49866930-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3 prime UTR variant
orthologous variants: 99394920-G-A

49866930-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3 prime UTR variant
orthologous variants: 99394920-G-T

http://identifiers.org/hco/12/GRCh38#49866943-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99394933-C-A

49866943-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3 prime UTR variant
orthologous variants: 99394933-C-T

49866993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3 prime UTR variant
orthologous variants: 99394981-T-C

http://identifiers.org/hco/12/GRCh38#49866995-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99394982-C-A

49866995-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3 prime UTR variant
orthologous variants: 99394982-C-T

49866997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3 prime UTR variant
orthologous variants: 99394984-G-T

http://identifiers.org/hco/12/GRCh38#49867046-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99395033-C-A

49867046-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3 prime UTR variant
orthologous variants: 99395033-C-T

http://identifiers.org/hco/12/GRCh38#49867054-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99395041-C-A

http://identifiers.org/hco/12/GRCh38#49867070-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#99395059-C-A

49867182-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3 prime UTR variant
orthologous variants: 99395095-G-A

49867182-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3 prime UTR variant
orthologous variants: 99395095-G-T

http://identifiers.org/hco/12/GRCh38#49867479-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#99395300-C-A

49867508-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 99395329-G-T

http://identifiers.org/hco/12/GRCh38#49867512-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#99395333-C-A

49867522-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3 prime UTR variant
orthologous variants: 99395352-G-A

49867522-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3 prime UTR variant
orthologous variants: 99395352-G-T

49867538-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 99395367-T-C

49867547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 99395376-G-A

49867547-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 99395376-G-T

49867548-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 99395377-G-A

49867548-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 99395377-G-C

49867548-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 99395377-G-T

http://identifiers.org/hco/12/GRCh38#49867647-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99395482-C-A

49867731-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 99395570-A-G

http://identifiers.org/hco/12/GRCh38#49867735-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#99395574-C-A

49867762-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 99395619-G-A

49867934-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3 prime UTR variant
orthologous variants: 99395737-T-C

49867934-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3 prime UTR variant
orthologous variants: 99395737-T-G

http://identifiers.org/hco/12/GRCh38#49867937-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99395740-C-A

49867937-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3 prime UTR variant
orthologous variants: 99395740-C-T

49867983-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 99395782-A-G

49867983-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 99395782-A-T

49868006-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3 prime UTR variant
orthologous variants: 99395809-G-A

49868006-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3 prime UTR variant
orthologous variants: 99395809-G-T

49868046-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3 prime UTR variant
orthologous variants: 99395848-A-G

49868046-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3 prime UTR variant
orthologous variants: 99395848-A-T

http://identifiers.org/hco/12/GRCh38#49868066-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99395869-A-C

49868073-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 99395876-G-A

49868384-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3 prime UTR variant
orthologous variants: 99396140-A-G

49868385-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3 prime UTR variant
orthologous variants: 99396141-G-A

49868385-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3 prime UTR variant
orthologous variants: 99396141-G-T

49868399-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3 prime UTR variant
orthologous variants: 99396155-A-G

http://identifiers.org/hco/12/GRCh38#49868433-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99396188-C-A

49868433-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3 prime UTR variant
orthologous variants: 99396188-C-T

49868500-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3 prime UTR variant
orthologous variants: 99396253-A-G

49868500-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3 prime UTR variant
orthologous variants: 99396253-A-T

49868508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3 prime UTR variant
orthologous variants: 99396259-T-C

49868532-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3 prime UTR variant
orthologous variants: 99396273-A-G

49868547-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3 prime UTR variant
orthologous variants: 99396289-G-A

49868562-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3 prime UTR variant
orthologous variants: 99396304-T-A

49868562-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3 prime UTR variant
orthologous variants: 99396304-T-C

http://identifiers.org/hco/12/GRCh38#49868592-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99396334-C-A

49868592-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3 prime UTR variant
orthologous variants: 99396334-C-G

49868592-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3 prime UTR variant
orthologous variants: 99396334-C-T

49868600-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3 prime UTR variant
orthologous variants: 99396342-C-T

49868661-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3 prime UTR variant
orthologous variants: 99396377-G-A

49868661-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3 prime UTR variant
orthologous variants: 99396377-G-C

49868661-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3 prime UTR variant
orthologous variants: 99396377-G-T

49868704-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3 prime UTR variant
orthologous variants: 99396407-T-C

49868706-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3 prime UTR variant
orthologous variants: 99396409-T-A

49868706-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3 prime UTR variant
orthologous variants: 99396409-T-C

http://identifiers.org/hco/12/GRCh38#49868770-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99396478-C-A

http://identifiers.org/hco/12/GRCh38#49869102-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#99396719-C-A

