-T-A

64044783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106290531-T-C

http://identifiers.org/hco/17/GRCh38#64045328-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106290993-C-A

64045353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 106291015-G-A

64045353-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 106291015-G-C

64045537-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106291196-T-C

64045538-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106291197-G-C

64045603-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106291308-G-A

64045603-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106291308-G-T

64045638-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106291336-C-G

64045638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106291336-C-T

64045791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106291491-G-A

64045974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106291650-A-G

64046248-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106292066-A-G

64046299-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106292296-C-T

64046980-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106292872-G-A

http://identifiers.org/hco/17/GRCh38#64047745-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106294173-C-A

64047745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106294173-C-T

http://identifiers.org/hco/17/GRCh38#64047808-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106294232-C-A

64048013-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106294425-T-A

http://identifiers.org/hco/17/GRCh38#64048486-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106296155-A-C

64048547-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106296211-G-C

64048913-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106296481-G-T

64048920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106296488-G-A

64048920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106296488-G-T

64049074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106296567-G-A

64049222-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106296710-G-A

64049222-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106296710-G-T

64049225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106296713-A-G

http://identifiers.org/hco/17/GRCh38#64049255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106296739-C-A

64049255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106296739-C-T

64051576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106297177-C-T

64051584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106297185-T-C

http://identifiers.org/hco/17/GRCh38#64051589-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106297190-A-C

64051589-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106297190-A-G

64051677-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106297260-T-G

64051891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106297386-G-A

64051892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106297387-G-A

64051939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106297427-G-A

64052301-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106297662-C-G

64052649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106297762-T-C

64052755-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106297845-C-T

64053168-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106298230-G-T

64053230-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106298278-T-C

http://identifiers.org/hco/17/GRCh38#64053236-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106298284-C-A

64053236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106298284-C-T

64053249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106298299-C-T

64053262-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106298312-A-G

64053262-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106298312-A-T

64053376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 106298426-A-G

64054271-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106298907-C-G

64054271-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106298907-C-T

64054277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106298913-G-A

64054535-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106299233-C-T

64054808-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106299786-T-A

64054808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106299786-T-C

64054854-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106299835-T-A

64054854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106299835-T-C

http://identifiers.org/hco/17/GRCh38#64054863-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106299844-C-A

64054863-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106299844-C-T

64054871-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106299852-A-T

64054879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106299860-A-G

64055170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106300138-A-G

64055203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106300172-C-T

64055279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106300243-T-C

http://identifiers.org/hco/17/GRCh38#64055401-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106300360-C-A

64055411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106300373-G-A

http://identifiers.org/hco/17/GRCh38#64055593-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106300587-C-A

http://identifiers.org/hco/17/GRCh38#64055616-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106300644-C-A

64055642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106300667-A-G

64055847-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106300893-T-A

64055847-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106300893-T-G

64055945-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106300985-T-C

64055981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106301012-A-G

http://identifiers.org/hco/17/GRCh38#64056000-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106301031-C-A

64056000-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106301031-C-G

64056000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106301031-C-T

64056074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106301098-G-A

64056074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106301098-G-T

64056105-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106301129-T-C

64056199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106301205-G-A

64056390-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106301226-G-C

64056422-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106301238-G-A

64056597-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106301371-T-G

http://identifiers.org/hco/17/GRCh38#64056873-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106301601-C-A

64056873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106301601-C-T

64056953-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106301676-A-G

http://identifiers.org/hco/17/GRCh38#64056994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106301719-C-A

64056994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106301719-C-T

http://identifiers.org/hco/17/GRCh38#64057680-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106302335-C-A

64057680-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106302335-C-G

64057734-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106302384-G-T

64057754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106302404-G-T

64058181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106302807-G-A

64058245-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106302867-G-A

64058326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106302942-T-C

64058665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106303673-T-C

http://identifiers.org/hco/17/GRCh38#64059427-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106304871-A-C

64059622-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106304993-G-C

64060621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106305328-A-G

64060623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106305330-T-C

64060632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106305338-T-C

http://identifiers.org/hco/17/GRCh38#64060646-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106305352-A-C

64060646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106305352-A-G

64060646-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106305352-A-T

http://identifiers.org/hco/17/GRCh38#64060663-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106305365-C-A

http://identifiers.org/hco/17/GRCh38#64060733-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106305438-C-A

