16067168-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: 3 prime UTR variant
orthologous variants: 26409804-A-T

http://identifiers.org/hco/5/GRCh38#16067287-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#26409688-C-A

16067301-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: 3 prime UTR variant
orthologous variants: 26409677-A-G

16067403-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: 3 prime UTR variant
orthologous variants: 26409569-T-C

http://identifiers.org/hco/5/GRCh38#16067493-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#26409481-A-C

16067517-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 26409457-T-C

16067706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: 3_prime_UTR_variant, missense_variant, undefined
orthologous variants: 26409268-T-C

16067727-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: 3_prime_UTR_variant, missense_variant
orthologous variants: 26409247-T-C

16067928-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26409046-T-C

16068083-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26408902-T-C

16068167-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26408835-G-T

16068285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26408736-T-C

16068297-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26408724-T-G

16068331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26408699-T-C

16068362-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26408662-A-G

16068449-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26408518-G-C

16068449-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26408518-G-T

16068518-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26408451-G-A

16068606-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26408374-A-G

16068617-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26408363-T-C

16068678-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26408290-A-T

16068766-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26408196-G-T

16068770-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26408192-C-T

16068808-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26408147-G-A

16068904-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26408049-G-T

16068940-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26408013-A-T

16069113-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26407877-T-C

http://identifiers.org/hco/5/GRCh38#16069174-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#26407816-A-C

16069318-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26407685-T-C

16069331-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26407672-T-C

16069638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26407356-A-G

16069759-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26407236-C-T

16069810-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26407097-T-C

16070004-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26406906-A-G

16070195-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26406717-G-A

http://identifiers.org/hco/5/GRCh38#16070320-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#26406599-A-C

16070320-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26406599-A-G

http://identifiers.org/hco/5/GRCh38#16070365-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#26406554-C-A

16070365-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26406554-C-T

16070527-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26406401-G-A

16070617-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26406312-T-A

16070806-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26406172-G-A

16070806-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26406172-G-T

16070980-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26406014-C-T

16071461-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26405563-G-A

16071560-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26405464-T-A

16071679-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26405320-G-A

16073396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26403204-A-G

16073787-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26402929-A-G

16073820-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26402913-T-C

16074713-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26402680-T-A

http://identifiers.org/hco/5/GRCh38#16074764-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#26402627-A-C

http://identifiers.org/hco/5/GRCh38#16074879-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#26402482-C-A

16074879-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26402482-C-G

16075136-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26402256-A-T

16075155-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26402237-A-G

16075227-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26402232-T-G

16075349-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26402146-C-T

16075507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26402009-G-A

http://identifiers.org/hco/5/GRCh38#16075567-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#26401935-A-C

16075587-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26401868-G-T

16075624-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26401828-G-C

16075883-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26401594-G-T

16075929-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26401559-T-C

16080320-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26400036-C-T

16080508-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26399852-C-T

16080597-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26399757-G-T

16080603-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26399751-T-C

http://identifiers.org/hco/5/GRCh38#16080645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#26399722-C-A

16080702-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26399666-C-T

16080789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26399579-T-C

16080818-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26399560-C-T

16081068-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26399089-C-T

http://identifiers.org/hco/5/GRCh38#16081086-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#26399071-C-A

16081220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26398923-T-C

16081220-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26398923-T-G

16081457-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26398656-T-C

16081835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26398248-C-T

16081898-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26398186-G-A

16081995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26397632-C-T

16082069-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26397563-T-C

16082129-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26397500-T-C

16082152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26397477-G-A

16082160-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26397471-G-A

16082198-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26397433-G-A

16082294-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26397340-G-C

16082299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26397335-G-A

16082433-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26397203-A-T

16082448-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26397186-C-T

16082455-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26397179-C-T

16082536-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26397101-C-G

16082778-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26396893-A-T

16082828-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26396843-C-T

16083038-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26396652-G-C

16083058-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26396622-G-A

16083058-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26396622-G-T

16083083-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26396597-T-G

16083084-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26396596-G-C

16083088-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26396571-G-C

16083220-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26396426-T-G

16083289-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26396364-G-C

16083299-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26396354-T-C

http://identifiers.org/hco/5/GRCh38#16083628-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#26395998-C-A

http://identifiers.org/hco/5/GRCh38#16083652-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#26395974-A-C

