41188380-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 92294726-G-A

http://identifiers.org/hco/12/GRCh38#41188719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: stop_gained, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#92295062-C-A

41188719-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: missense_variant, undefined
orthologous variants: 92295062-C-G

41188719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: synonymous_variant, undefined
orthologous variants: 92295062-C-T

41188739-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: missense_variant, undefined
orthologous variants: 92295081-A-G

41188743-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: synonymous_variant, undefined
orthologous variants: 92295085-G-A

41188743-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: missense_variant, undefined
orthologous variants: 92295085-G-T

http://identifiers.org/hco/12/GRCh38#41188767-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: stop gained
orthologous variants: http://identifiers.org/mco/15/GRCm39#92295109-C-A

41188767-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: synonymous variant
orthologous variants: 92295109-C-T

http://identifiers.org/hco/12/GRCh38#41188781-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92295123-C-A

41188781-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: missense variant
orthologous variants: 92295123-C-G

41188781-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: missense variant
orthologous variants: 92295123-C-T

http://identifiers.org/hco/12/GRCh38#41188782-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92295124-C-A

41188782-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: synonymous variant
orthologous variants: 92295124-C-T

41188787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: missense variant
orthologous variants: 92295128-G-A

41188787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: missense variant
orthologous variants: 92295128-G-T

http://identifiers.org/hco/12/GRCh38#41188947-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: synonymous variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92295253-C-A

41188947-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: synonymous variant
orthologous variants: 92295253-C-G

41189074-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: missense variant
orthologous variants: 92295360-G-A

41189074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: missense variant
orthologous variants: 92295360-G-T

41189129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92295411-G-A

41189129-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92295411-G-C

41189129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92295411-G-T

http://identifiers.org/hco/12/GRCh38#41189138-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92295416-C-A

41189138-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92295416-C-G

41189138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92295416-C-T

41189155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92295433-G-A

41189155-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92295433-G-T

41189170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92295446-G-A

41189170-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92295446-G-C

41189309-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92295545-A-G

41189460-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92295679-G-A

http://identifiers.org/hco/12/GRCh38#41189614-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92295749-C-A

41189615-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92295750-C-T

41189762-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92295855-A-T

41189811-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92295884-G-C

41190121-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92296156-A-T

41190258-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92296284-T-G

41190399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92296463-A-G

41190608-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, undefined
orthologous variants: 92296744-T-G

41191318-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92297519-G-A

41191318-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92297519-G-C

41191318-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92297519-G-T

41191429-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92297596-G-T

41191443-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92297613-T-C

http://identifiers.org/hco/12/GRCh38#41191444-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92297614-A-C

41191444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92297614-A-G

41191447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92297617-T-C

http://identifiers.org/hco/12/GRCh38#41191473-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92297643-C-A

41191473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: missense variant
orthologous variants: 92297643-C-T

41191475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: synonymous variant
orthologous variants: 92297645-A-G

http://identifiers.org/hco/12/GRCh38#41191505-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92297675-C-A

41191505-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: synonymous variant
orthologous variants: 92297675-C-T

41191535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: synonymous variant
orthologous variants: 92297705-A-G

41191669-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92297776-T-C

41192388-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92298041-C-G

41192434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92298099-C-T

41192536-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92298196-A-G

41192581-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92298240-G-A

41192638-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92298290-G-A

41192948-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92298609-G-T

41192983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92298705-A-G

41192994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92298716-C-T

41193123-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92298874-G-T

41193179-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92298925-A-G

41193377-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92299135-T-C

41193878-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92299597-A-G

41194046-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92299776-A-T

http://identifiers.org/hco/12/GRCh38#41194100-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: stop gained
orthologous variants: http://identifiers.org/mco/15/GRCm39#92299829-C-A

41194100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: missense variant
orthologous variants: 92299829-C-T

http://identifiers.org/hco/12/GRCh38#41194245-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92299977-A-C

41194245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92299977-A-G

41194271-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92299998-G-T

41194276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92300000-G-A

41194276-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92300000-G-C

41194291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92300015-A-G

41194853-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92300253-G-A

41194896-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92300293-A-G

41195028-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92300403-G-T

41195029-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92300404-T-C

41195141-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92300513-A-G

http://identifiers.org/hco/12/GRCh38#41195324-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92300711-C-A

41195326-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92300713-G-A

41195326-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92300713-G-C

41195340-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92300727-A-G

41195444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92300814-C-T

41195466-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92300852-A-G

http://identifiers.org/hco/12/GRCh38#41195611-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92300962-A-C

41195611-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92300962-A-G

41195666-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92301001-G-A

41195822-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92301115-C-T

http://identifiers.org/hco/12/GRCh38#41195948-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92301217-C-A

41196003-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92301267-T-C

41196005-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92301269-G-A

41196058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92301326-G-A

41196058-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92301326-G-T

http://identifiers.org/hco/12/GRCh38#41196100-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92302541-C-A

41196100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92302541-C-T

41196159-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92302608-C-G

41196265-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92302718-G-A

41196968-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92303449-G-C

41196973-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92303454-T-G

41197068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92303636-C-T

41197163-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92303793-G-C

41197163-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92303793-G-T

http://identifiers.org/hco/12/GRCh38#41197218-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92303841-A-C

41197218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92303841-A-G

41197458-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92304071-T-G

41197468-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92304081-A-G

41197521-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92304134-A-G

41197553-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92304167-A-T

41219263-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92304463-G-A

41219587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92311397-G-A

41219708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92311514-C-T

41219753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92311542-A-G

41219887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92311673-T-C

http://identifiers.org/hco/12/GRCh38#41219905-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92311690-C-A

41219949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92311737-G-A

41219971-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92311757-T-C

41220132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92311900-C-T

41220163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92311930-G-A

41220285-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92312047-C-T

41220787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92312482-A-G

41221127-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92312904-G-A

41221158-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92312930-C-T

41221185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92312936-A-G

41221186-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92312937-C-T

41227078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92313821-A-G

41227867-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92314029-G-A

41228205-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92314270-T-A

41228307-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92314361-A-G

41228560-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92314582-G-A

41228953-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92314950-A-T

41229027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92315028-A-G

41229062-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92315063-T-C

41229099-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92315096-T-A

41229129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92315125-T-C

41229131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92315127-T-C

41229466-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92315368-G-C

41229566-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92315455-C-G

41229566-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92315455-C-T

41229623-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92315511-A-G

41229811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92315727-A-G

41229972-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92315890-G-T

41230114-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92316017-C-T

41230115-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92316018-A-G

41230165-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92316051-C-T

41230217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92316099-G-A

41230289-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92316156-C-T

41230369-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92316215-G-T

http://identifiers.org/hco/12/GRCh38#41230495-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92316319-C-A

41230495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92316319-C-T

41230498-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92316322-T-G

41230594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92317300-G-A

41230594-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92317300-G-T

41230910-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92317565-A-G

41231191-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92317839-A-G

41231200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92317848-T-C

41231268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92317917-A-G

http://identifiers.org/hco/12/GRCh38#41231353-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92318000-C-A

41231353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92318000-C-T

41234022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92318693-G-A

41234072-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92318790-T-C

41234095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92318811-G-A

41234137-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92318860-G-T

http://identifiers.org/hco/12/GRCh38#41234157-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92318880-A-C

41234284-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92318999-T-A

41234524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92319236-G-A

41234524-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92319236-G-T

http://identifiers.org/hco/12/GRCh38#41234677-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92319384-A-C