64060733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106305438-C-T

64060887-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106306580-G-T

64061012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106306694-G-A

64061798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106307564-C-T

64061977-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106307711-C-G

64061977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106307711-C-T

64061981-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106307715-C-G

64062008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106307742-T-C

64062011-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106307745-C-T

64062023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106307757-A-G

64062470-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106308072-G-A

64062617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106308219-C-T

64062987-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106308594-T-C

64063034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106308641-C-T

http://identifiers.org/hco/17/GRCh38#64063347-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#106308855-C-A

64063653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106309367-A-G

64063665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106309379-C-T

http://identifiers.org/hco/17/GRCh38#64063859-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106309529-C-A

64063859-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106309529-C-T

64063885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106309556-G-T

64063957-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106309632-T-A

64064167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106309833-A-G

64064172-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106309838-G-C

64064172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106309838-G-T

64064225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106309880-T-C

64064391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106310142-G-A

64065014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106310658-G-A

64065014-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106310658-G-C

64065087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106310726-A-G

64065089-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106310728-A-G

64065092-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106310731-T-C

64065097-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106310736-A-T

64065143-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106310780-A-T

http://identifiers.org/hco/17/GRCh38#64065166-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106310798-C-A

http://identifiers.org/hco/17/GRCh38#64065221-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106310857-C-A

64065313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106310951-T-C

64065313-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106310951-T-G

http://identifiers.org/hco/17/GRCh38#64065314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106310952-C-A

64065314-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106310952-C-G

http://identifiers.org/hco/17/GRCh38#64065362-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106311013-C-A

64065362-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106311013-C-G

64065362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106311013-C-T

http://identifiers.org/hco/17/GRCh38#64065665-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106311293-C-A

64065668-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106311296-T-C

64065678-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106311306-G-C

64065918-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106311664-G-A

64065996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106311738-C-T

64065998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106311740-A-G

64066061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106311799-G-A

64066108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106311822-G-A

64066108-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106311822-G-C

64066120-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106311836-G-T

64066128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106311843-G-A

http://identifiers.org/hco/17/GRCh38#64066249-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106312012-C-A

64066290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106312164-T-C

64066313-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106312194-T-G

64066551-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106312388-T-A

64066551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106312388-T-C

64066581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106312421-T-C

64066581-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106312421-T-G

64066585-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106312425-C-T

64066597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106312439-G-A

64066597-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106312439-G-C

64066638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106312493-G-A

http://identifiers.org/hco/17/GRCh38#64066639-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106312494-C-A

64066835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106312696-C-T

64066904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106312765-A-G

64066940-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 106312799-G-C

64066940-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 106312799-G-T

64066964-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106312818-G-A

64067013-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106312863-G-C

64067013-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106312863-G-T

64067027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106312877-G-A

64067027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106312877-G-T

64067179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106313005-G-A

64067869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106313991-T-C

64067880-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106314003-T-A

64067898-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106314021-T-A

64067898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106314021-T-C

64067898-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106314021-T-G

64067944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106314066-G-T

http://identifiers.org/hco/17/GRCh38#64067953-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106314075-C-A

http://identifiers.org/hco/17/GRCh38#64067969-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106314091-A-C

64067969-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106314091-A-G

64068114-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106314158-A-G

64068167-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106314203-G-T

64068194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106314217-G-A

64068194-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106314217-G-C

64068203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106314226-G-A

64068209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106314232-A-G

64068209-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106314232-A-T

64068337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106314355-G-A

64068337-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106314355-G-C

64068337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106314355-G-T

http://identifiers.org/hco/17/GRCh38#64068508-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106314479-A-C

64068726-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106314955-G-A

64068819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106315050-C-T

http://identifiers.org/hco/17/GRCh38#64069035-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106315266-A-C

64069315-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106315556-C-G

64069471-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106315750-T-C

64069632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106315915-G-A

64069717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106315990-G-A

64069923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106316348-T-C

64070004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106316649-G-A

http://identifiers.org/hco/17/GRCh38#64070552-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106317156-C-A

64071919-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106317577-G-C

64071919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106317577-G-T

64071920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106317578-G-A

64071920-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106317578-G-C

http://identifiers.org/hco/17/GRCh38#64071949-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106317609-C-A

64071949-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106317609-C-G

64071949-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106317609-C-T

64071955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106317615-G-A

64072024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106317682-A-G

64072107-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 106317765-A-G

64072117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106317776-A-G

64072128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106317788-T-C

64072140-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106317800-T-C

http://identifiers.org/hco/17/GRCh38#64072172-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106317842-C-A

http://identifiers.org/hco/17/GRCh38#64072182-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106317852-C-A

