66998542-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103027166-A-G

66998651-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103027242-A-G

66998823-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103027379-G-A

66998863-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103027417-T-C

66999199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103027676-G-A

66999199-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103027676-G-T

66999234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103027716-T-C

66999579-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103028040-T-C

66999677-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103028138-G-A

66999783-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103028226-A-G

http://identifiers.org/hco/1/GRCh38#66999882-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103028274-C-A

66999882-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103028274-C-T

66999951-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103028335-T-C

67000477-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103028490-G-T

67000976-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103028885-A-T

67000977-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103028886-C-T

67000978-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103028887-G-A

67001039-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103028958-G-T

67001147-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103029038-A-G

67001147-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103029038-A-T

67001181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103029070-G-A

67001181-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103029070-G-T

67001206-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103029079-T-C

http://identifiers.org/hco/1/GRCh38#67001226-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103029096-C-A

67001226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103029096-C-T

http://identifiers.org/hco/1/GRCh38#67001265-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103029135-C-A

http://identifiers.org/hco/1/GRCh38#67001311-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103029179-C-A

http://identifiers.org/hco/1/GRCh38#67001349-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103029213-C-A

67002990-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103029467-T-C

67003050-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103029519-C-T

67003117-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103029562-A-G

67003127-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103029572-T-C

67003176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103029610-C-T

67003225-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103029658-C-T

http://identifiers.org/hco/1/GRCh38#67003305-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103029759-C-A

67003313-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103029767-G-A

67003313-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103029767-G-T

67003406-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103029850-G-T

http://identifiers.org/hco/1/GRCh38#67003450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103029890-C-A

67003566-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103029995-G-A

67003593-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103030017-A-G

http://identifiers.org/hco/1/GRCh38#67003670-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103030073-C-A

67003670-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103030073-C-G

67003670-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103030073-C-T

67003672-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103030075-T-C

http://identifiers.org/hco/1/GRCh38#67003739-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103030137-A-C

http://identifiers.org/hco/1/GRCh38#67003871-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103030239-C-A

67003871-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103030239-C-T

67004021-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: 3_prime_UTR_variant, intron_variant, splice_region_variant
orthologous variants: 103030633-G-A

67004021-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: 3_prime_UTR_variant, intron_variant, splice_region_variant
orthologous variants: 103030633-G-T

http://identifiers.org/hco/1/GRCh38#67004245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103030830-C-A

67004245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103030830-C-T

http://identifiers.org/hco/1/GRCh38#67004246-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103030831-A-C

http://identifiers.org/hco/1/GRCh38#67004258-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103030843-C-A

67004314-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: 3_prime_UTR_variant, splice_donor_variant
orthologous variants: 103030862-A-G

67004315-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: 3_prime_UTR_variant, splice_donor_variant
orthologous variants: 103030863-C-G

67004315-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: 3_prime_UTR_variant, splice_donor_variant
orthologous variants: 103030863-C-T

67004516-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103031031-T-A

67004516-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103031031-T-C

67004516-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103031031-T-G

67004550-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103031050-T-A

67004550-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103031050-T-C

67004585-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103031089-T-C

67004590-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103031094-T-C

67004629-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103031132-A-T

67004689-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103031162-A-G

67004731-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103031204-T-C

67005356-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103031641-T-C

67005457-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103031720-G-A

67007277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103034488-T-C

67007379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103034592-T-C

67007461-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103034674-C-T

67007620-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103034776-A-G

67008086-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 103034858-T-A

67008907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103041823-C-T

67008998-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103041920-T-A

67008998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103041920-T-C

67009003-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103041925-T-C

67009023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103041945-A-G

67009023-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103041945-A-T

67009026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103041950-G-A

67009026-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103041950-G-T

67009060-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103041994-A-G

67009218-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103042152-T-A

67009218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103042152-T-C

http://identifiers.org/hco/1/GRCh38#67009273-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103042198-A-C

http://identifiers.org/hco/1/GRCh38#67009274-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103042199-C-A

67009274-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103042199-C-G

67009274-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103042199-C-T

http://identifiers.org/hco/1/GRCh38#67009283-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103042210-A-C

67009283-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103042210-A-G

http://identifiers.org/hco/1/GRCh38#67009307-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103042232-A-C

67009307-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103042232-A-T

67009372-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103042295-C-G

67009372-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103042295-C-T

67018039-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103044603-C-T

67018196-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103044732-T-C

67018196-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103044732-T-G

67018417-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103044929-A-G

http://identifiers.org/hco/1/GRCh38#67018436-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103044948-C-A

67018907-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103045336-A-T

67019037-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103045428-T-G

67020106-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103046578-A-G

67020143-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103046663-T-C

http://identifiers.org/hco/1/GRCh38#67020232-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103046854-C-A

67020232-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103046854-C-T

67020234-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103046856-C-T

http://identifiers.org/hco/1/GRCh38#67020283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103046894-C-A

67020304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103046915-T-C

67020359-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103046974-T-C

67020366-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103046981-T-C

67020458-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103047073-G-A

67020544-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103047153-G-T

67020702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103047294-C-T

67020824-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103047409-G-C

67020940-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103047519-C-T

67021162-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103047638-G-C

67021404-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103047900-G-A

67021404-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103047900-G-T

67021439-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103047920-T-C

67021439-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103047920-T-G

67021469-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103047952-G-T

67021619-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103048113-A-T

67021706-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103048498-G-A

67021706-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103048498-G-C

67021712-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103048504-G-C

67021712-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103048504-G-T

http://identifiers.org/hco/1/GRCh38#67021740-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103048532-C-A