41234677-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92319384-A-T

41234801-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92319996-G-T

41234842-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92320037-C-T

41235251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92320419-A-G

41235318-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92320484-A-G

41235489-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92320627-C-T

41235534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92320674-T-C

41235823-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92320945-A-G

41236389-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92321692-C-T

41236743-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92322022-G-T

41239657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92322880-A-G

41239735-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92322953-C-G

41262854-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92330872-T-C

41262962-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92331631-T-C

41262970-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92331639-T-C

41262985-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92331654-A-G

41263128-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92331870-G-C

41263771-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92332031-G-A

41263865-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92332124-G-A

41263866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92332125-G-A

41263866-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92332125-G-T

41263871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92332130-T-C

http://identifiers.org/hco/12/GRCh38#41263957-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92332212-C-A

http://identifiers.org/hco/12/GRCh38#41263963-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92332297-A-C

41263963-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92332297-A-G

41264034-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92332356-A-G

41264238-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92332572-A-G

41264558-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92332754-C-G

41264585-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92332766-T-A

41264585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92332766-T-C

41264683-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92332858-T-G

http://identifiers.org/hco/12/GRCh38#41265308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92333082-C-A

41265308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92333082-C-T

41265481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92333208-G-A

41265481-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92333208-G-C

41265860-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92333656-G-A

41265860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92333656-G-T

41265908-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92333702-T-A

http://identifiers.org/hco/12/GRCh38#41265950-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92333745-C-A

http://identifiers.org/hco/12/GRCh38#41265951-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92333746-C-A

41266363-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92333836-G-T

41266380-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92333851-G-T

41266592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92334438-T-C

41266592-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92334438-T-G

41266615-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92334461-A-T

41266967-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92334744-G-A

41266982-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92334759-C-G

41267017-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92334792-A-T

http://identifiers.org/hco/12/GRCh38#41267020-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92334795-C-A

41267932-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92335499-A-G

41267994-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92335561-C-T

41268181-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92335747-T-C

http://identifiers.org/hco/12/GRCh38#41268402-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92335947-C-A

41268432-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92335971-G-A

41268432-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92335971-G-C

41268540-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92336078-T-C

41268605-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92336146-G-T

41268878-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92336413-T-C

41268919-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92336441-C-T

41269081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92336593-A-G

41269314-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92336823-C-T

41269727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92337335-T-C

41269741-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92337349-G-A

41270057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92338237-A-G

41270111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92338276-C-T

41270123-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92338288-C-T

41270147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92338312-A-G

41270161-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92338325-A-G

41270161-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92338325-A-T

41270194-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92338387-G-A

41270477-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92338618-C-T

41270573-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92338712-A-G

41270641-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92338787-G-C

41271051-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92339187-T-C

41271186-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92339329-T-A

41271443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92339577-G-A

41271779-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92339910-C-T

41271810-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92339938-T-G

41271987-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92340113-T-A

41272245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92340367-A-G

41272627-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92340898-G-A

41272709-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92340979-T-C

41272787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92341049-G-A

41272818-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92341077-G-A

41272818-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92341077-G-T

41273097-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92341305-T-C

41273202-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92341405-A-G

41273203-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92341406-T-C

41273789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92342048-T-C

http://identifiers.org/hco/12/GRCh38#41273840-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92342099-C-A

41273923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92342180-G-A

41273984-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92342246-A-T

41274014-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92342281-C-T

41274037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92342304-T-C

41274093-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92342344-C-T

41274614-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92342787-T-C

41274616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92342789-T-C

http://identifiers.org/hco/12/GRCh38#41274657-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92342817-C-A

41274777-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92342941-T-G

http://identifiers.org/hco/12/GRCh38#41274855-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92343013-A-C

41275243-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92343389-T-A

41275319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92343450-A-G

41275558-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92343650-T-C

41275613-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92343705-T-G

41275971-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92344023-G-T

41276020-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92344070-G-A

41276065-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92344111-G-C

41276143-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92344235-G-A

41276159-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92344257-A-G

41276206-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92344293-G-T

41276236-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92344323-T-G

41276402-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92344478-A-T

http://identifiers.org/hco/12/GRCh38#41276403-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92344479-C-A

41276403-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92344479-C-T

41276408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92344484-G-A

41276434-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92344508-G-A

41276651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92345112-A-G

41276651-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92345112-A-T

41276762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92345221-G-A

41276891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92345335-C-T

http://identifiers.org/hco/12/GRCh38#41277085-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92345522-C-A

41277185-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92345613-T-C

41277250-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92345676-T-G

41277362-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92345802-C-G

41277362-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92345802-C-T

41277429-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92345859-A-G

41277460-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92345895-T-C

http://identifiers.org/hco/12/GRCh38#41277484-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92345923-A-C

41277492-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92345930-G-C

http://identifiers.org/hco/12/GRCh38#41277555-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92345993-C-A

41277555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92345993-C-T

41278045-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92346387-A-G

41278315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92346631-G-A

http://identifiers.org/hco/12/GRCh38#41278383-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92346698-A-C

41278834-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92347055-G-A

41278919-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92347138-G-A

41279319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92347663-A-G

41279333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92347698-G-A

41279440-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92347802-C-T

41279541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92347886-G-A

41279541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92347886-G-T

41279603-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92347955-A-T

http://identifiers.org/hco/12/GRCh38#41279629-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92347981-A-C

http://identifiers.org/hco/12/GRCh38#41286830-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92349364-C-A

41286830-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92349364-C-T

41286838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92349372-T-C

41287238-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92349748-C-T

41287385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92349869-G-A

41287392-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92349876-G-A

41287435-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92349919-C-T

41287436-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92349920-G-A

41287482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92349964-T-C

41287541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92350020-T-C

http://identifiers.org/hco/12/GRCh38#41287789-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92350262-A-C

41287956-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92350427-T-A

41288024-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92350491-A-T

41288210-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92350672-C-G

41288366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92350826-C-T

41288367-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92350827-T-A

41288367-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92350827-T-C

41288394-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92350854-T-A

41288424-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92350884-G-A

41288478-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92350938-A-T

41288903-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92351349-C-T

41288907-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92351353-T-A

41289064-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92351998-G-A

41289064-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92351998-G-C

41289089-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92352025-T-C

41289156-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92352089-G-T

41289529-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92352461-G-A

41289643-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92352537-G-A

41289653-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92352551-G-T

41289897-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92352771-G-A

41290088-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92352936-G-T

41290108-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92352953-G-C

41290123-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92352968-T-C

41290267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92353067-A-G

http://identifiers.org/hco/12/GRCh38#41290941-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92355216-A-C

41290987-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92355263-T-G

41290998-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92355274-G-A

41291172-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92355443-T-A

41291299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92355974-G-A

http://identifiers.org/hco/12/GRCh38#41291318-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92355993-A-C

41291352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92356024-C-T

41291360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92356032-T-C

41291362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92356034-G-A

41291381-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92356053-G-T

41291579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92356240-C-T

41291792-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92356276-G-C

41291950-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92356411-G-A

41291957-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92356418-A-T

41292015-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92356446-T-C

41292300-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92356694-C-G

41292300-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92356694-C-T

41293333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92356977-A-G

41293790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92357381-G-A

41293790-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92357381-G-T

41294196-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92357717-G-T

http://identifiers.org/hco/12/GRCh38#41294295-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92357811-A-C

41294621-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92358873-T-C

41294621-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92358873-T-G

41294759-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92359010-T-A

41297439-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92359869-A-G

41297857-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92360571-T-C

41297912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92360619-T-C

http://identifiers.org/hco/12/GRCh38#41297958-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92360656-A-C

41297980-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92360678-T-C

41298197-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92360846-T-C

41298418-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92361095-G-C

41298422-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92361099-C-T

41298725-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92361307-C-T

41298734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92361316-T-C

http://identifiers.org/hco/12/GRCh38#41298790-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92361369-A-C

41298790-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92361369-A-G

41298859-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92361440-A-T

41298920-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92361509-C-T

41298966-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92361551-C-T

41299740-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92362793-T-A

41299981-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92363018-T-G

41300045-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92363076-T-C

http://identifiers.org/hco/12/GRCh38#41300249-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92363257-A-C