64072182-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106317852-C-T

64072230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106317913-G-A

64072230-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106317913-G-C

64072230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106317913-G-T

64072447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106318107-G-A

64072448-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106318108-T-C

http://identifiers.org/hco/17/GRCh38#64072641-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106318283-A-C

64072641-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106318283-A-G

64072922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106318528-A-G

64072924-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106318530-C-T

64072987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106318591-G-A

64074165-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106318819-C-G

64074372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106319006-C-T

64074449-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106319087-G-A

64074521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106319158-C-T

64074848-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106319491-C-G

http://identifiers.org/hco/17/GRCh38#64074992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106319640-C-A

64074992-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106319640-C-T

64075002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106319649-G-A

64075017-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106319664-T-A

64075017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106319664-T-C

64075017-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106319664-T-G

64075022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106319669-A-G

http://identifiers.org/hco/17/GRCh38#64075101-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106319760-C-A

64075101-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106319760-C-T

64075112-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106319770-A-T

http://identifiers.org/hco/17/GRCh38#64075135-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106319793-C-A

64075135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106319793-C-T

64075164-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106319829-G-A

64075164-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106319829-G-C

64075164-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106319829-G-T

64075230-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106319895-G-A

64075230-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106319895-G-T

64075266-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106319931-A-G

64075267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106319932-G-A

64075267-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106319932-G-C

64075267-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106319932-G-T

64075564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106320244-C-T

64075578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106320258-A-G

64075655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106320322-C-T

64075658-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106320325-C-T

64075705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106320382-G-A

64075882-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106320520-T-C

64076294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106320865-G-T

64077027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106321215-T-C

64077152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106321342-C-T

64077402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106321588-A-G

64079354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106325084-A-G

http://identifiers.org/hco/17/GRCh38#64079463-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106325203-C-A

64079578-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106325671-G-A

64079578-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106325671-G-T

http://identifiers.org/hco/17/GRCh38#64079757-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106325836-C-A

64079830-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106325905-G-A

64079830-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106325905-G-C

64079964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106326025-C-T

http://identifiers.org/hco/17/GRCh38#64080292-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106326585-A-C

http://identifiers.org/hco/17/GRCh38#64080352-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106326639-C-A

http://identifiers.org/hco/17/GRCh38#64080382-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106326674-C-A

64080382-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106326674-C-G

64080382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106326674-C-T

64080440-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106326730-T-C

64080559-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106327734-A-G

64080559-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106327734-A-T

64080572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106327747-A-G

http://identifiers.org/hco/17/GRCh38#64080580-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#106327755-C-A

64080580-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106327755-C-T

http://identifiers.org/hco/17/GRCh38#64080642-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106327800-A-C

64080642-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106327800-A-G

64080642-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106327800-A-T

http://identifiers.org/hco/17/GRCh38#64080644-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106327802-A-C

64080644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106327802-A-G

64080644-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106327802-A-T

64080738-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106327879-A-T

64080759-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106327900-G-A

64080759-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106327900-G-T

http://identifiers.org/hco/17/GRCh38#64080847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106327986-C-A

http://identifiers.org/hco/17/GRCh38#64080882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106328020-C-A

64080882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106328020-C-T

http://identifiers.org/hco/17/GRCh38#64080934-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106328063-C-A

64080934-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106328063-C-T

64081342-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106328798-C-G

64081342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106328798-C-T

64082004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106329592-A-G

64082057-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106329645-G-T

64082248-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106329792-C-G

64082248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106329792-C-T

64082260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106329804-T-C

64082285-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106329829-A-G

64082388-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106329932-T-C

64082564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106330121-T-C

64082662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 106330216-G-A

64082804-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106330339-C-G

http://identifiers.org/hco/17/GRCh38#64083022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106330571-C-A

64083133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106330797-G-A

64084019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106331511-C-T

64085639-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106335088-A-T

64086387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106335604-C-T

64086427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106335647-A-G

64086495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106335689-A-G

64086591-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106335770-G-C

http://identifiers.org/hco/17/GRCh38#64086612-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106335812-C-A

64086612-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106335812-C-G

64086612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106335812-C-T

http://identifiers.org/hco/17/GRCh38#64086617-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106335817-C-A

64086617-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106335817-C-T

http://identifiers.org/hco/17/GRCh38#64086632-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106335832-C-A

