10980914-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 3 prime UTR variant
orthologous variants: 41336119-T-A

10981702-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 3 prime UTR variant
orthologous variants: 41336726-T-A

10981702-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 3 prime UTR variant
orthologous variants: 41336726-T-C

10981722-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 3 prime UTR variant
orthologous variants: 41336746-G-A

10981722-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 3 prime UTR variant
orthologous variants: 41336746-G-T

10981758-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 3 prime UTR variant
orthologous variants: 41336783-T-A

10981982-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 3 prime UTR variant
orthologous variants: 41336967-A-G

10982250-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 3 prime UTR variant
orthologous variants: 41337194-A-T

10982592-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 3 prime UTR variant
orthologous variants: 41337464-G-T

http://identifiers.org/hco/6/GRCh38#10982727-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41337579-C-A

http://identifiers.org/hco/6/GRCh38#10982736-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41337589-C-A

http://identifiers.org/hco/6/GRCh38#10982845-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41337766-C-A

http://identifiers.org/hco/6/GRCh38#10982857-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41337778-C-A

10982906-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 3 prime UTR variant
orthologous variants: 41337818-A-G

10983204-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 3 prime UTR variant
orthologous variants: 41338230-G-A

10983241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 3 prime UTR variant
orthologous variants: 41338270-G-A

10983251-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 3 prime UTR variant
orthologous variants: 41338280-G-T

10983255-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 3 prime UTR variant
orthologous variants: 41338284-G-T

10983458-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 3 prime UTR variant
orthologous variants: 41338475-A-T

10983508-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 3 prime UTR variant
orthologous variants: 41338522-G-A

10983508-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 3 prime UTR variant
orthologous variants: 41338522-G-T

http://identifiers.org/hco/6/GRCh38#10983708-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41338676-C-A

10983708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 3 prime UTR variant
orthologous variants: 41338676-C-T

10983740-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 3 prime UTR variant
orthologous variants: 41338708-A-G

10983740-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 3 prime UTR variant
orthologous variants: 41338708-A-T

http://identifiers.org/hco/6/GRCh38#10983747-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41338715-A-C

10983773-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 3 prime UTR variant
orthologous variants: 41338762-A-G

10983773-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 3 prime UTR variant
orthologous variants: 41338762-A-T

10984008-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41338988-G-T

10987880-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41339379-A-T

10988739-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41339793-T-C

http://identifiers.org/hco/6/GRCh38#10988768-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41339813-C-A

10988782-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41339827-T-C

10988788-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41339831-G-T

10988978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41340026-A-G

10988986-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41340034-A-T

http://identifiers.org/hco/6/GRCh38#10989199-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41340171-C-A

10989693-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41340319-T-C

10989708-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: missense variant
orthologous variants: 41340334-C-T

10989718-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: missense variant
orthologous variants: 41340344-T-A

10989799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: synonymous variant
orthologous variants: 41340425-G-A

10989985-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41340597-T-C

10990011-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41340628-T-C

10990213-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41340819-G-A

10990213-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41340819-G-T

10990283-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41340874-C-T

10990311-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 41340898-A-G

10990378-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: synonymous variant
orthologous variants: 41340965-A-G

10990387-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: synonymous variant
orthologous variants: 41340974-A-G

10990387-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: stop gained
orthologous variants: 41340974-A-T

10990448-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron_variant, splice_region_variant
orthologous variants: 41341035-A-G

http://identifiers.org/hco/6/GRCh38#10990491-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41341074-C-A

10990491-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41341074-C-T

10990510-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41341093-A-G

10990678-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41341253-G-A

10990678-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41341253-G-C

10990685-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41341260-A-G

10991504-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41341468-A-T

10991781-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41341700-A-G

10991981-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41341771-C-T

10992333-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41342557-A-G

10992376-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41342606-A-G

10994534-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41342976-T-C

10994572-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41343022-T-C

http://identifiers.org/hco/6/GRCh38#10994588-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41343035-C-A

