108559960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 5 prime UTR variant
orthologous variants: 42152575-G-A

108559960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 5 prime UTR variant
orthologous variants: 42152575-G-T

http://identifiers.org/hco/6/GRCh38#108560029-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42152506-C-A

108560029-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42152506-C-T

108560759-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42151833-T-C

108560759-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42151833-T-G

http://identifiers.org/hco/6/GRCh38#108560770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42151822-C-A

108560770-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42151822-C-G

108560770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42151822-C-T

http://identifiers.org/hco/6/GRCh38#108560832-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42151763-C-A

108560832-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42151763-C-G

108560832-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42151763-C-T

108560893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42151696-T-C

108560961-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 42151628-T-C

108561043-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 42151572-G-A

108561043-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 42151572-G-C

108561043-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 42151572-G-T

108561106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 42151532-G-A

108561106-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 42151532-G-C

108561106-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 42151532-G-T

108561131-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 42151508-G-A

108561131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 42151508-G-T

http://identifiers.org/hco/6/GRCh38#108561219-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42151417-C-A

108561219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 42151417-C-T

108561553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 42151086-G-A

108561557-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 42151082-G-A

108561573-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 42151066-G-A

108561573-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 42151066-G-T

http://identifiers.org/hco/6/GRCh38#108561610-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42151029-A-C

108561610-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 42151029-A-G

108561610-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 5_prime_UTR_variant, synonymous_variant
orthologous variants: 42151029-A-T

108561623-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 42151016-G-A

108561728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 5_prime_UTR_variant, missense_variant
orthologous variants: 42150911-C-T

108561845-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 42150794-G-A

108561889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 42150753-G-A

108561889-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 42150753-G-C

108561889-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 42150753-G-T

http://identifiers.org/hco/6/GRCh38#108561893-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42150749-C-A

108561893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 42150749-C-T

http://identifiers.org/hco/6/GRCh38#108561898-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42150744-A-C

108561910-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 42150732-G-C

108561912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 42150730-G-A

108561912-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 42150730-G-C

108561912-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 42150730-G-T

108561960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 42150692-A-G

108561986-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 42150661-C-T

108562201-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron_variant, undefined
orthologous variants: 42150449-G-C

108562462-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42150223-C-G

108562462-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42150223-C-T

http://identifiers.org/hco/6/GRCh38#108562532-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42150156-C-A

108564197-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron_variant, undefined
orthologous variants: 42148726-C-G

108564197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron_variant, undefined
orthologous variants: 42148726-C-T

http://identifiers.org/hco/6/GRCh38#108564666-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#42148135-A-C

108565007-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42147830-A-T

108565061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42147810-T-C

108565290-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42147609-C-G

108565361-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42147540-T-C

108565453-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42147464-C-T

http://identifiers.org/hco/6/GRCh38#108565477-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42147440-A-C

108565515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42147403-T-C

108565534-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42147381-C-T

108565639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42147305-C-T

108565838-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42147144-T-A

108565933-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42147053-T-C

108566237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron_variant, undefined
orthologous variants: 42146765-T-C

http://identifiers.org/hco/6/GRCh38#108566422-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42146595-A-C

108566727-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42146392-G-A

108566790-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42146310-A-T

108566822-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42146278-G-A

108566822-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42146278-G-T

108566847-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42146253-A-T

108567109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42146014-A-G

http://identifiers.org/hco/6/GRCh38#108567296-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42145840-C-A

108567319-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 42145817-G-A

108567407-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 42145729-G-A

108567564-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42145581-A-G

108568437-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 42145300-T-A

108568484-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 42145258-G-T

108569203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 42144675-G-A

108569910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42144125-G-A

108569910-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42144125-G-C

108570814-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42143901-T-G

108570831-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42143887-T-C

108570851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42143867-T-C

108573433-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42142317-G-C

http://identifiers.org/hco/6/GRCh38#108574315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42141770-C-A

