34478915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: 3 prime UTR variant
orthologous variants: 103281199-A-G

34479041-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: 3 prime UTR variant
orthologous variants: 103281072-G-C

34479376-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: 3 prime UTR variant
orthologous variants: 103280719-T-G

http://identifiers.org/hco/11/GRCh38#34479397-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103280694-C-A

34479447-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: 3 prime UTR variant
orthologous variants: 103280642-C-G

34479490-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: 3 prime UTR variant
orthologous variants: 103280591-G-T

34479864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: 3 prime UTR variant
orthologous variants: 103280388-G-A

34479864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: 3 prime UTR variant
orthologous variants: 103280388-G-T

34479869-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: 3 prime UTR variant
orthologous variants: 103280383-T-C

34479885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: 3 prime UTR variant
orthologous variants: 103280370-T-C

34479987-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: 3 prime UTR variant
orthologous variants: 103280269-T-A

34480035-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: 3 prime UTR variant
orthologous variants: 103280222-T-A

34480035-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: 3 prime UTR variant
orthologous variants: 103280222-T-C

34480137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: 3 prime UTR variant
orthologous variants: 103280084-T-C

34480151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: 3 prime UTR variant
orthologous variants: 103280070-T-C

http://identifiers.org/hco/11/GRCh38#34480214-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103280007-C-A

34480214-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: 3 prime UTR variant
orthologous variants: 103280007-C-T

34480249-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: missense variant
orthologous variants: 103279972-T-C

34480411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, undefined
orthologous variants: 103279811-G-A

34480411-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, undefined
orthologous variants: 103279811-G-T

http://identifiers.org/hco/11/GRCh38#34480443-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103279779-C-A

34480443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron variant
orthologous variants: 103279779-C-T

http://identifiers.org/hco/11/GRCh38#34480452-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103279771-C-A

34480657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron variant
orthologous variants: 103279565-T-C

34480678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron variant
orthologous variants: 103279545-G-A

34480678-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron variant
orthologous variants: 103279545-G-T

34480711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron variant
orthologous variants: 103279506-C-T

34480762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron variant
orthologous variants: 103279453-A-G

34480982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron variant
orthologous variants: 103279233-A-G

34482329-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron variant
orthologous variants: 103277907-G-T

34482330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron variant
orthologous variants: 103277906-G-A

34482330-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron variant
orthologous variants: 103277906-G-C

34482330-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron variant
orthologous variants: 103277906-G-T

34482340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron variant
orthologous variants: 103277896-A-G

http://identifiers.org/hco/11/GRCh38#34482342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103277894-C-A

34482342-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron variant
orthologous variants: 103277894-C-T

34482506-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 103277768-T-C

http://identifiers.org/hco/11/GRCh38#34482592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103277704-C-A

34482592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103277704-C-T

34482643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103277666-G-T

34484544-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103276201-T-C

34484545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103276200-C-T

34484812-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103275943-A-G

34485040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103275728-A-G

34485076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103275691-C-T

34485108-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103275659-T-A

34485290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103275454-G-T

34485304-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103275440-C-G

34485319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103275428-T-C

34485459-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103275304-A-G

34485580-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103275187-G-A

34485685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103275094-C-T

34485765-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103275000-G-A

34486282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103274540-A-G

34486539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103274296-G-A

34486551-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103274276-T-G

34486582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103274245-G-A

34486588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103274239-G-A

34486588-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103274239-G-C

34489454-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103273720-A-T

34489624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103273563-T-C

34489634-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103273553-G-A

34489634-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103273553-G-C

http://identifiers.org/hco/11/GRCh38#34489724-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103273447-C-A

34489726-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103273445-T-C

http://identifiers.org/hco/11/GRCh38#34489742-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103273429-C-A

34489742-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103273429-C-G

34489742-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103273429-C-T

34489894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103273306-G-T

34489927-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103273272-T-C

34489931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103273268-A-G

http://identifiers.org/hco/11/GRCh38#34489951-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103273248-C-A

34489951-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103273248-C-G

http://identifiers.org/hco/11/GRCh38#34489994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103273208-C-A

34489994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103273208-C-T

34490063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 103273140-G-T

34490202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103272997-T-C

34490202-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103272997-T-G

34490243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103272954-G-A

34490328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103272876-C-T

34490466-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103272745-C-T

34490983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103272325-G-T

34490987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103272321-G-A

34491005-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103272303-C-T

34491016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103272293-G-A

http://identifiers.org/hco/11/GRCh38#34491029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103272280-C-A