41300316-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92363318-A-G

41300998-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92363975-A-G

41300998-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92363975-A-T

41301090-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92364065-A-T

41301192-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92364172-A-G

41301204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92364184-C-T

41301424-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92364373-T-G

41301706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92364610-G-A

41301706-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92364610-G-T

41301732-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92364636-T-C

41302009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92364800-G-A

41302140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92364942-A-G

41302362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92365215-G-A

41302431-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92365273-T-G

41302520-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92365370-T-A

41302593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92365432-T-C

41302706-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92365541-T-G

41302775-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92365606-T-A

41303001-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92365932-G-C

41303088-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92366009-T-C

41303148-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92366062-A-G

41303320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92366237-G-A

41303367-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92366284-G-C

41303371-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92366288-T-C

41303416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92366329-A-G

41303476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92366389-T-C

41303804-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92366703-C-T

41304047-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92366914-G-T

41304411-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92367232-T-C

41304526-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92367417-T-C

41304595-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92367485-G-A

41304753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92367640-A-G

41304837-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92367722-T-G

41310268-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92373685-G-A

41310346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92373761-A-G

http://identifiers.org/hco/12/GRCh38#41310399-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92373811-C-A

41310436-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92373846-G-T

41310904-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92374347-A-G

41310951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92374394-T-C

41310956-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92374399-G-A

41311076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92374519-C-T

41311082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92374526-T-C

41311082-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92374526-T-G

41311514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92375002-G-A

41311783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92375288-A-G

41314720-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92376212-G-T

41314768-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92376271-A-G

41314995-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92376479-G-A

41315026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92376507-G-T

41315068-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92376531-G-C

41315185-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92376647-C-T

41315672-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92377124-A-G

41315730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92377180-T-C

41315776-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92377221-T-G

41315803-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92377247-T-C

41316150-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92377590-G-C

41316174-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92377614-T-C

41316224-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92377664-G-T

41316313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92377727-G-A

41316886-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92378259-G-T

41318325-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92378697-A-G

http://identifiers.org/hco/12/GRCh38#41318458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92378823-C-A

41318458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92378823-C-T

41318599-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92378914-C-T

41320678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92379145-G-A

41320678-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92379145-G-C

41320681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92379148-C-T

41320720-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92379185-G-A

41320872-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92379332-A-G

41320967-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92379445-T-C

41321196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92380211-G-A

41321239-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92380266-A-G

41321259-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92380286-G-A

41321964-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92380930-A-T

41321989-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92380955-A-G

41321989-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92380955-A-T

41321999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92380966-G-A

41321999-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92380966-G-T

41322441-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92381803-A-T

41322462-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92381821-A-G

41322462-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92381821-A-T

41322975-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92383423-G-A

41323101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92383545-A-G

41323102-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92383546-C-G

41323117-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92383562-C-G

41323167-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92383612-C-T

41323255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92383681-G-T

41323291-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92383715-G-A

41323291-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92383715-G-C

41323330-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92383753-T-A

41323356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92383779-A-G

41323445-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92383881-G-A

41323620-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92384057-T-A

41324009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92384408-A-G

41324049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92384465-T-C

41324076-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92384488-G-C

41324278-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92384669-T-C

http://identifiers.org/hco/12/GRCh38#41324544-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92384929-A-C

http://identifiers.org/hco/12/GRCh38#41324753-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92385059-A-C

41324973-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92385257-C-T

41325225-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92385818-T-C

41325282-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92385876-T-C

41325353-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92385938-A-G

41325390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92385971-C-T

41326617-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92387503-T-A

http://identifiers.org/hco/12/GRCh38#41326721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92387601-C-A

41326757-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92387634-C-G

41327144-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92388022-C-G

41327386-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92388256-G-A

41327386-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92388256-G-C

41327430-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92388304-G-A

41328085-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92388908-G-T

41328217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92389043-G-A

41328217-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92389043-G-T

41328220-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92389046-G-A

41328275-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92389099-T-C

41328278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92389102-G-A

41328314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92389116-A-G

41328734-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92389332-T-C

41328981-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92389569-T-A

41329372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92390232-C-T

41329669-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92390505-G-A

41329707-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92390542-G-T

41329785-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92390603-T-G

41329884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92390686-T-C

41329917-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92390718-A-G

http://identifiers.org/hco/12/GRCh38#41330065-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92390848-C-A

41330148-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92390928-C-G

41330148-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92390928-C-T

41330981-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92391595-A-G

41331010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92391624-A-G

41331022-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92391636-G-T

41331240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92391846-A-G

41331255-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92391860-A-G

41333236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92392749-G-A

41333236-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92392749-G-T

41333265-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92392778-T-A

41333265-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92392778-T-C

41333481-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92392937-C-T

41333549-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92392944-C-T

http://identifiers.org/hco/12/GRCh38#41333588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92392962-C-A

41333602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92392976-G-A

41333602-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92392976-G-T

41333666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92393031-A-G

41333821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92393140-C-T

41333895-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92393212-A-G

41333930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92393237-G-A

41334047-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92393369-T-C

41334196-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92393518-C-T

http://identifiers.org/hco/12/GRCh38#41334375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92393695-C-A

41334375-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92393695-C-G

41334414-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92393725-G-A

41334414-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92393725-G-T

41334425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92393736-G-T

41334503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, undefined
orthologous variants: 92393803-C-T

41334553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92393852-G-T

41335494-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92394645-G-T

41335787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92394920-A-G

41336160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92395309-A-G

41336185-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92395334-A-G

41336256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92395386-T-C

41336480-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92395558-A-G

41337372-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92395884-A-G

41337610-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92396131-G-T

http://identifiers.org/hco/12/GRCh38#41337746-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92396241-C-A

41343938-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92396956-G-C

http://identifiers.org/hco/12/GRCh38#41344111-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92397146-A-C

41344111-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92397146-A-G

41344111-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92397146-A-T

41344161-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92397194-C-T

41344262-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92397294-C-T

41344451-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92397472-A-G

http://identifiers.org/hco/12/GRCh38#41344532-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92397542-A-C

41344628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92397627-T-C

41344813-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92397780-T-A

41345115-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92398179-T-C

41345125-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92398189-G-T

http://identifiers.org/hco/12/GRCh38#41345268-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92398333-C-A

41345434-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92398525-G-C

41345507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92398595-G-A

41345509-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92398597-T-C

http://identifiers.org/hco/12/GRCh38#41345590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92398736-C-A

41345637-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92398786-C-T

41345680-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92398827-C-T

http://identifiers.org/hco/12/GRCh38#41345726-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92398879-C-A

41345726-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92398879-C-G

41346136-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92399278-T-A

41347112-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92400776-A-T

41347127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92400790-T-C

41347245-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92400861-A-G

41347268-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92400874-A-G

41347415-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92401004-C-T

http://identifiers.org/hco/12/GRCh38#41348211-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92401993-C-A

41348211-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92401993-C-T

41348360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92402138-T-C

41349121-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92406572-T-A

41349224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92406660-T-C

41349248-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92406682-T-G

41349610-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92406998-C-T

41349798-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92407156-T-A

41349921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92407279-T-C

41349956-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92407314-A-T

41349963-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92407321-G-A

41349982-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92407340-T-A

41349982-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92407340-T-C

41350160-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92407526-A-G

41350311-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92407674-G-T

41350353-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92407710-G-C

41350538-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92407925-A-G

41350765-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92408121-A-G

41352208-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92408540-G-A

41352278-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92408612-G-A

41352278-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92408612-G-T

41352311-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92408649-A-T

41352340-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92408678-C-G

41352408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92408746-G-A

41352485-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92408823-T-C

41352690-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92409042-G-A

http://identifiers.org/hco/12/GRCh38#41352721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92409073-C-A

