64894616-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 6312255-A-G

64894628-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 6312243-G-A

64894628-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 6312243-G-C

64894641-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: 3 prime UTR variant
orthologous variants: 6312230-T-C

64894804-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: 3 prime UTR variant
orthologous variants: 6312064-G-T

64894811-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: 3 prime UTR variant
orthologous variants: 6312057-G-T

64895109-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: missense variant
orthologous variants: 6311729-G-A

64895121-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: missense variant
orthologous variants: 6311717-A-G

http://identifiers.org/hco/11/GRCh38#64895354-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6311488-C-A

64895354-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 6311488-C-T

64895446-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 6311396-G-A

64895446-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 6311396-G-C

64895446-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 6311396-G-T

64895483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron variant
orthologous variants: 6311369-G-A

http://identifiers.org/hco/11/GRCh38#64895527-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6311337-C-A

64895527-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron variant
orthologous variants: 6311337-C-T

64895569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron variant
orthologous variants: 6311302-G-A

64895569-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron variant
orthologous variants: 6311302-G-T

64896217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron variant
orthologous variants: 6310341-G-A

64896313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron variant
orthologous variants: 6310277-G-T

64896342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron variant
orthologous variants: 6310253-A-G

64896381-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron variant
orthologous variants: 6310233-G-C

64896399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron variant
orthologous variants: 6310216-C-T

64896408-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron variant
orthologous variants: 6310207-A-G

64896725-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron variant
orthologous variants: 6309035-G-A

64896877-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 6308884-G-C

64896958-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron variant
orthologous variants: 6308842-G-A

64896958-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron variant
orthologous variants: 6308842-G-T

64897106-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 6308782-C-T

http://identifiers.org/hco/11/GRCh38#64897325-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6308740-A-C

64897325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 6308740-A-G

http://identifiers.org/hco/11/GRCh38#64897356-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6308711-C-A

64897365-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 6308702-A-T

64897386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 6308681-G-A

64897404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 6308669-G-A

64897404-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 6308669-G-C

64897404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 6308669-G-T

64897433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6308640-T-C

64897433-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6308640-T-G

64897554-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6308541-G-T

64897783-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron variant
orthologous variants: 6308338-G-A

http://identifiers.org/hco/11/GRCh38#64897975-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: splice acceptor variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6308161-C-A

64897975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: splice acceptor variant
orthologous variants: 6308161-C-T

64898003-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron variant
orthologous variants: 6308133-A-G

http://identifiers.org/hco/11/GRCh38#64898345-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6307822-C-A

64898345-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: synonymous variant
orthologous variants: 6307822-C-T

64898398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 6307771-G-A

64898398-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 6307771-G-T

http://identifiers.org/hco/11/GRCh38#64898442-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6307746-C-A

64898444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron variant
orthologous variants: 6307744-A-G

64898445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron variant
orthologous variants: 6307743-G-A

64898445-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron variant
orthologous variants: 6307743-G-T

http://identifiers.org/hco/11/GRCh38#64898447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6307741-C-A

64898511-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron variant
orthologous variants: 6307732-G-A

64898511-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron variant
orthologous variants: 6307732-G-T

64898540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron variant
orthologous variants: 6307703-G-T

64898711-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 6307595-G-A

64898711-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: 3_prime_UTR_variant, synonymous_variant
orthologous variants: 6307595-G-C

http://identifiers.org/hco/11/GRCh38#64898754-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6307552-C-A

64898754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 6307552-C-T

64898850-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 6307460-G-T

64898886-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron variant
orthologous variants: 6307427-G-A

64900802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6306471-G-A

64900802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6306471-G-T

64900823-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6306460-G-C

64900823-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6306460-G-T

http://identifiers.org/hco/11/GRCh38#64901002-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6306299-C-A

64901002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6306299-C-T

64901232-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6306233-G-T

64901282-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6306200-C-G

64901515-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6306076-C-T

64901597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6306053-G-T

64901963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 6305854-G-A

64901963-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 6305854-G-T

64902278-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6305548-C-T

64902286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6305540-C-T

64902295-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6305528-G-T

64902358-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6305465-G-A

64902358-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6305465-G-C

64902380-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6305443-C-T

http://identifiers.org/hco/11/GRCh38#64902420-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6305402-C-A

64902420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6305402-C-T

64902562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6305247-T-C

64902694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6305122-G-A

64902723-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6305096-G-T

http://identifiers.org/hco/11/GRCh38#64902763-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6305060-C-A

64902763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6305060-C-T

64903131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6304781-A-G

64903172-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6304758-G-A

64903172-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6304758-G-T

64903235-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6304720-T-G

64903313-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6304669-C-G

64903313-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: 6304669-C-T

64903391-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6304595-T-C

http://identifiers.org/hco/11/GRCh38#64903419-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6304567-C-A

64903508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6304542-C-T

64903509-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6304541-G-A

64903509-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6304541-G-T

64903513-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6304537-A-G

64903540-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6304504-G-A

64903540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6304504-G-T

64903703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6304344-G-T

64905538-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6303671-G-T

64905693-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6303503-C-T

64905796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6303414-G-A

64905796-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6303414-G-T

64905805-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6303405-T-C

http://identifiers.org/hco/11/GRCh38#64905950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6303258-C-A

64905950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6303258-C-T

http://identifiers.org/hco/11/GRCh38#64906077-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6303133-C-A

http://identifiers.org/hco/11/GRCh38#64906155-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6303054-C-A

64906273-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6302945-A-G

64906273-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6302945-A-T

http://identifiers.org/hco/11/GRCh38#64906424-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6302827-C-A

http://identifiers.org/hco/11/GRCh38#64906466-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6302785-C-A