108574349-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42141731-G-C

108574439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42141672-C-T

108574763-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42141360-A-G

http://identifiers.org/hco/6/GRCh38#108574801-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42141323-A-C

108574817-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42141307-C-T

108575073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42141052-G-A

108575073-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42141052-G-T

108575201-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42140882-C-G

108575292-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42140796-T-G

108575357-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42140731-T-A

108575754-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42140134-A-G

108576001-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42139872-A-G

108576183-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42139701-A-G

http://identifiers.org/hco/6/GRCh38#108576554-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42139212-A-C

108577020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42138491-T-C

108577084-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42138420-G-C

108577186-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42138321-T-A

108577635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42138126-A-G

108577685-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42138076-C-T

108577887-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42137839-C-G

108577887-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42137839-C-T

108577972-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42137751-A-G

108578034-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42137689-T-C

108578048-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42137675-A-G

108578048-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42137675-A-T

108578190-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42137541-A-G

108578261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42137455-G-A

108578638-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42136841-G-T

108578854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42136638-C-T

108579546-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42136020-C-T

108579844-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42135764-G-T

108579994-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42135654-T-C

108580618-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42135365-T-C

http://identifiers.org/hco/6/GRCh38#108580907-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42135055-A-C

108581100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42134847-A-G

108581369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42134644-G-T

108581487-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42134531-T-G

108581644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42134389-T-C

108581746-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42134286-A-G

108581813-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42134219-A-T

108581900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42134133-G-A

108581912-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42134121-T-G

108582112-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42134085-A-T

108582199-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42134001-A-G

108582217-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42133992-C-T

108582574-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42133618-C-G

108582705-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42133524-T-C

108583162-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42133068-A-G

108583168-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42133060-T-C

108583470-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42132759-G-C

http://identifiers.org/hco/6/GRCh38#108583838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42132446-C-A

108584308-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42131640-T-C

108584663-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42131309-T-A

108584694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42131278-A-G

108584871-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42131105-A-T

108584952-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42131050-A-G

108585433-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42130917-T-C

108585505-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42130831-G-A

108585602-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42130733-A-G

108585961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42130379-G-A

108586122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42130227-T-C

108586215-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42130134-A-G

108588233-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42128733-G-T

http://identifiers.org/hco/6/GRCh38#108588402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42128475-C-A

108588739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42128179-A-G

http://identifiers.org/hco/6/GRCh38#108588791-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42128126-A-C

108588791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 42128126-A-G

108589067-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42127802-G-A

108589696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 42127200-T-C

108589820-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42127127-G-C

108590717-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42126784-A-G

108591485-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42125996-C-G

108591508-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42125974-A-G

108591694-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42125783-A-G

108591716-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42125761-A-G

108591797-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42125685-G-A

108592204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42125311-G-A

108592379-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42125170-C-T

108592689-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42124896-T-G

108592754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42124827-C-T

108592791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42124806-T-C

108593025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42124589-A-G

108593027-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42124587-G-A

108593027-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42124587-G-T

108593126-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42124486-G-C

108593159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42124461-G-A

108593159-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42124461-G-C

108593229-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42124385-T-C

108593240-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42124374-G-C

108594569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42123832-C-T

108594680-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42123722-G-A

108594789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42123610-A-G

http://identifiers.org/hco/6/GRCh38#108595019-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42123361-C-A

108595019-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42123361-C-T

108595389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42123005-G-A

108595417-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42122977-C-G

108595473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42122920-A-G

108595866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42122539-G-A

108595892-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42122513-A-G

http://identifiers.org/hco/6/GRCh38#108595945-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42122468-A-C

108596295-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42122132-G-A

108596424-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42122019-T-A

108596424-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42122019-T-G

108596440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42122002-G-A

108596486-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42121958-T-A

108596565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42121883-C-T

108596628-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42121836-T-G

http://identifiers.org/hco/6/GRCh38#108596864-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42121605-A-C