41352721-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92409073-C-T

41352906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92409266-A-G

41352915-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92409275-A-G

41352960-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92409310-G-A

41353012-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92409357-G-A

41353061-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92409468-G-C

41353085-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92409485-T-C

41353364-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92409693-G-T

41353543-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92409838-G-T

41353682-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92409959-G-C

41353733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92410021-T-C

41353864-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92410149-G-C

41353879-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92410171-G-A

41353879-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92410171-G-T

41354141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92411086-C-T

41354207-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92411152-A-T

41354541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92411649-A-G

http://identifiers.org/hco/12/GRCh38#41354695-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92411783-C-A

http://identifiers.org/hco/12/GRCh38#41354764-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92411852-C-A

41354787-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92411875-G-T

41354868-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92411962-A-G

41355214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92412269-G-A

41355256-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92412311-T-C

41355308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92412362-G-A

http://identifiers.org/hco/12/GRCh38#41356445-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92413442-C-A

http://identifiers.org/hco/12/GRCh38#41356610-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92413610-A-C

http://identifiers.org/hco/12/GRCh38#41356666-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92413670-A-C

41356905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92413908-T-C

41357152-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92414109-C-G

41357236-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92414188-C-T

41357272-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92414212-T-C

41357346-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92414268-C-T

41357420-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92414366-C-T

41357431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92414377-C-T

41357522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92414462-G-A

41357600-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92414540-T-A

41357758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92414676-G-A

41357809-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92414721-C-T

41357813-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92414725-C-T

41357823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92414735-C-T

http://identifiers.org/hco/12/GRCh38#41358241-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92415089-C-A

41358359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92415169-A-G

41358436-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92415246-A-T

41358500-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92415303-T-C

41358838-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92415581-G-A

http://identifiers.org/hco/12/GRCh38#41358874-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92415612-A-C

41360494-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92417573-C-T

41360732-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92417744-G-A

41361105-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92418014-T-A

41361367-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92418303-A-T

41361812-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92418752-G-A

41361813-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92418753-T-A

41361827-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92418767-G-C

41362375-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92419323-C-T

http://identifiers.org/hco/12/GRCh38#41362682-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92419759-A-C

41362912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92419950-G-A

http://identifiers.org/hco/12/GRCh38#41363187-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92420224-C-A

41363808-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, undefined
orthologous variants: 92420540-G-C

41363893-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92420602-C-G

41363893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92420602-C-T

41363909-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92420618-T-C

41363913-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92420622-C-T

http://identifiers.org/hco/12/GRCh38#41364157-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92420820-A-C

41364166-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92420829-C-T

41364168-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92420831-T-A

41364196-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92420855-G-A

41364305-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92420956-T-C

41364365-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92421016-T-G

41364536-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92421155-G-A

41364862-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92421467-T-A

41364862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92421467-T-C

41364912-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92421512-T-C

41364961-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92421568-C-G

41365003-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92421609-T-C

41365027-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92421633-A-G

41365140-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92422222-T-G

41365170-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92422255-G-A

41365170-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92422255-G-T

41365239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92422319-C-T

41365240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92422320-A-G

41365377-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92422450-T-A

41365416-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92422489-A-G

41365443-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92422516-C-G

41366493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92423561-T-C

41366722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92423789-T-C

http://identifiers.org/hco/12/GRCh38#41367732-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92424431-A-C

41367732-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92424431-A-G

41367763-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92424461-G-A

41367773-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92424472-G-T

http://identifiers.org/hco/12/GRCh38#41367789-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92424488-A-C

http://identifiers.org/hco/12/GRCh38#41368130-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92424716-A-C

41368245-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92424843-T-A

41368458-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92424983-T-C

41368706-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92425217-A-G

41368725-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92425255-T-A

41368842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92425409-G-A

41369038-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92425618-T-C

http://identifiers.org/hco/12/GRCh38#41369045-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92425623-C-A

41369116-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92425694-C-T

41369130-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92425704-A-G

41369174-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92425745-G-A

41369174-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92425745-G-T

41369177-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92425748-T-A

41369249-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: -G-T

41369283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: -A-G

41369828-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: -G-A

41369828-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: -G-C

41382439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92437740-T-C

41382497-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92437786-G-C

http://identifiers.org/hco/12/GRCh38#41382605-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92437895-A-C

41382605-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92437895-A-T

41382832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92438455-A-G

41382889-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92438510-T-G

41383334-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92438925-A-G

41388522-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92441344-A-T

41388593-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92441412-A-T

41388705-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92441537-G-A

41388821-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92441652-A-T

41388838-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92441666-A-T

41388904-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92441719-T-G

41389005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92441828-T-C

http://identifiers.org/hco/12/GRCh38#41389099-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92441902-A-C

41389154-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92441953-C-G

41389165-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92441964-A-G

41389224-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92442011-G-T

41390077-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92445755-G-A

41390179-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92445844-C-G

41390381-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92446058-G-C

41390418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92446095-C-T

http://identifiers.org/hco/12/GRCh38#41390529-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92446205-C-A

41390541-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92446217-T-G

41390697-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92446369-G-A

41390697-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92446369-G-C

41390736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92446409-G-A

41390736-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92446409-G-C

41390944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92446622-A-G

41391030-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92446708-C-G

41391033-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92446712-G-A

41391033-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92446712-G-C

41391144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92446817-C-T

http://identifiers.org/hco/12/GRCh38#41391214-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92446925-A-C

41391218-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92446929-A-G

41391309-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92447018-T-A

41391310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92447019-G-A

41391426-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92447134-C-T

41391430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92447138-C-T

41391443-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92447156-G-A

41391545-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92447251-C-T

41391552-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92447258-T-A

41391602-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92447298-T-G

41391683-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92447405-T-C

41391716-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92447438-A-T

41392145-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92447838-G-A

41392158-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92447851-T-C

41392167-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92447860-A-G

41392209-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92447900-G-T

41392600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92448259-C-T

41392621-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92448280-G-T

41393000-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92449150-C-T

41393033-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92449183-A-G

41393067-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92449217-T-A

41393171-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92449321-A-G

41393273-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92449423-G-C

http://identifiers.org/hco/12/GRCh38#41393373-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92449536-C-A

41393385-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92449548-T-C

41393423-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92449586-T-C

41393423-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92449586-T-G

41397067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92455571-C-T

41397123-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92455628-G-A

41397123-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92455628-G-T

41397375-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92455868-T-C

41397999-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92456486-C-T

http://identifiers.org/hco/12/GRCh38#41398396-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92457871-C-A

41398437-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92457913-A-G

41398473-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92458011-C-T

41398547-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92458075-A-T

41398814-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92458246-G-T

41398854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92458284-C-T

41398889-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92458322-C-T

41399228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92459075-G-A

41399296-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92459173-T-C

41399300-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92459177-A-G

41399327-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92459204-G-A

41399336-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92459213-T-G

41400035-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92459516-T-A

41400145-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92459624-C-G

41400151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92459631-T-C

41400151-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92459631-T-G

41400311-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92459797-T-A

41400486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92459972-A-G

41400645-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92460128-A-G

41400847-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92460332-A-G

41400935-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92460408-T-C

http://identifiers.org/hco/12/GRCh38#41400988-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92460461-A-C

41401077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92460551-A-G

41401091-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92460565-A-G

41401195-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92460644-C-G

41401195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92460644-C-T

41401213-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92460662-C-G

41401319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92460764-A-G

41403570-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92461435-T-A

41403570-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92461435-T-G

41403753-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92461577-T-G

41406379-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92468237-T-A

41406462-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92468319-G-A

41406462-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92468319-G-C

41406962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92468542-G-A

41407189-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92468742-G-C

41407299-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92468894-T-A

41407299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92468894-T-C

41407513-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92469108-G-A

41407944-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92469536-A-G

41408330-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92469908-G-A

41408391-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92469976-T-A

41408397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92469982-T-C

41408397-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92469982-T-G

41408408-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92469993-C-T

41408519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92470105-G-A

41408584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92470175-A-G

41408914-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92470688-T-C

41408996-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92470772-G-A

41409017-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92470793-T-A

41409689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 92471757-G-T

41409758-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 92471828-G-A

41409758-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 92471828-G-T

41409823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 92471889-C-T

http://identifiers.org/hco/12/GRCh38#41409848-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92471911-C-A