64906485-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6302766-A-T

64906491-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6302760-G-C

64906582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6302675-T-C

64906679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6302591-G-A

64906799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6302471-C-T

http://identifiers.org/hco/11/GRCh38#64906845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6302428-C-A

64906845-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6302428-C-T

64906883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6302348-G-T

http://identifiers.org/hco/11/GRCh38#64907103-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6302036-C-A

64907103-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6302036-C-T

64907113-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6302026-A-G

http://identifiers.org/hco/11/GRCh38#64907240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6301905-C-A

64907240-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6301905-C-G

64907240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6301905-C-T

64907329-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6301817-G-C

64907343-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6301803-G-A

64907343-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6301803-G-C

64907343-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6301803-G-T

64907350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6301796-C-T

64907417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: non_coding_transcript_exon_variant, splice_acceptor_variant, synonymous_variant
orthologous variants: 6301732-T-C

64907697-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6301483-G-C

64907775-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6301402-T-G

64907929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6301276-T-C

64908034-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6301176-G-A

http://identifiers.org/hco/11/GRCh38#64908852-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6300856-C-A

http://identifiers.org/hco/11/GRCh38#64908878-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6300842-C-A

64908878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6300842-C-T

64908967-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6300803-G-T

64909040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6300734-G-A

64909219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6300589-C-T

64909255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6300553-C-T

64909306-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6300502-G-T

64909389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6300419-G-A

64909389-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6300419-G-T

64909934-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6300042-G-A

64909934-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6300042-G-T

64909938-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6300037-G-T

64909946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6300029-G-A

64909946-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6300029-G-C

64909946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6300029-G-T

64909959-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6300016-A-G

http://identifiers.org/hco/11/GRCh38#64910060-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: non_coding_transcript_exon_variant, stop_gained
orthologous variants: http://identifiers.org/mco/19/GRCm39#6299935-C-A

64910060-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6299935-C-T

64910082-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 6299913-C-T

64910086-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6299909-A-T

64910181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 6299814-G-T

64910190-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 6299805-T-A

64910190-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 6299805-T-C

64910216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6299776-G-A

64910267-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6299707-G-C

http://identifiers.org/hco/11/GRCh38#64910676-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6298257-C-A

64910676-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6298257-C-G

64910747-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6298188-G-A

64910747-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6298188-G-T

http://identifiers.org/hco/11/GRCh38#64910781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6298158-C-A

64910781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6298158-C-T

64910979-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6297966-G-C

64911009-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6297938-C-G

64911026-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6297922-T-C

64911300-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6297642-G-A

64911300-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6297642-G-T

http://identifiers.org/hco/11/GRCh38#64911377-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6297344-C-A

64911377-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6297344-C-G

64911377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6297344-C-T

64911440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6297285-A-G

64911725-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6297036-G-C

64911725-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6297036-G-T

64911844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: missense_variant, non_coding_transcript_exon_variant, splice_region_variant
orthologous variants: 6296918-G-A

http://identifiers.org/hco/11/GRCh38#64911845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6296917-C-A

64911952-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6296810-C-G

64911952-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6296810-C-T

http://identifiers.org/hco/11/GRCh38#64911961-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6296801-C-A

64911961-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6296801-C-T

64912035-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6296725-C-T

http://identifiers.org/hco/11/GRCh38#64912240-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6296525-C-A

64912240-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6296525-C-T

64912290-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6296476-C-G

64912592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6296183-T-C

http://identifiers.org/hco/11/GRCh38#64912636-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6296166-C-A

64912636-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6296166-C-G

64912636-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6296166-C-T

64912677-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6296139-T-A

64912677-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6296139-T-C

64912680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6296131-G-A

64912680-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6296131-G-T

64913048-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6295711-G-A

64913048-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6295711-G-T

http://identifiers.org/hco/11/GRCh38#64913086-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6295673-C-A

64913086-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6295673-C-G

64913086-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6295673-C-T

64913273-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6295615-G-A

64913273-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6295615-G-T

http://identifiers.org/hco/11/GRCh38#64913418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6295470-C-A

64913477-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6295418-T-C

64913530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6295390-G-A

64913530-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6295390-G-T

64913709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6295265-C-T

64913711-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6295263-T-A

64913711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6295263-T-C

64913828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6295169-C-T

64913837-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 6295160-C-T

64914056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6294892-G-A

64914056-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6294892-G-T

http://identifiers.org/hco/11/GRCh38#64914063-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6294885-C-A

64914063-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6294885-C-G

64914063-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6294885-C-T

64914251-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6294696-G-A

64914251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6294696-G-T

http://identifiers.org/hco/11/GRCh38#64914270-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6294677-C-A

64914270-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6294677-C-T

http://identifiers.org/hco/11/GRCh38#64914304-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6294652-C-A

http://identifiers.org/hco/11/GRCh38#64914306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6294650-C-A

64914313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6294643-G-A

64914313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 6294643-G-T

64914348-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 6294607-G-A

64914348-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 6294607-G-T

http://identifiers.org/hco/11/GRCh38#64914623-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6294331-A-C

64914678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6294297-A-G

64914884-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6294014-T-G

64914967-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6293794-A-G

64914990-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6293746-C-T

http://identifiers.org/hco/11/GRCh38#64915202-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6293545-C-A

64915614-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6293152-A-G

http://identifiers.org/hco/11/GRCh38#64915628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/19/GRCm39#6293145-C-A

64915631-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6293142-A-G

64915654-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6293119-T-C

64915852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6293033-G-A

64915863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 6293022-T-C

64916131-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6292787-C-T

64916243-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6292653-G-A

64916587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6292350-G-A

64916637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 6292301-C-T

64917154-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6291805-T-A

64917155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6291804-G-A

64917155-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 29028
most severe consequence: 5_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 6291804-G-T