219002861-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74941245-A-G

219002861-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 74941245-A-T

http://identifiers.org/hco/2/GRCh38#219002961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74941351-C-A

219002961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 74941351-C-T

219003060-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 74941424-G-A

219003095-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74941461-C-G

219003802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74942174-G-T

http://identifiers.org/hco/2/GRCh38#219003987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74942291-C-A

219003987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 74942291-C-T

http://identifiers.org/hco/2/GRCh38#219004203-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74942480-A-C

219004236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 74942510-C-T

http://identifiers.org/hco/2/GRCh38#219004290-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74942546-C-A

219004317-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 74942570-G-A

http://identifiers.org/hco/2/GRCh38#219004411-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74942664-C-A

219004411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 74942664-C-T

219004552-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74942821-T-G

http://identifiers.org/hco/2/GRCh38#219005582-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: http://identifiers.org/mco/1/GRCm39#74943327-C-A

http://identifiers.org/hco/2/GRCh38#219005600-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74943345-C-A

219005600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 74943345-C-T

http://identifiers.org/hco/2/GRCh38#219005683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74943430-C-A

http://identifiers.org/hco/2/GRCh38#219005882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74943596-C-A

219005882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74943596-C-T

219005912-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74943625-G-T

219005941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74943654-G-A

219005941-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74943654-G-T

219005976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74943747-G-A

219005976-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74943747-G-C

219005976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74943747-G-T

http://identifiers.org/hco/2/GRCh38#219005998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74943769-C-A

219005998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74943769-C-T

http://identifiers.org/hco/2/GRCh38#219006264-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74944029-C-A

219006264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74944029-C-T

219006288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74944052-C-T

http://identifiers.org/hco/2/GRCh38#219006344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74944087-C-A

219006344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74944087-C-T

219006348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74944091-G-A

219006348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74944091-G-T

219006411-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74944154-C-G

219006458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 74944198-G-A

219006458-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 74944198-G-C

219006472-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 74944212-T-C

219006492-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 74944232-T-C

219006549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74944284-C-T

219006895-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74944328-G-T

http://identifiers.org/hco/2/GRCh38#219006899-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74944332-C-A

219006927-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74944360-A-G

219008989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74944712-C-T

http://identifiers.org/hco/2/GRCh38#219009014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74944733-C-A

219009014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74944733-C-T

219009092-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 74944811-C-T

219009110-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 74944829-C-T

219009176-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74944894-G-A

219009176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74944894-G-T

219009228-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74944941-C-G

219009228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74944941-C-T

219009241-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74944954-A-G

219009241-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74944954-A-T

http://identifiers.org/hco/2/GRCh38#219009330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74945042-C-A

219009330-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74945042-C-G

219009429-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 74945141-G-C

219009609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74945218-G-T

219009612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74945221-A-G

219009683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74945292-G-A

219009736-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74945345-T-G

219009791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74945399-T-C

219009791-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74945399-T-G

219009796-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74945404-T-C

219009796-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74945404-T-G

219010057-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 74945584-G-A

219010094-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74945621-G-A

219010094-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74945621-G-C

http://identifiers.org/hco/2/GRCh38#219010416-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74946366-C-A

219010416-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74946366-C-T

219010501-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74946445-G-A

219010501-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74946445-G-T

219010662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 74946603-T-C

219010780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74946739-C-T

http://identifiers.org/hco/2/GRCh38#219010805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74946764-C-A

219010805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, synonymous_variant
orthologous variants: 74946764-C-T

219010823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 74946782-G-A

219010823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 74946782-G-T

219010859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 74946818-G-A

219010859-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 74946818-G-C

http://identifiers.org/hco/2/GRCh38#219010955-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant, stop_gained
orthologous variants: http://identifiers.org/mco/1/GRCm39#74946914-A-C

219010955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 74946914-A-G

219012920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74949342-G-A

219013206-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74949552-T-G

219013237-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74949581-C-T

219013525-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 74949868-C-G

219013525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 74949868-C-T

219013665-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74949992-G-C

219013665-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74949992-G-T

http://identifiers.org/hco/2/GRCh38#219013767-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74950075-A-C