49869131-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 99396749-G-C

49869131-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 99396749-G-T

http://identifiers.org/hco/12/GRCh38#49869263-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#99396882-C-A

49869263-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 99396882-C-T

49869393-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 99397011-A-G

49869478-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 99397081-T-C

49869519-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3 prime UTR variant
orthologous variants: 99397119-G-A

49869519-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3 prime UTR variant
orthologous variants: 99397119-G-T

http://identifiers.org/hco/12/GRCh38#49869544-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#99397145-C-A

49869544-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 99397145-C-T

49869559-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 99397160-G-A

49869559-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3_prime_UTR_variant, undefined
orthologous variants: 99397160-G-T

49869824-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3 prime UTR variant
orthologous variants: 99397406-C-T

http://identifiers.org/hco/12/GRCh38#49869835-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99397413-C-A

49869835-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3 prime UTR variant
orthologous variants: 99397413-C-T

http://identifiers.org/hco/12/GRCh38#49869989-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99397548-C-A

49869989-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3 prime UTR variant
orthologous variants: 99397548-C-T

http://identifiers.org/hco/12/GRCh38#49870006-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99397571-C-A

49870006-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3 prime UTR variant
orthologous variants: 99397571-C-T

49870010-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3 prime UTR variant
orthologous variants: 99397576-G-A

49870010-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3 prime UTR variant
orthologous variants: 99397576-G-T

49870036-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3 prime UTR variant
orthologous variants: 99397606-A-T

49870053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3 prime UTR variant
orthologous variants: 99397623-C-T

49870178-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3 prime UTR variant
orthologous variants: 99397694-T-C

49870241-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3 prime UTR variant
orthologous variants: 99397757-G-A

49870241-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3 prime UTR variant
orthologous variants: 99397757-G-T

http://identifiers.org/hco/12/GRCh38#49870280-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99397796-C-A

49870280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3 prime UTR variant
orthologous variants: 99397796-C-T

http://identifiers.org/hco/12/GRCh38#49870284-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99397800-C-A

49870284-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3 prime UTR variant
orthologous variants: 99397800-C-T

49870321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3 prime UTR variant
orthologous variants: 99397837-C-T

http://identifiers.org/hco/12/GRCh38#49870330-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3 prime UTR variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99397846-C-A

49870330-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3 prime UTR variant
orthologous variants: 99397846-C-T

49870421-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 99397946-T-C

49870421-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 99397946-T-G

49870442-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 99397966-G-A

49870442-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 3_prime_UTR_variant, NMD_transcript_variant
orthologous variants: 99397966-G-T

49870704-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99398222-A-T

49870785-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99398266-G-T

49870786-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99398267-G-A

49870786-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99398267-G-T

49870884-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99398381-G-A

49870915-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99398412-T-A

49871079-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99398584-G-A

49871079-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99398584-G-C

49871106-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99398629-G-A

49871128-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99398650-G-A

49871164-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99398678-C-G

49871198-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99398712-C-T

49871541-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99399024-A-G

49871585-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99399067-A-G

49872026-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99399167-G-A

49872179-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99399281-G-C

49872234-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99399342-T-C

49872381-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99399496-G-A

49872466-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99399588-G-A

49872634-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99399749-G-C

49872781-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99399859-T-C

49872794-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99399873-G-A

http://identifiers.org/hco/12/GRCh38#49873273-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99400303-A-C

49873399-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99400392-G-T

49873587-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 99400582-G-A

49873658-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99400652-G-C

49873730-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99400712-C-G

49873819-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 99400787-C-G

49873836-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 99400804-T-C

49873946-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 99400946-A-G

49874296-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99401475-C-T

49874321-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99401502-C-T

49874322-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99401503-G-A

49874982-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99402403-G-A

49875133-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99402542-G-A

49875133-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99402542-G-T

http://identifiers.org/hco/12/GRCh38#49875315-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99402712-C-A

49881689-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99403444-G-A

49881709-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99403425-G-T

49881782-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99403361-G-A

49881890-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99403248-C-T

49882173-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99403007-G-A

49882181-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99402999-G-A

http://identifiers.org/hco/12/GRCh38#49882586-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99403755-C-A

49882784-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99403935-A-G

49882821-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99403969-C-T

http://identifiers.org/hco/12/GRCh38#49883062-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99404201-A-C