10994588-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41343035-C-T

10994594-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41343041-T-A

10994849-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41343283-A-G

http://identifiers.org/hco/6/GRCh38#10994853-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41343287-C-A

http://identifiers.org/hco/6/GRCh38#10994855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41343289-C-A

http://identifiers.org/hco/6/GRCh38#10994877-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41343309-C-A

10994877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41343309-C-T

10995047-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: synonymous variant
orthologous variants: 41343462-G-A

http://identifiers.org/hco/6/GRCh38#10995061-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: missense variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41343476-C-A

10995196-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41343609-G-T

10995229-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41343628-G-C

10995254-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41343648-T-C

http://identifiers.org/hco/6/GRCh38#10995306-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41343684-C-A

10995306-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41343684-C-T

10995307-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41343685-T-C

http://identifiers.org/hco/6/GRCh38#10995308-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41343686-C-A

10995308-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41343686-C-G

10995664-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41343922-C-T

10998419-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 41344138-A-T

10998497-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 41344211-G-A

10998634-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 41344321-T-C

10998659-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: 41344347-G-A

http://identifiers.org/hco/6/GRCh38#10998787-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 3_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41344463-C-A

10999031-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41344690-C-T

10999142-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41344798-T-C

10999142-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41344798-T-G

10999624-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41344984-T-G

10999816-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41345129-C-G

10999869-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41345183-G-C

11000218-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41345525-T-C

11000648-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41345824-C-T

11000959-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41346058-T-C

11000966-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41346065-G-T

11001008-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41346107-G-C

11001031-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41346121-T-C

11001152-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41346161-G-A

11001187-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41346177-T-A

11001230-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41346209-G-C

11001425-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41346384-G-A

11001425-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41346384-G-T

11001939-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41346910-A-G

11004217-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41347337-G-A

11004317-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41347438-C-G

11004451-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41347556-A-T

11004633-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41347713-G-A

11004664-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41347738-A-G

11004751-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41347799-A-G

11004958-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41347982-A-G

11005450-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: synonymous variant
orthologous variants: 41348201-T-C

11005483-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: synonymous variant
orthologous variants: 41348234-T-A

11005483-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: synonymous variant
orthologous variants: 41348234-T-C

11005483-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: synonymous variant
orthologous variants: 41348234-T-G

11005507-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: synonymous variant
orthologous variants: 41348258-A-G

11005583-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41348334-G-T

11005590-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41348341-G-C

11005590-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41348341-G-T

11005611-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41348360-G-C

11005611-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41348360-G-T

11005633-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41348382-T-C

11005633-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41348382-T-G

http://identifiers.org/hco/6/GRCh38#11005637-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41348385-A-C

http://identifiers.org/hco/6/GRCh38#11008766-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41349804-C-A

11008766-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41349804-C-T

11008814-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41349825-A-G

http://identifiers.org/hco/6/GRCh38#11008855-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41349861-C-A

11008869-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41349875-G-A

11008908-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41349903-T-C

11008978-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41349965-A-G

11009054-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41350040-T-C

11010509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41350414-C-T

11010601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41350482-G-T

http://identifiers.org/hco/6/GRCh38#11010609-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41350490-A-C

11010609-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41350490-A-G

11010696-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41350576-G-A

11010696-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41350576-G-T

http://identifiers.org/hco/6/GRCh38#11010728-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41350593-C-A

11010728-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41350593-C-T

11010733-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41350598-G-A

11010737-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41350602-T-C

11010847-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41350696-T-G

11010856-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41350705-T-C

11010856-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41350705-T-G

http://identifiers.org/hco/6/GRCh38#11010890-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41350743-A-C

11010890-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41350743-A-G

11010893-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41350746-T-A

11010893-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41350746-T-C

http://identifiers.org/hco/6/GRCh38#11010904-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41350756-C-A