219013788-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74950096-C-T

219013805-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74950113-G-A

219013805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74950113-G-T

219013821-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74950130-G-A

219013836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74950144-G-A

219013836-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74950144-G-C

219014255-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74950519-G-A

219014255-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74950519-G-C

219014255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74950519-G-T

219014268-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74950532-T-A

219014283-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74950547-T-C

219014283-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74950547-T-G

219014287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74950551-G-A

219014287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74950551-G-T

http://identifiers.org/hco/2/GRCh38#219014420-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74951621-A-C

http://identifiers.org/hco/2/GRCh38#219014425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74951626-C-A

219014425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74951626-C-T

219014427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74951628-G-A

219014568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74951749-A-G

http://identifiers.org/hco/2/GRCh38#219014590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74951770-C-A

219014608-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74951794-G-T

219014643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74951829-C-T

219014682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74951870-C-T

219016092-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron variant
orthologous variants: 74953400-A-G

219016167-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron variant
orthologous variants: 74953460-G-A

219017042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron variant
orthologous variants: 74954050-G-A

219017307-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron variant
orthologous variants: 74954331-G-A

219017405-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron variant
orthologous variants: 74954438-G-T

219017436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron variant
orthologous variants: 74954468-G-A

219017479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron variant
orthologous variants: 74954503-G-A

http://identifiers.org/hco/2/GRCh38#219018251-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74954842-C-A

219018251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron variant
orthologous variants: 74954842-C-T

http://identifiers.org/hco/2/GRCh38#219018291-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74954889-A-C

219018291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74954889-A-G

219018291-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74954889-A-T

219018412-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74955129-C-G

219018412-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74955129-C-T

219018426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74955143-T-C

219018450-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74955163-A-G

219018455-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74955168-G-C

219018494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74955203-G-A

219018494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74955203-G-T

http://identifiers.org/hco/2/GRCh38#219018496-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74955205-C-A

219018600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74955316-T-C

219018817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74955697-T-C

219018837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74955713-C-T

http://identifiers.org/hco/2/GRCh38#219018860-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74955729-C-A

219018860-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74955729-C-T

http://identifiers.org/hco/2/GRCh38#219018883-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74955752-C-A

219018883-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74955752-C-T

219018924-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74955792-G-A

219018924-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74955792-G-T

http://identifiers.org/hco/2/GRCh38#219018949-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74955814-A-C

219018985-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 74955848-C-G

219019544-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: synonymous variant
orthologous variants: 74956347-G-A

219019694-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: synonymous variant
orthologous variants: 74956497-C-T

219019730-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron variant
orthologous variants: 74956533-G-A

219019730-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron variant
orthologous variants: 74956533-G-T

http://identifiers.org/hco/2/GRCh38#219019817-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74956575-C-A

219019817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron variant
orthologous variants: 74956575-C-T

219020080-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, undefined
orthologous variants: 74956813-C-G

http://identifiers.org/hco/2/GRCh38#219020081-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#74956814-A-C

219020685-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron variant
orthologous variants: 74957119-T-G

219020740-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron variant
orthologous variants: 74957175-G-T

219020779-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron variant
orthologous variants: 74957204-T-C

http://identifiers.org/hco/2/GRCh38#219020918-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74957296-A-C

219020918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron variant
orthologous variants: 74957296-A-G

219020961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron variant
orthologous variants: 74957342-C-T

http://identifiers.org/hco/2/GRCh38#219021038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74957405-C-A

219021038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron variant
orthologous variants: 74957405-C-T

http://identifiers.org/hco/2/GRCh38#219021048-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74957415-C-A

219021048-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron variant
orthologous variants: 74957415-C-G

219021067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron variant
orthologous variants: 74957438-C-T

219021099-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron variant
orthologous variants: 74957476-C-G

219021099-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron variant
orthologous variants: 74957476-C-T

219021111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron variant
orthologous variants: 74957482-T-C

219021149-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron variant
orthologous variants: 74957522-T-C

219021212-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: missense variant
orthologous variants: 74957585-A-G

219021299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron variant
orthologous variants: 74957685-G-A

219021453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron variant
orthologous variants: 74957801-T-C

219021915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: synonymous variant
orthologous variants: 74958128-G-A

219022305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: synonymous variant
orthologous variants: 74958477-A-G

http://identifiers.org/hco/2/GRCh38#219022350-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74958526-C-A

219022350-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron variant
orthologous variants: 74958526-C-G

219022350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron variant
orthologous variants: 74958526-C-T

219022374-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron variant
orthologous variants: 74958552-T-G

