50396242-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: 3 prime UTR variant
orthologous variants: 117412392-G-T

http://identifiers.org/hco/5/GRCh38#50396328-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#117412313-C-A

50396453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: 3 prime UTR variant
orthologous variants: 117412224-G-A

50396564-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: 3 prime UTR variant
orthologous variants: 117412164-T-C

50396854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: 3 prime UTR variant
orthologous variants: 117411881-A-G

50396860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: 3 prime UTR variant
orthologous variants: 117411875-G-A

50396860-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: 3 prime UTR variant
orthologous variants: 117411875-G-C

50397260-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: 3 prime UTR variant
orthologous variants: 117411500-T-C

50397266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: 3 prime UTR variant
orthologous variants: 117411494-T-C

50397358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: 3 prime UTR variant
orthologous variants: 117411402-T-C

50397416-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: 3 prime UTR variant
orthologous variants: 117411343-T-A

50397433-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: 3 prime UTR variant
orthologous variants: 117411326-T-A

50397434-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: 3 prime UTR variant
orthologous variants: 117411325-T-C

50397466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: 3 prime UTR variant
orthologous variants: 117411294-A-G

50397466-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: 3 prime UTR variant
orthologous variants: 117411294-A-T

50397514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: 3 prime UTR variant
orthologous variants: 117411248-G-A

50397514-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: 3 prime UTR variant
orthologous variants: 117411248-G-T

50397724-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: 3 prime UTR variant
orthologous variants: 117411095-T-C

50397941-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: 3 prime UTR variant
orthologous variants: 117410874-T-C

50398001-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: 3 prime UTR variant
orthologous variants: 117410817-G-T

http://identifiers.org/hco/5/GRCh38#50398103-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#117410685-A-C

50398125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 117410665-G-T

http://identifiers.org/hco/5/GRCh38#50398268-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#117410522-C-A

50398340-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 117410469-G-T

50398508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 117410312-A-G

50398515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 117410305-T-C

http://identifiers.org/hco/5/GRCh38#50398533-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#117410271-C-A

50398584-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 117410226-T-G

50398671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 117410146-T-C

50398745-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 117410073-T-A

50398745-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 117410073-T-C

50398903-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 117409945-T-A

50398952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 117409896-A-G

50399225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 117409647-T-C

50399234-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 117409632-T-A

50399234-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 117409632-T-G

50399334-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117409549-G-T

50399430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117409455-G-A

50399431-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117409454-T-C

50399431-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117409454-T-G

50399432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117409453-T-C

50399658-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117409179-A-G

50399793-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117408752-T-C

http://identifiers.org/hco/5/GRCh38#50399805-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#117408730-C-A

50399805-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117408730-C-T

50399842-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117408650-A-G

50399842-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117408650-A-T

50399916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 117408576-G-A

http://identifiers.org/hco/5/GRCh38#50399917-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#117408575-C-A

50399917-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 117408575-C-T

50400016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117408477-T-C

http://identifiers.org/hco/5/GRCh38#50400018-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#117408475-C-A

50400018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117408475-C-T

50400072-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117408421-T-G

50400464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117408075-T-C

50400651-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117407836-T-A

50400814-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117407658-T-C

50401088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117407368-T-C

50401238-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117407178-T-C

50401275-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117407134-C-T

50401346-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117407033-T-C

50401388-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117406927-C-G

50401388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117406927-C-T

50401433-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117406869-A-G

50401479-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117406823-T-C

50401803-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117406545-T-A

50401807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117406542-A-G

http://identifiers.org/hco/5/GRCh38#50402138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#117405651-C-A

50402138-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117405651-C-G

50402142-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117405649-G-A

50402142-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117405649-G-T

http://identifiers.org/hco/5/GRCh38#50402239-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#117405539-C-A

50402239-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117405539-C-G

http://identifiers.org/hco/5/GRCh38#50402251-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#117405528-C-A