34491029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103272280-C-T

34491063-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103272242-T-C

34491147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103272159-C-T

34491282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103272040-T-C

34491385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103271955-T-C

http://identifiers.org/hco/11/GRCh38#34491934-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103271332-C-A

http://identifiers.org/hco/11/GRCh38#34491962-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103271304-C-A

34491962-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103271304-C-T

34491995-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103271275-T-A

34491995-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103271275-T-C

http://identifiers.org/hco/11/GRCh38#34492006-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103271264-C-A

34492028-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103271244-C-T

34492047-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103271225-A-G

34492062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103271210-T-C

34492152-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103270965-C-T

34492154-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103270963-A-G

34492159-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103270958-G-T

34492172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103270945-G-A

http://identifiers.org/hco/11/GRCh38#34492439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103270738-C-A

34492439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103270738-C-T

34492604-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103270555-C-T

34492653-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103270512-G-T

34492677-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103270491-G-T

34492681-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103270488-T-C

http://identifiers.org/hco/11/GRCh38#34492688-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103270481-C-A

34492725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103270443-T-C

34492812-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103270351-G-T

34492824-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103270339-T-C

http://identifiers.org/hco/11/GRCh38#34493029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#103270205-C-A

34493029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 103270205-C-T

http://identifiers.org/hco/11/GRCh38#34493202-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103270031-A-C

34493202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103270031-A-G

http://identifiers.org/hco/11/GRCh38#34493242-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103269993-C-A

http://identifiers.org/hco/11/GRCh38#34493297-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103269935-C-A

34493297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103269935-C-T

http://identifiers.org/hco/11/GRCh38#34493316-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103269917-C-A

34493316-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103269917-C-G

34493328-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 103269905-A-T

http://identifiers.org/hco/11/GRCh38#34493439-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103269803-C-A

34493553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 103269699-T-C

34493799-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103269470-T-C

34494057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103269231-C-T

34494070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103269218-C-T

34494228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103269057-C-T

34494235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103269050-A-G

34494324-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103268964-A-G

34494689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103268568-T-C

34495104-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103268038-T-A

34495104-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103268038-T-C

34495509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103267637-T-C

34495519-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103267627-C-G

http://identifiers.org/hco/11/GRCh38#34496009-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/2/GRCm39#103267021-A-C

34496065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 103266976-C-T

34496177-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103266886-G-C

34496213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103266847-C-T

34496402-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 103266636-A-G

34497296-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103265771-G-A

34497383-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103265679-C-T

34497572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103265514-G-A

34497582-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103265505-C-G

34497628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103265459-G-A

34497641-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103265447-A-T

34497678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103265407-G-A

34500284-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103265227-G-A

34500771-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103264783-A-G

34500849-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103264706-C-G

34501015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103264297-T-C

34501034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103264278-A-G

34501284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103264032-C-T

34501396-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103263923-C-T

http://identifiers.org/hco/11/GRCh38#34501543-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103263786-A-C

34501690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103263430-C-T

34501821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103263297-A-G

http://identifiers.org/hco/11/GRCh38#34501867-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103263255-A-C

34501883-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103263241-G-A

34501914-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103263206-T-A

http://identifiers.org/hco/11/GRCh38#34502047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103263124-C-A

34502047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103263124-C-T

34502211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103262949-A-G

34502249-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103262911-T-G

34502375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103262813-T-C

34502516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103262784-T-C

34502733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103262669-G-A

34502733-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103262669-G-C

34502733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103262669-G-T

34502950-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103262455-T-G

34504184-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103261999-G-C

34504362-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103261838-C-G

34504419-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103261616-G-A

34504419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103261616-G-T

34504535-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103261488-G-A

http://identifiers.org/hco/11/GRCh38#34504628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103261383-C-A

34504628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103261383-C-T

34504673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103261336-G-A

34504802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103261207-G-A

34505589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103260795-T-C

34505589-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103260795-T-G

34505592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103260792-T-C

34505612-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103260773-C-G

34505612-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103260773-C-T

34505655-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 103260730-T-G

34505767-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103260619-A-G

34505818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103260568-G-A

34505818-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103260568-G-C

34505818-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103260568-G-T

34505827-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103260559-G-C

34505827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103260559-G-T

34505846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103260540-T-C

34505884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103260520-G-A

34505884-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103260520-G-C

34505884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103260520-G-T

http://identifiers.org/hco/11/GRCh38#34505956-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103260443-A-C

34506842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103260255-A-G

http://identifiers.org/hco/11/GRCh38#34506862-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103260233-A-C

34507012-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103260092-C-G

http://identifiers.org/hco/11/GRCh38#34507098-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103260020-A-C