219022431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron variant
orthologous variants: 74958602-T-C

219022590-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron variant
orthologous variants: 74958749-A-T

219022935-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron variant
orthologous variants: 74959294-C-G

219023056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron variant
orthologous variants: 74959405-G-A

219023056-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron variant
orthologous variants: 74959405-G-T

219023225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: synonymous variant
orthologous variants: 74959563-G-A

219023225-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: synonymous variant
orthologous variants: 74959563-G-T

219023266-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: missense variant
orthologous variants: 74959604-G-A

219023355-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: missense variant
orthologous variants: 74959693-G-A

219023396-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: missense variant
orthologous variants: 74959734-C-G

219023442-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron variant
orthologous variants: 74959779-A-G

219023457-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron variant
orthologous variants: 74959795-G-T

219023838-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron variant
orthologous variants: 74960400-T-G

219023927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron variant
orthologous variants: 74960494-G-A

http://identifiers.org/hco/2/GRCh38#219024122-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74960697-C-A

http://identifiers.org/hco/2/GRCh38#219024142-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74960717-C-A

219024142-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: missense variant
orthologous variants: 74960717-C-G

219024142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: missense variant
orthologous variants: 74960717-C-T

http://identifiers.org/hco/2/GRCh38#219024155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74960730-C-A

219024183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: synonymous variant
orthologous variants: 74960758-G-A

219024183-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: synonymous variant
orthologous variants: 74960758-G-T

219024243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: synonymous variant
orthologous variants: 74960818-G-A

219024258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: splice_region_variant, synonymous_variant
orthologous variants: 74960833-T-C

219024285-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron variant
orthologous variants: 74960866-G-A

219024285-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron variant
orthologous variants: 74960866-G-T

219024305-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron variant
orthologous variants: 74960885-A-G

219024337-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron variant
orthologous variants: 74960916-G-A

219024337-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron variant
orthologous variants: 74960916-G-T

219025570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron variant
orthologous variants: 74961740-G-A

219025972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron variant
orthologous variants: 74962034-A-G

219026024-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: missense_variant, splice_region_variant
orthologous variants: 74962089-T-C

219026103-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: stop gained
orthologous variants: 74962168-G-T

219026115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: stop gained
orthologous variants: 74962180-G-T

219026148-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: missense variant
orthologous variants: 74962213-G-C

http://identifiers.org/hco/2/GRCh38#219026233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74962295-C-A

219026233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron variant
orthologous variants: 74962295-C-T

219026265-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron variant
orthologous variants: 74962327-G-T

219026753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74962765-G-A

219026753-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74962765-G-T

219026770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74962793-C-T

219026825-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74962831-G-A

219026825-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74962831-G-T

219026929-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74962936-G-A

219026929-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74962936-G-C

219026929-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74962936-G-T

219026935-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74962942-G-A

http://identifiers.org/hco/2/GRCh38#219027497-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74963799-C-A

219027497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 74963799-C-T

219027568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74963860-C-T

219027614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 74963912-G-A

219027643-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 74963945-C-T

219027715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74964017-G-A

219027715-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74964017-G-T

219027944-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 74964246-G-A

219027944-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74964246-G-C

219027944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74964246-G-T

219028091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74964397-A-G

219028095-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74964401-C-T

219028158-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74964475-G-A

219028158-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74964475-G-T

219028231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 74964562-G-A

219028322-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74964653-G-C

219028322-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74964653-G-T

219028341-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 74964672-G-A

219028466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74964796-G-A

219028466-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74964796-G-T

http://identifiers.org/hco/2/GRCh38#219028532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74964840-C-A

219028532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74964840-C-T

http://identifiers.org/hco/2/GRCh38#219028540-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74964846-C-A

219028540-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74964846-C-T

219028713-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74965026-G-A

http://identifiers.org/hco/2/GRCh38#219029164-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74965342-C-A

219029313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74965505-T-C

219029327-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74965518-C-T

219029348-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74965539-G-C

219029574-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 74965761-C-T

http://identifiers.org/hco/2/GRCh38#219029603-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: http://identifiers.org/mco/1/GRCm39#74965790-C-A

219029603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74965790-C-T

219029659-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74965846-A-G

219029659-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 74965846-A-T

219029764-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74965970-C-G

http://identifiers.org/hco/2/GRCh38#219029845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/1/GRCm39#74966041-C-A

