68867387-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109820520-A-T

68867411-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109820544-T-A

68867412-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109820545-G-T

http://identifiers.org/hco/17/GRCh38#68867460-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109820593-C-A

68867460-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109820593-C-G

68867460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109820593-C-T

68867514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109820619-G-A

68867671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109820720-A-G

68867780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109825066-G-A

68867780-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109825066-G-C

68867780-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109825066-G-T

68867885-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109825168-T-C

68867930-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109825202-G-T

68867941-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109825214-A-T

68867942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109825215-G-A

68867942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 109825215-G-T

68868144-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 109825398-A-T

68868251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109825502-G-A

http://identifiers.org/hco/17/GRCh38#68868455-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109825698-A-C

68868458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109825701-G-A

68868458-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109825701-G-T

68868533-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109825752-G-A

68868756-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109825963-G-A

68869687-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 109826529-T-C

68869783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 109826625-A-G

68869826-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109826653-T-A

68869826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109826653-T-C

68869836-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109826663-T-A

68869836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109826663-T-C

68875016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109826935-G-A

http://identifiers.org/hco/17/GRCh38#68875151-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109827062-C-A

68875206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 109827114-T-C

68875206-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 109827114-T-G

68875223-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 109827131-C-T

68875225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 109827133-T-C

68875225-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 109827133-T-G

68875283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 109827191-G-A

68875283-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 109827191-G-C

68875301-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 109827209-T-G

68875302-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 109827210-G-A

68875302-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 109827210-G-T

68875319-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 109827227-T-A

68875319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 109827227-T-C

68875410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 109827322-G-A

68875417-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 109827329-T-G

68875433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 109827345-A-G

http://identifiers.org/hco/17/GRCh38#68875525-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109827435-A-C

68875540-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 109827450-T-A

68875540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 109827450-T-C

68875547-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 109827457-C-T

68875984-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 109827778-G-A

68876128-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 109827891-T-G

http://identifiers.org/hco/17/GRCh38#68876169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109827929-C-A

68876169-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 109827929-C-T

68876170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 109827930-G-A

68876228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 109827995-G-A

68876228-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 109827995-G-T

68876320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 109828079-G-A

68876320-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 109828079-G-T

68876356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 109828116-T-C

68876368-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 109828132-G-T

68876507-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 109828580-C-T

68876557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 109828630-G-A

68876567-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109828640-G-C

68876572-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109828645-G-C

http://identifiers.org/hco/17/GRCh38#68877399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109829166-C-A

68877399-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109829166-C-G

68877399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109829166-C-T

http://identifiers.org/hco/17/GRCh38#68877433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109829185-C-A

68877433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109829185-C-T

http://identifiers.org/hco/17/GRCh38#68877484-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109829236-C-A

68877484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109829236-C-T

68877489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109829239-G-A

68877614-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 109829360-G-A

68877635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 109829381-C-T

68877644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 109829390-C-T

68877721-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109829467-G-A

68877774-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109829500-G-A

68877774-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109829500-G-C

68877774-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109829500-G-T

http://identifiers.org/hco/17/GRCh38#68877909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109829642-C-A

68877909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109829642-C-T

http://identifiers.org/hco/17/GRCh38#68877914-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109829656-A-C

68878004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109829746-A-G

http://identifiers.org/hco/17/GRCh38#68878005-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109829747-C-A

68878020-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109829762-A-G

http://identifiers.org/hco/17/GRCh38#68878048-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109829791-A-C

68878106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109829849-G-A

68878191-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109829932-G-C

68878406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109830186-G-T

68878407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109830187-A-G

http://identifiers.org/hco/17/GRCh38#68878408-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109830188-C-A

68878408-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109830188-C-G

68878426-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109830240-G-T

68878499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109830310-C-T

68878749-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109830762-A-G

http://identifiers.org/hco/17/GRCh38#68878813-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109830830-C-A

http://identifiers.org/hco/17/GRCh38#68878916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109830945-C-A

68878924-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109830953-T-C

http://identifiers.org/hco/17/GRCh38#68878929-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109830958-C-A

