http://identifiers.org/hco/13/GRCh38#40932328-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79819630-C-A

40932328-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 79819630-C-T

40932526-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 79819442-G-A

40932526-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 79819442-G-T

http://identifiers.org/hco/13/GRCh38#40932528-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79819440-C-A

40933159-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 79818459-T-C

40933216-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 79818407-G-A

40933216-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 79818407-G-T

40933256-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 79818371-G-A

40933256-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 79818371-G-T

40933266-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 79818361-T-G

40933270-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 79818357-T-C

40933416-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 79818213-G-A

40933695-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 79817944-A-G

40933711-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant, undefined
orthologous variants: 79817928-G-C

40933780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 79817859-G-A

40933939-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 79817703-G-C

40933939-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 79817703-G-T

http://identifiers.org/hco/13/GRCh38#40934067-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79817584-A-C

40935111-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79815616-T-C

40937067-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79814325-C-T

40937106-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79813348-T-C

40937251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79813203-A-G

40937322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79813138-T-C

40937438-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79813030-C-T

http://identifiers.org/hco/13/GRCh38#40940451-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79811622-A-C

40940709-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79811315-C-T

40940775-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79811252-G-T

40941077-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 79810903-A-G

40941078-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 79810902-C-T

40941122-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 79810858-G-A

40941122-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 79810858-G-C

40941131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 79810849-T-C

40941165-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 79810815-T-C

40941208-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, synonymous_variant
orthologous variants: 79810772-C-T

40941209-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 79810771-C-G

40941210-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 79810770-T-C

40941222-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 79810758-C-G

40941425-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79810544-C-G

40941425-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79810544-C-T

40941529-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79810448-T-C

40941958-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79809998-C-T

40943063-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 79808242-T-A

40943333-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79807975-G-A

40943782-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79806992-A-G

40943907-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant, missense_variant
orthologous variants: 79806677-G-A

40943998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79806586-T-C

40944049-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79806539-T-A

40944049-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79806539-T-C

40944116-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79806476-G-T

40944175-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79806300-T-C

40944219-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79806252-G-T

40948722-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79805706-T-C

40948902-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79805182-T-C

40950440-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79804208-G-T

40950681-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79803806-C-T

40950877-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79803627-T-C

40951064-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79803327-T-C

40951487-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79802849-T-A

40951487-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79802849-T-C

http://identifiers.org/hco/13/GRCh38#40951526-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79802814-C-A

40951526-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79802814-C-T

40958862-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 79798339-T-C

http://identifiers.org/hco/13/GRCh38#40959087-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79798126-C-A

http://identifiers.org/hco/13/GRCh38#40961134-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79795683-A-C

40962031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79794821-T-C

40963960-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79789712-T-C

http://identifiers.org/hco/13/GRCh38#40964195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79789454-C-A

40964195-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79789454-C-T

40964294-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79789342-G-A

40964365-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79789272-A-G

40965843-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79787704-C-T

40966039-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79787534-T-G

40970035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79781115-A-G

40970053-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79781094-T-A

40970134-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79781013-C-T

40970819-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79780251-C-T

40971226-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79779833-T-A

40971226-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79779833-T-C

40977701-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79778446-C-T

40977743-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79778420-C-T

40977984-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79778192-T-C

40978076-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79778104-A-G

40978602-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79777518-G-A

40978789-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79777206-G-A

http://identifiers.org/hco/13/GRCh38#40978792-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79777200-C-A

http://identifiers.org/hco/13/GRCh38#40978798-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79777194-A-C

40979296-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79776640-T-G

40979645-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79776296-C-T

40980430-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79775280-C-T

40980580-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79775133-T-A

40980580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79775133-T-C

40980733-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79774980-A-G

40980794-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79774918-C-T

40980921-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79774819-G-A

http://identifiers.org/hco/13/GRCh38#40981044-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79774713-A-C

40981050-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79774707-C-G

40981050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79774707-C-T

40981131-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79774633-T-C

40981158-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79774606-G-C

40981244-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79774517-T-C

40981317-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79774466-C-T

40981368-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79774439-T-C

http://identifiers.org/hco/13/GRCh38#40981404-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79774402-A-C

40981404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79774402-A-G

40981580-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79774236-A-G

40981618-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79774197-A-G

40981775-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79774052-T-C

40981836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79773991-G-A

40981836-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79773991-G-T

40981910-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79773923-G-A

40981910-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79773923-G-T

http://identifiers.org/hco/13/GRCh38#40981921-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79773915-C-A

http://identifiers.org/hco/13/GRCh38#40981924-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79773912-A-C