16083890-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26395787-G-A

16083890-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26395787-G-C

16083987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26395723-A-G

http://identifiers.org/hco/5/GRCh38#16084732-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#26394355-C-A

16084815-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26394276-T-C

16084903-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26394188-T-A

16085013-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26394046-C-T

16085158-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26393885-A-G

16085159-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26393884-G-A

16085159-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26393884-G-C

http://identifiers.org/hco/5/GRCh38#16085342-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#26393743-C-A

16085771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26393425-T-C

16085794-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26393402-T-C

16085894-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26393390-C-T

16086609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26392873-A-G

16086808-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26392607-T-C

http://identifiers.org/hco/5/GRCh38#16086815-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#26392600-C-A

16086851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26392554-T-C

16086923-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26392484-G-A

16087106-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26392312-C-G

16087628-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26391830-T-C

http://identifiers.org/hco/5/GRCh38#16087731-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#26391736-A-C

16087902-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26391484-A-T

16088085-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26391308-C-G

16088215-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26391177-T-C

16088304-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26391097-T-C

16088345-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26390580-T-C

16088359-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26390566-A-G

16088519-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26390398-T-C

16088521-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26390396-C-T

http://identifiers.org/hco/5/GRCh38#16088559-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#26390358-A-C

16088789-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26390155-T-C

http://identifiers.org/hco/5/GRCh38#16089074-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#26389882-C-A

16089092-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26389864-C-G

16089100-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26389856-A-G

16089100-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26389856-A-T

16089624-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26389236-T-A

16089715-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26389146-G-A

16089791-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26389068-T-C

16089838-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26389022-G-C

16090078-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26388805-G-A

16090219-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26388622-T-C

16090271-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26388600-T-C

16090372-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26388529-G-T

16090470-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26388432-A-T

16090514-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26388392-G-A

16090600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26388309-A-G

16090628-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26388275-C-T

16090775-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26388142-G-A

16090775-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26388142-G-T

http://identifiers.org/hco/5/GRCh38#16090815-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#26388098-C-A

16090815-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron variant
orthologous variants: 26388098-C-T

16091117-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26387794-G-A

16091117-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26387794-G-C

16091117-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26387794-G-T

16091146-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26387759-T-C

http://identifiers.org/hco/5/GRCh38#16091149-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#26387756-C-A

http://identifiers.org/hco/5/GRCh38#16091200-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#26387705-C-A

16091200-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26387705-C-T

16091342-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26387563-G-C

16091658-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26387259-T-C

16091720-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26387201-C-T

16092226-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26386726-C-T

http://identifiers.org/hco/5/GRCh38#16092331-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#26386607-C-A

16092352-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26386590-T-G

16093139-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26385739-G-A

16093243-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26385625-C-T

16093338-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26385527-T-C

16093341-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26385524-T-G

16093465-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26385403-G-A

16093520-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26385363-C-T

16093662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26385227-C-T

http://identifiers.org/hco/5/GRCh38#16093756-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#26385134-A-C

16093756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26385134-A-G

16093787-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26385106-C-T

16093867-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26385044-T-C

http://identifiers.org/hco/5/GRCh38#16094014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#26384889-C-A

16094114-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26384788-G-A

16094152-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26384749-A-G

16094157-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26384744-G-C

16094321-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26384584-G-A

16094349-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26384568-A-G

16094539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26383605-G-A

16094686-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26383474-T-C

16094855-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26383361-C-G

16094855-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26383361-C-T

http://identifiers.org/hco/5/GRCh38#16095132-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#26380818-C-A