219029845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 74966041-C-T

219029921-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 74966103-G-T

219029947-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74966131-G-C

219029947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74966131-G-T

219029950-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74966134-C-G

219029950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 74966134-C-T

219030146-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 74966333-T-G

219030179-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 74966366-G-A

219030179-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 74966366-G-T

http://identifiers.org/hco/2/GRCh38#219030188-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74966375-A-C

219030220-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74966413-A-G

http://identifiers.org/hco/2/GRCh38#219030328-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74966514-C-A

219030328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74966514-C-T

http://identifiers.org/hco/2/GRCh38#219030329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74966515-C-A

219030358-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74966543-C-T

219030378-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74966561-A-T

219030410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74966571-G-T

http://identifiers.org/hco/2/GRCh38#219030592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74966667-C-A

219030592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74966667-C-T

219030925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74967016-G-A

219031029-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74967098-T-A

219031029-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74967098-T-G

http://identifiers.org/hco/2/GRCh38#219031036-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74967104-C-A

219031036-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74967104-C-T

219031037-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74967105-A-G

219031063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74967131-G-T

219031152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, synonymous_variant, undefined
orthologous variants: 74967210-G-A

219031152-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained, undefined
orthologous variants: 74967210-G-C

219031152-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, stop_gained, undefined
orthologous variants: 74967210-G-T

http://identifiers.org/hco/2/GRCh38#219031223-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74967281-C-A

219031223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: 5_prime_UTR_variant, intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74967281-C-T

219031515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 74967519-C-T

219031682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74967686-G-A

http://identifiers.org/hco/2/GRCh38#219031742-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74967753-A-C

http://identifiers.org/hco/2/GRCh38#219032321-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74968280-C-A

219032321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74968280-C-T

219032368-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74968312-G-A

219032368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74968312-G-T

219032390-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74968331-G-A

219032390-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74968331-G-C

219032390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74968331-G-T

219032399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74968340-G-T

219032402-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74968343-C-G

219032402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74968343-C-T

219032419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74968360-G-T

219032424-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74968365-T-C

219032600-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74968545-C-G

219032609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74968554-G-T

http://identifiers.org/hco/2/GRCh38#219032633-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74968578-A-C

219032633-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74968578-A-G

http://identifiers.org/hco/2/GRCh38#219035440-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74970967-A-C

http://identifiers.org/hco/2/GRCh38#219035441-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74970968-A-C

219035485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 74971008-C-T

http://identifiers.org/hco/2/GRCh38#219035737-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74971232-C-A

219035737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74971232-C-T

219038272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74972131-G-A

219038272-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74972131-G-T

219038281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74972140-G-A

219038281-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74972140-G-T

219038332-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74972188-G-A

219038356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74972210-G-A

219038356-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74972210-G-C

219038356-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74972210-G-T

219038576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 74972401-G-A

219038576-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, splice_region_variant, synonymous_variant
orthologous variants: 74972401-G-C

http://identifiers.org/hco/2/GRCh38#219038686-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74972486-C-A

219038686-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74972486-C-T

219038804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74972607-G-A

219038804-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74972607-G-C

219038804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74972607-G-T

http://identifiers.org/hco/2/GRCh38#219038842-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74972645-C-A

219038845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 74972648-T-C

http://identifiers.org/hco/2/GRCh38#219039937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74973417-C-A

219040017-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74973489-T-C

http://identifiers.org/hco/2/GRCh38#219040119-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74973612-C-A

219040119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74973612-C-T

http://identifiers.org/hco/2/GRCh38#219040310-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74973797-C-A

219040334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74973819-C-T

219040373-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74973842-G-A

219040373-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74973842-G-T

219040376-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74973845-G-T

http://identifiers.org/hco/2/GRCh38#219040683-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74974143-C-A

219040683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74974143-C-T

http://identifiers.org/hco/2/GRCh38#219040705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/1/GRCm39#74974165-C-A

219040705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74974165-C-T

219040752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74974207-G-T

219040991-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74974280-A-G

219041200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74974470-T-C

219041284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74974567-G-A

219041284-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74974567-G-C

219041284-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74974567-G-T

219041289-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74974570-G-A

219041289-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74974570-G-T

219041378-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 74974637-T-C

219041446-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 74974703-C-T

219041524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 74974759-G-A

219041534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 25325
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 74974769-C-T