40981924-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79773912-A-G

40981924-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79773912-A-T

40981946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79773891-A-G

40981946-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79773891-A-T

40981959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 79773878-T-C

40982183-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 79773660-G-A

40982223-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 79773616-G-C

40982223-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 79773616-G-T

40982320-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79773523-A-T

40982565-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79773321-G-A

40982622-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79773266-A-G

40982992-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79772901-T-A

40982992-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79772901-T-C

40983352-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79772548-T-A

40983353-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79772547-C-G

40983395-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron_variant, undefined
orthologous variants: 79772506-G-A

40983486-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79772423-G-A

40983740-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79772003-T-C

40983929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79771784-T-C

40984659-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79771298-T-C

40985091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79770916-T-C

http://identifiers.org/hco/13/GRCh38#40985111-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79770897-A-C

40985239-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79770765-T-C

40985267-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79770737-A-G

40985270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79770734-A-G

40985411-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79770603-G-A

40985879-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79770054-A-G

40986499-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79769413-T-C

40988204-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79767982-A-G

40988538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79767587-T-C

40989156-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79767284-T-C

40993888-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79765565-A-G

40994010-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron_variant, undefined
orthologous variants: 79765459-A-G

40994010-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron_variant, undefined
orthologous variants: 79765459-A-T

40994736-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron_variant, undefined
orthologous variants: 79764961-G-A

40994964-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79764764-C-T

40999596-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79762147-T-C

40999715-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79762053-A-G

40999716-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79762052-C-G

41000072-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79761148-A-G

http://identifiers.org/hco/13/GRCh38#41003982-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79760892-A-C

41004220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79760675-T-C

41004422-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79760505-T-C

41004883-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79759551-T-A

41004883-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79759551-T-C

41004921-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79759508-G-C

http://identifiers.org/hco/13/GRCh38#41005376-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79758897-A-C

http://identifiers.org/hco/13/GRCh38#41005432-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79758762-A-C

41006013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79758128-C-T

41007140-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79757444-G-A

41007481-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79756755-G-A

41007673-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79756597-T-C

41007732-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79756521-T-A

41013491-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79755683-A-G

41017722-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79754597-A-G

41017793-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79754531-G-A

41017880-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79754442-G-A

http://identifiers.org/hco/13/GRCh38#41018065-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79754266-A-C

41018544-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79753824-A-G

http://identifiers.org/hco/13/GRCh38#41018556-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79753812-A-C

http://identifiers.org/hco/13/GRCh38#41019104-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#79753326-A-C

41019117-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron_variant, undefined
orthologous variants: 79753313-C-G

41019180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron_variant, undefined
orthologous variants: 79753252-A-G

41019789-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79752701-A-G

41019898-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79752592-T-C

41019949-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79752555-A-G

41048801-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79731712-A-T

41048936-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79731588-T-A

41049525-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79730928-G-T

41049961-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79730419-T-A

http://identifiers.org/hco/13/GRCh38#41049976-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79730404-A-C

41049976-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79730404-A-G

41050937-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79728292-G-C

http://identifiers.org/hco/13/GRCh38#41052022-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79727244-C-A

41052042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79727224-G-A

41052105-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79727175-A-G

41052921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79726512-T-C

41052921-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79726512-T-G

41052946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79726488-A-G

41052972-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79726462-C-T

41053413-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79726323-C-T

41053500-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79726248-G-T

41053540-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79726211-C-G

41053541-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79726210-C-T

41053557-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79726199-A-G

http://identifiers.org/hco/13/GRCh38#41054137-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79725476-C-A

41054200-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79725264-G-A

41054341-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79725124-A-G

41054359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79725106-T-C

41054517-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron_variant, undefined
orthologous variants: 79724964-C-G

http://identifiers.org/hco/13/GRCh38#41054554-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79724925-C-A

41054900-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79724615-C-T

41054943-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79724569-G-A

http://identifiers.org/hco/13/GRCh38#41055133-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79724418-C-A

41055133-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79724418-C-T

41055199-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79724393-T-C

41055257-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79724317-A-G

41055308-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79724268-C-T

41055417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79724157-C-T

41055494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79724082-G-A

41055555-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79724032-A-G

41055585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79724011-A-G

http://identifiers.org/hco/13/GRCh38#41055772-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79723959-C-A