11010904-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41350756-C-T

http://identifiers.org/hco/6/GRCh38#11010916-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41350768-C-A

11010916-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41350768-C-T

http://identifiers.org/hco/6/GRCh38#11010977-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41350827-A-C

11011125-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41350905-G-C

11011131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41350911-G-T

11011473-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41350999-A-G

11011568-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41351079-C-T

http://identifiers.org/hco/6/GRCh38#11011874-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41351397-C-A

11011987-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41351509-C-T

11012056-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41351582-G-A

11012166-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41351681-G-A

11012170-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41351685-A-G

11012203-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41351715-A-G

11012223-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41351733-A-G

11012376-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41351882-G-C

11012915-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41352328-G-A

11012934-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41352347-A-G

http://identifiers.org/hco/6/GRCh38#11013174-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41352559-C-A

11015354-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41352827-G-A

http://identifiers.org/hco/6/GRCh38#11015458-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41352915-C-A

http://identifiers.org/hco/6/GRCh38#11015476-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41352933-C-A

11015476-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41352933-C-T

http://identifiers.org/hco/6/GRCh38#11015490-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41352947-C-A

11015498-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41352951-G-A

11015498-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41352951-G-T

11015530-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41352981-T-C

11015553-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41352996-T-C

11015600-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 41353033-A-G

11015601-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 41353034-G-A

11015601-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 41353034-G-T

http://identifiers.org/hco/6/GRCh38#11015624-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#41353055-C-A

11015710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 41353109-A-G

11015729-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 41353128-A-G

11015754-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 41353152-G-C

11015754-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 41353152-G-T

http://identifiers.org/hco/6/GRCh38#11015757-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#41353155-C-A

11015862-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 41353247-A-G

11016512-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41353630-T-G

11016672-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41353736-C-T

11021133-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41354110-C-G

11021159-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41354131-C-T

11021285-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41354256-G-C

11021317-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41354284-T-G

11021823-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41354815-C-T

11021911-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41354900-C-G

11021920-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41354909-G-A

11022091-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41355206-T-C

11022210-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41355314-G-C

11022210-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41355314-G-T

11022398-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41355462-G-A

http://identifiers.org/hco/6/GRCh38#11022443-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41355479-A-C

11022464-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41355500-C-T

11022525-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41355558-T-C

11022647-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41355670-G-C

11022798-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41355878-C-T

11023203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41356878-G-A

11023206-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41356881-C-G

11023263-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41356938-G-C

11023428-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41357115-T-C

11023533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41357223-T-C

11023553-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41357243-C-T

11023612-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41357282-A-T

11023691-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41357356-C-G

11023710-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41357375-A-G

11023712-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41357377-T-A

11023737-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41357398-C-T

11023778-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41357437-T-C

11023877-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41357524-C-T

11023905-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41357551-T-C

11023981-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41357598-C-G

11023994-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41357608-G-A

11024002-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41357616-C-T

11024256-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41357820-C-T

11024340-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41357901-T-C

11025036-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41358514-G-T

11025277-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41358689-T-C

11026144-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41359458-G-C

11026302-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41359614-T-C

11026325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41359642-G-A

11026381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41359702-G-A

11026403-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41359723-G-A

11028013-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41360852-G-T

11028180-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41361005-T-G

11028188-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41361013-T-C

11028433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41361202-C-T

11028495-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41361264-A-G

11028924-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: 5_prime_UTR_variant, intron_variant
orthologous variants: 41361614-A-T

11029573-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41362143-G-T

11029697-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41362264-G-C

11029697-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41362264-G-T

11029769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41362436-G-A

11029981-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41362591-G-A

11030014-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41362620-G-A

11030238-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41362735-G-A

11030400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41362892-T-C

11030436-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41362921-A-G

http://identifiers.org/hco/6/GRCh38#11031100-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41363393-A-C

http://identifiers.org/hco/6/GRCh38#11031124-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41363417-A-C