50402264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117405516-A-G

50402331-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117405447-A-G

50402380-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117405407-T-A

50402380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117405407-T-C

50402454-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117405354-C-T

50402475-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117405333-C-G

50402480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117405320-A-G

50402558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117405218-A-G

50403050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117404230-A-G

50403097-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117404184-C-G

50403169-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117404142-A-G

50403257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 117404054-T-C

50403302-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 117404009-C-T

50403307-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 117404004-T-A

50403387-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 117403924-T-G

http://identifiers.org/hco/5/GRCh38#50403420-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#117403891-A-C

50403505-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117403806-A-G

50403568-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117403740-G-A

50403568-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117403740-G-T

50403579-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117403729-G-A

50403579-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117403729-G-T

50403598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117403710-T-C

50403712-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117403593-G-C

50403952-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117403411-T-G

50403967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117403396-T-C

50403982-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117403389-C-T

50404063-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117403321-G-A

50404070-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117403314-A-G

50404075-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117403309-T-A

50404179-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117403222-T-C

50404644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117402761-T-C

50404650-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117402755-A-T

50404872-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117402570-T-C

http://identifiers.org/hco/5/GRCh38#50405103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#117402352-C-A

50405632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117401488-T-C

50405633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117401487-C-T

http://identifiers.org/hco/5/GRCh38#50405655-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#117401465-C-A

50405655-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117401465-C-T

http://identifiers.org/hco/5/GRCh38#50405729-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#117401052-A-C

http://identifiers.org/hco/5/GRCh38#50405837-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#117400944-C-A

50405916-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117400864-G-A

50405916-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117400864-G-T

50406092-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117400675-T-G

50406171-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117400617-T-C

50406284-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117400510-G-C

50406288-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117400506-C-G

50406316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117400480-A-G

50406366-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117400369-G-A

50406427-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117400298-T-A

50406427-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117400298-T-C

50406509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117400219-T-C

50406510-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117400218-G-A

50407673-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117396341-G-C

50407683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117396322-C-T

50407741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117396264-G-A

50407787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117396218-G-A

50407800-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117396212-G-A

50407898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117396116-A-G

50407956-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117396060-T-A

50408081-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117395998-T-C

50408147-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117395938-C-G

50408147-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117395938-C-T

50408245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117395781-A-G

http://identifiers.org/hco/5/GRCh38#50408325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#117395613-C-A

http://identifiers.org/hco/5/GRCh38#50408616-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#117395378-A-C

50408829-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117395189-A-G

50409021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117394997-G-A

50409824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117392745-C-T

50409887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117392688-T-C

50409912-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117392663-A-G

50410150-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117392460-C-T

50410165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117392446-T-C

50410313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117392301-G-T

50410368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117392257-T-C

50410389-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117392239-T-A

50410671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117386504-A-G

50410823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117386355-T-C

http://identifiers.org/hco/5/GRCh38#50410876-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: non_coding_transcript_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#117386321-C-A

50411094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117386099-A-G

50411124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117386067-T-C

50411141-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117386050-T-A

http://identifiers.org/hco/5/GRCh38#50411155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#117386036-C-A

50411161-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117386030-T-C

50411161-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117386030-T-G

50411167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117386024-A-G

50411237-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 117385952-G-C

50411239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 117385950-T-C

http://identifiers.org/hco/5/GRCh38#50411313-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#117385876-C-A

50411313-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 117385876-C-G

http://identifiers.org/hco/5/GRCh38#50411348-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#117385841-A-C

50411645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117385337-G-A

50411645-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117385337-G-T

50411658-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117385321-G-A

50411658-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117385321-G-T

50411662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117385317-G-A

50411662-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117385317-G-C

50411662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 117385317-G-T

50414902-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117380520-G-C

50415025-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117380385-G-C

http://identifiers.org/hco/5/GRCh38#50415092-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#117380319-C-A

