51208100-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54071480-G-T

51208162-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54071542-T-G

51208165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54071547-G-A

51208165-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54071547-G-T

51208177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54071559-T-C

51208311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54071669-A-G

51208320-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54071678-T-C

51208449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54071802-A-G

51208636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54071941-G-T

51208717-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54071997-T-A

http://identifiers.org/hco/15/GRCh38#51208733-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54072013-C-A

51208733-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54072013-C-T

51208766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54072044-C-T

51208804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54072072-T-C

51208871-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54072125-A-G

http://identifiers.org/hco/15/GRCh38#51208910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54072164-C-A

51208921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54072175-G-A

51208921-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54072175-G-T

http://identifiers.org/hco/15/GRCh38#51208931-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54072184-A-C

51208978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54072224-A-G

51208978-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54072224-A-T

http://identifiers.org/hco/15/GRCh38#51209029-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54072269-A-C

51209700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54072991-T-C

51209707-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54072998-A-T

51209810-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54073097-G-T

http://identifiers.org/hco/15/GRCh38#51209973-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54073220-C-A

51210196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54073400-G-A

51210196-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54073400-G-T

51210248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54073452-G-A

51210326-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54073611-C-T

51210330-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54073615-G-T

51210334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54073619-A-G

51210429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54073704-G-A

51210429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54073704-G-T

http://identifiers.org/hco/15/GRCh38#51210448-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54073717-C-A

51210448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54073717-C-T

http://identifiers.org/hco/15/GRCh38#51210462-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54073735-A-C

51210462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54073735-A-G

51210477-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54073750-G-T

51210483-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54073756-C-T

51210488-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54073761-A-G

http://identifiers.org/hco/15/GRCh38#51210658-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54073890-A-C

51210658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54073890-A-G

http://identifiers.org/hco/15/GRCh38#51210704-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54073936-C-A

51210704-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54073936-C-T

51210711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54073943-G-A

51210711-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54073943-G-T

http://identifiers.org/hco/15/GRCh38#51210730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54073962-C-A

51210730-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54073962-C-T

51210796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54074029-G-A

51210796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54074029-G-T

51210804-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54074037-T-A

51210804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54074037-T-C

http://identifiers.org/hco/15/GRCh38#51211014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54074247-C-A

51211014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54074247-C-T

51211136-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54074358-T-A

51211137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54074359-G-A

51211137-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54074359-G-T

51211139-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54074361-G-C

51211139-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54074361-G-T

http://identifiers.org/hco/15/GRCh38#51211570-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54074879-C-A

51211583-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54074891-T-C

51211596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54074904-T-C

51211653-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54074954-G-T

51211663-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54074960-G-A

51211663-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54074960-G-C

51211663-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54074960-G-T

http://identifiers.org/hco/15/GRCh38#51211758-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54075048-C-A

51211758-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54075048-C-G

51211758-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54075048-C-T

http://identifiers.org/hco/15/GRCh38#51211788-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54075083-C-A

51211793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54075088-A-G

51211814-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54075109-C-G

51212003-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54075522-G-T

51212016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54075531-G-A

http://identifiers.org/hco/15/GRCh38#51212128-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54075627-C-A

51212128-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54075627-C-T

51212133-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54075632-T-C

51212199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54075690-G-A

51212199-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54075690-G-T

51212234-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54075719-T-A

51212234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54075719-T-C

51212313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 54075784-C-T

51212588-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54076059-G-A

51212588-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54076059-G-C

51212588-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54076059-G-T

51212708-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54076074-G-A

51212708-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54076074-G-T

http://identifiers.org/hco/15/GRCh38#51212709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54076075-C-A

51212727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54076093-G-A

51213719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54077041-C-T

51213742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54077063-T-C

51213758-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54077089-A-T

51214044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54077375-C-T

51214897-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54078924-G-T

http://identifiers.org/hco/15/GRCh38#51214924-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54078957-A-C

51214938-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54078971-G-A

51214938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54078971-G-T

http://identifiers.org/hco/15/GRCh38#51215281-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54079298-C-A