41409850-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 92471913-A-G

41409851-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 92471914-G-T

http://identifiers.org/hco/12/GRCh38#41409881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92471943-C-A

http://identifiers.org/hco/12/GRCh38#41409955-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92471996-C-A

41409978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92472005-C-T

41410096-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92472158-C-T

41410361-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92472426-G-A

41410473-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92472540-T-C

41410512-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92472579-A-G

41410647-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92472687-G-A

41410730-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92472761-C-G

41411360-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92473027-G-A

41411409-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92473069-T-C

http://identifiers.org/hco/12/GRCh38#41411456-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92473111-C-A

41411825-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 92473471-A-G

41411920-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92473563-G-C

41411966-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92473593-G-A

41412287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 92474047-G-T

41412299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92474059-G-A

41412339-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92474100-G-A

41412339-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92474100-G-T

41412437-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 92474177-T-C

41414682-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92474691-T-C

41414895-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92474884-G-A

http://identifiers.org/hco/12/GRCh38#41414933-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#92474924-C-A

41414933-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92474924-C-T

41414970-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92474961-A-G

41415886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92475706-T-C

41416218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92476041-C-T

41416258-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92476075-G-A

41416266-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92476079-T-G

41416287-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92476100-G-T

41416653-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92476163-A-G

41416742-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92476247-G-A

41416745-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92476253-T-G

41416750-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92476258-C-T

41416842-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92476389-T-C

41417013-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92476477-G-A

41417123-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92476584-T-A

41417356-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92476792-A-G

41417491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92476902-C-T

41417555-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92476963-T-C

http://identifiers.org/hco/12/GRCh38#41417724-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92477123-A-C

41417724-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92477123-A-G

41418009-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92477420-T-A

41418138-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92477552-T-A

41418339-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92477741-T-A

41418377-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92477779-C-T

http://identifiers.org/hco/12/GRCh38#41418564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92478023-C-A

41418571-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92478030-T-C

http://identifiers.org/hco/12/GRCh38#41418793-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92478260-A-C

41419227-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92478688-C-T

41420034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92479499-C-T

41420039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92479504-T-C

http://identifiers.org/hco/12/GRCh38#41420246-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92479709-C-A

41420258-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92479721-T-C

41420351-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92479802-A-G

http://identifiers.org/hco/12/GRCh38#41420463-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92479912-A-C

41420463-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92479912-A-G

41420513-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92479968-T-C

41420578-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92480023-C-T

http://identifiers.org/hco/12/GRCh38#41421751-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92480465-A-C

41421793-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92480509-A-G

41421795-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92480511-A-G

41421866-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92480642-T-G

41421887-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92480663-T-C

41421965-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92480739-G-A

41421965-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92480739-G-T

41422165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92480939-T-C

41423544-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92481684-T-A

41423693-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92481823-A-G

41423970-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92482087-T-A

41424336-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92482449-T-C

41424549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92482651-G-A

41424612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92482704-T-C

41424734-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92482824-T-G

41424827-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92482922-G-A

41424827-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92482922-G-C

41424850-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92482943-G-A

41424863-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92482956-G-A

http://identifiers.org/hco/12/GRCh38#41424872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92482965-C-A

41424872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92482965-C-T

41424881-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92482974-G-T

41425469-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92483516-G-A

41425530-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92483584-G-C

41425668-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92483705-A-G

41426116-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92484070-G-A

41426219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92484170-C-T

http://identifiers.org/hco/12/GRCh38#41426453-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92484353-C-A

41426472-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92484372-T-G

41426480-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92484380-G-A

41426480-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92484380-G-T

41426579-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92484491-A-T

41426646-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92484569-A-G

41426760-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92484673-A-G

http://identifiers.org/hco/12/GRCh38#41426813-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92484727-A-C

41426813-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92484727-A-T

41426859-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92484771-G-C

41427050-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92484908-A-T

http://identifiers.org/hco/12/GRCh38#41427466-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92485306-C-A

41428116-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92486406-A-G

41428152-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92486441-C-G

41428225-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92486513-A-G

41428298-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92486554-T-G

41428356-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92486612-T-G

41428393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92486649-A-G

41428919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92487017-A-G

41429020-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92487111-T-C

41429034-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92487118-C-T

41429093-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92487178-T-C

41429348-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92487567-A-G

41429614-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92487849-G-T

41429652-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92487886-C-T

41429665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92487898-T-C

41429843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92488045-A-G

41430010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92488187-C-T

41430178-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92488350-G-A

41431402-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92488790-C-T

41431429-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92488806-G-A

41431429-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92488806-G-C

http://identifiers.org/hco/12/GRCh38#41431432-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92488809-C-A

41431455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92488832-C-T

41431472-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92488840-G-A

41431506-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92488876-C-T

41431533-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92488903-T-A

41431552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92488921-G-T

41431790-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92489129-G-A

41431797-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92489136-T-G

41431799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92489138-C-T

41431815-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92489157-T-A

41432098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92489452-A-G

41432169-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92489519-T-G

41432248-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92489599-C-T

http://identifiers.org/hco/12/GRCh38#41432375-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92489681-C-A

41432530-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92489816-A-T

41432600-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92489885-G-A

41432601-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92489886-C-T

41432662-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92489935-G-A

41432761-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92490030-G-A

41432884-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92490141-G-C

41432894-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92490150-G-A

41432922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92490177-G-A

41432947-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92490202-G-T

41433390-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92490640-C-T

41433403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92490653-A-G

41433450-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92490701-A-T

41433469-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92490711-C-T

41433553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92490775-G-A

41433612-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92490812-T-C

41433655-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92490832-A-G

41433659-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92490836-C-T

41434315-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92492049-T-C

41434347-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92492076-T-C

http://identifiers.org/hco/12/GRCh38#41434468-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92492211-C-A

41434549-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92492292-G-A

41434560-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92492303-A-T

41435064-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92492764-C-G

41435108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92492808-G-A

http://identifiers.org/hco/12/GRCh38#41435828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92493194-C-A

http://identifiers.org/hco/12/GRCh38#41435840-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92493206-A-C

41435912-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92493273-C-T

41436683-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92493969-G-A

41437141-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92494432-C-T

41437856-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 92495147-T-G

http://identifiers.org/hco/12/GRCh38#41438033-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92495340-C-A

41438035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92495342-A-G

41438035-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92495342-A-T

http://identifiers.org/hco/12/GRCh38#41438113-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92495424-C-A

41438113-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92495424-C-T

41438515-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92495850-T-C

41438714-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92496056-G-C

41439018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92496389-C-T

41439373-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92496751-G-C

41439483-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92496864-G-A

http://identifiers.org/hco/12/GRCh38#41439504-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92496913-C-A

41439568-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92496970-A-T

41439902-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92497303-C-T

41440017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92497407-G-A

41440181-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92497696-A-G

41440325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92497866-C-T

41440468-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92497983-C-G

41440468-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92497983-C-T

41440524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92498039-G-A

41440618-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92498132-G-A

41440865-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92498378-C-G

41440870-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92498383-T-C

41440913-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92498426-T-C

41441061-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92498561-T-C

41441080-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92498580-G-A

http://identifiers.org/hco/12/GRCh38#41441213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92498691-C-A

41441264-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92498741-C-T

41441310-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92498786-A-G

41441649-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92499451-T-C

http://identifiers.org/hco/12/GRCh38#41441687-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92499497-C-A