16095498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26380518-G-A

16095613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26380437-T-C

16095613-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26380437-T-G

16096126-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26379965-A-G

16096133-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26379958-C-G

16096162-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26379921-C-G

16096186-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26379897-T-C

16096230-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26379866-A-G

16096308-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26379783-G-A

http://identifiers.org/hco/5/GRCh38#16096333-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#26379756-A-C

16096333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26379756-A-G

16096645-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26379493-G-A

16096656-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26379482-G-A

16097151-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26379022-T-C

http://identifiers.org/hco/5/GRCh38#16097450-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#26378746-C-A

16097450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26378746-C-T

16097522-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26378674-C-G

16097522-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26378674-C-T

16099717-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26378115-G-A

16099807-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26378025-A-T

16100617-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26377563-G-A

16101451-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26377245-T-A

16101673-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26377038-C-T

16101685-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26377026-G-T

16101700-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26377011-T-C

16101763-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26376959-C-T

16101842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26376890-G-A

16102177-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26375196-G-A

16102178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26375195-T-C

16102288-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26375085-G-A

16102971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26375073-C-T

16102974-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26375070-C-T

http://identifiers.org/hco/5/GRCh38#16103014-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#26375033-C-A

16103189-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26374895-A-G

16103365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26374721-T-C

16103670-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26374453-T-C

16103689-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26374433-T-C

16103748-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26374365-A-G

16103842-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26374281-G-A

http://identifiers.org/hco/5/GRCh38#16103881-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#26374250-C-A

16103896-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26374235-T-G

16103998-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26374140-T-C

16104138-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26374006-C-T

16104203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26373957-C-T

16104292-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26373892-C-T

16104396-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26373782-A-G

16104897-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26373265-T-C

http://identifiers.org/hco/5/GRCh38#16104948-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#26373177-A-C

16104987-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26373145-A-G

16105406-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26372796-C-T

16105556-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26372641-A-T

16105735-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26372073-G-A

16105838-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26371996-T-A

http://identifiers.org/hco/5/GRCh38#16105907-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#26371951-C-A

16105907-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26371951-C-T

16105935-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26371922-T-A

16105936-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26371921-C-T

16106221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26371616-G-A

16106369-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26371470-C-T

16106403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26371436-A-G

16106444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26371386-C-T

16106505-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26371314-T-C

16106514-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26371306-T-C

16106555-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26371263-C-T

16106636-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26371193-T-C

16106646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26371183-C-T

16106657-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26371172-T-C

16106657-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26371172-T-G

16106747-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26371105-G-C

16107059-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26370665-C-T

16107121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26370621-C-T

16107466-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26370288-T-G

16108475-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26370119-G-A

16108475-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26370119-G-C

16108493-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26370094-G-A

16108493-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26370094-G-T

16108577-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26370012-T-A

16108577-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26370012-T-G

16108610-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26369973-G-A

16108961-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26369491-G-A

16109052-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26369395-A-G

http://identifiers.org/hco/5/GRCh38#16109206-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#26369283-A-C

http://identifiers.org/hco/5/GRCh38#16109233-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#26369249-C-A

16109233-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26369249-C-T

16109276-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26369209-G-A

16109290-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26369195-T-C

16109290-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26369195-T-G

16109370-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26369119-A-G

16109575-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26368979-T-C

16109632-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26368924-G-A

16109702-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26368860-C-G

16109988-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26368562-A-G

16110019-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26368531-G-T

16113166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26367048-G-A

16113209-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26367005-T-C

16113228-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26366986-A-G

16113240-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26366974-A-G

16114243-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26366588-T-C

16114277-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26366553-C-G

16114277-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26366553-C-T

16114607-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26366266-T-G

16114637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26366239-G-A

16114851-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26366165-T-C

16114895-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26366124-A-T

http://identifiers.org/hco/5/GRCh38#16115121-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#26365917-A-C