68878929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109830958-C-T

68878943-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109830972-A-G

68879389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109831428-G-T

68880944-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109831496-T-C

68881042-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109831581-T-A

http://identifiers.org/hco/17/GRCh38#68881084-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109831606-C-A

68881235-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109831755-A-G

68881264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109831778-G-A

68881264-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109831778-G-T

http://identifiers.org/hco/17/GRCh38#68881284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109831797-C-A

68881284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109831797-C-T

68881492-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109832011-C-G

68881557-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109832067-T-A

68881719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109832226-G-T

68881879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 109832388-G-A

68881891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 109832400-C-T

68882151-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109832637-T-G

68882191-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109832673-T-A

68882460-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109832897-A-T

68882502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109832940-T-C

68882511-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109832949-T-A

68882524-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109832962-A-T

68882617-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 109833081-A-G

68882803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109833269-G-A

68882803-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109833269-G-T

68882810-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109833276-G-A

68882810-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109833276-G-T

http://identifiers.org/hco/17/GRCh38#68882843-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109833315-C-A

68882843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109833315-C-T

68883746-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109836543-A-T

68883894-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109836696-G-C

68883894-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109836696-G-T

68883896-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109836698-G-A

68883896-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109836698-G-C

68883896-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109836698-G-T

68883922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109836727-G-A

68883922-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109836727-G-T

68883923-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109836728-A-G

http://identifiers.org/hco/17/GRCh38#68884224-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109836983-A-C

68884224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109836983-A-G

http://identifiers.org/hco/17/GRCh38#68884239-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109836997-A-C

68884239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109836997-A-G

68884239-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109836997-A-T

68884272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109837018-A-G

68884282-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109837028-A-G

http://identifiers.org/hco/17/GRCh38#68884317-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109837057-C-A

68884323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 109837063-G-A

68884356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 109837096-A-G

http://identifiers.org/hco/17/GRCh38#68884365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109837105-C-A

68884365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 109837105-C-T

68884375-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: 3_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 109837112-A-G

68884428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 109837169-A-G

68884445-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 109837186-A-G

68884480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 109837221-G-A

68884480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 109837221-G-T

http://identifiers.org/hco/17/GRCh38#68884490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109837231-C-A

68884618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 109837344-A-G

68884660-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 109837391-A-G

68884685-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 109837417-G-C

68884685-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 109837417-G-T

http://identifiers.org/hco/17/GRCh38#68884707-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109837438-C-A

68884707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 109837438-C-T

http://identifiers.org/hco/17/GRCh38#68884735-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109837464-C-A

68884850-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, missense_variant
orthologous variants: 109837576-C-T

http://identifiers.org/hco/17/GRCh38#68884872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109837608-C-A

68884894-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron variant
orthologous variants: 109837630-T-A

68884955-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron variant
orthologous variants: 109837691-T-A

68884970-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron variant
orthologous variants: 109837706-T-A

http://identifiers.org/hco/17/GRCh38#68884974-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109837710-C-A

68884974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron variant
orthologous variants: 109837710-C-T

68884976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron variant
orthologous variants: 109837712-T-C

68884976-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron variant
orthologous variants: 109837712-T-G

68885178-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron variant
orthologous variants: 109837873-G-T

68885232-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: synonymous variant
orthologous variants: 109837927-A-G

68885253-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: synonymous variant
orthologous variants: 109837948-G-A

68885274-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: synonymous variant
orthologous variants: 109837969-G-A

68885338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron variant
orthologous variants: 109838035-T-C

68885502-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron variant
orthologous variants: 109838393-A-G

68886766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron variant
orthologous variants: 109839934-G-A

68886766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron variant
orthologous variants: 109839934-G-T

http://identifiers.org/hco/17/GRCh38#68886883-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109840279-C-A

68886900-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 109840296-A-G

68886962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 109840543-G-A

68886962-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 109840543-G-T

68886974-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 109840555-A-G

68886974-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 109840555-A-T

http://identifiers.org/hco/17/GRCh38#68886998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109840579-C-A

http://identifiers.org/hco/17/GRCh38#68887141-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109840722-C-A