49883359-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99404469-T-G

49883533-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99404641-T-C

49885111-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99405823-G-A

49885458-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99406137-C-T

49885459-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99406138-G-A

49885503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99406187-C-T

49885557-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99406260-C-T

49886102-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99407509-G-A

49886115-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99407522-G-T

49886408-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99407785-G-A

49886950-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99408098-C-T

49887176-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99408275-C-T

49887178-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99408277-C-T

49887279-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99408360-C-T

http://identifiers.org/hco/12/GRCh38#49887280-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99408361-C-A

49887280-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99408361-C-T

http://identifiers.org/hco/12/GRCh38#49887489-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99408567-C-A

http://identifiers.org/hco/12/GRCh38#49887564-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99408630-C-A

49887564-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99408630-C-T

49887568-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99408633-A-G

49887568-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99408633-A-T

49887598-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99408662-T-C

49887635-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99408749-G-A

49887988-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99409366-C-T

49888070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99409435-C-T

49888282-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 99409635-C-T

49888451-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99409792-G-A

49888541-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99409860-G-A

49888541-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99409860-G-T

49888699-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99410029-G-C

49888997-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99410282-G-A

49888997-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99410282-G-T

49888999-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99410284-G-A

http://identifiers.org/hco/12/GRCh38#49889021-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99410305-C-A

49889021-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99410305-C-T

49889032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99410317-G-A

49889032-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99410317-G-C

49889032-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99410317-G-T

49889067-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99410342-T-G

49889207-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 99410477-G-C

49889221-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99410490-G-A

49889221-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99410490-G-T

49889224-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99410493-A-G

49889239-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99410501-C-G

49889239-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99410501-C-T

49889322-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99410556-T-C

49889342-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99410560-A-G

http://identifiers.org/hco/12/GRCh38#49889363-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99410581-C-A

49889363-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99410581-C-T

http://identifiers.org/hco/12/GRCh38#49889368-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99410586-C-A

49889368-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99410586-C-T

49889407-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99410620-A-G

49889508-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 99410689-T-C

49889553-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 99410734-G-A

49889553-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 99410734-G-T

49889595-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99410766-G-T

49889636-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99410805-G-T

49889637-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99410809-G-A

49889637-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99410809-G-T

http://identifiers.org/hco/12/GRCh38#49889645-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99410817-C-A

49889674-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99410847-T-C

49889674-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99410847-T-G

http://identifiers.org/hco/12/GRCh38#49889690-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99410861-C-A

49889690-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99410861-C-G

49889690-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99410861-C-T

49889703-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99410874-T-A

49889703-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99410874-T-C

49889703-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99410874-T-G

49889710-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99410881-G-A

49889710-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99410881-G-C

49889710-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99410881-G-T

49889886-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99410990-T-C

http://identifiers.org/hco/12/GRCh38#49889978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99411096-C-A

49890032-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99411159-G-A

49890032-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99411159-G-C

49890032-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99411159-G-T

http://identifiers.org/hco/12/GRCh38#49890038-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99411164-C-A

49890038-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99411164-C-T

49890056-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99411182-G-T

49890070-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99411196-C-G

49890070-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99411196-C-T

49890082-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99411207-T-A

49890082-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99411207-T-C

http://identifiers.org/hco/12/GRCh38#49890213-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99411325-C-A

49890213-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99411325-C-T

49890232-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99411344-T-C

49890234-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99411346-T-A

49890535-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99411655-A-G

49890580-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99411697-T-C

49890580-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99411697-T-G

http://identifiers.org/hco/12/GRCh38#49890618-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99411737-C-A

49890618-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99411737-C-T

49890632-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99411751-T-C

49890632-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99411751-T-G

http://identifiers.org/hco/12/GRCh38#49890638-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99411758-C-A

49890638-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99411758-C-T

49890646-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99411766-C-T

49890647-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99411767-T-A

49890654-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99411774-C-G

49890922-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99411959-G-A

49890922-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99411959-G-T

49890955-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99411993-G-A

http://identifiers.org/hco/12/GRCh38#49890978-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99412016-C-A

49890978-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99412016-C-T

http://identifiers.org/hco/12/GRCh38#49891035-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99412239-A-C

49891035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99412239-A-G

49891035-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99412239-A-T

49891053-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99412270-C-T

49891162-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99412377-C-T

http://identifiers.org/hco/12/GRCh38#49891210-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99412418-C-A

49891210-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99412418-C-T

49891367-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99412534-C-T

49891554-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99413464-G-A

http://identifiers.org/hco/12/GRCh38#49891575-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99413482-C-A

