155476867-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28386421-C-T

155476941-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28386488-G-A

155476942-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28386489-G-T

http://identifiers.org/hco/7/GRCh38#155477080-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#28386645-A-C

155477114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28386678-G-A

155482978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 28389304-A-G

155483161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 28389447-C-T

155483240-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 28389525-T-G

155483241-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 28389526-T-C

155483415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 28389672-A-G

155483443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 28389700-G-A

http://identifiers.org/hco/7/GRCh38#155488538-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#28395229-C-A

155488706-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28395374-G-T

http://identifiers.org/hco/7/GRCh38#155488750-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#28395438-C-A

155488864-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28395538-G-A

155488864-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28395538-G-T

155489280-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28395802-G-A

155489280-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28395802-G-C

155489395-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28395873-T-C

155489435-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28395911-T-C

http://identifiers.org/hco/7/GRCh38#155489598-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#28396031-C-A

http://identifiers.org/hco/7/GRCh38#155489599-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#28396032-C-A

155489602-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28396035-T-G

155489766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28396137-A-G

155489975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28396304-C-T

155490253-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28396497-G-C

155490294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28396534-G-A

155490351-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28396610-C-T

http://identifiers.org/hco/7/GRCh38#155490621-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#28396865-A-C

155490729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28396948-C-T

155491036-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28397194-G-C

155491038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28397196-T-C

http://identifiers.org/hco/7/GRCh38#155491130-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#28397258-C-A

155491269-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28397386-C-G

155491391-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28397486-G-A

155491392-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28397487-G-T

155491440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28397521-G-A

155491480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28397567-G-A

155491480-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28397567-G-C

155491492-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28397579-T-G

155492542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28399048-A-G

155493534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28400355-T-C

155493652-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28400483-A-G

155493792-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28400589-G-C

155494256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28400909-C-T

155494350-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28400989-C-T

155494378-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28401017-G-A

155494378-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28401017-G-C

155494531-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28401147-A-T

155495114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28401514-C-T

155495119-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28401519-C-T

155495462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28401790-C-T

155495478-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28401806-G-T

155497348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28403284-T-C

155497467-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28403404-C-T

155497471-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28403408-G-A

155497655-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28403569-G-C

155498142-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28403946-C-G

155498142-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28403946-C-T

155498317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28404085-C-T

155498502-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28404237-G-C

155498734-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28404448-C-T

155498799-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28404510-T-G

155499035-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28404701-C-G

155499138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28404787-T-C

http://identifiers.org/hco/7/GRCh38#155499213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#28404857-C-A

155499292-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28404918-T-C

155499563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28405237-A-G

155499660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28405475-C-T

155500366-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28406107-T-G

155500401-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28406138-C-G

155500447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28406183-T-C

http://identifiers.org/hco/7/GRCh38#155500630-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#28406306-C-A

155500695-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28406358-T-G

155500779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28406456-C-T

155500882-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28406542-A-T

155500949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28406599-G-A

155501002-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28406634-G-A

155501002-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 28406634-G-T

155501685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 28407111-A-G

155501685-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 28407111-A-T

155501698-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 28407124-T-G

http://identifiers.org/hco/7/GRCh38#155501706-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#28407132-C-A

155501778-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 28407199-G-T

155501808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 28407242-G-A

155501808-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 28407242-G-T

155501853-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 28407276-G-T

http://identifiers.org/hco/7/GRCh38#155501914-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#28407335-C-A

http://identifiers.org/hco/7/GRCh38#155501923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#28407344-C-A

http://identifiers.org/hco/7/GRCh38#155501963-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#28407372-C-A

155502011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 28407415-G-T

155502012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 28407416-G-A

155502012-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 28407416-G-T

http://identifiers.org/hco/7/GRCh38#155502013-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#28407417-A-C