41441705-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92499516-G-T

41441707-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92499518-C-T

41442138-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92499828-T-C

http://identifiers.org/hco/12/GRCh38#41442199-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92499872-C-A

41442199-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92499872-C-T

41442312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92499942-C-T

41442353-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92499980-T-C

41442413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92500043-G-A

http://identifiers.org/hco/12/GRCh38#41442472-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92500109-C-A

41442951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92500540-C-T

41443037-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92500626-G-T

41443564-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92501607-G-A

41443902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92501919-T-C

41444246-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92502233-A-G

41444248-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92502235-G-A

41444248-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92502235-G-T

41444279-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92502267-G-A

41444413-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92502418-G-A

41444473-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92502473-T-G

41444530-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92502528-G-A

41444543-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92502540-G-A

41444811-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92502782-A-G

http://identifiers.org/hco/12/GRCh38#41444878-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92502928-A-C

41444951-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92503036-T-G

41445179-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92503363-C-T

41445316-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92503500-G-T

http://identifiers.org/hco/12/GRCh38#41445812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92503957-C-A

41445897-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92504032-T-A

41445910-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92504038-T-G

41445938-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92504066-A-G

41445951-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92504079-C-T

http://identifiers.org/hco/12/GRCh38#41448016-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92505394-A-C

41448016-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92505394-A-G

http://identifiers.org/hco/12/GRCh38#41448039-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92505413-C-A

http://identifiers.org/hco/12/GRCh38#41448152-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92505496-C-A

41448358-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92505688-G-T

41448622-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92505905-G-A

41449482-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92506459-T-A

41449859-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92506805-G-T

41449900-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92506846-G-A

http://identifiers.org/hco/12/GRCh38#41449933-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92506880-A-C

41449981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92506929-C-T

41450015-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92506963-C-T

41450028-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92506976-G-T

41450068-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92507015-T-C

http://identifiers.org/hco/12/GRCh38#41450120-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92507058-A-C

41450210-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92507132-T-G

41450224-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92507148-T-C

41450264-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92507187-A-G

41450311-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92507234-G-A

41450311-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92507234-G-T

41450426-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92507326-T-C

41450548-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92507452-T-G

41450594-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92507487-G-A

41451160-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92507655-G-C

41451227-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92507717-G-C

41451453-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92507913-T-C

41451556-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92508013-T-G

41451648-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92508080-C-G

41451648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92508080-C-T

41451684-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92508113-T-G

41451692-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92508120-T-G

41451803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92508200-G-A

41451849-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92508242-G-A

41451884-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92508285-A-G

41452050-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92508457-A-G

41452106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92508506-G-A

41452964-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92508788-A-G

41452964-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92508788-A-T

41453008-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92508829-A-G

41453174-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92508998-A-G

41453376-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92509187-T-C

http://identifiers.org/hco/12/GRCh38#41453681-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92509486-A-C

41453681-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92509486-A-G

41453702-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92509508-G-C

41453766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92509572-C-T

41453800-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92509606-A-T

41454025-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92509820-A-G

41454122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92509918-G-A

41454135-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92509931-C-T

41454353-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92510148-G-A

41454679-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92510489-C-T

41454738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92510547-T-C

http://identifiers.org/hco/12/GRCh38#41454936-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92510734-A-C

41455015-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92510814-G-A

41455263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92511058-C-T

41455319-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92511110-A-G

41455359-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92511149-A-T

41455572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92511368-T-C

41455620-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92511421-C-T

41455945-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92516229-A-G

http://identifiers.org/hco/12/GRCh38#41456044-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92516311-C-A

41456044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92516311-C-T

41456066-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92516332-C-T

41456080-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92516346-C-T

41456219-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92516504-C-G

41456219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92516504-C-T

http://identifiers.org/hco/12/GRCh38#41456311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92516596-C-A

41456577-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92516791-G-C

41456801-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92516863-G-A

41457084-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92517138-A-G

41457118-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92517172-A-G

41457119-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92517173-T-C

41457129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92517183-G-A

41457247-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92517319-G-A

41457271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92517339-G-A

41457439-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92517468-C-T

41457492-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92517523-T-G

41457495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92517526-A-G

41457700-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92517724-G-C

41457856-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92517866-A-G

41459411-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92519783-A-G

41459547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92519920-G-A

41459783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92520154-T-C

http://identifiers.org/hco/12/GRCh38#41459904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92520285-C-A

41459953-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 92520342-G-A

41459953-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant, splice_region_variant
orthologous variants: 92520342-G-T

41460199-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92520613-G-T

41460854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92521670-C-T

41460878-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92521696-G-A

41460993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92521809-A-G

http://identifiers.org/hco/12/GRCh38#41460994-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92521810-C-A

41461009-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92521825-T-A

41461057-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92521872-C-T

41461824-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92522266-C-G

41461983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92522395-T-C

41462033-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92522446-C-G

41462046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92522459-C-T

41462339-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92522751-A-G

41462505-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92522915-T-G

41462763-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92523122-T-C

41462826-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92523184-T-C

http://identifiers.org/hco/12/GRCh38#41463111-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92523444-A-C

http://identifiers.org/hco/12/GRCh38#41463128-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92523460-A-C

41463192-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92523517-C-T

41463200-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92523525-T-C

http://identifiers.org/hco/12/GRCh38#41463556-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92523741-C-A

41463592-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92523776-G-A

41463665-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92523815-T-C

41463736-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92523863-A-T

41463973-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92524081-G-A

41464184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92524267-G-A

41464184-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92524267-G-T

41464251-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92524416-C-T

41464434-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92524630-T-A

41464519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92524712-G-A

41464539-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92524734-T-C

41465432-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92525823-T-C

41465493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92525884-T-C

http://identifiers.org/hco/12/GRCh38#41465548-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92525933-C-A

41465686-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92526066-G-A

41465819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92526203-C-T

41466214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92526569-G-A

41466245-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92526600-G-T

41466749-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92527110-G-T

41466802-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92527114-G-T

41466837-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92527150-G-A

41467320-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92527611-G-A

http://identifiers.org/hco/12/GRCh38#41467360-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92527653-C-A

41467471-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92527759-A-G

41467482-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92527771-T-C

41467523-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92527810-A-G

41467538-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92527825-T-G

41467644-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92527919-A-T

41467751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92528008-C-T

41467773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92528030-C-T

41467847-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92528103-C-T

41468093-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92528313-A-G

41468125-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92528345-T-C

41468270-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92528413-C-G

41468317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92528460-C-T

http://identifiers.org/hco/12/GRCh38#41468389-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92528496-C-A

http://identifiers.org/hco/12/GRCh38#41468590-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92529984-C-A

41468760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92530143-G-A

41468773-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92530156-C-T

41468901-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92530198-C-T

41469004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92530240-G-A

41469004-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92530240-G-T

41469031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92530250-C-T

http://identifiers.org/hco/12/GRCh38#41469291-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92530524-C-A

41469444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92530673-A-G

http://identifiers.org/hco/12/GRCh38#41470940-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92531948-C-A

41470940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92531948-C-T

41471065-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92532091-T-G

41471161-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92532211-G-A

41471161-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92532211-G-T

41471270-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92532327-G-C

41471675-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92532647-T-C

41471806-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92532824-T-A

41471875-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92532893-G-C

41471974-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92532988-G-T

41472018-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92533145-T-G

41472025-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92533152-G-A

41472025-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92533152-G-C

41472025-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92533152-G-T

41472120-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92533233-C-T

41472147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92533259-G-A

41472153-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92533265-G-C

41472164-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92533276-C-G

41472164-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92533276-C-T

http://identifiers.org/hco/12/GRCh38#41472387-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92533076-A-C

41472387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92533076-A-G

41472785-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92533476-A-G

41473032-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92533797-C-G

41473032-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92533797-C-T

http://identifiers.org/hco/12/GRCh38#41473091-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92533871-A-C