67021740-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103048532-C-T

http://identifiers.org/hco/1/GRCh38#67022038-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103048881-A-C

67022136-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103048974-T-G

67022511-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103049270-T-C

67022700-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103049443-T-G

67022702-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103049445-G-A

67022702-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103049445-G-C

67023270-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103050201-A-G

67023478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103050405-C-T

67030832-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103051148-A-G

67031441-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103051665-G-A

67031441-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103051665-G-T

67031461-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103051691-A-T

67031465-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103051695-A-G

67031498-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103051714-G-C

67031696-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103054403-A-G

67032039-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron_variant, synonymous_variant
orthologous variants: 103054722-G-A

67032184-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103054860-G-A

67032184-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103054860-G-T

67037802-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103055429-G-A

67037850-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103055463-A-T

67037892-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103055505-G-A

67037975-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103055754-C-T

67038101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103055857-A-G

67038462-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103056441-T-C

67038524-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103056505-G-A

67038671-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103056646-T-C

67038805-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103057800-G-T

67038828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103057820-T-C

67038867-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103057858-C-G

67038969-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103057954-T-A

67038969-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103057954-T-C

67039186-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103058117-T-A

67039270-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103058203-G-A

67040633-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron_variant, undefined
orthologous variants: 103058956-C-T

67040655-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103058973-G-A

67040655-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103058973-G-T

67040942-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103060667-C-T

67041007-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103060726-A-G

67041342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103061057-G-A

67041342-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103061057-G-C

67041342-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103061057-G-T

67041469-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103061168-T-C

67041493-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103061189-T-C

67041495-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103061191-C-G

67041496-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103061192-T-C

67041742-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103061383-T-C

http://identifiers.org/hco/1/GRCh38#67041890-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103061493-C-A

67041914-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103061518-G-A

67042078-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103062149-A-G

67042144-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103062223-A-G

67042153-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103062232-G-T

67042218-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103062285-G-A

67042218-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103062285-G-T

67042311-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: synonymous variant
orthologous variants: 103062378-T-C

67044766-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103062588-A-G

67045002-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103062734-T-C

67045002-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103062734-T-G

67045009-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103062741-G-A

67045218-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103062942-T-G

67045275-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103063028-G-A

67045275-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103063028-G-C

67045828-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103063765-T-C

67046152-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103064059-A-T

67046238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103064145-G-A

67046262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103064167-G-A

67046273-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103064178-T-C

67046312-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103064233-T-C

67046530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103064435-A-G

67046640-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103064541-G-T

67046679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103064575-G-A

67047254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103065296-T-C

67047254-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103065296-T-G

67047518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103065554-G-A

67047518-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103065554-G-T

67047646-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103065907-T-C

67048142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103066343-T-C

67048153-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103066354-G-A

67048258-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103066360-G-C

67048770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103067029-C-T

67049440-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103067455-A-G

67049728-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103067674-T-C

http://identifiers.org/hco/1/GRCh38#67049870-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103067810-A-C

67049870-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103067810-A-G

67049870-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103067810-A-T

67049912-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103067855-G-A

67049912-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103067855-G-C

67049912-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103067855-G-T

http://identifiers.org/hco/1/GRCh38#67049998-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103067893-C-A

67049998-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103067893-C-T

67050094-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103067969-A-G

67050360-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103068231-T-C

67050417-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103068484-T-C

67050419-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103068486-G-T

67050535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103068600-A-G

67050550-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103068615-G-C

67050550-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103068615-G-T

67050596-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103068669-C-T

67050616-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103068693-T-A

67050616-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103068693-T-C

67050616-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103068693-T-G

http://identifiers.org/hco/1/GRCh38#67050636-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103068708-A-C

67050636-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103068708-A-T

67051048-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103069097-T-C

67051061-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103069110-G-A

67051096-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103069142-A-G

67051176-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103069230-G-T

67051404-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103069653-A-G

67051431-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103069680-C-T

67051861-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103070178-G-T

67051901-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103070215-T-C

67051919-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103070269-G-C

67051919-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103070269-G-T

67052122-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103070470-T-C

http://identifiers.org/hco/1/GRCh38#67052234-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103070573-A-C

67052414-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103070698-A-G

67052482-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103070806-C-T

67052484-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103070808-C-T

67052527-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103070831-T-G

67052703-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103070985-A-G

67052899-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103071199-G-A

67052931-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103071231-C-T

67053004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103071304-A-G

67053025-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103071332-C-G

67053075-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103071378-A-G

67053092-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103071395-G-A

67053131-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103071436-G-C

67053131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103071436-G-T

67053132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103071437-G-T

67053399-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103071700-C-T

67053417-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103071716-C-G

67053417-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103071716-C-T

http://identifiers.org/hco/1/GRCh38#67053562-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103071780-A-C

67053571-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: 103071791-G-A

http://identifiers.org/hco/1/GRCh38#67053617-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103071810-A-C

67054077-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: 5 prime UTR variant
orthologous variants: 103072233-T-A

67054077-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: 5 prime UTR variant
orthologous variants: 103072233-T-C

67054081-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: 5 prime UTR variant
orthologous variants: 103072237-A-G

http://identifiers.org/hco/1/GRCh38#67054102-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103072296-A-C

67054102-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: 5 prime UTR variant
orthologous variants: 103072296-A-G

http://identifiers.org/hco/1/GRCh38#67054124-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: 5 prime UTR variant
orthologous variants: http://identifiers.org/mco/4/GRCm39#103072344-C-A

67054124-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: 5 prime UTR variant
orthologous variants: 103072344-C-G

67054124-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 20800
most severe consequence: 5 prime UTR variant
orthologous variants: 103072344-C-T