108597073-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42121468-A-G

108597079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42121462-G-A

108597163-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42121402-T-A

108597264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42121312-A-G

108597751-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42121110-G-T

108597872-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42121006-G-A

108603853-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42119222-T-G

108603918-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42119163-T-G

108604026-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42119060-A-T

108605913-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42118361-A-G

108606003-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42118282-T-C

108606569-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42117797-C-T

108607674-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42117033-T-G

108607749-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42116961-C-G

108607873-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42116855-C-T

108608202-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42116626-G-A

108608719-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42116266-G-A

108608969-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42116128-G-A

108609757-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42115171-T-C

108609785-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42115127-T-C

108609822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42115084-T-C

http://identifiers.org/hco/6/GRCh38#108609965-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42114901-A-C

http://identifiers.org/hco/6/GRCh38#108609993-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42114873-A-C

108610502-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42114420-G-A

108610598-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42114349-A-G

108610711-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42114251-C-T

108610756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42114213-C-T

108610801-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42114168-T-C

108610850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42114119-A-G

108611318-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42113496-C-T

108611638-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42113232-T-C

108619264-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42109366-G-A

108619395-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42109249-C-T

108619710-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42108835-T-A

108619804-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42108740-T-C

108619857-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42108687-C-T

108620196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42108346-G-A

108620196-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42108346-G-C

108620229-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42108313-G-C

108620518-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42108045-G-C

108620704-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42107900-G-T

http://identifiers.org/hco/6/GRCh38#108621334-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42107303-C-A

http://identifiers.org/hco/6/GRCh38#108621792-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42105203-A-C

108622428-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42104909-T-A

108622445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42104892-G-A

http://identifiers.org/hco/6/GRCh38#108622447-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42104890-C-A

108622541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42104834-A-G

108622920-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42104469-A-G

108622954-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42104451-G-T

108623055-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42104356-G-A

108623203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42104036-G-A

108623649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42103588-T-C

108623650-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42103587-G-A

108623736-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42103494-A-G

108623869-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42103366-A-G

108626925-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42102307-T-A

108626929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42102303-T-C

108627061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42102181-G-A

108627124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42102126-T-C

108629337-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42101531-G-C

108629391-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42101487-A-G

108630870-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42100865-C-T

108630929-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42100807-T-A

108630947-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42100789-T-G

108632342-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42098212-C-G

108632386-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42098166-T-C

108632427-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42098131-A-G

108632906-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42097827-C-T

108632921-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42097812-G-T

108633087-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42097754-C-G

108633243-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42097621-T-A

108633288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42097578-C-T

108633433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42097489-C-T

108633627-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42097349-G-T

108633659-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42097316-G-T

http://identifiers.org/hco/6/GRCh38#108633838-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42097141-C-A

108634071-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42096949-A-G

http://identifiers.org/hco/6/GRCh38#108634173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42096855-C-A

108634231-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42096823-C-T

108634240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42096814-G-A

108634240-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42096814-G-C

108634280-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42096793-A-T

108634434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42096652-G-A

108634551-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42096562-T-C

108636573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42095662-A-G

108636783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42095473-A-G

108636818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42095444-G-A

108636870-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42095391-C-G

108637689-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42094510-G-C

108638108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42093905-G-A

108638161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42093853-G-A

108638193-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42093825-G-A

108638346-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42093656-G-T

108638719-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42093379-T-C

108638872-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42093240-T-A

108639003-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42093108-C-T

108639040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42093084-C-T

108639309-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42092958-C-T

108639394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42092877-G-A

http://identifiers.org/hco/6/GRCh38#108639425-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42092851-C-A

108641360-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42092502-A-G

108641467-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42092421-T-C

108641504-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42092389-C-G

108641504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42092389-C-T

108641745-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42092162-C-G

108641745-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42092162-C-T

108642671-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42091493-C-T

108642737-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42091434-G-A

108642855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42091364-C-T

108642879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42091335-A-G

http://identifiers.org/hco/6/GRCh38#108642918-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42091297-A-C