16115530-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26365489-A-G

16116362-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26365074-T-G

16116444-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26365004-A-G

http://identifiers.org/hco/5/GRCh38#16116464-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#26364983-C-A

16116511-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26364936-A-G

16116621-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26364880-A-G

16116713-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26364805-T-A

16117011-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26364524-T-G

16117093-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26364443-G-A

16117208-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26364334-A-T

16117334-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26364205-T-C

16118121-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26362636-C-T

http://identifiers.org/hco/5/GRCh38#16118139-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#26362618-A-C

16118414-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26362362-G-C

16118563-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26362176-T-A

16118563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26362176-T-C

16118601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26362137-G-A

16118675-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26362073-G-A

http://identifiers.org/hco/5/GRCh38#16118690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#26362058-C-A

16118783-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26361963-T-A

16118783-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26361963-T-C

16119129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26361697-G-A

16119129-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26361697-G-C

16119385-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26361632-A-G

16119718-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26361416-A-G

16119877-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26361210-G-C

16120046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26361033-G-A

16120903-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26360328-C-G

http://identifiers.org/hco/5/GRCh38#16120924-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#26360307-C-A

16121069-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26360158-G-A

16121271-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26359959-G-A

16121427-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26359828-G-A

16121866-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26359418-C-G

16121922-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26359361-A-G

16123406-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26358900-G-A

16123892-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26358441-T-A

16123931-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26358403-G-A

16123931-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26358403-G-C

16125217-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26357896-G-T

16125382-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26357736-T-A

16126126-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26357115-C-T

16126132-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26357109-C-T

16126510-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26355315-T-C

16126618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26355215-C-T

16127366-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26354471-C-T

16127478-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26353985-C-T

16127846-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26353624-C-T

16127889-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26353581-G-A

16128135-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26353353-T-C

16128137-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26353351-T-C

16128180-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26353323-A-G

16128368-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26353162-T-A

16128381-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26353149-T-C

16128491-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26353064-G-A

http://identifiers.org/hco/5/GRCh38#16128664-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#26352736-C-A

16128777-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26352509-A-T

http://identifiers.org/hco/5/GRCh38#16129072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#26352206-C-A

16129124-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26352168-A-T

16129297-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26352015-A-G

16129458-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26351868-A-G

16129635-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26351701-A-G

16129948-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26351422-C-T

16130111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26351257-G-A

16130111-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26351257-G-C

16130525-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26350839-C-T

16130937-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26350428-A-G

16131116-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26350272-T-C

16131379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26349538-T-C

16131425-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26349496-A-G

16131640-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26349331-C-T

16131724-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26349283-C-T

16131915-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26349036-T-C

16132052-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26348902-A-T

16132100-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26348856-G-A

16132101-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26348855-A-G

16132201-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26348753-G-A

16132352-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26348619-C-T

http://identifiers.org/hco/5/GRCh38#16132742-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#26348260-A-C

16135592-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26348073-T-C

http://identifiers.org/hco/5/GRCh38#16135793-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#26347910-C-A

16135793-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26347910-C-T

16135820-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26347883-A-G

16135905-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26347844-A-G

16136486-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26347185-A-G

16136844-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26346891-C-T

16137037-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26346710-T-C

16139575-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26346381-A-G

16140412-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26344800-G-A

http://identifiers.org/hco/5/GRCh38#16140425-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#26344787-A-C

16140487-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26344723-T-A

16140487-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26344723-T-G

16140578-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26344638-A-G

http://identifiers.org/hco/5/GRCh38#16140721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#26344487-C-A

16140721-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26344487-C-G

16143170-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26342654-T-C

16143198-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26342631-T-A

http://identifiers.org/hco/5/GRCh38#16143255-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#26342580-C-A