51215581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54079838-G-T

51215649-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54079905-C-G

51215699-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54079956-G-C

http://identifiers.org/hco/15/GRCh38#51215951-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54080172-C-A

http://identifiers.org/hco/15/GRCh38#51215962-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54080183-C-A

http://identifiers.org/hco/15/GRCh38#51218333-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54080429-C-A

51218333-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54080429-C-T

51218336-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54080432-G-A

51218336-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54080432-G-T

51218401-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54080494-T-A

51218436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54080524-A-G

51218498-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54080583-A-T

51218900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54080904-C-T

51218976-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54080978-T-C

51219034-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54081033-G-C

51220055-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54082173-C-T

http://identifiers.org/hco/15/GRCh38#51220154-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54082225-A-C

http://identifiers.org/hco/15/GRCh38#51221705-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54082603-C-A

51221705-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54082603-C-G

51221705-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54082603-C-T

51221755-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54082640-T-A

51221775-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54082661-G-T

http://identifiers.org/hco/15/GRCh38#51221791-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54082677-C-A

51221791-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54082677-C-G

51221791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54082677-C-T

51221831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54082713-G-A

51221831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54082713-G-T

http://identifiers.org/hco/15/GRCh38#51222066-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54082940-C-A

http://identifiers.org/hco/15/GRCh38#51222144-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54083004-A-C

51222144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54083004-A-G

http://identifiers.org/hco/15/GRCh38#51222224-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54083628-C-A

51222224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54083628-C-T

http://identifiers.org/hco/15/GRCh38#51222287-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54083704-C-A

51222287-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54083704-C-T

51222289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54083706-C-T

51222455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 54083866-C-T

51222457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 54083868-T-C

51222594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54084606-G-A

51222594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54084606-G-T

51222662-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54084673-T-C

51222723-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54084739-G-C

51222723-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54084739-G-T

51223475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54085465-G-A

51223475-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54085465-G-T

51224680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54085549-C-T

51224693-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54085562-G-C

http://identifiers.org/hco/15/GRCh38#51224783-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54085655-C-A

51224953-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54085804-T-C

51225305-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54086095-G-A

51226333-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54086801-G-C

51226643-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54086967-G-T

51227724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54087415-A-G

51227951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54087638-T-C

51227954-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54087641-G-A

51227954-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54087641-G-C

51227954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54087641-G-T

51227991-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54087735-T-A

51227991-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54087735-T-C

51227995-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54087738-T-A

51228024-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54087767-A-G

51228028-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54087771-A-G

51228028-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54087771-A-T

51228032-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54087775-T-C

http://identifiers.org/hco/15/GRCh38#51228074-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54087815-A-C

http://identifiers.org/hco/15/GRCh38#51229452-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54088309-A-C

51233147-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54090441-T-A

51233263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54090536-G-A

51233753-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54091077-A-T

51234072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54091385-T-C

51234095-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54091407-A-G

http://identifiers.org/hco/15/GRCh38#51234370-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54091672-C-A

51234370-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54091672-C-T

51234455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54091743-C-T

51234593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54091866-T-C

51235040-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54092292-A-G

51235170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54092408-G-A

51235170-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54092408-G-T

51235257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54092497-G-T

51235373-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54092588-C-T

51236176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54093293-C-T

51236320-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54093353-T-A

http://identifiers.org/hco/15/GRCh38#51236359-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54093385-C-A

51236759-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54093728-T-A

51236759-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54093728-T-G

http://identifiers.org/hco/15/GRCh38#51237345-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54094381-A-C

51237346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54094382-A-G

51237411-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54094450-C-T

51237526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54094552-G-A

51237762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54094778-A-G

51237950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54095327-G-A

51238063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54095424-C-T

51238194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54095569-G-A

51238378-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54095753-T-A

51238498-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54095848-C-T

51238811-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54096873-G-A

51238851-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54096913-A-G

51239109-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54097132-C-G

51239427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54097406-A-G

51239753-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54097760-C-T

51239791-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54097798-C-T

51239792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54097799-G-A

51239792-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54097799-G-T

51239828-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54097835-A-G

51239834-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54097842-G-C

51239891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54097902-C-T

http://identifiers.org/hco/15/GRCh38#51240065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54098056-C-A