68887141-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109840722-C-G

http://identifiers.org/hco/17/GRCh38#68887142-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109840726-A-C

68887142-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109840726-A-G

68887150-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109840734-G-C

68887179-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109840759-G-T

http://identifiers.org/hco/17/GRCh38#68887396-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: http://identifiers.org/mco/11/GRCm39#109840923-A-C

68887586-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109841114-T-A

68887586-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109841114-T-C

68887586-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109841114-T-G

68887600-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109841128-T-G

68887612-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109841140-T-A

68887614-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109841142-T-A

68887614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109841142-T-C

68887614-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109841142-T-G

68891470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109841429-T-C

68891534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 109841500-C-T

68891555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 109841521-C-T

68891638-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109841592-T-A

68891774-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109841716-A-G

68891848-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109841797-T-G

http://identifiers.org/hco/17/GRCh38#68891895-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109841845-A-C

68892094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109842017-A-G

68893218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109842293-G-A

68893552-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109843071-G-C

68894074-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 109843302-T-C

68894182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 109843388-T-C

68894212-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 109843418-T-C

68894296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 109843502-C-T

http://identifiers.org/hco/17/GRCh38#68894362-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109843573-C-A

68894471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109843830-A-G

68894622-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109843974-T-C

68894692-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109844047-G-T

68894703-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109844060-G-A

68894703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109844060-G-T

68895125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109844553-G-T

68895132-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109844560-T-C

68895400-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109844814-A-G

http://identifiers.org/hco/17/GRCh38#68895558-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109844934-A-C

68902689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109845839-G-A

http://identifiers.org/hco/17/GRCh38#68903019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109846333-C-A

68903019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109846333-C-T

68903038-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109846352-C-G

http://identifiers.org/hco/17/GRCh38#68903153-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109846473-C-A

68903153-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109846473-C-G

68903153-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109846473-C-T

68903290-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109847878-C-G

68903354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 109847942-A-G

68903357-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 109847945-T-A

68903357-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 109847945-T-G

http://identifiers.org/hco/17/GRCh38#68903503-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109848088-C-A

68903539-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109848124-G-C

68903539-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109848124-G-T

68903541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109848132-G-A

68903541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109848132-G-T

http://identifiers.org/hco/17/GRCh38#68903569-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109848155-C-A

68903569-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109848155-C-G

68903569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109848155-C-T

68903601-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109848192-A-G

68904919-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109849671-G-C

68904988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109849737-T-C

68905032-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109849781-T-A

http://identifiers.org/hco/17/GRCh38#68905102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109849851-C-A

68905242-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109849966-C-T

http://identifiers.org/hco/17/GRCh38#68905272-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109849996-C-A

68905272-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109849996-C-T

68905908-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109852449-G-T

68906006-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109852547-T-C

68906059-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 109852635-T-A

68906059-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 109852635-T-C

68906182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109852757-G-A

68906182-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109852757-G-T

68906194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109852769-A-G

68906199-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109852777-G-T

http://identifiers.org/hco/17/GRCh38#68906260-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109852837-C-A

68906260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109852837-C-T

68906386-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109852953-T-G

68906414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109852984-A-G

68906441-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109853002-C-T

68906552-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109853110-C-T

68906573-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109853131-A-T

68907545-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109853219-A-G

68907572-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109853243-A-G

68907576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109853247-C-T

http://identifiers.org/hco/17/GRCh38#68907643-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109853308-C-A

68907690-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109853357-A-G

68907813-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 109853480-A-G

http://identifiers.org/hco/17/GRCh38#68907816-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109853483-A-C

68907816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 109853483-A-G

68907816-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 109853483-A-T

68907837-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 109853504-T-G

68907947-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109853606-T-G

68907986-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109853643-T-A

68907986-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109853643-T-C

68908140-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109853673-C-T

68908153-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109853686-T-C

68908449-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109853963-T-C

68908566-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109854064-G-C

68908645-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109854145-C-G

68908744-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109854235-T-G

68908809-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109854300-T-A

68908907-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109854394-A-T

http://identifiers.org/hco/17/GRCh38#68908987-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109854473-C-A