108642925-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42091290-T-C

108642925-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42091290-T-G

108643118-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42090832-T-G

http://identifiers.org/hco/6/GRCh38#108643261-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42090561-C-A

http://identifiers.org/hco/6/GRCh38#108643504-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42090371-A-C

108645598-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42090239-G-A

108645614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42090221-T-C

108645811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42089906-A-G

108645931-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42089782-A-G

108647040-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42088204-G-A

108647466-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42087834-A-T

108647528-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42087778-A-T

108647671-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42087526-A-G

108647891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42087260-C-T

108648390-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42086467-G-T

108650344-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42085144-C-G

108650382-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42085106-C-T

108650567-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42084479-G-C

108650663-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42084374-A-G

108650817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42084264-T-C

108650929-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron_variant, undefined
orthologous variants: 42084149-A-G

108651049-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42083924-G-T

108651491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42083614-A-G

108651630-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron_variant, undefined
orthologous variants: 42083483-G-C

108651766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron_variant, undefined
orthologous variants: 42083370-A-G

108651788-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron_variant, undefined
orthologous variants: 42083357-G-A

108651795-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron_variant, undefined
orthologous variants: 42083350-T-C

108652062-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron_variant, undefined
orthologous variants: 42083086-G-A

108652085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron_variant, undefined
orthologous variants: 42083063-T-C

108652127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42083019-G-A

108652494-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42082936-T-G

108652644-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42082801-C-T

108652660-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42082793-T-A

108652774-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42082690-C-G

108653108-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42082428-C-G

108653166-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42082366-C-G

108653260-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42082278-A-G

108653673-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42081825-G-A

108653689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42081809-G-A

108653927-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42081553-G-A

108654190-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42081296-G-A

108654213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42081273-A-G

108654392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42081108-A-G

108654393-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42081107-T-C

108654396-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42081104-T-C

108654474-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42081057-C-T

108654763-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42080805-A-T

http://identifiers.org/hco/6/GRCh38#108654792-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42080775-A-C

108654827-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42080729-T-C

108654925-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42080631-T-A

108654929-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42080627-C-T

108655822-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42079970-C-G

108655822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42079970-C-T

108655883-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron_variant, undefined
orthologous variants: 42079909-A-G

108655886-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron_variant, undefined
orthologous variants: 42079906-T-G

108655904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42079888-A-G

108655925-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42079867-A-G

108655963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42079829-A-G

108655978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42079816-G-A

108655992-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42079802-G-T

108656149-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42079706-G-A

http://identifiers.org/hco/6/GRCh38#108656326-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#42079492-C-A

108656438-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 42079370-G-T

108656443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 42079365-G-A

108656456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 42079353-T-C

108656493-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 42079317-C-T

108656520-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 42079289-A-G

108656551-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42079258-T-A

108656570-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42079245-G-A

108656584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42079235-A-G

http://identifiers.org/hco/6/GRCh38#108656635-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42079189-C-A

108656636-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42079188-A-T

108656637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42079187-G-A

108656681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42079147-A-G

108656911-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42078852-G-A

108657054-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42078707-A-G

108657064-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42078679-A-G

108657106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42078654-A-G

108657137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42078644-T-C

108657179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42078618-C-T

108657193-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42078607-C-T

108657200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42078600-G-A

108657284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42078523-C-T

108657422-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42078427-A-G

http://identifiers.org/hco/6/GRCh38#108657620-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42078273-C-A

108658371-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42077421-A-G

108658392-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42077402-T-G

108659454-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42077005-T-C

108659583-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42076899-C-T

108659608-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42076876-A-G

108659844-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42076691-G-A

108659847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42076688-A-G

108659992-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42076572-G-A

108660363-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42076239-A-T

108661457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron_variant, undefined
orthologous variants: 42075832-G-A

108661547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron_variant, undefined
orthologous variants: 42075754-A-G