49891575-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99413482-C-T

49891979-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99413824-A-G

49892162-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99413987-G-A

49892162-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99413987-G-C

49892219-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99414044-C-T

49892355-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99414107-T-G

49893248-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99414893-T-C

49893579-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99415143-A-G

49893903-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99415537-G-A

49893903-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99415537-G-T

49894127-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99415759-A-G

49894158-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99415793-C-G

49894240-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99415849-G-A

49894444-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 99416041-C-T

49894609-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 99416161-G-C

49894649-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99416200-C-T

49894756-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99416263-C-T

49894769-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99416276-G-A

49895018-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 99416474-C-T

49895325-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99416687-C-T

49895334-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99416696-C-T

http://identifiers.org/hco/12/GRCh38#49895397-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99416730-C-A

49895482-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99416822-A-G

49895650-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99416988-C-T

49896776-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99417991-T-G

http://identifiers.org/hco/12/GRCh38#49896965-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99418139-C-A

49896965-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99418139-C-G

49896965-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99418139-C-T

49897105-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99418254-G-C

49897129-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99418275-G-A

49897129-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99418275-G-T

49897211-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99418330-G-T

49897357-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99418435-G-A

49897357-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99418435-G-T

49897375-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99418452-G-T

49897391-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99418468-G-T

49897429-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99418503-C-T

49897455-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99418527-T-C

49897609-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 99418674-G-A

49897609-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant, splice_region_variant
orthologous variants: 99418674-G-T

49897611-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99418676-T-C

49897697-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99418775-T-C

49897701-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99418779-G-A

49897701-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99418779-G-T

49897708-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99418785-T-C

49897854-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99418904-T-G

49897866-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99418916-G-A

49897866-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99418916-G-T

49897881-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99418931-G-A

49897881-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99418931-G-T

49898058-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, missense_variant
orthologous variants: 99419121-T-G

49898203-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99419254-G-A

http://identifiers.org/hco/12/GRCh38#49898212-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99419263-C-A

49898212-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99419263-C-G

http://identifiers.org/hco/12/GRCh38#49898329-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99419372-C-A

49898359-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99419400-G-A

49898758-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99419525-G-C

49898953-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99419634-C-T

49898962-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99419643-G-A

49899214-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99419860-G-A

49899265-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99419905-C-T

49899342-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99419985-G-A

49899383-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99420026-T-C

49899383-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99420026-T-G

49900124-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99421112-G-A

49900131-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99421119-A-G

49900132-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99421120-G-A

49900132-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant
orthologous variants: 99421120-G-T

49900173-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 99421152-T-C

49900175-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 99421154-G-T

http://identifiers.org/hco/12/GRCh38#49900193-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99421172-C-A

49900199-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant, synonymous_variant
orthologous variants: 99421178-G-A

49900209-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant, missense_variant
orthologous variants: 99421188-C-T

49900257-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 99421240-G-C

49900257-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 99421240-G-T

49900277-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 99421260-G-A

49900277-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 99421260-G-C

49900277-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 99421260-G-T

49900285-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 99421267-T-C

49900291-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 99421273-A-G

49900291-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 99421273-A-T

http://identifiers.org/hco/12/GRCh38#49900295-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: http://identifiers.org/mco/15/GRCm39#99421277-C-A

49900295-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant
orthologous variants: 99421277-C-T

49900316-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 99421298-T-C

49900316-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 99421298-T-G

49900503-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 99421779-C-T

49900577-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 99421844-C-T

http://identifiers.org/hco/12/GRCh38#49900649-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#99421914-C-A

49900823-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 99422279-T-C

49900993-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 99422441-T-C

49901043-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 99422488-T-C

http://identifiers.org/hco/12/GRCh38#49901076-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#99422517-C-A

http://identifiers.org/hco/12/GRCh38#49901082-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#99422523-C-A

49901098-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 99422550-A-G

49901102-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 99422554-T-C

49901119-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 99422571-G-A

49901119-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 99422571-G-T

49901140-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 99422592-A-G

49901281-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 99422736-C-T

49901302-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, synonymous_variant, undefined
orthologous variants: 99422757-A-G

http://identifiers.org/hco/12/GRCh38#49901391-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#99422845-C-A

49901391-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 99422845-C-T

http://identifiers.org/hco/12/GRCh38#49901392-A-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#99422846-A-C

49901392-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 99422846-A-G

49901392-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 99422846-A-T

49901400-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 99422854-T-A

49901400-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 99422854-T-C

49901400-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 99422854-T-G

49901403-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 99422857-A-G

49901403-A-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 99422857-A-T

http://identifiers.org/hco/12/GRCh38#49901418-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#99422873-C-A