68908993-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109854479-T-A

68909296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109854730-C-T

68909376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109854849-T-C

68909671-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109855118-G-A

68909786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109855230-G-A

68917408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 109855814-G-A

68917408-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 109855814-G-T

68917465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109855871-A-G

68917471-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109855875-A-T

http://identifiers.org/hco/17/GRCh38#68917498-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109855902-C-A

http://identifiers.org/hco/17/GRCh38#68917518-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109855923-C-A

68917518-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109855923-C-T

68917575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109855979-A-G

68917584-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109855988-T-A

68917584-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109855988-T-C

68917585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109855989-A-G

68917585-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109855989-A-T

68917700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109856091-A-G

68917700-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109856091-A-T

68917753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109856144-C-T

68917790-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109856181-C-T

68917839-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109856225-T-A

http://identifiers.org/hco/17/GRCh38#68917875-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109856259-C-A

68917979-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109857436-G-T

http://identifiers.org/hco/17/GRCh38#68918018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109857479-C-A

68918018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109857479-C-T

68918019-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109857480-A-G

68918249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109857705-G-A

http://identifiers.org/hco/17/GRCh38#68918250-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109857706-C-A

68918307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109857760-T-C

68918344-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109857793-C-G

68918420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 109857848-G-A

68918420-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 109857848-G-T

68918432-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 109857860-G-C

68918432-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 109857860-G-T

http://identifiers.org/hco/17/GRCh38#68918433-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109857861-A-C

68918433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 109857861-A-G

68918433-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 109857861-A-T

68918439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 109857867-T-C

http://identifiers.org/hco/17/GRCh38#68918447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109857875-C-A

68918447-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 109857875-C-G

68918447-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 109857875-C-T

68918468-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 109857896-T-C

http://identifiers.org/hco/17/GRCh38#68918917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109858072-C-A

68918917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109858072-C-T

68918983-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109858103-G-C

68918988-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109858108-G-C

68918995-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109858115-A-G

68919060-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109858196-T-A

68919183-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109858311-T-C

68919183-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109858311-T-G

http://identifiers.org/hco/17/GRCh38#68919185-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109858313-C-A

68919185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109858313-C-T

68919201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109858327-A-G

68919201-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109858327-A-T

68919205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109858331-T-C

http://identifiers.org/hco/17/GRCh38#68919226-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109858350-A-C

68919226-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109858350-A-T

68919276-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109858391-C-G

68919276-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109858391-C-T

68919296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109858411-T-C

68919296-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109858411-T-G

68919297-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109858412-G-A

68919297-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109858412-G-C

68919297-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109858412-G-T

68919392-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 109858507-G-C

68919392-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 109858507-G-T

68919497-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109858614-A-G

68919517-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109858640-A-G

68919517-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109858640-A-T

68920529-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109859750-A-G

68921388-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 109859894-T-G

68921452-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 109859958-T-C

68921485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 109859991-T-C

http://identifiers.org/hco/17/GRCh38#68921488-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109859994-C-A

68921488-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 109859994-C-T

68921576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109860090-G-A

68921576-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109860090-G-C

68921576-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109860090-G-T

http://identifiers.org/hco/17/GRCh38#68921740-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109860180-A-C

68921774-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109860215-A-T

http://identifiers.org/hco/17/GRCh38#68921914-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109860359-A-C

68921941-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109860386-A-T

68921943-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109860388-A-T

http://identifiers.org/hco/17/GRCh38#68922033-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109860481-C-A

68922033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109860481-C-T

68922147-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109860599-A-T

68922307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 109860709-A-G

68922335-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109860736-T-C

68922336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109860737-T-C

68922405-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109860804-T-C

68922414-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109860813-T-A

68922414-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109860813-T-C

68922538-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109860910-G-A

68922553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109860913-G-A

68922554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109860914-G-T

68922598-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109860959-G-T

68922690-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109861050-T-C

68922734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109861094-C-T

68922910-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109861249-T-C

68922987-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109861351-G-A

68922987-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109861351-G-C

http://identifiers.org/hco/17/GRCh38#68923197-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109861534-A-C