41057704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79722254-T-C

41057758-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79722197-T-C

41057786-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79722170-T-C

http://identifiers.org/hco/13/GRCh38#41057814-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79722154-A-C

41058601-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79721166-T-C

41059362-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79720353-G-A

41059914-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79719808-T-G

41060136-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron_variant, undefined
orthologous variants: 79719615-G-A

41060136-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron_variant, undefined
orthologous variants: 79719615-G-T

http://identifiers.org/hco/13/GRCh38#41060169-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79719581-C-A

http://identifiers.org/hco/13/GRCh38#41060329-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79719497-A-C

41060512-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79719325-G-C

41060515-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79719322-G-T

41060704-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79719209-G-A

41060704-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79719209-G-C

41060719-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79719194-A-G

41060719-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79719194-A-T

http://identifiers.org/hco/13/GRCh38#41060727-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79719186-A-C

41060727-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79719186-A-G

41060727-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79719186-A-T

http://identifiers.org/hco/13/GRCh38#41060814-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#79719101-C-A

41060814-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron_variant, undefined
orthologous variants: 79719101-C-G

41060814-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron_variant, undefined
orthologous variants: 79719101-C-T

41060815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron_variant, undefined
orthologous variants: 79719100-T-C

http://identifiers.org/hco/13/GRCh38#41060819-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/14/GRCm39#79719096-A-C

41060819-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron_variant, undefined
orthologous variants: 79719096-A-G

41060821-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79719094-A-G

41060821-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79719094-A-T

41060826-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79719087-G-A

41060826-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79719087-G-C

41060826-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: intron variant
orthologous variants: 79719087-G-T

41060843-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: 5_prime_UTR_variant, undefined
orthologous variants: 79719070-A-G

http://identifiers.org/hco/13/GRCh38#41060890-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79719053-C-A

41060890-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: 5 prime UTR variant
orthologous variants: 79719053-C-G

41060890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: 5 prime UTR variant
orthologous variants: 79719053-C-T

41060906-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: 5 prime UTR variant
orthologous variants: 79719041-G-A

41060906-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: 5 prime UTR variant
orthologous variants: 79719041-G-C

41060906-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: 5 prime UTR variant
orthologous variants: 79719041-G-T

http://identifiers.org/hco/13/GRCh38#41060960-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79718992-A-C

41060960-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: 5 prime UTR variant
orthologous variants: 79718992-A-G

41061016-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: 5 prime UTR variant
orthologous variants: 79718950-G-A

41061016-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: 5 prime UTR variant
orthologous variants: 79718950-G-T

41061030-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: 5 prime UTR variant
orthologous variants: 79718936-G-A

41061030-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: 5 prime UTR variant
orthologous variants: 79718936-G-T

41061041-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: 5 prime UTR variant
orthologous variants: 79718925-A-G

http://identifiers.org/hco/13/GRCh38#41061086-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79718884-C-A

41061147-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: 5 prime UTR variant
orthologous variants: 79718836-G-A

http://identifiers.org/hco/13/GRCh38#41061182-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79718802-A-C

41061202-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: 5 prime UTR variant
orthologous variants: 79718782-C-G

41061202-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: 5 prime UTR variant
orthologous variants: 79718782-C-T

http://identifiers.org/hco/13/GRCh38#41061204-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79718780-C-A

41061204-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: 5 prime UTR variant
orthologous variants: 79718780-C-G

41061204-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: 5 prime UTR variant
orthologous variants: 79718780-C-T

http://identifiers.org/hco/13/GRCh38#41061209-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/14/GRCm39#79718775-A-C

41061209-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: 5 prime UTR variant
orthologous variants: 79718775-A-G

41061225-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: 5 prime UTR variant
orthologous variants: 79718759-C-G

41061225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: 5 prime UTR variant
orthologous variants: 79718759-C-T

41061228-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: 5 prime UTR variant
orthologous variants: 79718756-G-A

41061228-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: 5 prime UTR variant
orthologous variants: 79718756-G-T

41061235-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: 5 prime UTR variant
orthologous variants: 79718749-G-A

41061435-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: 5 prime UTR variant
orthologous variants: 79718566-G-A

41061435-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 3316
most severe consequence: 5 prime UTR variant
orthologous variants: 79718566-G-T