50415567-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117379339-G-T

50415842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117379072-T-C

50415863-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117379051-A-G

50415916-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117379003-A-G

50416007-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117378916-G-A

50416007-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117378916-G-C

50416222-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117378722-C-T

50416303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117378645-C-T

50417211-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117377443-A-G

50417231-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117377421-C-G

50424925-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117372577-G-A

50425247-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117372191-T-G

50425476-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117371959-T-G

50425594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117371869-G-A

50425870-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117371741-G-T

50426248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117371530-T-C

50426319-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117371460-C-T

50426527-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117371221-A-G

50428096-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117369400-T-G

http://identifiers.org/hco/5/GRCh38#50428127-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#117369367-A-C

http://identifiers.org/hco/5/GRCh38#50428259-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#117369222-C-A

50428259-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117369222-C-G

50428259-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117369222-C-T

50428274-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117369207-T-A

50428274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117369207-T-C

50430218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117368775-G-A

50430218-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117368775-G-C

http://identifiers.org/hco/5/GRCh38#50430468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#117368517-C-A

50430614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117368381-T-C

50430857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117368218-T-C

http://identifiers.org/hco/5/GRCh38#50430912-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#117368162-A-C

50430999-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117368065-G-C

http://identifiers.org/hco/5/GRCh38#50431447-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#117367406-A-C

50431620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117367206-A-G

50431982-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117366845-T-G

50431993-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117366834-A-T

50432416-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117365056-T-C

50432447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117365025-T-C

http://identifiers.org/hco/5/GRCh38#50434296-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#117364269-A-C

http://identifiers.org/hco/5/GRCh38#50434300-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#117364265-C-A

50434303-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117364262-C-T

50434426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117364133-C-T

50434502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117364062-G-A

50434580-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117363991-G-C

50435128-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117362540-T-C

50435250-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117362419-C-T

50435273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117362396-T-C

50435324-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117362347-G-A

50435384-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117362297-T-A

50435384-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117362297-T-G

50436418-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117361140-G-A

50436450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117361067-T-C

50436653-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117360887-C-T

50436794-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117360768-C-G

50436837-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117360727-T-G

50436863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117360704-G-A

50436958-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117360625-A-T

50436981-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117360602-T-C

50437638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117360547-A-G

50437927-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117360293-A-T

50437928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117360292-T-C

50438197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117359869-T-C

50438278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117359813-T-C

50438368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117359722-C-T

50438533-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117359525-C-G

http://identifiers.org/hco/5/GRCh38#50438847-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#117359123-C-A

50438870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117359101-C-T

50438924-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117359059-A-T

50438955-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117359028-G-T

http://identifiers.org/hco/5/GRCh38#50440638-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#117357894-A-C

http://identifiers.org/hco/5/GRCh38#50440713-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#117357828-A-C

50440902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117357638-T-C

http://identifiers.org/hco/5/GRCh38#50440907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#117357627-C-A

50440907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117357627-C-T

50440999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117357535-G-A

50440999-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117357535-G-C

50440999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117357535-G-T

http://identifiers.org/hco/5/GRCh38#50441025-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#117357508-C-A

50441025-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117357508-C-T

50441098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 117357433-G-A

50441098-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 117357433-G-C

50441098-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant, synonymous_variant
orthologous variants: 117357433-G-T

http://identifiers.org/hco/5/GRCh38#50441198-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#117357339-C-A

50441198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117357339-C-T

http://identifiers.org/hco/5/GRCh38#50441206-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#117357331-C-A

50441206-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117357331-C-G

50441206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117357331-C-T

50441279-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117357257-T-A

50441279-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117357257-T-C

50441279-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117357257-T-G

50441308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117357228-G-A

50441308-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117357228-G-C

50441308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 117357228-G-T

50441383-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117357148-G-A

http://identifiers.org/hco/5/GRCh38#50441388-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#117357143-C-A

50441388-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117357143-C-T

50441389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117357142-G-A

50441389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117357142-G-T

50441476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117357062-T-C

50441505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117357020-G-A

50441505-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117357020-G-C

50441505-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117357020-G-T

http://identifiers.org/hco/5/GRCh38#50441565-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#117356966-A-C

50441566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 117356965-C-T

50441985-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117356568-G-A

50441985-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117356568-G-C

50442922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117353534-G-A

50442955-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 117353501-A-G

50443162-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30465
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 117353222-T-C