68923197-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109861534-A-G

68923819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109861788-A-G

68924132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109862039-A-G

68924239-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109862155-G-A

68924272-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109862180-G-A

68924275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109862183-G-A

68924320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109862208-T-C

68924320-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109862208-T-G

68924334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109862222-A-G

68924351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109862232-A-G

68924367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109862248-G-T

68924376-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109862257-G-A

http://identifiers.org/hco/17/GRCh38#68924382-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109862264-A-C

68924395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109862277-T-C

68924432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109862314-T-C

68924566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109862379-G-A

68924566-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109862379-G-T

68924567-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109862380-A-G

68924573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109862386-A-G

68924589-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109862401-T-C

68924589-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109862401-T-G

http://identifiers.org/hco/17/GRCh38#68924595-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109862407-C-A

68924595-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109862407-C-G

68924624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109862434-G-A

68924624-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109862434-G-T

68924667-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109862478-T-A

68924674-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109862485-C-T

68924676-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109862487-T-C

68924752-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 109862562-T-C

http://identifiers.org/hco/17/GRCh38#68924765-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109862575-C-A

68924765-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 109862575-C-T

68924766-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 109862576-G-A

68924766-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: missense_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 109862576-G-C

68924812-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 109862622-T-G

68924862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 109862672-A-G

68924883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109862693-A-G

68924884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109862694-G-T

68924885-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109862695-A-G

68924894-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109862704-T-C

68924896-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109862706-T-C

http://identifiers.org/hco/17/GRCh38#68924941-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109862739-C-A

68924945-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109862743-G-A

68924945-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109862743-G-C

68924945-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109862743-G-T

68924960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109862762-G-T

68924971-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109862773-T-A

68924971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109862773-T-C

68924976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109862782-A-G

68924976-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109862782-A-T

68924991-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109862797-G-A

68924991-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109862797-G-T

http://identifiers.org/hco/17/GRCh38#68925017-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109862810-C-A

68925017-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109862810-C-T

68925701-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109863353-T-G

68925918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109863509-T-C

68926023-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109863610-T-C

68927462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109863934-G-A

68927609-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109864089-T-C

68927859-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109864440-G-A

68927859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109864440-G-T

68927885-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109864466-G-A

68927885-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109864466-G-T

http://identifiers.org/hco/17/GRCh38#68927899-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109864480-A-C

68927899-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109864480-A-G

68927899-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109864480-A-T

68928011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 109864592-T-C

68928049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 109864630-G-T

http://identifiers.org/hco/17/GRCh38#68928158-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109864736-C-A

68928160-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109864738-T-A

68928160-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109864738-T-C

68928163-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109864741-T-C

68928164-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109864742-A-G

68928182-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109864765-T-C

68928182-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109864765-T-G

68928359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109864896-G-A

68928850-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109865151-T-C

http://identifiers.org/hco/17/GRCh38#68928897-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109865198-C-A

68928977-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109865276-T-G

http://identifiers.org/hco/17/GRCh38#68928983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109865282-C-A

68928983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109865282-C-T

68929053-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 109865338-G-A

68929110-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 109865395-G-T

68929132-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 109865417-A-G

68929285-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109865572-A-T

68929323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109865610-G-A

68929323-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109865610-G-T

68929326-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109865613-T-A

68929326-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109865613-T-C

68929573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 109865828-A-G

68929581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 109865836-G-A

68929588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 109865843-G-A

68929588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 109865843-G-T

68929746-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109866001-T-C

68929746-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109866001-T-G

http://identifiers.org/hco/17/GRCh38#68929748-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109866003-A-C

68929748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109866003-A-G

68929753-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109866008-G-A

68929753-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109866008-G-T

http://identifiers.org/hco/17/GRCh38#68929811-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109866114-C-A

68929811-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109866114-C-G

68929811-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109866114-C-T

68929832-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109866135-G-A

68929832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109866135-G-T

68929845-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109866148-T-C

68930598-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109866432-C-T

68930774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109866603-C-T

68930923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109866766-T-C

68931180-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109867002-C-T

68932247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109867223-T-C

68932275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109867250-G-A

68932275-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109867250-G-T

68932281-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 109867256-G-A

68932281-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 109867256-G-T

68932303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 109867278-C-T

68932329-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 109867304-C-T

68932410-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, stop_gained
orthologous variants: 109867385-G-T

http://identifiers.org/hco/17/GRCh38#68932470-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109867445-A-C