11031720-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41364016-T-C

11031832-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41364111-T-C

11031961-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41364178-T-G

11031973-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41364190-T-C

11032021-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41364238-A-G

11032156-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41364353-A-G

11032373-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41364550-A-T

http://identifiers.org/hco/6/GRCh38#11032374-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41364551-C-A

11032524-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41364675-A-T

11033054-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41364978-C-G

11033130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41365036-G-A

11033169-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41365068-T-A

11033422-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41365270-C-G

11033450-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41365297-C-T

11033563-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41365411-T-A

11033563-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41365411-T-C

11033596-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41365446-A-G

11033673-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41365539-T-G

11033686-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41365558-A-T

http://identifiers.org/hco/6/GRCh38#11033721-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41365593-C-A

11033983-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41365861-T-C

11034014-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41365885-T-A

http://identifiers.org/hco/6/GRCh38#11034047-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41365918-A-C

11034195-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41366057-A-G

11035112-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41366289-G-C

http://identifiers.org/hco/6/GRCh38#11035125-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41366302-A-C

11035195-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41366365-T-C

11035197-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41366367-C-T

11035210-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41366380-C-G

http://identifiers.org/hco/6/GRCh38#11035300-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41366496-A-C

11036010-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41366619-T-C

11036014-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41366623-T-C

http://identifiers.org/hco/6/GRCh38#11036055-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41366664-A-C

11036055-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41366664-A-G

http://identifiers.org/hco/6/GRCh38#11036107-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41366694-C-A

11036107-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41366694-C-G

11036107-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41366694-C-T

11036252-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41366812-G-A

11037313-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron_variant, undefined
orthologous variants: 41367458-T-C

11037321-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41367466-G-C

11037584-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41367809-A-G

http://identifiers.org/hco/6/GRCh38#11037902-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41368252-A-C

11037902-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41368252-A-G

11037922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41368274-G-A

11038052-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41368407-T-C

11038060-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41368415-T-A

11038501-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41368998-T-A

11038677-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41369227-T-G

11038748-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41369290-C-T

11039090-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41369826-G-T

11039104-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron_variant, undefined
orthologous variants: 41369840-A-G

11039348-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41370077-T-C

11039379-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41370090-T-C

11039558-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41370162-A-G

11039758-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41370225-T-G

11039809-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41370276-T-C

11039878-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41370320-C-T

11039918-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41370363-T-C

http://identifiers.org/hco/6/GRCh38#11039950-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41370395-A-C

11040125-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41370587-G-A

11040435-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41371045-G-C

11040447-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41371057-T-A

11040447-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41371057-T-C

http://identifiers.org/hco/6/GRCh38#11040488-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: http://identifiers.org/mco/13/GRCm39#41371112-A-C

11041107-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41371689-G-A

11041107-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41371689-G-T

11041124-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41371706-G-C

11041157-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41371718-C-G

11041375-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41371913-G-C

11041431-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41371971-G-A

11041600-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41372253-T-C

11041756-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41372381-A-G

11041821-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41372447-T-A

11041821-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41372447-T-C

11041843-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41372472-T-C

11041983-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41372586-C-T

11042022-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41372623-G-A

11042023-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41372624-A-G

11042759-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41372976-C-G

11043007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron variant
orthologous variants: 41373191-T-C

11044095-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron_variant, undefined
orthologous variants: 41373691-G-A

11044095-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron_variant, undefined
orthologous variants: 41373691-G-C

11044095-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron_variant, undefined
orthologous variants: 41373691-G-T

http://identifiers.org/hco/6/GRCh38#11044156-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/13/GRCm39#41373760-C-A

11044156-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron_variant, undefined
orthologous variants: 41373760-C-G

11044156-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 14416
most severe consequence: intron_variant, undefined
orthologous variants: 41373760-C-T