64086632-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106335832-C-G

64086632-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106335832-C-T

64086879-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106336067-C-T

64087177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106336391-T-C

64087587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106338856-G-A

64087666-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106338980-T-C

64087683-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106339001-T-G

64088057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106339380-G-A

64088073-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106339392-T-C

64088073-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106339392-T-G

64088263-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106339581-C-G

64088263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106339581-C-T

http://identifiers.org/hco/17/GRCh38#64088518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106339797-C-A

64088877-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106339928-C-G

64088877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106339928-C-T

64088988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106340033-T-C

64088999-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106340043-A-G

64090089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106340705-T-C

64090673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106341373-G-A

64090969-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106342620-C-T

http://identifiers.org/hco/17/GRCh38#64091385-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106343010-C-A

64091447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106343072-T-C

64091557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106343166-G-A

64091600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106343209-G-A

64091801-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106343439-T-G

64091826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106343463-T-C

64091884-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106343520-C-T

64091970-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106343593-G-A

64092310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106343882-G-A

64092326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106343896-G-A

64092346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106343915-C-T

64093257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106344138-G-T

http://identifiers.org/hco/17/GRCh38#64094687-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106346499-A-C

64094687-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106346499-A-T

http://identifiers.org/hco/17/GRCh38#64095085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106347026-C-A

http://identifiers.org/hco/17/GRCh38#64095231-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106347219-C-A

64095235-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106347223-C-G

64095268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106347253-A-G

http://identifiers.org/hco/17/GRCh38#64095397-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106347464-C-A

64095962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106347936-C-T

64097311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106348665-T-C

64097398-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106348894-C-T

64097581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106349247-G-A

64097602-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106349274-C-G

64097603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106349275-A-G

64097832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106349475-T-C

http://identifiers.org/hco/17/GRCh38#64098218-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106349831-C-A

64098218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106349831-C-T

64098229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 106349842-T-C

64098230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 106349843-A-G

64098267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106349877-A-G

http://identifiers.org/hco/17/GRCh38#64098312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106349920-C-A

64098312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106349920-C-T

64098336-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106349945-A-G

64098360-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106349969-G-C

http://identifiers.org/hco/17/GRCh38#64098392-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106350001-C-A

64098392-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106350001-C-G

http://identifiers.org/hco/17/GRCh38#64098407-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106350025-C-A

64098407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106350025-C-T

http://identifiers.org/hco/17/GRCh38#64098408-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106350026-C-A

http://identifiers.org/hco/17/GRCh38#64098455-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106350073-C-A

http://identifiers.org/hco/17/GRCh38#64098630-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106350437-C-A

64098630-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106350437-C-T

64098724-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106350526-T-G

64099372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106352565-A-G

64099390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106352581-G-A

64099487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106352677-C-T

64099783-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106352964-C-T

64099900-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106353077-A-T

64100399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106353366-G-T

64100957-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106353572-G-C

64101335-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106354217-A-G

64101561-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106354452-G-A

64101845-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106354750-G-T

http://identifiers.org/hco/17/GRCh38#64101988-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106354932-C-A

64102946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106355837-G-A

64102946-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106355837-G-C

64102946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106355837-G-T

64106328-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106356824-G-C

64106513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106356986-C-T

64106520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106356993-C-T

64106527-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106357000-A-T

64106531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106357004-G-A

64107102-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106358668-C-T

64107133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106358911-T-C

64107261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106359030-G-A

64107261-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106359030-G-C

64107941-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106359366-T-A

64108288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106359690-C-T

http://identifiers.org/hco/17/GRCh38#64108333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106359734-C-A

64108358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106359759-T-C

64108393-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106359777-G-A

64108687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106359957-T-C

64109260-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106360273-G-A

64109614-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106360584-A-T

64109910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106360867-C-T

http://identifiers.org/hco/17/GRCh38#64110051-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106361231-A-C

64110597-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106361805-G-C

64110736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106362434-A-G

64111055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106362721-A-G

http://identifiers.org/hco/17/GRCh38#64111296-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106362826-A-C

64111296-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106362826-A-G

64111359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106362882-T-C

64111359-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106362882-T-G

64111396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106362957-T-C

64111503-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106363060-A-G

64112468-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106363702-A-T

64114581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106365758-T-C

64114586-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106365763-G-A

64114682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106365866-T-C

64114923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106366064-T-C

64114943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106366084-A-G

64115081-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106366191-C-T

64115189-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106366285-G-C

64115236-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106366332-A-G

http://identifiers.org/hco/17/GRCh38#64115375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106366475-C-A