155502013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 28407417-A-G

155502013-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 28407417-A-T

155502156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 28407557-C-T

155502246-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 28407655-G-T

155502498-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 28407872-A-G

155502557-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 28407925-T-A

155502557-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 28407925-T-G

155502567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 28407934-G-A

155502567-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 28407934-G-T

http://identifiers.org/hco/7/GRCh38#155502623-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#28407993-C-A

155502687-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 28408057-C-T

155502983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28408335-T-C

155502983-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28408335-T-G

155503011-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: 3_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28408358-A-G

http://identifiers.org/hco/7/GRCh38#155503033-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#28408380-C-A

155503033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: 3_prime_UTR_variant, non_coding_transcript_exon_variant
orthologous variants: 28408380-C-T

155503081-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 28408410-T-G

155503161-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28408480-T-A

155503245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28408549-A-G

155503304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28408609-C-T

155503392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28408680-T-C

155503424-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28408713-T-G

155503524-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28408817-T-C

155503631-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28408879-T-C

155504514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28409672-T-C

155504541-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28409695-T-A

155504855-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28409953-G-A

155505153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28410588-G-T

155505206-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28410640-C-T

155505469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28410841-T-C

155505648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28411010-C-T

155505753-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28411124-T-C

155506207-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28411510-G-A

155506295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28411598-C-T

http://identifiers.org/hco/7/GRCh38#155506474-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#28411782-C-A

155506474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28411782-C-T

155506506-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28411815-G-A

155506506-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28411815-G-T

155506792-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28412062-T-C

155506796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28412066-G-A

155506796-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28412066-G-C

155506797-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28412067-A-T

http://identifiers.org/hco/7/GRCh38#155506862-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/5/GRCm39#28412147-C-A

155506976-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28412244-G-A

155506976-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28412244-G-T

155506998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant, undefined
orthologous variants: 28412263-C-T

155507120-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant, undefined
orthologous variants: 28412385-T-A

155507165-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28412428-G-A

155507165-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28412428-G-T

155507192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28412454-A-G

155507192-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28412454-A-T

155507308-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 28412567-C-G

155507340-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28412597-G-C

155507415-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28412762-A-G

155507553-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28412856-A-G

http://identifiers.org/hco/7/GRCh38#155507721-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#28413060-A-C

155507831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28413164-G-A

155507831-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28413164-G-C

155508135-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28413469-A-G

http://identifiers.org/hco/7/GRCh38#155508241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#28413551-C-A

155508345-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28413637-A-T

155508430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28413728-G-A

http://identifiers.org/hco/7/GRCh38#155508445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#28413743-C-A

155508445-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28413743-C-T

155508704-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28413964-A-G

155508731-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28413991-C-T

155509043-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: 5_prime_UTR_variant, missense_variant, non_coding_transcript_exon_variant
orthologous variants: 28414271-C-T

155509629-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28414643-C-T

155509682-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28414694-G-C

155510011-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28414985-G-T

155510257-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28415231-T-C

155510294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28415258-G-A

155510294-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28415258-G-C

155510294-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 28415258-G-T

http://identifiers.org/hco/7/GRCh38#155510551-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#28415432-C-A

155510551-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28415432-C-T

155510569-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28415455-G-A

155510723-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28415589-C-T

155510854-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28415686-G-A

155511068-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28415884-G-A

155511077-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28415891-T-A

155511357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28416141-G-A

155512034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28416709-A-G

155512261-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28416948-A-G

155512338-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28417020-C-T

155512410-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28417091-A-G

155512426-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28417107-C-G

155512541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28417226-T-C

155512762-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28417457-A-G

155512802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28417498-G-A

155512912-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28417607-T-A

http://identifiers.org/hco/7/GRCh38#155512981-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#28417679-A-C

http://identifiers.org/hco/7/GRCh38#155513200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#28417882-C-A

155513280-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28417960-A-T

http://identifiers.org/hco/7/GRCh38#155513639-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#28418275-A-C

155513694-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28418359-G-A

http://identifiers.org/hco/7/GRCh38#155513725-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#28418390-C-A