51240065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54098056-C-T

51240066-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54098057-G-A

51240066-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54098057-G-C

51240526-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54098451-C-G

51240526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54098451-C-T

http://identifiers.org/hco/15/GRCh38#51240557-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54098481-A-C

51240565-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54098491-A-G

51240565-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54098491-A-T

51240680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54098577-C-T

51240827-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54098686-G-C

http://identifiers.org/hco/15/GRCh38#51240909-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54098756-C-A

http://identifiers.org/hco/15/GRCh38#51241561-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54099436-C-A

51241561-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54099436-C-T

http://identifiers.org/hco/15/GRCh38#51241671-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54099515-C-A

51241826-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54099607-T-G

51242134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54099917-C-T

51242170-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54099952-G-T

51242197-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54099979-T-A

http://identifiers.org/hco/15/GRCh38#51242231-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54100013-A-C

51242305-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54100060-T-A

51242305-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54100060-T-G

http://identifiers.org/hco/15/GRCh38#51242326-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54100081-A-C

51242326-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54100081-A-G

51242327-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54100082-T-A

51242327-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54100082-T-C

51242327-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54100082-T-G

51242333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54100088-A-G

51242353-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54100114-A-T

http://identifiers.org/hco/15/GRCh38#51242358-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54100119-A-C

51242358-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54100119-A-G

51242358-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54100119-A-T

51242367-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54100128-G-A

51242367-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54100128-G-C

51242367-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54100128-G-T

51242684-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54100416-C-T

51242781-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 54100554-T-A

51242781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 54100554-T-C

51242807-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant
orthologous variants: 54100580-G-T

51242980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54100760-C-T

51243024-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54100800-G-T

51243502-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54101312-T-C

51243581-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54101389-G-T

51243603-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54101410-G-T

51244053-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54102028-C-G

51248155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54108258-T-C

http://identifiers.org/hco/15/GRCh38#51248337-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54108438-C-A

51248337-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54108438-C-T

51248343-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54108444-A-G

51248344-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54108445-C-T

51248721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54108874-C-T

51248919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54109095-A-G

51248919-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54109095-A-T

51249368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54109594-C-T

51249452-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54109654-C-T

51249470-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54109672-G-C

51249706-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54110178-C-T

51249921-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54110357-A-T

http://identifiers.org/hco/15/GRCh38#51250033-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54110461-C-A

51250342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54110689-G-A

51250678-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54110968-C-T

51250978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54111220-G-A

51250978-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54111220-G-C

51251522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54111655-C-T

51251666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54111821-G-A

http://identifiers.org/hco/15/GRCh38#51251983-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#54112122-C-A

51251983-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54112122-C-G

51252086-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54112223-G-C

51252270-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54112386-G-T

51252422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54112547-C-T

51252446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54112571-G-A

51252460-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54112585-A-T

51252535-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54112668-T-C

51252582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54112714-T-C

51252588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54112720-C-T

51253270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54114232-T-C

51255025-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54117942-T-C

51255047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54117956-T-C

51255102-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54117999-T-A

51255528-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54118367-G-A

51255528-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54118367-G-T

51255647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54118475-C-T

51255666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54118494-G-A

51255666-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54118494-G-C

51255832-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54119061-G-T

http://identifiers.org/hco/15/GRCh38#51256199-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54119389-C-A

51256435-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54119729-G-C

51256491-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54119782-G-C

51256735-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54120022-C-T

51259428-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54122050-G-A

51259428-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54122050-G-T

51259565-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54122166-G-T

51259944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54122583-A-G

http://identifiers.org/hco/15/GRCh38#51260436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54123070-C-A

51260436-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54123070-C-T

51260481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54123115-C-T

51263028-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54125670-T-C

http://identifiers.org/hco/15/GRCh38#51263223-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54125817-A-C