64115375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106366475-C-T

64116048-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106367229-C-G

64116292-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106367508-G-C

64116468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106367854-C-T

64116595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106367972-G-A

64116699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106368049-G-A

64117559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106368179-G-A

64120194-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106369546-C-T

64120218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106369569-C-T

64120700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106370010-T-C

64120877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106370163-A-G

http://identifiers.org/hco/17/GRCh38#64121043-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#106370498-C-A

64121043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106370498-C-T

64121864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106370923-G-A

64121864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106370923-G-T

64121867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106370926-G-A

64122195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106371221-C-T

64122373-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106371311-A-G

64122655-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106371576-T-C

64123198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106372649-G-A

64123381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106372833-T-C

64123482-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106372919-C-G

http://identifiers.org/hco/17/GRCh38#64123501-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106372937-C-A

64123936-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106373419-G-A

64124102-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106373587-T-A

64124102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106373587-T-C

64124905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106373933-T-C

64124905-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106373933-T-G

64124986-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106374015-T-G

64125220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106374233-T-C

64125571-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106374388-C-T

64125623-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 106374432-G-C

64126130-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106374977-C-T

http://identifiers.org/hco/17/GRCh38#64126162-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106375009-C-A

64126187-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106375034-C-T

64126195-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106375042-C-G

64126385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106375228-T-C

64126444-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106375289-T-C

http://identifiers.org/hco/17/GRCh38#64126502-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106375340-A-C

64126851-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106376044-G-A

64126925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106376122-A-G

64126941-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106376138-C-T

64127102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106376259-G-A

http://identifiers.org/hco/17/GRCh38#64127375-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106376510-A-C

64127375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106376510-A-G

64127377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106376512-T-C

64128343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106376834-T-C

64128554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106377025-C-T

http://identifiers.org/hco/17/GRCh38#64128590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106377060-C-A

64128600-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106377071-T-A

64128675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106377148-G-A

64128675-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106377148-G-T

64128764-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106377275-G-A

64128764-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106377275-G-C

64128839-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106377350-G-C

64128839-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106377350-G-T

64128939-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106377455-T-C

64129026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106377543-G-A

64129026-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106377543-G-C

64129064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106377581-T-C

64129308-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106377805-A-G

64129343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106377843-C-T

64129356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106377856-G-A

64129356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106377856-G-T

64129359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106377859-G-A

64129359-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106377859-G-T

http://identifiers.org/hco/17/GRCh38#64129371-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106377884-A-C

64129371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106377884-A-G

64129371-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106377884-A-T

64129438-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106377955-G-A

64129438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106377955-G-T

64129446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106377968-C-T

64129464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106377986-T-C

64129621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106378146-G-A

64129621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106378146-G-T

64129723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 106378228-C-T

64129812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106378290-G-A

64129812-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 106378290-G-T

http://identifiers.org/hco/17/GRCh38#64129882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106378355-C-A

64129882-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 106378355-C-G

64129882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 106378355-C-T

64129944-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 106378411-T-A

64129944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 106378411-T-C

64129944-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 106378411-T-G

http://identifiers.org/hco/17/GRCh38#64130012-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#106378485-C-A

64130012-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 106378485-C-G

64130012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant, undefined
orthologous variants: 106378485-C-T

64130065-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 106378557-G-A

64130065-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 106378557-G-T

http://identifiers.org/hco/17/GRCh38#64130302-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#106378791-A-C

64130302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 106378791-A-G

64130302-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 106378791-A-T

64130305-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 106378794-G-C

64130331-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 5 prime UTR variant
orthologous variants: 106378820-G-A

64130331-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 5 prime UTR variant
orthologous variants: 106378820-G-T

64130343-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 5 prime UTR variant
orthologous variants: 106378832-T-C

64130343-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 5 prime UTR variant
orthologous variants: 106378832-T-G

64130361-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 106378849-A-G

64130418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106378903-G-A

64130444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 106378930-G-A

64130444-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 106378930-G-T

64130447-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 106378933-G-A

64130447-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 106378933-G-T

64130463-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106378951-G-A

64130554-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106379003-C-T

64130587-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 106379030-T-A

64130587-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 106379030-T-G

http://identifiers.org/hco/17/GRCh38#64130645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#106379093-C-A

64130645-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106379093-C-G

64130645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106379093-C-T

64130695-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 106379124-G-T

64130706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 106379134-T-C

http://identifiers.org/hco/17/GRCh38#64130757-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/11/GRCm39#106379186-C-A

64130757-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 106379186-C-T

64130765-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3449
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 106379195-T-C