108662075-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42075196-G-T

108662156-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42075119-C-G

108662156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42075119-C-T

108662231-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42075052-G-A

108662564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42074792-G-A

108662577-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42074778-G-A

108662657-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42074722-C-T

108662674-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42074707-A-G

108663082-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42074333-A-T

108663109-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42074244-A-G

108663263-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42074030-A-G

http://identifiers.org/hco/6/GRCh38#108663497-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron_variant, synonymous_variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42073853-C-A

108663497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron_variant, missense_variant
orthologous variants: 42073853-C-T

108663788-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron_variant, missense_variant
orthologous variants: 42073562-A-G

108663809-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron_variant, missense_variant
orthologous variants: 42073541-C-G

108663950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron_variant, missense_variant
orthologous variants: 42073400-G-A

108663968-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron_variant, missense_variant
orthologous variants: 42073382-A-G

108664013-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron_variant, missense_variant
orthologous variants: 42073337-A-G

108664013-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron_variant, missense_variant
orthologous variants: 42073337-A-T

108664052-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron_variant, missense_variant
orthologous variants: 42073298-C-G

108664052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron_variant, missense_variant
orthologous variants: 42073298-C-T

108664217-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron_variant, missense_variant
orthologous variants: 42073133-A-G

108664350-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron_variant, missense_variant
orthologous variants: 42073000-G-A

108664423-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron_variant, missense_variant
orthologous variants: 42072927-T-A

108665005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42072356-G-A

108665005-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42072356-G-T

108665029-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42072343-G-A

108665029-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42072343-G-C

108665029-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42072343-G-T

108665044-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42072331-G-C

108665260-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42072170-C-T

108665261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42072169-G-A

108665261-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42072169-G-T

http://identifiers.org/hco/6/GRCh38#108665267-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42072163-C-A

108666926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42071367-C-T

108667070-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42071211-G-A

108667176-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42071110-T-C

108667637-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42070735-T-G

108671157-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42070240-A-G

108671345-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42070057-G-A

108671346-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42070056-T-A

108671515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42069915-T-C

108671640-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42069822-T-C

108671644-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42069818-A-G

108671784-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42069716-G-C

108672676-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42068917-G-T

108672786-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42068837-C-T

108672985-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42068664-T-G

108673208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42068484-C-T

108673369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42068380-C-T

108673654-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42068151-G-A

108673716-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron_variant, undefined
orthologous variants: 42068097-G-A

http://identifiers.org/hco/6/GRCh38#108673912-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/10/GRCm39#42067952-C-A

108673990-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42067879-G-A

108674189-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42067718-C-G

108674362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42067569-C-T

108674408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42067531-C-T

108674410-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42067530-G-A

108674470-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42067467-T-C

108674537-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42067410-G-A

108674682-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42067286-G-A

108674684-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42067284-G-A

108675649-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42065488-A-G

108675683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42065455-C-T

108675767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42065382-C-T

108675830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42065323-C-T

108675876-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42065267-G-C

108676576-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42064780-C-G

108676576-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42064780-C-T

108676578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42064778-A-G

108676697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42064702-G-A

108676837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42064600-G-A

108677248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42064238-T-C

108677388-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42064102-G-A

108677434-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42064058-G-C

108677440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42064052-G-A

http://identifiers.org/hco/6/GRCh38#108677988-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42063528-A-C

108677989-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42063527-A-T

108678008-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42063508-T-C

108679489-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42062605-T-C

108679570-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42062518-C-T

108679733-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42062374-G-T

108679736-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42062371-G-T

108679743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42062364-G-A

108679743-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42062364-G-T

108679781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: intron variant
orthologous variants: 42062331-T-C

108679988-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 3 prime UTR variant
orthologous variants: 42062130-T-C

108679997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 3 prime UTR variant
orthologous variants: 42062121-G-A

108679997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 3 prime UTR variant
orthologous variants: 42062121-G-T

108680012-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 3 prime UTR variant
orthologous variants: 42062106-A-G

108680128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 3 prime UTR variant
orthologous variants: 42062001-G-A

108680128-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 3 prime UTR variant
orthologous variants: 42062001-G-T