155514356-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28419246-G-A

155515162-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28419769-C-G

155515483-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28420035-A-G

155515510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28420062-C-T

155515689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28420171-G-T

155519861-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28423613-G-A

155519861-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28423613-G-T

155519909-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28423652-C-T

155521262-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28425613-T-C

155521412-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28425757-C-G

155521425-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28425765-T-C

155521426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28425766-C-T

155521806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28426349-G-A

155522544-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28427043-C-G

155522544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28427043-C-T

155522701-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28427166-A-T

155522941-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28427352-T-A

155524914-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28434640-C-G

155524914-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28434640-C-T

155524944-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28434658-G-T

155525171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28434890-A-G

155525171-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28434890-A-T

155526356-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28437284-C-T

155526420-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28437319-G-A

155526426-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28437325-G-A

155526455-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28437354-C-G

155526528-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28437404-T-C

155526529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28437405-G-A

155526552-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28437431-T-C

155526598-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28437476-T-A

155526715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28437580-C-T

http://identifiers.org/hco/7/GRCh38#155526732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#28437590-C-A

155526784-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28437643-C-T

155526824-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28437683-G-C

155526872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28437746-G-A

155531575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28441180-A-G

http://identifiers.org/hco/7/GRCh38#155531658-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#28441259-C-A

155533680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28443117-C-T

155533705-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28443140-T-G

155533742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 28443160-T-C

155533770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 28443188-T-C

155533833-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 28443240-G-A

155533842-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 28443249-T-A

155533842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_exon_variant
orthologous variants: 28443249-T-C

http://identifiers.org/hco/7/GRCh38#155533919-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#28443308-A-C

155533919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28443308-A-G

155533919-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28443308-A-T

http://identifiers.org/hco/7/GRCh38#155533923-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#28443312-C-A

155533923-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28443312-C-T

155534033-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28443419-C-T

155534065-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28443449-C-T

155534303-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, undefined
orthologous variants: 28443663-G-A

155534476-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, undefined
orthologous variants: 28443840-A-G

155534511-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28443866-C-G

155534558-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28443920-C-T

155534603-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28443964-C-T

155534612-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28443967-A-G

155534996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 28444300-G-A

155538603-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28446181-A-G

155538612-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28446192-G-A

155538661-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28446236-T-C

155538794-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28446352-T-G

155539046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28446548-C-T

155539224-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28446704-C-T

155539360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28446781-A-G

155543448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28449058-G-A

155543448-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28449058-G-T

155543458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28449068-A-G

155543463-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28449073-G-C

155543972-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28449459-C-G

155543972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28449459-C-T

155544232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28449633-G-A

155545262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, undefined
orthologous variants: 28450127-G-A

155545392-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28450273-C-T

http://identifiers.org/hco/7/GRCh38#155545825-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#28450700-C-A

155545825-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28450700-C-T

155545950-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 28450825-A-G

155546034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28450901-A-G

155546071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28450952-A-G

155546867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28451613-T-C

155546941-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28451663-A-G

155546960-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, undefined
orthologous variants: 28451682-C-T

155547098-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28451825-G-A

155547098-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28451825-G-C

155547108-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28451838-C-T

http://identifiers.org/hco/7/GRCh38#155547145-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#28451871-C-A

155547145-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28451871-C-T

155547292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28452013-C-T

155547352-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28452097-G-A

155549675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron variant
orthologous variants: 28453527-T-C

http://identifiers.org/hco/7/GRCh38#155554551-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: intron_variant, splice_donor_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#28455678-A-C

155554592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 28455720-G-A

155554592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 28455720-G-T

155554597-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 28455725-G-A

155554597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 28455725-G-T

155554665-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 28455802-C-T

http://identifiers.org/hco/7/GRCh38#155554710-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/5/GRCm39#28455839-C-A

155554846-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 28455952-G-C

155554846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 28455952-G-T

155554852-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 28455957-G-A

155554852-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 28455957-G-T

155554939-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 27786
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 28456044-C-T