41473117-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92533898-C-T

41473155-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92533939-G-A

41473155-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92533939-G-T

http://identifiers.org/hco/12/GRCh38#41473821-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92534235-C-A

41473821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92534235-C-T

41473928-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92534334-A-G

41474052-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92534453-C-T

41474235-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92534586-T-C

41474618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92536214-C-T

41474692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92536263-G-A

41474701-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92536272-A-G

41474760-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92536331-G-A

41474794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92536351-G-A

41474972-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92536553-T-C

41475038-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92536624-T-A

41475042-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92536628-T-C

41475322-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92536876-T-A

41475442-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92537005-A-T

http://identifiers.org/hco/12/GRCh38#41475778-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92537324-C-A

41475872-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92537410-C-G

41475872-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92537410-C-T

41476703-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92538107-G-T

41476912-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92538317-C-G

41477120-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92538516-T-A

41477542-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92538936-C-T

41477610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92539003-G-A

41477610-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92539003-G-T

41477658-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92539042-G-T

41477807-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92539185-T-G

41477819-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92539197-T-G

41477845-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92539216-A-G

41477908-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, stop_gained
orthologous variants: 92539282-T-A

41477908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 92539282-T-C

41477993-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92539358-A-G

41478038-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92539407-G-T

41478058-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92539427-T-C

41478707-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92539914-G-A

41478808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92540005-G-A

41479151-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92540340-T-A

41479178-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92540366-A-G

41479178-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92540366-A-T

41479230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92540421-A-G

41479307-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92540504-C-T

41479828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92540992-T-C

41479854-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92541019-C-T

41479877-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92541040-G-A

41479885-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92541048-T-G

41479993-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92541142-G-A

41479993-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92541142-G-C

41480035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92541179-A-G

41480039-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92541187-T-C

41480144-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92541274-C-T

41480374-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92541550-A-G

41481231-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92542990-A-G

http://identifiers.org/hco/12/GRCh38#41481380-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92543104-C-A

41481406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92543130-C-T

41481766-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92543473-T-G

http://identifiers.org/hco/12/GRCh38#41482029-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92543722-A-C

41482683-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92550451-T-A

http://identifiers.org/hco/12/GRCh38#41482733-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92550496-A-C

41483003-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92550752-T-C

41483044-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92550774-C-T

41483187-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92550915-T-A

http://identifiers.org/hco/12/GRCh38#41483195-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92550923-A-C

41483195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92550923-A-G

41483200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92550927-C-T

41483205-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92550932-T-C

41483272-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92551060-A-G

41483495-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92551395-C-T

http://identifiers.org/hco/12/GRCh38#41483541-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92551440-C-A

41483541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92551440-C-T

41483561-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92551460-A-T

http://identifiers.org/hco/12/GRCh38#41483997-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92551923-A-C

41483997-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92551923-A-G

41484053-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92551977-C-G

41484053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92551977-C-T

41484056-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92551980-C-T

41484254-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92552136-G-A

41484254-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92552136-G-C

41484302-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92552183-G-T

41484354-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92552220-A-G

41484380-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92552245-T-C

41484389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92552254-G-A

41484579-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92552432-C-T

41485392-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92552660-T-C

41485428-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92552696-A-G

41485599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92552792-G-A

41485630-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92552824-G-T

41485901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92552935-T-C

41486037-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92553006-T-A

http://identifiers.org/hco/12/GRCh38#41486477-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92554004-A-C

41486492-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92554018-G-T

41486567-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92554075-G-A

41486704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92554212-G-A

41486723-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92554231-G-A

41486770-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92554278-T-C

41486787-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92554373-G-A

41486933-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92554601-G-A

41486933-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92554601-G-T

41486973-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92554634-A-G

41487023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92554687-A-G

41487037-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92554701-C-T

41487106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92554764-G-A

41487118-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92554776-T-G

41487594-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92555222-C-T

41487623-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92555250-T-C

41487627-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92555254-T-C

41488004-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92555591-G-A

41488004-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92555591-G-C

http://identifiers.org/hco/12/GRCh38#41488044-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92555629-C-A

41488112-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92555683-G-A

41488126-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92555696-G-A

41488126-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92555696-G-C

41488152-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92555721-C-G

41488184-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92555750-T-A

41488353-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92555913-C-T

41488449-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92556011-A-G

41488450-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92556012-C-G

41488450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92556012-C-T

41488451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92556013-G-A

41488451-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92556013-G-T

41488540-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92556092-G-T

41488568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92556121-C-T

41488572-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92556125-A-T

41488884-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92556395-T-C

41489514-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92556648-G-C

41489557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92556689-A-G

41489560-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92556692-G-C

41489576-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92556708-G-A

41489692-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92556812-A-T

41489719-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92556831-G-T

41489735-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92556850-A-T

41489873-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92556991-T-G

41489979-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92557101-G-A

41490147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92557318-G-A

41490220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92557392-T-C

41490323-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92557486-T-G

http://identifiers.org/hco/12/GRCh38#41490328-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92557491-C-A

http://identifiers.org/hco/12/GRCh38#41490344-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92557507-C-A

41490354-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92557517-T-C

41490387-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92557551-C-T

41490456-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92557626-T-A

41490456-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92557626-T-C

41490854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92558170-A-G

41490919-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92558233-A-G

41491673-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92558460-A-T

41491784-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92558562-T-C

41492022-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92558797-A-G

41492058-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92558833-G-C

41492131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92558932-T-C

41492289-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92559073-A-G

41492290-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92559074-G-T

41492320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92559104-A-G

41492396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92559213-A-G

41492444-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92559256-G-A

41492514-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92559634-T-G

41492547-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92559656-A-G

41492558-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92559667-G-C

41492558-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92559667-G-T

41492559-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92559668-C-T

41492686-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92559795-G-T

41492766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92559882-C-T

http://identifiers.org/hco/12/GRCh38#41492798-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92559914-C-A

41492916-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92560030-T-C

41492960-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92560074-G-T

41493175-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92560290-G-A

41493407-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92560520-C-T

41493442-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92560555-T-C

41493497-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92560601-C-T

41493554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92560752-G-A

41493624-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92560824-C-G

41493662-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92560861-G-C

41493662-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92560861-G-T

41493729-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92560925-C-T

41493753-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92560947-A-G

41494773-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92561336-G-A

41494786-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92561348-A-G

41494809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92561372-A-G

41494862-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92561425-T-G

41494963-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92561526-T-C

41495074-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92561604-A-G

41495315-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92561861-G-A

41495333-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92561874-T-C

http://identifiers.org/hco/12/GRCh38#41495388-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92561936-A-C

41495407-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92561955-T-C

41495504-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92562045-C-T

41495508-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92562049-T-A

41495509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92562050-C-T

41495814-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92562344-C-G

41495814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92562344-C-T

http://identifiers.org/hco/12/GRCh38#41495828-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92562358-C-A

41495828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92562358-C-T

41495893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92562418-C-T

41497267-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92563140-G-A

41497288-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92563167-C-T

http://identifiers.org/hco/12/GRCh38#41497414-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92563296-C-A

41497414-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92563296-C-T

41497415-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92563297-G-A

41497456-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92563339-A-T

41497725-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92563611-T-C

41498909-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92565504-G-T

41498916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92565511-C-T

41500076-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92567291-C-T

41500313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92567495-G-A

41500343-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92567525-C-T

41500422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92567600-T-C

41500601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92568253-T-C

41500678-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92568324-A-G

41500735-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92568403-G-T

41500797-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92568460-C-T

41500926-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92568582-C-G

41500926-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92568582-C-T

http://identifiers.org/hco/12/GRCh38#41500954-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92568610-C-A