16143255-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26342580-C-T

16143512-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26342361-C-T

16144159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26341039-C-T

16144250-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26340938-T-C

16144389-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26340797-G-A

16144438-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26340739-A-G

16144441-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26340736-A-G

16144454-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26340726-A-G

16144464-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26340716-T-C

http://identifiers.org/hco/5/GRCh38#16144479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#26340711-C-A

16144744-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26340442-A-G

16152075-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26339199-T-A

16152075-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26339199-T-G

16152142-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26339132-G-C

16152177-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26339095-T-C

16152249-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26339027-C-T

16152498-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26338760-A-T

16152742-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26338532-G-T

16152761-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26338508-T-C

16152847-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26338422-T-G

16152996-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26338279-T-A

http://identifiers.org/hco/5/GRCh38#16153080-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#26338202-A-C

16153080-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26338202-A-G

16153527-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26337122-T-C

http://identifiers.org/hco/5/GRCh38#16153532-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#26337117-A-C

16153582-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26337066-T-C

16153625-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26337023-T-C

16153635-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26337013-T-A

16153638-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26337010-A-G

16153692-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26336956-T-C

16153716-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26336932-C-T

http://identifiers.org/hco/5/GRCh38#16154872-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#26336209-C-A

16154908-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26336172-G-A

16155003-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26336121-G-C

16155218-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26335924-C-T

16155299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26335805-G-A

16155299-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26335805-G-T

http://identifiers.org/hco/5/GRCh38#16155302-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#26335802-A-C

16157188-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26333633-G-C

http://identifiers.org/hco/5/GRCh38#16157654-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#26333186-C-A

16157654-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26333186-C-T

16157666-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26333174-A-G

16157730-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26333108-T-C

16157951-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26332889-T-A

16157989-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26332861-G-A

16158155-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26332683-T-C

16158219-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26332616-T-A

16158373-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26332412-G-T

16158451-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26332307-T-C

16159358-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26328748-T-C

16159358-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26328748-T-G

16159449-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26328678-C-T

16159780-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26328361-C-T

16159882-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26328261-A-G

http://identifiers.org/hco/5/GRCh38#16160085-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#26328053-A-C

16160197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26327953-C-T

16160978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26327397-C-T

16160982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26327393-G-A

16161419-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26327175-C-T

16161738-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26326858-T-C

16161893-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26326704-C-T

16162057-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26326545-A-G

http://identifiers.org/hco/5/GRCh38#16163195-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#26326235-C-A

16163554-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26325850-T-C

16163554-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26325850-T-G

16163621-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26325782-G-A

16163667-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26325733-T-A

16163667-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26325733-T-C

16163689-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26325711-G-T

16163748-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26325658-T-G

http://identifiers.org/hco/5/GRCh38#16163849-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#26325558-C-A

16163849-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26325558-C-T

16164061-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26325436-C-T

16164109-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26325392-T-G

16164232-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26325267-G-A

16164244-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26325255-C-G

16164591-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26324987-T-C

16166846-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26324152-T-C

16166947-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26324051-G-A

16167083-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26323965-T-A

16167157-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26323942-C-T

16167373-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26323731-G-C

16167971-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26323168-C-T

16168040-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26321789-C-T

16168115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26321727-G-T

16168237-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26321598-T-C

16168337-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26321507-T-C

16168494-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26321345-G-A

16168580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26321254-T-C

16168596-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26321240-G-A

16168599-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26321237-G-C

16168639-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26321210-C-T

16168662-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26321186-C-T

16168822-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26321037-T-C

16169476-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26320453-T-C

16169590-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26320340-T-A

16169598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26320332-T-C

16169792-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26320138-G-A

16169809-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26320121-A-G

16170042-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26319902-G-A

16170045-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26319900-T-G

16170048-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26319897-A-T

16170053-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26319892-T-C

16170220-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26319741-T-C

16170304-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26319663-C-T

16170530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26319441-T-C

16170817-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26319178-T-C

16170896-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26319105-C-T

16171075-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26318945-G-A

16171360-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26318831-C-T

16171394-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26318804-T-A

16171453-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26318746-A-G

16171624-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26318631-T-C

16171780-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26318504-G-A

16171881-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26318412-C-T

16172013-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26318274-T-C

16172120-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26318162-T-C

http://identifiers.org/hco/5/GRCh38#16172141-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#26318140-A-C