108680173-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 3 prime UTR variant
orthologous variants: 42061956-G-T

108680287-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 3 prime UTR variant
orthologous variants: 42061843-A-G

108680392-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 3 prime UTR variant
orthologous variants: 42061731-T-A

http://identifiers.org/hco/6/GRCh38#108680463-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42061660-C-A

108680463-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 3 prime UTR variant
orthologous variants: 42061660-C-T

108680536-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 3 prime UTR variant
orthologous variants: 42061588-G-T

108680620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 3 prime UTR variant
orthologous variants: 42061505-C-T

108680621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 3 prime UTR variant
orthologous variants: 42061504-A-G

http://identifiers.org/hco/6/GRCh38#108680633-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42061495-C-A

108680702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 3 prime UTR variant
orthologous variants: 42061437-C-T

108680734-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 3 prime UTR variant
orthologous variants: 42061405-T-A

108680777-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 3 prime UTR variant
orthologous variants: 42061379-T-A

108680777-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 3 prime UTR variant
orthologous variants: 42061379-T-C

108680777-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 3 prime UTR variant
orthologous variants: 42061379-T-G

108680807-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 3 prime UTR variant
orthologous variants: 42061349-A-G

108680843-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 3 prime UTR variant
orthologous variants: 42061323-G-C

108680850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 3 prime UTR variant
orthologous variants: 42061316-A-G

108681244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 3 prime UTR variant
orthologous variants: 42060889-T-C

108681323-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 3 prime UTR variant
orthologous variants: 42060811-T-C

108681323-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 3 prime UTR variant
orthologous variants: 42060811-T-G

108682004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 42060171-A-G

108682093-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 3 prime UTR variant
orthologous variants: 42060081-A-T

108682280-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 3 prime UTR variant
orthologous variants: 42059905-G-T

108682308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 3 prime UTR variant
orthologous variants: 42059891-G-A

108682308-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 3 prime UTR variant
orthologous variants: 42059891-G-T

108682368-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 3 prime UTR variant
orthologous variants: 42059838-G-C

http://identifiers.org/hco/6/GRCh38#108682499-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42059787-C-A

108682499-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 3 prime UTR variant
orthologous variants: 42059787-C-T

108682539-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 3 prime UTR variant
orthologous variants: 42059747-C-T

http://identifiers.org/hco/6/GRCh38#108682572-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42059712-C-A

http://identifiers.org/hco/6/GRCh38#108682605-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42059675-C-A

108682605-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 3 prime UTR variant
orthologous variants: 42059675-C-T

http://identifiers.org/hco/6/GRCh38#108682641-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42059639-C-A

108682641-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 3 prime UTR variant
orthologous variants: 42059639-C-T

108682683-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 3 prime UTR variant
orthologous variants: 42059597-C-T

108682737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 3 prime UTR variant
orthologous variants: 42059547-T-C

http://identifiers.org/hco/6/GRCh38#108683003-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42059315-C-A

108683003-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 3 prime UTR variant
orthologous variants: 42059315-C-G

108683209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 3 prime UTR variant
orthologous variants: 42059129-T-C

108683239-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 3 prime UTR variant
orthologous variants: 42059116-C-G

http://identifiers.org/hco/6/GRCh38#108683427-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/10/GRCm39#42058954-C-A

108683520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 3 prime UTR variant
orthologous variants: 42058927-C-T

108683831-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 3 prime UTR variant
orthologous variants: 42058762-G-A

108683831-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 3 prime UTR variant
orthologous variants: 42058762-G-T

108683835-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 3 prime UTR variant
orthologous variants: 42058758-G-T

108683959-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 3 prime UTR variant
orthologous variants: 42058636-G-A

108683959-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 3 prime UTR variant
orthologous variants: 42058636-G-T

108684394-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 3 prime UTR variant
orthologous variants: 42058185-G-A

108684635-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3821
most severe consequence: 3 prime UTR variant
orthologous variants: 42057965-C-T