34507234-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103259886-G-A

34507506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103259644-G-A

34507837-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103259314-T-A

34507843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103259309-A-G

34507843-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103259309-A-T

34509488-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103258494-G-T

34509647-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103258367-A-G

34509876-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103258153-A-G

34509877-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103258152-A-G

34509949-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103258082-T-C

34509955-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103258076-A-T

http://identifiers.org/hco/11/GRCh38#34510334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103257692-C-A

34510334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103257692-C-T

34510346-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103257680-G-T

34510365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103257661-C-T

34510531-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103257506-T-G

34510536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103257501-G-A

http://identifiers.org/hco/11/GRCh38#34510559-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103257495-C-A

34511142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103257056-C-T

34511219-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103256984-A-G

34511505-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 103256743-T-A

34511638-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 103256621-T-G

34511650-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 103256610-G-C

34511650-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 103256610-G-T

34511825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 103256492-A-G

http://identifiers.org/hco/11/GRCh38#34511903-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103256413-A-C

34511903-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron variant
orthologous variants: 103256413-A-G

34511944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron variant
orthologous variants: 103256231-A-G

34512077-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron variant
orthologous variants: 103256104-C-T

34512098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron variant
orthologous variants: 103256085-G-A

34512304-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron variant
orthologous variants: 103255886-A-G

http://identifiers.org/hco/11/GRCh38#34512314-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103255877-C-A

34512314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron variant
orthologous variants: 103255877-C-T

34512367-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron variant
orthologous variants: 103255829-G-C

34512818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron_variant, undefined
orthologous variants: 103255393-C-T

34512933-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron variant
orthologous variants: 103255278-C-G

34512933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron variant
orthologous variants: 103255278-C-T

34513552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron variant
orthologous variants: 103254654-C-T

34513561-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron variant
orthologous variants: 103254647-G-T

34513572-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron variant
orthologous variants: 103254636-G-A

34513737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 103254468-T-C

34513752-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 103254453-G-A

34513752-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 103254453-G-T

34514150-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron variant
orthologous variants: 103254086-A-G

34514696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron variant
orthologous variants: 103253269-A-G

34515169-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron variant
orthologous variants: 103252300-T-C

34515827-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron variant
orthologous variants: 103251955-G-T

34516796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron variant
orthologous variants: 103251177-G-A

34517104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron variant
orthologous variants: 103250693-A-G

34517104-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron variant
orthologous variants: 103250693-A-T

34517387-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron variant
orthologous variants: 103250441-T-C

34517539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron variant
orthologous variants: 103250279-C-T

34517577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron variant
orthologous variants: 103250238-G-A

34518069-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron variant
orthologous variants: 103249906-A-G

34518273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron variant
orthologous variants: 103249741-T-C

34518286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron variant
orthologous variants: 103249731-C-T

34518292-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron variant
orthologous variants: 103249725-G-C

34518681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron variant
orthologous variants: 103248919-A-G

34518775-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron variant
orthologous variants: 103248850-C-T

34518887-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron variant
orthologous variants: 103248759-A-G

34518900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron variant
orthologous variants: 103248746-G-A

34519022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron variant
orthologous variants: 103248610-G-A

http://identifiers.org/hco/11/GRCh38#34519328-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103247571-C-A

34519328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron variant
orthologous variants: 103247571-C-T

34519435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron variant
orthologous variants: 103247475-T-C

34519475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron variant
orthologous variants: 103247427-A-G

34519486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron variant
orthologous variants: 103247418-G-A

34519528-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron variant
orthologous variants: 103247379-T-A

34521123-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron variant
orthologous variants: 103246256-G-C

34521350-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron variant
orthologous variants: 103246022-C-G

34521722-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron variant
orthologous variants: 103245441-C-T

34521756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron variant
orthologous variants: 103245407-A-G

34521812-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron variant
orthologous variants: 103245330-T-A

34521863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron variant
orthologous variants: 103245279-A-G

34521959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron variant
orthologous variants: 103245225-T-C

34523107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron variant
orthologous variants: 103244019-C-T

34523931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron variant
orthologous variants: 103243251-C-T

34524085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron variant
orthologous variants: 103243132-T-C

34524229-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron variant
orthologous variants: 103243002-C-T

34524550-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron variant
orthologous variants: 103242682-A-G

http://identifiers.org/hco/11/GRCh38#34524635-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/2/GRCm39#103242603-C-A

34524730-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron variant
orthologous variants: 103242519-A-G

34524746-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: intron variant
orthologous variants: 103242505-C-T

34524937-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: 5 prime UTR variant
orthologous variants: 103242307-G-A

34524989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3320
most severe consequence: 5 prime UTR variant
orthologous variants: 103242255-C-T