16172266-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26318018-T-C

16172475-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26317802-A-G

16172478-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26317799-G-T

16172565-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26317721-C-T

16172624-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26317670-A-G

16172644-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26317650-T-C

16173221-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26317145-A-G

http://identifiers.org/hco/5/GRCh38#16173304-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#26317054-C-A

16173390-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26316971-T-G

16173448-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26316906-G-A

16174137-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26315455-G-A

http://identifiers.org/hco/5/GRCh38#16174283-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#26315244-C-A

16174478-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26315089-T-A

16174614-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26314912-C-G

16174614-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26314912-C-T

16174817-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26314699-G-A

16174903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26314618-G-A

http://identifiers.org/hco/5/GRCh38#16175017-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#26314495-C-A

16175251-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26314296-A-G

16175413-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26314149-A-G

16175541-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26314047-T-C

16175928-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26313097-A-T

16176202-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26312846-T-C

16176453-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26312514-G-A

16176597-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26312334-C-T

16176625-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26312307-G-A

16176715-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26312226-C-T

16176771-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26312172-T-C

16176794-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26312107-G-T

16176799-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26312102-C-T

16177161-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26311755-T-A

http://identifiers.org/hco/5/GRCh38#16177583-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#26311350-A-C

16177583-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26311350-A-G

16177583-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26311350-A-T

http://identifiers.org/hco/5/GRCh38#16177593-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#26311340-A-C

16177613-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26311320-T-A

16177613-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26311320-T-C

16177613-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26311320-T-G

16177657-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26311275-A-G

http://identifiers.org/hco/5/GRCh38#16177688-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#26311244-A-C

16177699-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26311233-G-A

16177699-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26311233-G-T

16177796-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26311140-C-T

16177838-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26311098-T-C

16177841-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26311095-C-G

16177841-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: missense_variant, non_coding_transcript_exon_variant
orthologous variants: 26311095-C-T

http://identifiers.org/hco/5/GRCh38#16177966-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#26310949-C-A

16177966-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26310949-C-G

http://identifiers.org/hco/5/GRCh38#16178015-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#26310896-A-C

http://identifiers.org/hco/5/GRCh38#16178028-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#26310883-C-A

16178803-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 26310066-G-A

16178821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 26310048-T-C

http://identifiers.org/hco/5/GRCh38#16178996-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#26309925-C-A

16178996-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 26309925-C-G

16178996-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant, undefined
orthologous variants: 26309925-C-T

16179046-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 26309869-G-A

16179046-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 26309869-G-T

16179274-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, missense_variant, non_coding_transcript_variant, undefined
orthologous variants: 26309623-T-C

16179599-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26309322-G-A

16179599-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: 5_prime_UTR_variant, intron_variant, non_coding_transcript_variant
orthologous variants: 26309322-G-T

16179817-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26309106-G-T

16179854-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26309079-A-G

16180108-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26308819-G-A

16180146-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26308777-G-A

16180146-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26308777-G-T

http://identifiers.org/hco/5/GRCh38#16180245-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#26308691-C-A

16180245-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26308691-C-T

16180262-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26308672-G-A

16180265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26308667-C-T

16180297-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26308620-C-T

16180332-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26308593-T-G

16180365-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26308564-T-C

16180383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26308546-T-C

16180408-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26308530-T-C

16180545-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26308434-T-C

16180545-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_variant
orthologous variants: 26308434-T-G

16180751-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 33609
most severe consequence: intron_variant, non_coding_transcript_exon_variant, non_coding_transcript_variant
orthologous variants: 26308217-C-T