68932470-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 109867445-A-G

68932473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 109867448-A-G

68932581-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109867558-T-C

68932597-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109867573-T-C

68932597-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109867573-T-G

68932668-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109867644-G-A

68932671-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109867647-C-G

68932744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109867716-A-G

68932771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109867742-G-A

68932823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109867791-C-T

68932976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109868407-G-T

http://identifiers.org/hco/17/GRCh38#68932992-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109868423-C-A

68933023-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109868454-G-A

68933023-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109868454-G-C

68933023-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109868454-G-T

http://identifiers.org/hco/17/GRCh38#68933047-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109868482-C-A

68933047-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109868482-C-T

68933097-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109868532-G-A

68933097-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109868532-G-T

68933098-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109868533-A-T

68933102-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109868537-T-A

68933102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109868537-T-C

68933109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109868543-G-A

68933109-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109868543-G-T

http://identifiers.org/hco/17/GRCh38#68933246-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109868674-A-C

http://identifiers.org/hco/17/GRCh38#68933340-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109868749-C-A

68933340-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109868749-C-T

68936806-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109870578-A-G

68936806-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109870578-A-T

68936808-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109870582-T-A

http://identifiers.org/hco/17/GRCh38#68936905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109870640-C-A

68936941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109870678-A-G

68937080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 109870814-T-C

68937128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109870865-G-A

68937128-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109870865-G-C

68937137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109870874-T-C

http://identifiers.org/hco/17/GRCh38#68937139-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109870876-A-C

68937236-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109870983-C-G

68937236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109870983-C-T

68937255-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109871006-A-T

68937479-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109871192-G-A

68937559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109871520-G-A

68940774-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 109871692-A-T

68940849-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 109871767-A-T

68940852-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 109871770-T-A

68940869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 109871787-G-A

68940869-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 109871787-G-T

68940955-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 109871873-A-T

http://identifiers.org/hco/17/GRCh38#68940996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109871954-C-A

68940996-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109871954-C-G

68941003-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109871961-A-T

http://identifiers.org/hco/17/GRCh38#68941018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109871976-C-A

68941018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109871976-C-T

68941884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109872451-G-A

68941884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109872451-G-T

http://identifiers.org/hco/17/GRCh38#68941934-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109872499-C-A

68942491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109873214-C-T

http://identifiers.org/hco/17/GRCh38#68942557-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109873277-A-C

68942599-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109873303-C-G

68942599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109873303-C-T

68946368-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109880639-T-A

http://identifiers.org/hco/17/GRCh38#68946411-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109880682-A-C

68946458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109880729-T-C

68946532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109880798-C-T

68946623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109880890-T-C

68946626-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109880894-T-C

68947080-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109881003-T-C

68947086-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109881009-T-C

68951684-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109883714-A-T

68951685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109883715-G-A

68951750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109883785-A-G

68951939-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109883969-G-A

68952044-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109884080-T-C

68952162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109884190-T-C

68952531-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109884299-C-T

68952547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109884315-A-G

68952650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109884400-C-T

http://identifiers.org/hco/17/GRCh38#68952695-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109884445-C-A

68952702-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109884452-A-G

68952762-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109884514-C-G

68952869-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109884593-G-C

68952960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109884740-G-A

68952993-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109884770-C-T

68953138-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109884919-C-G

68953174-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109884952-C-T

http://identifiers.org/hco/17/GRCh38#68953206-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109884983-C-A

68953259-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109885026-C-G

68953348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109885094-A-G

http://identifiers.org/hco/17/GRCh38#68953356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/11/GRCm39#109885097-C-A

68953356-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109885097-C-G

68953421-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109885150-A-G

68953477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109885212-C-T

68953569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109885298-C-T

68953584-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109885306-G-C

68954831-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 109886075-G-C

68954940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 109886177-C-T

68955350-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 38
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 109886568-T-C