41500954-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92568610-C-T

41500961-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92568632-T-G

41501016-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92568691-T-C

41501019-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92568694-A-T

41501396-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92569220-A-T

41501692-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92569506-G-A

41501740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92569570-T-C

41501776-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92569606-A-G

41502228-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92570087-C-T

41502249-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92570119-G-A

41502286-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92570157-C-T

41502287-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92570158-G-A

41502421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92570280-T-C

41502546-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92570383-A-G

http://identifiers.org/hco/12/GRCh38#41502615-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92570454-C-A

41502615-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92570454-C-G

41502660-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92570474-C-G

41502660-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92570474-C-T

41502682-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92570496-C-T

41502749-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92570563-T-C

41502788-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92570631-G-T

41502796-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92570639-G-A

41502871-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92570765-T-C

41502919-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92570817-G-C

41503017-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92570912-G-A

41503074-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92570969-G-T

41503186-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92571079-G-A

41503504-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92571412-T-C

41504323-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92572770-G-A

41504597-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92573012-T-G

41504620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92573035-A-G

41504706-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92573124-A-T

41504719-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92573137-C-T

41505045-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92573434-G-C

41505077-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92573463-C-G

41505100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92573486-C-T

41505111-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92573497-C-T

41505225-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92573603-G-A

41505225-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92573603-G-C

41505543-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92573858-C-G

41505720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92574024-T-C

http://identifiers.org/hco/12/GRCh38#41505965-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92574279-A-C

41505994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92574308-G-A

41506005-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92574987-T-C

http://identifiers.org/hco/12/GRCh38#41506325-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92575282-C-A

41506325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92575282-C-T

41506342-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92575295-T-C

41506346-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92575299-A-G

41506582-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: missense variant
orthologous variants: 92575508-G-A

41506716-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92575642-T-C

http://identifiers.org/hco/12/GRCh38#41506730-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92575656-C-A

http://identifiers.org/hco/12/GRCh38#41506740-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92575666-C-A

41506741-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92575667-C-T

41506767-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92575694-G-A

41506767-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92575694-G-T

41506963-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92575885-G-T

41507124-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92576036-T-A

41507124-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92576036-T-C

41507201-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92576114-A-G

41507261-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92576174-T-C

41508115-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92577309-A-T

41508139-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92577333-A-G

41508207-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92577390-C-G

41508268-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92577431-T-C

41508284-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92577447-T-C

41508457-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92577598-A-G

41508485-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92577633-C-T

http://identifiers.org/hco/12/GRCh38#41508510-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92577658-C-A

41508510-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92577658-C-T

http://identifiers.org/hco/12/GRCh38#41508551-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92577704-C-A

41508653-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92577778-G-A

41508791-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92577938-A-G

41509236-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron variant
orthologous variants: 92578064-G-A

41509593-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 92578128-T-C

41509599-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 92578134-T-C

41509639-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 92578162-A-T

41509640-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 92578163-G-C

41509640-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 92578163-G-T

41509711-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 92578223-T-C

http://identifiers.org/hco/12/GRCh38#41509727-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92578239-A-C

41509727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 92578239-A-G

41509745-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_exon_variant
orthologous variants: 92578257-A-G

41509862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 92578373-T-C

http://identifiers.org/hco/12/GRCh38#41509889-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92578400-C-A

41509889-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 92578400-C-G

http://identifiers.org/hco/12/GRCh38#41509894-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92578405-C-A

41509894-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 92578405-C-G

41509894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 92578405-C-T

41509898-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: non_coding_transcript_exon_variant, synonymous_variant
orthologous variants: 92578409-A-G

41509968-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92578473-T-C

41510002-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92578504-A-G

http://identifiers.org/hco/12/GRCh38#41510010-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92578512-C-A

41510269-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92578766-A-G

41510656-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92579130-A-G

41510657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92579131-T-C

41511089-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92579551-T-G

41511194-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92579648-A-G

41511310-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92579753-G-A

http://identifiers.org/hco/12/GRCh38#41511468-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92579898-A-C

41511735-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92580165-C-G

41511794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92580210-C-T

http://identifiers.org/hco/12/GRCh38#41511812-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92580228-C-A

41511812-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92580228-C-G

41511913-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92580325-C-G

41512051-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92580463-T-G

41512468-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92580985-G-A

41512522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92581185-G-T

41512571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92581383-G-A

41512579-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92581391-T-G

41512731-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92581608-T-A

41512731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92581608-T-C

41512749-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92581627-C-T

41512981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92581853-G-A

41513041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92581913-A-G

41513079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92581948-G-A

41513163-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92582029-G-A

http://identifiers.org/hco/12/GRCh38#41513176-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92582043-A-C

41513176-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92582043-A-G

41513176-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92582043-A-T

41513261-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92582128-G-A

41513649-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92582600-G-A

41513809-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92582760-G-T

41513891-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92582861-C-T

41513905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92582869-T-C

41513909-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92582873-G-C

41514068-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92583037-A-G

41514117-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92583085-G-T

41514246-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92583194-C-T

http://identifiers.org/hco/12/GRCh38#41514263-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92583211-A-C

41514372-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92583302-A-T

41514409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92583339-A-G

41514434-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92583435-C-T

41514437-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92583440-G-T

41514482-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92583485-C-G

41514532-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92583527-C-T

41514596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92583587-T-C

41514624-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92583616-G-A

41514791-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92583785-G-A

41514860-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92583853-G-T

41515010-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 92584368-C-T

41515069-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92584428-C-T

41515089-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92584453-C-G

41515100-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92584464-C-T

41515349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92584667-C-T

41515417-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92584745-G-A

41515417-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92584745-G-T

41515440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92584783-A-G

41515460-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92584803-C-T

41515846-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92585179-G-T

41515977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92585303-C-T

41516012-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92585338-C-T

41516129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92585442-T-C

http://identifiers.org/hco/12/GRCh38#41516173-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92585481-C-A

41516440-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92585904-G-A

41516462-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92585926-T-A

41516592-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92586060-C-G

http://identifiers.org/hco/12/GRCh38#41516608-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92586086-C-A

41516720-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92586196-T-A

41516823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92586281-C-T

41516862-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92586321-C-G

41516940-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92586410-A-G

41516942-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92586412-G-A

41517188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92586650-T-C

41517282-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92586743-C-G

41517552-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92587017-G-T

41517571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92587035-G-A

41517754-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92587244-C-T

41517784-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92587272-C-G

41517846-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92587328-A-G

http://identifiers.org/hco/12/GRCh38#41517857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92587343-C-A

41517859-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92587345-A-G

41518003-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92587486-A-T

41518009-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92587492-A-G

41518160-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92587651-G-C

41518313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92587818-T-C

41518522-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92588718-A-G

41518593-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92588782-A-T

41518948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92589195-C-T

41519107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92589356-G-A

41519213-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92589465-A-G

41519258-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92589506-T-G

http://identifiers.org/hco/12/GRCh38#41519709-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92590306-C-A

http://identifiers.org/hco/12/GRCh38#41519716-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92590313-A-C

http://identifiers.org/hco/12/GRCh38#41519720-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92590317-C-A

41519980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92590630-C-T

http://identifiers.org/hco/12/GRCh38#41520010-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92590656-C-A

41520159-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92590809-T-G

41520184-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92590834-A-G

41520254-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92590869-G-C

41520283-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92590899-G-A

41520361-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92590965-G-T

http://identifiers.org/hco/12/GRCh38#41520387-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92590989-A-C

41520387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92590989-A-G

41520409-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92591008-A-G

41520432-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92591031-G-T

41520501-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92591147-C-T

41520647-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92591268-C-T

41520733-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92591348-T-C

41520798-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92591413-G-A

41520830-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92591445-A-G

http://identifiers.org/hco/12/GRCh38#41520835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#92591450-C-A

41520835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92591450-C-T

41521027-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92591590-T-C

41521155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92591713-T-C

41521178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92591747-T-C

41521454-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92593814-G-T

41521907-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92594240-G-T

41521949-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 30552
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 92594294-G-A