51263624-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54126200-C-G

51263624-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54126200-C-T

51263866-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54126403-G-T

51263984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54126518-T-C

51264000-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54126534-G-T

51264580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54127083-T-C

51264729-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54127217-G-A

51264744-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54127231-C-T

51264918-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54127364-A-G

51265059-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54127449-A-G

51265127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54127519-A-G

51270189-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54128633-T-G

51270237-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54128677-A-G

51270356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54128794-T-C

51270359-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54128797-C-T

51270360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54128798-G-A

51270360-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54128798-G-C

51270360-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54128798-G-T

51271461-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54129805-A-G

51271572-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54129890-A-T

51271597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54129915-C-T

51272417-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54131368-T-G

51272431-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54131382-C-G

51272695-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54131666-G-C

51272911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54131828-G-A

51273341-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54131969-C-G

51273345-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54131974-C-G

http://identifiers.org/hco/15/GRCh38#51273469-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54132091-C-A

51273531-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54132156-G-A

51273633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54132246-C-T

51273649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54132262-C-T

51275425-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54133702-T-G

51275511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54133786-A-G

51275684-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54133963-A-G

51275699-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54133978-T-C

51276070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54134282-A-G

51276286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54134477-C-T

51276360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54134553-T-C

51276767-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54134973-T-A

http://identifiers.org/hco/15/GRCh38#51276789-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54134995-A-C

http://identifiers.org/hco/15/GRCh38#51276831-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54135011-C-A

51277319-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54135405-T-C

51277460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54135538-C-T

51277629-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54135742-G-A

51277629-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54135742-G-T

51277960-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54136063-T-G

51278892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54136967-G-A

51278920-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54136993-G-T

51279008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54137084-T-C

http://identifiers.org/hco/15/GRCh38#51279076-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54137150-C-A

51279122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54137187-T-C

51279122-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54137187-T-G

51279189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54137442-A-G

51279249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54137516-C-T

51279346-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54137616-A-T

51279465-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54137728-C-T

51279713-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54138026-G-C

51280050-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54138317-T-C

51280461-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54138417-G-T

51281113-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54139109-C-G

51281115-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54139111-C-T

51281247-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54139213-T-C

http://identifiers.org/hco/15/GRCh38#51281265-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54139233-A-C

51281275-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54139243-A-G

51281489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54139474-G-A

51281605-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54139572-G-A

51286815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54141158-T-C

51286844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54141180-G-A

51286927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54141266-G-A

51286989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54141318-C-T

http://identifiers.org/hco/15/GRCh38#51287697-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54142145-C-A

51287715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54142159-G-A

51288403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54143595-T-C

http://identifiers.org/hco/15/GRCh38#51288497-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54143680-C-A

51288829-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54144003-C-T

51288864-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54144038-A-G

51289012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54144178-A-G

51289575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54144793-A-G

51289928-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54145125-A-T

51290286-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54145440-G-A

51290607-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54146175-A-G

51291495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54147175-A-G

http://identifiers.org/hco/15/GRCh38#51291770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54147451-C-A

51292319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54147975-C-T

51292354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54148010-T-C

51292432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54148072-G-A

51292625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54148238-G-A

51292891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54148494-C-T

51293004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54148611-G-T

51293431-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54148833-A-T

51295119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54149025-G-A

51295157-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54149059-A-T

51295275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54149176-G-A

51295443-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54149333-C-T

51295480-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54149370-T-C

51295761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54149637-T-C

51295770-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54149646-C-G

51295770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54149646-C-T

http://identifiers.org/hco/15/GRCh38#51295813-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54149694-C-A

51296130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54149966-G-A

51296130-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54149966-G-C

51296854-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54150705-C-G

51297389-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54151181-C-G

51297389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54151181-C-T

51298464-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54152272-G-A

51298536-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54152345-C-T

51298575-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54152411-G-T

51298653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54152489-C-T

51299731-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54153864-T-A

51299731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54153864-T-C

51299977-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54154032-T-C

51300280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54154149-G-A

51300375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54154234-C-T

51300379-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54154238-G-A

51300998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54154808-C-T

51301079-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54154886-A-G

51301512-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54155418-G-T

51301651-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54155548-C-T

51302188-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54156243-C-T

51302392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54156418-A-G

51302453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54156480-T-C

51302489-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54156514-G-A

51303069-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54157095-T-A

51306546-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54161742-T-C

51306631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54161826-A-G

51306920-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54162091-C-G

51306920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54162091-C-T

51307473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54162464-C-T

51307724-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54162696-G-C

51308128-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54163182-G-T

51308239-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54163300-C-G

51311469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron variant
orthologous variants: 54170516-G-A