49901418-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 99422873-C-G

49901418-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 99422873-C-T

49901441-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 99422896-T-C

49901507-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 99422959-G-A

49901507-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 99422959-G-T

49901563-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 99422995-A-G

http://identifiers.org/hco/12/GRCh38#49901566-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#99422998-C-A

http://identifiers.org/hco/12/GRCh38#49901604-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#99423029-C-A

49901660-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 99423085-T-C

49901664-T-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 99423089-T-A

49901758-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 99423562-A-G

49901768-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 99423566-C-G

http://identifiers.org/hco/12/GRCh38#49901778-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#99423576-C-A

49901884-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 99423664-G-C

49901884-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 99423664-G-T

49901940-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 99423708-T-G

49901946-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 99423714-G-A

49901946-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 99423714-G-C

49901946-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 99423714-G-T

http://identifiers.org/hco/12/GRCh38#49902036-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#99423765-C-A

http://identifiers.org/hco/12/GRCh38#49902179-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#99423904-C-A

49902299-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 99424006-G-A

49902299-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 99424006-G-T

http://identifiers.org/hco/12/GRCh38#49902312-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#99424019-C-A

49902312-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 99424019-C-T

49902397-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 99424095-T-C

49902458-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 99424128-G-T

http://identifiers.org/hco/12/GRCh38#49902487-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#99424163-C-A

49902487-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 99424163-C-T

http://identifiers.org/hco/12/GRCh38#49902509-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#99424196-C-A

49902509-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 99424196-C-T

http://identifiers.org/hco/12/GRCh38#49902513-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#99424200-C-A

49902513-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 99424200-C-T

49902539-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 99424225-G-A

49902615-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 99424298-G-A

49902690-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 99424350-G-T

http://identifiers.org/hco/12/GRCh38#49902719-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#99424398-C-A

http://identifiers.org/hco/12/GRCh38#49902774-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#99424452-C-A

49902774-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 99424452-C-T

49902837-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 99424507-G-C

49902921-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 99424581-T-C

49902921-T-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 99424581-T-G

49902923-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 99424583-T-C

http://identifiers.org/hco/12/GRCh38#49902952-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#99424612-C-A

49902983-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 99424643-G-A

49902983-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 99424643-G-T

49903007-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 99424666-T-C

49903035-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 99424700-A-G

49903063-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 99424728-G-T

49903076-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 99424741-G-T

49903325-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 99425001-G-A

49903439-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 99425099-G-C

http://identifiers.org/hco/12/GRCh38#49903634-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#99425312-C-A

49903685-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 99425364-G-A

49903696-T-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: NMD_transcript_variant, intron_variant, undefined
orthologous variants: 99425376-T-C

49903799-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 99425482-G-A

49903799-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 99425482-G-T

49903836-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 99425519-G-A

49903836-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 99425519-G-C

49903836-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 5_prime_UTR_variant, NMD_transcript_variant, intron_variant, undefined
orthologous variants: 99425519-G-T

http://identifiers.org/hco/12/GRCh38#49903910-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#99425593-C-A

49903910-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99425593-C-T

http://identifiers.org/hco/12/GRCh38#49904030-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#99425711-C-A

49904030-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: intron_variant, undefined
orthologous variants: 99425711-C-T

http://identifiers.org/hco/12/GRCh38#49904072-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#99425736-C-A

49904072-C-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: intron_variant, undefined
orthologous variants: 99425736-C-G

49904087-A-G
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: intron_variant, undefined
orthologous variants: 99425751-A-G

http://identifiers.org/hco/12/GRCh38#49904098-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: intron_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#99425762-C-A

49904098-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: intron_variant, undefined
orthologous variants: 99425762-C-T

49904099-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: intron_variant, undefined
orthologous variants: 99425763-G-A

49904104-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: intron_variant, undefined
orthologous variants: 99425768-G-C

49904104-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: intron_variant, undefined
orthologous variants: 99425768-G-T

49904130-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: intron_variant, undefined
orthologous variants: 99425792-G-A

49904130-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: intron_variant, undefined
orthologous variants: 99425792-G-C

49904130-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: intron_variant, undefined
orthologous variants: 99425792-G-T

http://identifiers.org/hco/12/GRCh38#49904203-C-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: http://identifiers.org/mco/15/GRCm39#99425860-C-A

49904203-C-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99425860-C-T

49904206-G-A
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99425862-G-A

49904206-G-C
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99425862-G-C

49904206-G-T
type: SNV
type: Insertion
type: Deletion
type: Indel
type: Substitution
hgnc id: 17067
most severe consequence: 5_prime_UTR_variant, intron_variant, undefined
orthologous variants: 99425862-G-T