51311839-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron variant
orthologous variants: 54171223-G-A

51312022-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron variant
orthologous variants: 54171386-C-T

http://identifiers.org/hco/15/GRCh38#51312108-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54171464-C-A

51312132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron variant
orthologous variants: 54171480-G-A

51312132-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron variant
orthologous variants: 54171480-G-C

51312158-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron variant
orthologous variants: 54171500-A-T

51312364-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 54171664-C-T

51312365-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 54171665-G-A

51312365-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 54171665-G-T

http://identifiers.org/hco/15/GRCh38#51312422-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: http://identifiers.org/mco/9/GRCm39#54171722-C-A

51312447-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_exon_variant, undefined
orthologous variants: 54171743-A-G

http://identifiers.org/hco/15/GRCh38#51312875-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54172120-C-A

51312875-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54172120-C-T

51312891-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54172135-G-A

51312891-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54172135-G-C

51312910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54172151-G-A

51312910-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54172151-G-T

51312997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54172218-G-A

51313013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54172234-G-A

51313013-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54172234-G-T

51313106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54172315-G-T

51313107-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54172316-T-C

51313111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 54172320-T-C

http://identifiers.org/hco/15/GRCh38#51313309-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54172466-C-A

http://identifiers.org/hco/15/GRCh38#51314219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54173391-C-A

51314606-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54173686-T-C

51314636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54173717-G-T

51317919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54174799-G-A

51318256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54175122-G-A

51318423-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54175346-A-G

http://identifiers.org/hco/15/GRCh38#51318601-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54175456-C-A

51318601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54175456-C-T

51318841-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 54176182-T-C

51319046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 54176386-C-T

51319079-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54176421-C-G

51319079-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54176421-C-T

51319099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54176441-G-A

51319107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54176449-C-T

http://identifiers.org/hco/15/GRCh38#51319143-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54176485-C-A

51319143-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54176485-C-T

51319457-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54177173-A-T

51319700-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54177410-A-G

51324023-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54179167-T-A

51324419-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54179513-T-C

51326787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54181242-G-A

51326987-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54181423-T-A

http://identifiers.org/hco/15/GRCh38#51326997-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54181433-A-C

51327038-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54181474-G-A

http://identifiers.org/hco/15/GRCh38#51329173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54181949-C-A

51329346-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54182100-A-T

http://identifiers.org/hco/15/GRCh38#51329405-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54182149-C-A

51329425-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54182169-G-C

51329589-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54182339-G-A

51329661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54182411-T-C

51329668-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54182418-C-T

51329791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54182537-G-A

51329791-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54182537-G-T

http://identifiers.org/hco/15/GRCh38#51333689-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54187583-C-A

51333770-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54187653-A-G

51334060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54187934-A-G

51334199-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54188075-T-G

51334251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54188116-G-A

51334311-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54188168-C-G

51334311-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54188168-C-T

51334600-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54188815-G-T

51334663-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54188876-G-T

51334686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54188898-G-A

51334686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54188898-G-T

51334913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54189124-C-T

51336542-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54189668-A-T

51336821-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54189945-G-T

51336860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54189983-G-A

51336860-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54189983-G-C

51336860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54189983-G-T

51336872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54189995-G-A

51336959-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54190082-G-C

51337569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54190683-G-A

51337750-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54190830-A-G

51337771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54190851-G-A

51337771-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54190851-G-T

51337804-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54190877-G-A

51337804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54190877-G-T

51337816-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant, splice_donor_variant
orthologous variants: 54190889-A-G

http://identifiers.org/hco/15/GRCh38#51337871-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54190924-C-A

51337871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54190924-C-T

51337892-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 54190944-G-T

51338004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54191043-G-A

51338004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54191043-G-T

51338005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54191044-G-T

http://identifiers.org/hco/15/GRCh38#51338031-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54191070-C-A

51338031-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54191070-C-G

http://identifiers.org/hco/15/GRCh38#51338032-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/9/GRCm39#54191071-C-A

51338032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 2594
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 54191071-C-T